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. 2026 Oct 8;19(10):e70456. doi: 10.1111/1751-7915.70456

Metabolic Design Patterns for a Regenerative Architecture

Rachel Armstrong 1,✉, Pablo Carbonell 2, Deshendran Moodley 3, Ioannis Ieropoulos 4, Jorge Barriuso 5
PMCID: PMC13650528  PMID: 42851018

ABSTRACT

The contemporary home remains trapped in a mechanistic paradigm of twentieth‐century resource consumption, where metabolic biological presence is considered irrelevant to the functioning of a building. Presenting the home as a conceptual vehicle for metabolically optimised living spaces in dense urban environments, this paper develops a conceptual framework of metabolic design patterns that enables the staged retrofit of bioreactors, from composters and fermenters to bioelectrical systems, into human‐occupied living spaces. By bringing circular resource processing into the heart of domestic life the principles for regenerative homes are established. Bioelectrical systems are given particular attention because they provide real‐time, connectable data through electricity as a medium for information, power, and chemical transformation simultaneously, forming a connective backbone for generating the metabolic design patterns. Three patterns are developed: Toilet as Hearth, Kitchen Garden, and Greywater Wetland, each integrating bioelectrical systems into the habitation programme to provide the respective architectural affordances. The framework proposes a staged retrofit pathway to implementation from passive sensing to neighbourhood metabolic exchange, supported by a conceptual anatomical atlas for diagnosing metabolic failures in established metabolic systems. This revaluation positions metabolic presence as a generative resource rather than a cost, directly addressing SDGs 6, 7, 9, 11 and 12.

Keywords: 12‐V DC infrastructure, bioelectrical systems, circular economy, living architecture, meta holobiont, metabolic design patterns, microbial fuel cells


This simplified diagram illustrates the three core Metabolic Design Patterns: Toilet as Hearth, Kitchen Garden, and Greywater Wetland, which form the foundation of a regenerative domestic infrastructure. Each pattern integrates bioelectrical systems (BES) and bioreactors into recognisable domestic programmes, transforming waste streams into resources while generating real‐time metabolic data. The patterns are linked through a shared 12‐V DC bus, which provides a safe, bidirectional interface between biological metabolism and low‐power electronics (e.g., 5G Wi‐Fi), and a recycled water loop that circulates treated effluent between patterns.

graphic file with name MBT2-19-e70456-g005.webp

1. Introduction

The twenty‐first century has been declared the Age of Biology (Hockfield 2019). Genomics, living materials, systems and synthetic biology have provided designers and engineers with tools that were unimaginable two decades ago. Yet the spaces we inhabit—homes, buildings, cities—continue to operate on a model of obligate resource consumption, where energy is imported, waste is exported, and the metabolic presence of inhabitants is treated as irrelevant to the functioning of the building. Today, the built environment is responsible for 39% of global carbon emissions: 28% operational and 11% embodied (World Green Building Council 2019).

Time‐activity patterns show that inhabitants of Western societies spend more than 80% of their time indoors, performing the work of life which renders their continuous metabolic presence the primary driver of resource consumption in the built environment (Nassikas et al. 2024; Leech et al. 2002). Resource circularity can be achieved when substrates currently regarded as waste from daily metabolic activities (urine, faeces, food scraps, water vapour, carbon dioxide) are recycled, repurposed and transformed into useful materials. In urban environments where access to land is limited, bioreactors offer a technological approach to closing the loop between consumption and regeneration, doing the work of the soil, and ultimately reversing the damaging footprint of the built environment through both operational and embodied energy contributions. Composters convert organic waste into soil conditioners, fermenters produce probiotic foods and preserve nutrients, and bioelectrical systems (BES) perform simultaneous decentralised waste treatment, milliwatt‐level energy recovery, and self‐powered, real‐time biosensing of water quality (Konig et al. 2015; Pasternak et al. 2018; Soemarie et al. 2021). Bioelectrical systems integrated into building infrastructure extract ultra‐low‐power energy from organic waste streams (Chao 2025). This low but steady output can trickle‐charge localised energy storage to power ambient building utilities such as low‐power LED nightlights or smart‐home sensors (Merino‐Jiménez et al. 2021). Similarly, reclaimed sludge (biosolids) from wastewater treatment can be incorporated into clay brick manufacturing, reducing kiln firing energy by up to 48% and mitigating the embodied carbon footprint of building materials (Mohajerani et al. 2019). Biogas captured from domestic anaerobic digesters using kitchen waste can be channelled into specialised cookstoves, reducing reliance on fossil gas or grid electricity for daily cooking (Ferdeș et al. 2022). Together, these approaches support the transition toward circular resource processing by embedding zero‐waste principles into architectural design and urban material flow planning (Lehmann 2011; Memon 2011). Thinking through home metabolism creates a system for more nuanced organic resource use where diverse inputs from urine to food scraps can be valued, counted, and integrated into future living space development (Zaman 2011; Kumar et al. 2011). Collectively and individually, these circular approaches directly contribute to multiple UN Sustainable Development Goals. By converting waste streams into resources, the framework advances SDG 6 (Clean Water and Sanitation) through decentralised wastewater treatment and water quality biosensing (Walter et al. 2018; Gajda et al. 2020; Randall and Naidoo 2018; Aguirre‐Sierra et al. 2016); SDG 7 (Affordable and Clean Energy) via low‐power energy recovery from organic waste (Ferdeș et al. 2022; Soemarie et al. 2021; Walter et al. 2018; Merino‐Jiménez et al. 2021; Prasad and Tripathi 2021); SDG 9 (Industry, Innovation and Infrastructure) through the integration of bioelectrical systems and living materials into building infrastructure (Pasternak et al. 2018; Merino‐Jiménez et al. 2021; Prasad and Tripathi 2021; Mohajerani et al. 2019; Atkinson et al. 2022; Fernandes et al. 2019); SDG 11 (Sustainable Cities and Communities) by enabling regenerative urban housing that reduces operational emissions and resource consumption (Mohajerani et al. 2019; Modesto et al. 2026; Habibi et al. 2022); and SDG 12 (Responsible Consumption and Production) by closing metabolic loops and transforming waste into valuable products (Randall and Naidoo 2018; Jadhav et al. 2022; Armstrong 2023). The metabolic design patterns developed below operationalise these goals through specific architectural programmes.

Bioreactors are already being integrated into the built environment through commercial products and architectural installations. Fermenting practices are commonplace (Blanchet et al. 2025; Meyer et al. 2026), and composters are established as increasingly sophisticated indoor devices (Merck 2026), while products like Carbelim's algae oxygen generators are entering the market as bio‐tech solutions for improving indoor air quality (Carbelim 2026). Standalone bioreactors such as composters and fermenters, therefore, provide the entry point at Technology Readiness Level (TRL) 9, while emerging Bioelectrical systems remain aspirational informatic backbones (TRL4). From an architectural perspective, established biotech precedents are already demonstrating their technical contributions to building performance. For example, ecoLogicStudio's algae curtain (Photo.Synth.Etica) provides an attractive green external building layer that absorbs approximately 1 kg (2.2 pounds) of carbon dioxide per day for every 2‐square‐meter section or standard module (Joonhwan 2023; Aouf 2021). Similarly, the 200 m2 of photobioreactor panels embedded in the Intelligent Building (BIQ) façade in Hamburg actively save 6 t of carbon dioxide per year (tCO 2 /a), where the microalgae also act as a dynamic sun shading system, achieving an average shading coefficient of 67%. Under operational tests, the BIQ façade maintains a comfortable average indoor illuminance of 1049.18 lux, satisfying standard lighting requirements for office environments (Habibi et al. 2022). These built precedents demonstrate that metabolic processes are already being distributed through indoor spaces and building envelopes, providing a socially acceptable premise for the staged retrofit proposed in this paper.

However, such bioreactors tend to operate in isolation from other bioreactors and building systems. Their social value remains observational rather than participatory. To develop spatial programs and generate architectural affordances, defined as the physical and spatial properties that invite or suggest certain human actions that are integrated into our living spaces to offer genuine cultural value (Manolakelli 2025), bioreactors must be understood and developed in relation to one another, through interfaces that meaningfully connect with human activity. Technical function alone, no matter how impressive, does not create the conditions for cultural adoption. A framework that networks bioreactors into recognisable domestic programmes is needed, transforming them from isolated appliances into integrated sites of daily ritual and shared responsibility. To establish a shared vocabulary across the disciplinary boundaries of architecture, microbiology, and engineering that inform this framework, the key terms are defined in Table 1.

TABLE 1.

Operational glossary of key terms used in this study.

Term Definition as used in this paper
Architectural affordance The spatial and physical properties of a bioreactor arrangement (e.g., visible MFC stack) that invite specific human actions, such as monitoring, feeding, or maintenance
Building Anatomy A conceptual model treating buildings as adaptive organisms that can be upgraded through additive, non‐destructive layers over time, enabling staged retrofits
Holobiont A host organism (human, plant, or pet) together with its entire community of associated symbiotic microorganisms (bacteria, fungi, viruses)
Metabolic design pattern A conceptual spatial framework that networks bioreactors (composters, MFCs, wetlands) into recognisable domestic programmes, linking waste processing with human rituals
Meta‐holobiont The composite entity formed by a building, its human/plant inhabitants, and the building's own Microbiome of the Built Environment (MBE), functioning as a single metabolic unit
Microbiome of the Built Environment (MBE) The distinct microbial community colonising the surfaces, air, and water systems of a building, shaped by architectural design and occupancy
Oikos The ancient Greek concept of the household as a complete economic and ecological unit, encompassing the dwelling, inhabitants, and shared resource management
Regenerative architecture An approach to building design that moves beyond sustainability (minimising harm) to actively restore ecological systems through integrated metabolic processes
Staged retrofit A phased upgrade pathway for existing buildings, progressing from passive sensing (Stage 1) to local processing (Stage 2) to neighbourhood exchange (Stage 3)

2. The Home as a Vehicle for Regenerative Living Spaces: The Oikos

The home is both a conceptual and practical vehicle for developing metabolically optimised living spaces. Revisiting the ancient Greek concept of oikos provides a foundational lens for the appropriate development of metabolic design patterns as part of a healthy household management strategy, the oikonomia (economy). This domestic sphere incorporates a person's entire relational web: family, friends, servants, employees, and neighbours, a community that is bound together by shared territory or cooperative tasks (Leshem 2016). By considering the household as a complete economic and ecological unit, the home becomes a customisable metabolic system that encompasses the dwelling, its inhabitants, and the management of resources within it.

Building on this first‐principles understanding, the notion of home as a customisable vehicle (the oikos) is flexible enough to embrace a range of residential configurations, from dense multi‐generational households to single occupant dwellings. The trend away from the traditional nuclear family and toward alternative co‐habitation arrangements is already underway. In the United States, an estimated 17% of recent households establishing shared dwellings did so to house multiple adult generations or aging parents, a sector now comprising approximately 4.5% of owner‐occupied housing stock (National Association of REALTORS 2025). This demographic creates a “sandwich generation” that balances resource allocation between dependent children and grandparents, a process that was shown to be economically efficient in Polish three‐generation households (Bartczak et al. 2021). The decision to co‐reside is driven by an interplay of financial circumstances, kinship systems, and health conditions (Hanum et al. 2024).

Conversely, the United Nations reports that ‘living alone’ is increasingly one of the standard living arrangements globally (Hanum et al. 2024). While single occupants often prefer to live independently to protect personal autonomy, their individual metabolic waste streams are fundamentally mismatched with the volumetric scales required to operate standalone, large‐scale bioelectrical stacks, producing a standard physiological average of only 1.5 L of urine daily (Randall and Naidoo 2018), Rather than trying to force an under‐capacity standalone system onto an isolated household, this scale mismatch becomes a practical invitation for networking resources. The metabolic design pattern framework developed here can address this scale gap by providing the spatial and metabolic rules for dense, flexible arrangements. Whether co‐residing under one roof (Bartczak et al. 2021), or living independently as networked, single‐occupant units, residents can be linked to hybrid, community‐scale shared metabolic services. Routing decentralised individual fixtures into localised neighbourhood‐scale chemical and energy exchange networks transforms isolated waste streams into spatial affordances that provide shared domestic wealth. This resource networking strategy actively supports the strategic move toward urban density and collective metabolic services, revealing that a home can be as vast, interconnected, and adaptable as the networks of care and metabolic cooperation that sustain it.

3. The Meta‐Holobiont: An Ontology for Living Systems

The transition to a regenerative oikos requires a phased integration of mature technologies (composting, fermentation) and emerging innovations (BES) as they reach commercial maturity. Integration demands active coordination across disparate systems with different operating logics, timescales, and interfaces, whose structured vocabulary is provided by an ontology, which specifies what constitutes the system, how components relate, and what defines function or failure (Armstrong and Moodley 2026). Without such a shared vocabulary, a composter and a bioelectrical system remain isolated appliances rather than integrated metabolic infrastructure. The ontology provides the common language through which diverse technologies can be understood as parts of a coherent whole.

Applying this to the built environment demands distinguishing two complementary ontologies. The architectural ontology addresses physical, spatial, and material dimensions (volumes, assemblies, plumbing, daylighting, circulation), while the computational‐engineering ontology formalises operational behaviour through sensor networks, feedback loops, mass‐energy balances, and control algorithms. Their overlap enables real‐time optimisation of metabolic flows (waste routes, bioreactor placement, thermal absorption). Without this synthesis, however, architecture remains an inert shell and engineering is just a set of abstract formulae. Achieving genuine metabolic function thus requires their integration.

Classical architecture answered questions of integrating form and function by modelling the home on a single human body, as encoded in Vitruvian Man: a unified, symmetrical structure arranged around a central order. The twenty‐first century, however, reinterprets the human body as a holobiont (Rohwer et al. 2002; Rohwer and Kelley 2004; Rosenberg et al. 2007) hosting trillions of symbiotic microorganisms, or microbiome (Whipps et al. 1988), upon which digestion, immunity, and even mood depend (Lederberg and McCray 2001). Extending this human‐centred analogy, the home hosts multiple holobionts (humans, pets, plants), each with its own microbiome, alongside the building's own microbiome of the built environment (MBE) (Kembel et al. 2012). The meta‐holobiont concept captures this complexity, accommodating co‐habiting and nested holobionts within the MBE in an interdependent relationship (Armstrong 2025). Consequently, the home becomes a composite entity: singular in metabolic coherence yet plural in its nested living constituents (Figure 1). This framework serves as a design program, providing architects with the conceptual tools to assemble metabolic processes that generate appropriate affordances while maintaining contemporary comfort and functionality.

FIGURE 1.

FIGURE 1

Home as metaholobiont. This schematic diagram presents the domestic building as a structural scaffold, analogous to a coral reef skeleton that supports a discrete ecological community. The architectural envelope is depicted housing a distinct Microbiome of the Built Environment (MBE). Within this built scaffold, nested holobionts, a human inhabitant, dog, and plant, are schematically represented with their own internal microbial communities (e.g., gut, skin, or rhizosphere microbiomes). Collectively, the entire dwelling and all its living constituents comprise the meta‐holobiont: A singular, metabolically coherent composite entity. This holistic framing positions the home as a living, adaptive system, providing the conceptual foundation for the staged integration of Metabolic Design Patterns that orchestrate resource circularity between microbial activity, human rituals, and building infrastructure.

The formal metabolic design pattern ontology systematically maps a building's structural and metabolic systems, akin to a medical atlas for diagnosis, enabling the identification of metabolic failures, which are points where resource flows are disrupted or where bioreactor performance falls below expected thresholds. An atlas alone, however, is static, describing a body at a single moment. The Building Anatomy model regards the building as a living, adaptive organism (Sönmez and Özçelik 2025), providing the necessary temporal dimension that the ontology requires for implementation by treating buildings as systems that can grow, respond, and be upgraded in additive layers, which are incremental interventions that add new capabilities to the building's existing fabric over time, increasing its complexity and functionality without requiring demolition or wholesale replacement. This layered, time‐based understanding is consistent with the meta‐holobiont that accommodates multiple co‐habiting and nested living systems across different temporal scales of intervention. Together, these three concepts converge: the meta‐holobiont supplies the structural model of the domestic entity itself, describing the building as a composite host that accommodates multiple nested holobionts and maintains a core metabolic complexity; the ontology supplies the systematic vocabulary and classification; Building Anatomy supplies the phased, non‐destructive pathway from current housing stock to regenerative living systems. Consequently, wholesale replacement of current domestic infrastructure is neither proposed nor necessary, since staged retrofits are made possible and the functional complexity of buildings can be increased over time without demolition.

Translating the meta‐holobiont to multi‐unit buildings, however, presents critical trade‐offs. Centralised processing offers economies of scale and simplified maintenance, whereas a hybrid approach might instead equip each unit with small‐scale bioreactors for sensing while centralising bulk waste treatment and energy recovery. The optimal configuration must be adapted to the specific context, including building size, occupancy, regulations, and community governance.

4. Metabolic Design Patterns: A Framework for Staged Retrofit

Professional architects often draw on Christopher Alexander's “A Pattern Language” as a practical handbook when designing spaces for particular functions (Alexander et al. 1977; Park and Newman 2017). This invaluable resource comprises 253 interconnected design solutions, ranging from entire towns down to room corners. Each pattern targets a recurring spatial problem, providing a flexible core solution that allows infinite unique variations while maintaining proven effectiveness (Park and Newman 2017). Operating as a spatial grammar, these patterns help create human‐centred environments which reflect how people naturally live and interact, empowering both professional architects and ordinary people to participate meaningfully in designing their own homes, streets, and communities. The pattern language is grounded in empirical human comfort, focusing on light, scale, connection to nature, and communal flow (Park and Newman 2017).

Operating across multiple scales, Alexander's framework demonstrates how large‐scale choices support small‐scale human needs and potentiate to achieve real change within the practice of the built environment. For example, Agricultural Valleys (Pattern 3) restrict urban sprawl to preserve local food production and natural cooling. Wings of Light (Pattern 107) use narrow building footprints to maximise natural ventilation and daylight. Light on Two Sides of Every Room (Pattern 159) places windows on two walls to create cross‐breezes that passively cool occupants (Alexander et al. 1977).

Metabolic design patterns extend this multi‐scale logic into a new territory: the sequencing of resource flows, the conversion of waste streams, and the orchestration of microbial activity (Armstrong 2023; Armstrong and Moodley 2026). Where Alexander's patterns addressed spatial organisation, metabolic patterns address the living processes that occur within that space (Barouni et al. 2026). They share Alexander's commitment to human‐centred design, but they also recognise that human comfort depends on more than light and air to include the metabolic health of the systems that sustain us, such as the cycling of water, nutrients, and energy through the domestic realm (Barouni et al. 2026; Cantin 2026). The spatial system remains present, but the affordances emerge through the networking of bioreactors across domestic space to assist citizens in their daily activities, enabling them to become active metabolic contributors within the network of domestic resource flows (Manolakelli 2025; Sönmez and Özçelik 2025). In this way, the adaptable, multi‐scale design vocabulary of metabolic design patterns can empower inhabitants to become active participants in circular resource flows, generating electricity, clean water, and fertiliser while strengthening bonds between inhabitants, communities, and the living systems that sustain them (Walter et al. 2018). This metabolic logic operates across three nested scales (Barouni et al. 2026). At the microbial scale (micro), the fundamental redox reactions are performed by specific microbial consortia (Bond and Lovley 2003; Gorby et al. 2006; Kato 2015). At the bioreactor scale (meso), the kinetics and efficiency of these reactions are determined by the physical configuration of stacks, membranes, and electrodes (Logan 2010; Abdallah et al. 2019; Tan et al. 2021; Jadhav et al. 2022). At the room scale (macro), architectural affordances are generated by the spatial arrangement and networking of bioreactors, producing recognisable programmes such as kitchens, toilets, and greywater wetlands that invite specific human activities (Alexander et al. 1977; Manolakelli 2025). Decisions made at the microbial level support bioreactor design, and that design in turn serves the human rituals of cooking, abluting, and cleaning (Blanchet et al. 2025; Modesto et al. 2026). Coherence across scales ensures that each room becomes a site where life's work is performed through a partnership between inhabitants and microbial communities (Armstrong 2025). Every pattern is simultaneously a metabolic node, an assembly of technologies, and a living ecology, with the whole system sustained by the logical progression of patterns across scales (Barouni et al. 2026; de Gerlache 2026).

5. Bioelectrical Systems as a Special Case: Networking Bioreactors Through Electricity

While a range of bioreactor technologies can participate in the metabolic design patterns framework, bioelectrical systems receive particular attention in this paper as they serve as an informatic and integrative backbone. By providing a direct link to electronic systems, BES offer a route for artificial intelligence to read the building's metabolism in real time. BES include MFCs (Potter 1911; Bennetto 1987) and microbial electrolysis cells (MECs), which cultivate electroactive microbes that exchange electrons with bioelectrodes (Kato 2015). These are surfaces where electroactive microbes form biofilms and exchange electrons via direct contact, conductive pili, or soluble electron shuttles (Gorby et al. 2006). This extracellular electron transfer (EET) can be harvested as electrical power (in MFC mode) or driven by applied voltage to synthesise valuable compounds (in MEC mode). The bidirectionality of this interface distinguishes the bioelectrode from a conventional electrode. Electrons can be supplied to or accepted from a circuit to drive synthetic reactions, forming a ‘living electronic’ component (Fang et al. 2024).

Unlike conventional electronics that rely on delocalised electron flow in metal wires, biological electron transport is always coupled to biochemical reactions, enabling parallel processing, self‐repair, and metabolic integration (Carbonell et al. 2026; Geerlings et al. 2020). This bidirectional capability allows a single infrastructural layer to harvest energy from waste and, when supplied with a small external voltage, direct microbes to produce hydrogen, fertiliser precursors, or platform chemicals, effectively turning the home into a flexible biofactory (Kadier et al. 2016). This capability allows BES to combine waste treatment, power generation, and biosensing within a single platform, a feat that no abiotic renewable technology can match. By using electron flow as a medium for information, power, and chemical transformation simultaneously, BES platforms generate real‐time, connectable data for monitoring system health, optimising operational performance, and feeding directly into neural networks (Logan and Rabaey 2012; Zhou et al. 2017; Jadhav et al. 2022; Atkinson et al. 2022; Hentati et al. 2025; Carbonell et al. 2026). In this way, the electrical signal itself encodes metabolic information, with fluctuations in voltage and current correlating with organic load, toxicity, and nutrient availability (Zhou et al. 2017). When integrated into a building's waste streams, it provides real‐time data that can be visualised, interpreted, and acted upon by inhabitants, translating the raw electrical output into architectural affordances that coordinate the spatial distribution of metabolic work with the temporal rituals of daily life (Zhou et al. 2017).

To realise these capabilities in practice, a 12‐V DC infrastructure is proposed as the interface between biological metabolism and low‐power electronics (Gajda et al. 2020; Prasad and Tripathi 2021). Experimental data from MFC stacks, sediment MFCs, and biohybrid systems consistently converge on 12V DC as a practical working principle, grounded in empirical evidence of compatibility between biological systems and low‐power electronics (Salgado 2009; Romero Mejía et al. 2012; Gajda et al. 2020; Gupta and Basile 2020; Prasad and Tripathi 2021). Direct coupling to a 12‐V DC bus avoids redundant AC‐to‐DC or DC‐to‐AC conversion losses whille leveraging continuous organic waste oxidation for off‐grid residential energy recovery (Romero Mejía et al. 2012; Sahoo et al. 2017). The 12‐V DC bus falls below the 60‐V DC threshold for human safety on dry skin in residential DC distribution networks (Sahoo et al. 2017; Gajda et al. 2020), as well as below the approximate 15‐to‐20‐V range observed to cause damage to some microbial biofilms in certain configurations (Gajda et al. 2020). Electrolysis and cell lysis occur above this threshold, leading to performance degradation. This is not a universal threshold, however, as microbial biofilm damage is determined by multiple interacting factors, which include current density, exposure duration, microbial community composition, biofilm thickness, and local pH conditions. The 12‐V threshold provides a conservative operating margin that prevents these damaging effects while remaining high enough to be stepped down or regulated to 5 V for logic circuits, which is sufficient to drive low‐power actuators, sensors, and communication devices (Prasad and Tripathi 2021; Pan and Bhattacharyya 2025).

Managing this complex, dynamic system requires a sophisticated mathematical and computational framework that bridges biological complexity and engineering control. The challenge of modelling biological systems lies in their inherent instability and non‐linearity, which resist simple mathematical description. Process‐based deterministic models using ordinary and partial differential equations can describe substrate consumption kinetics (Monod) and biomass growth, but they also carry inherent simplifying assumptions that limit their accuracy (Luo et al. 2016). Hybrid or grey‐box models of biological systems offer an improvement by combining mechanistic engineering models with statistical adjustments to account for biological instability and delayed responses, significantly improving predictive and structural validity. However, the most powerful approaches for biological systems are data‐driven. Artificial Neural Networks (ANNs), machine learning, and fuzzy logic can bypass the need for complete phenomenological knowledge by mapping highly non‐linear biological and physical interactions. Multilayer feedforward networks trained by Levenberg–Marquardt backpropagation are the gold standard for predicting real‐time reactor performance including COD removal, Coulombic efficiency, and power output, based on fluctuating abiotic inputs such as pH, conductivity, temperature, and influent organics (Gadkari 2022). Taken together, this mathematical toolkit transforms the bioelectrical interface into an actively controlled, self‐optimising metabolic backbone.

The electron itself is the critical signal (Zacharoff and El‐Naggar 2017). It is the measurable output that reveals the underlying biochemical transformations occurring within the MFCs (Zacharoff and El‐Naggar 2017; Apollon et al. 2026). While the models described above provide a framework for understanding and predicting system behaviour, the true test of their validity lies in field performance (Han et al. 2022; Apollon et al. 2026). In practice, electron flow is both a product of energy recovery and a real‐time data stream that encodes metabolic activity (Zacharoff and El‐Naggar 2017; Apollon et al. 2026). This makes power output a proxy for biological function (Corazao and Zauscher 2026; Apollon et al. 2026), and the ability to reliably measure and interpret this signal is what connects the theoretical models to practical implementation (Han et al. 2022; Corazao and Zauscher 2026; Apollon et al. 2026).

The feasibility of reaching the required 12 V from biological sources has been demonstrated through the PEE POWER system, as proof of principle of the networking infrastructure for developing metabolic design patterns (Savenije 2013). The system pioneered MFC stacks fuelled directly with undiluted human urine and was trialled at a major UK music festival in 2016, where a bespoke stack of 12 MFC modules with a displacement volume of 19.2 L was implemented as a self‐sufficient lit urinal system, continuously producing approximately 150 milliwatts from a cascade of four modules (Walter et al. 2018).

To benchmark this field performance against standardised engineering metrics, two normalised indices are introduced (Xiao et al. 2014; Jadhav et al. 2022). Normalised Energy Recovery (NER) is defined as the electrical energy recovered per unit of chemical oxygen demand (COD) removed, which is expressed as kilowatt‐hours per kilogram of COD (kWh/kgCOD) (Xiao et al. 2014; Jadhav et al. 2022). For the PEE POWER system, NER values in the range of 0.1–0.3 kWh/kgCOD have been reported for urine‐fed stacks (Ieropoulos et al. 2017). Coulombic Efficiency (CE) is the fraction of electrons recovered from the substrate as electrical current, expressed as a percentage that indicates how effectively the electroactive biofilm transfers electrons to the electrode (Liu et al. 2024). MFC systems typically achieve CE values ranging from 10% to 60% depending on substrate and reactor design (Logan 2010; Budania et al. 2024; Liu et al. 2024). These indices provide the technical grammar for evaluating the bioelectrical platform against established engineering benchmarks (Jadhav et al. 2022).

Extrapolating from field‐validated data to a theoretical 1000‐unit MFC stack with a volume of 115–300 L suggests a potential continuous power output of 24–48 watt‐hours per day, equivalent to 1–2 watts continuous (Armstrong 2023). This extrapolation must be treated with caution, as large MFC stacks frequently exhibit non‐linear scale‐up behaviour (Logan 2010; Greenman and Ieropoulos 2017; Tan et al. 2021; Jadhav et al. 2022). This is due to voltage reversal, hydraulic maldistribution, varying internal resistances between cells, biofilm heterogeneity, and electrical losses in series or parallel configurations (Ieropoulos et al. 2010; Tan et al. 2021; Jafary et al. 2026; Pan and Bhattacharyya 2025). Modular architectures mitigate these risks. Pilot‐scale studies, such as a 45‐unit parallel stack, have demonstrated near‐ideal scaling, producing 43 times the power of a single unit (Jafary et al. 2026), while 1000 L pilot systems have operated robustly for over three years (Abdallah et al. 2019; Jafary et al. 2026). The challenge is whether engineering and economic optimisations can keep pace with the non‐linear complexities that emerge at higher unit counts (Jadhav et al. 2022; Jafary et al. 2026). The 115–300 L volume range corresponds to the urine output of approximately 15–40 people per day, indicating that community‐scale rather than household‐scale deployment is the more appropriate target for the development of metabolic design patterns (Armstrong 2023). This conservative output is nevertheless potentially sufficient for LED lighting, 5G Wi‐Fi, and sensor networks (Walter et al. 2018; Prasad and Tripathi 2021; Apollon et al. 2026).

Operational stability presents further challenges. Biofouling and inorganic scaling of the cathode and membranes remain major barriers to long‐term performance, often cutting power by more than 90% if they are not cleaned aggressively (Jafary et al. 2026; Logan 2010). This fouling is compounded by biofilm heterogeneity across individual units, which introduces additional uncertainty. A further risk is voltage reversal in serial stacks, where individual cells invert polarity and consume power from the rest of the stack due to substrate starvation or kinetic imbalances (Tan et al. 2021; Jadhav et al. 2022). Together, these challenges pose significant obstacles to reliable long‐term operation. However, a counterbalancing feature of electroactive biofilms is their resilience, which addresses a critical concern for intermittent domestic use. Unlike abiotic systems that fail when starved of fuel, these biofilms can enter a dormant state during periods of low occupancy and resume electricity generation upon reactivation following a sigmoidal recovery pattern (Hentati et al. 2025). This biological buffer provides a mechanism against the occupancy gaps discussed later in this paper.

The bioelectrical platform does not need to operate in isolation. Its low‐power, 12‐V DC backbone is inherently networkable, enabling it to draw from and contribute to a broader energy system (Sahoo et al. 2017; Mukherjee et al. 2022; Onwuemezie and Gohari Darabkhani 2024). Other off‐grid renewable sources complement the bioelectrical platform (Rahman et al. 2016; Onwuemezie and Gohari Darabkhani 2024). While solar and wind provide higher power density and mature infrastructure for electricity generation, bioelectrical processes uniquely perform simultaneous waste remediation, water purification, and low‐voltage power generation within a circular metabolic loop (Logan and Rabaey 2012; Armstrong 2023; Onwuemezie and Gohari Darabkhani 2024). This complementarity suggests that a resilient off‐grid home would not rely on a single technology but instead integrate a hybrid system using solar or wind for high‐wattage loads, and bioelectrical systems for continuous low‐power functions plus waste‐to‐resource conversion (Rahman et al. 2016; Onwuemezie and Gohari Darabkhani 2024).

Bioelectrical systems, therefore, offer more than an alternative energy source by providing a living interface between domestic metabolic activity and building infrastructure (Armstrong 2023; Onwuemezie and Gohari Darabkhani 2024). By networking bioreactors through electrical signals, the coordination of resource flows, waste processing and power generation is enabled across the home (Mukherjee et al. 2022; Onwuemezie and Gohari Darabkhani 2024). This interconnectivity is the foundation for the metabolic design patterns developed below, where the ability to group and sequence bioreactors translates raw biological activity into recognisable domestic programmes that inhabitants can understand, maintain and participate in (Joshi 2019; Onwuemezie and Gohari Darabkhani 2024; Armstrong and Moodley 2026).

6. Three Metabolic Design Patterns

With these technical performance benchmarks established, it is now possible to examine how the bioelectrical platform translates into architectural programmes (Alexander et al. 1977; Andrews et al. 2024). Each metabolic design pattern operates across three interdependent scales. The fundamental redox reactions are performed by specific microbial consortia at the micro‐scale, while the meso‐scale concerns the physical configuration of bioreactors that determines kinetics, mass transport, and operational efficiency (Elsayed et al. 2026), and the macro‐scale addresses how the arrangement of bioreactors generates architectural affordances and recognisable domestic programmes (Alexander et al. 1977; Telhan 2025). Decisions made at the microbial level enable bioreactor design, and that design in turn serves the human rituals of cooking, abluting, and cleaning. Coherence across scales ensures that each pattern becomes a living ecology rather than a mere assembly of technologies. The patterns described below are conceptual frameworks, with the figures illustrating one possible configuration for each as a demonstration of the framework's flexibility in accommodating diverse spatial arrangements, bioreactor selections, and cultural contexts (Telhan 2025). Within these metabolic design patterns, microbiologists can contribute to the design of formal building programmes that integrate microbial metabolism into domestic space responsibly and programmatically (Telhan 2025; Elsayed et al. 2026).

7. The Toilet as Hearth Pattern

The Toilet as Hearth pattern reimagines sanitation as a productive act. At its core, it integrates an MFC stack with the toilet, using urine and faeces as feedstock to generate 12‐V DC power, treated water and biofertiliser (Figure 2). In doing so, it provides a concrete example of the meta‐holobiont principle by transforming the toilet from a passive waste conduit into a productive utility. Drawing on a growing body of literature on MFC stack configurations for sanitation applications (Ieropoulos et al. 2017; Walter et al. 2018; Gajda et al. 2020), the pattern targets a theoretical thousand‐unit stack, aiming for continuous power output in the range of 1–2 W (24–48 Wh/day). This is sufficient for low‐power LED lighting and 5G Wi‐Fi, while achieving 60%–90% COD removal and 1–3 log pathogen reduction (Ieropoulos et al. 2017). These performance targets correspond to NER values of 0.1–0.3 kWh/kgCOD, aligning with benchmarks provided by the field‐validated PEE POWER data.

FIGURE 2.

FIGURE 2

Metabolic design patterns for ‘Toilet as Hearth’. This schematic details the integration of a theoretical thousand‐unit microbial fuel cell (MFC) stack with domestic sanitation infrastructure. The pattern routes urine and faeces through an MFC series‐parallel configuration, which simultaneously performs 60%–90% chemical oxygen demand removal, 1–3 log pathogen reduction, and bioelectrogenesis. The recovered energy is conditioned onto the household's 12‑volt DC bus, sufficient to power LED lighting, Wi‑Fi routers, and sensor networks, while treated effluent and stabilised biofertiliser are returned as productive outputs. At the microscale, electroactive consortia (Geobacter, Shewanella) mediate extracellular electron transfer across the bioanode. Socially, the pattern leverages 5G connectivity to transform metabolic output into interactive, shareable digital media (e.g., real‑time performance selfies), demystifying sanitation by making the invisible work of microbes visible and celebratory. This reframes the toilet from a concealed waste conduit into a transparent community hearth, a productive focal point where inhabitants gather, coordinate feeding schedules, and collectively steward their own metabolic resources, reinforcing circular habits through ritualised engagement.

This vision is realised at the meso‐scale through a specific bioreactor sequence: urine collection, MFC stack in a series–parallel configuration, power conditioning, and load distribution. The toilet fixture sits adjacent to the stack, which is visible from the living space to encourage engagement and standardised interfaces connect the stack to the household 12 V DC bus and plumbing network. Currently at Technology Readiness Level 5–6 (Jadhav et al. 2022; Ieropoulos et al. 2024), the MFC stack requires further engineering optimisation for household deployment (Pan and Bhattacharyya 2025), although the composting and fermentation components of the broader pattern are immediately implementable at TRL 9.

The micro‐scale system is sustained by electroactive microbial consortia dominated by Geobacter sulfurreducens and Shewanella oneidensis on the anode, where electron transfer occurs through outer‐membrane cytochromes and conductive pili. This community adapts dynamically to changes in urine composition and loading rate.

The social programme and architectural affordances of this pattern operate at three scales that mirror the metabolic framework. For the individual resident, the visible MFC stack removes taboo around sanitation through transparent operation, while daily maintenance rituals provide structure, purpose, and emotional connection to the system. Within the household, family members coordinate the “feeding” schedule, creating shared responsibility and children learn circular economy principles through visible demonstration. At the community level, the public‐facing architectural treatment elevates sanitation to a visible community asset. The Urban Toilets challenge (Terraviva 2026), the Little Big Loo 2025 competition (Volume Zero Competitions 2025), and Toronto's TO the Loo competition (Amselem 2025) all demonstrate institutional recognition being conferred upon engaging sanitation design, where the toilet block becomes a community gathering place, comparable to a hearth around which the community gathers, shares resources, and celebrates collective achievement.

8. The Kitchen Garden Pattern

The Kitchen Garden pattern establishes the kitchen as the social heart of the home, positioned adjacent to dining and gathering spaces (Pattern 139, Pattern 184, Alexander et al. 1977). A core activity is fermentation, a practice that operates across cultures and connects modern technology with ancient food preservation techniques (Meah 2016). Through fermentation by Lactobacillus, the pattern directly supports the inhabitants' microbiome, which produces up to 90% of gut serotonin (Mittal et al. 2017). This ancient practice can be expressed in diverse cultural forms: Korean kimchi uses lactic acid bacteria (Jung et al. 2011), Japanese miso and natto rely on Aspergillus and Bacillus (Chan et al. 2021), Swiss Emmental is produced with Propionibacterium (Gagnaire et al. 2015), and French Roquefort is made with Penicillium (Gauthier et al. 2025).

At the heart of this system are two complementary bioelectrochemical processes (Figure 3). First MFCs convert organic waste in the kitchen into low‐power energy, while simultaneously producing catholyte, which is treated to become a nutrient‐rich solution for indoor hydroponics (Modesto et al. 2026). Second, MECs operating in electrolysis mode go beyond energy recovery. This second process harneses a small external voltage, which can be drawn from excess electricity generated by the MFCs or from renewable sources, to drive electrofermentation. MECs then synthesise novel organic compounds for domestic use, such as flavourings (e.g., esters) and detergents (e.g., rhamnolipids) (Andersen et al. 2014; Gong et al. 2020; de Rosset et al. 2024). This programmability creates a role for microbiologists and metabolic engineers to design and optimise the microbial consortia that produce these compounds (Nastro et al. 2025).

FIGURE 3.

FIGURE 3

Metabolic design patterns for ‘Kitchen Garden’: This schematic outlines the integration of a Microbial Electrolysis Cell (MEC) into the domestic food cycle. Drawing low‐voltage power (12 V DC) from the building's bioelectrical bus, potentially supplied by a co‐located MFC stack, the MEC drives the electrochemical conversion of nitrogen‐ and phosphate‐rich organic waste streams into concentrated hydroponic fertiliser. This nutrient extract is then circulated directly to indoor hydroponic cultivation systems, closing the loop between food scraps and fresh produce. At the microscale, specialised microbial consortia in the MEC perform parallel fermentative and electrosynthetic transformations, effectively linking ancient principles of microbial fermentation with modern bioelectrochemistry. The social programme culminates in a dining experience where resource circularity is rendered tangible: Harvested vegetables are prepared and consumed within sight of the fermenters and growing beds. This pattern embeds circular economy principles directly into daily culinary rituals, transforming meals into sensory, educational events that link gut‐microbiome health, cultural food traditions, and shared household responsibility.

In practical terms, the pattern operates through bioreactor sequences that begin with food waste collection and proceed through MEC treatment, nutrient extraction, hydroponic cultivation, and harvest. Spatially, this translates into a work triangle that connects waste collection, fermentation, and food preparation areas (Lee et al. 2025). The hydroponic growing area is fed by the catholyte produced by the MFCs, while inedible plant biomass returns to the bioreactors as feedstock, creating a continuous cycle of resource recovery (Ollár et al. 2022; Wouterszoon Jansen et al. 2023). This approach builds on emerging research on coupled bioelectrochemical–hydroponic systems (Modesto et al. 2026; Nath and Ieropoulos 2025; Ieropoulos and Moreno 2025), which have demonstrated the technical feasibility of integrating MFC/MEC platforms with plant cultivation through strategic nitrogen and carbon management.

The garden itself, the hydroponic growing area, is fed by the catholyte produced by the MFCs, creating a continuous cycle of resource recovery (Sato et al. 2023). Plants grown in this system provide fresh produce for the kitchen, while their inedible biomass returns to the bioreactors as feedstock. In this way, the Kitchen Garden pattern embodies the circular metabolism of the regenerative home: waste nourishes plants, plants nourish inhabitants, and inhabitants generate the waste that sustains the entire cycle (Greenman et al. 2024).

At the microbial level, the pattern is sustained by multiple consortia, where electroactive bacteria (Geobacter, Shewanella) populate the MEC, lactic acid bacteria (Lactobacillus, Leuconostoc) drive fermentation, and yeast ( Saccharomyces cerevisiae ) support leavening and alcohol fermentation.

9. The Greywater Wetland Pattern

Spatially, the Greywater Wetland pattern is encountered as a transition space between the bathroom and the garden (Figure 4), where MFC biosensors are embedded in a constructed wetland to harvest millivolt signals from electroactive biofilms. Installed as a visible, living installation, such as a green wall or indoor planter, it transforms what could be a purely mechanical system into an ecological feature. The bioreactor sequence is straightforward: greywater collection, treatment in the wetland with integrated MFC biosensors, and treated water output. This approach is supported by extensive literature on MFC‐based biosensors (e.g., Zhou et al. 2017), and by METland technology, a field‐validated precedent that has demonstrated effective wastewater treatment coupled with bioelectrochemical signal generation at pilot scale (Aguirre‐Sierra et al. 2016).

FIGURE 4.

FIGURE 4

Metabolic design patterns for ‘Greywater Wetland’: This schematic depicts a constructed wetland positioned as a transitional edge space between bathroom and garden, embedded with MFC‐based biosensors. Electroactive biofilms colonising the wetland's anodic zones generate millivolt‐scale signals that fluctuate in direct correlation with organic loading, toxicity, and nutrient availability, enabling real‐time, self‐powered water quality monitoring without external energy input. Treated greywater is polished through rhizosphere filtration before reuse in irrigation or domestic non‐potable applications. At the microscale, diverse biofilm communities and plant root exudates create complex rhizosphere microhabitats that sustain stable electrogenic activity. The social programme is framed as a contemplative garden experience: the visible wetland, with its flowing water and lush vegetation, provides sensory richness (sight, sound, smell) that counters the sterility of mechanical systems. This pattern cultivates environmental stewardship through daily plant tending and water monitoring, repositioning wastewater treatment as a visible, valued domestic ritual.

The pattern is characterised by its ability to translate raw millivolt fluctuations into actionable water quality data through neural network‐based biosensing. Rather than relying on peak current height alone, which can misrepresent concentrations, the neural networks process the entire current response profile to extract four distinct transient metrics: Peak Height (PH), Peak Area (PA), Acceleration Rate (AR), and Subsidence Rate (SR). This approach has been empirically validated: non‐fermentable substrates (acetate and butyrate) induce larger peak areas and peak heights than fermentable substrates (glucose and corn starch) (Feng, Barr, and Barr Jr. 2013), and ANNs employing the hyperbolic tangent sigmoid transfer function outperform those using non‐continuous transfer functions (Feng, Kayode, and Kayode Jr. 2013). Furthermore, ANNs using Peak Area (PA) provide a significantly more accurate correlation for real‐time COD concentrations, with R 2 = 0.99, and can identify specific recalcitrant chemical pollutants in mixed wastewater (Feng, Kayode, and Kayode Jr. 2013). This provides a solid mathematical and empirical foundation for how the proposed wetland translates these electrical outputs into architectural affordances.

At the microbial level, diverse biofilm communities, including electroactive bacteria, generate signals correlated with water quality (Bhattacharyya et al. 2023; Liu et al. 2025). These are supported by plant roots, which create rhizosphere microhabitats that support complex microbial interactions (Garbini et al. 2023). The richness of this living ecology, however, is also what makes household‐scale integration challenging. The pattern currently remains at TRL 5–6, indicating that further development is needed before widespread domestic deployment (Gupta et al. 2023).

The social programme and architectural affordances weave this metabolic function into human sensory experience, where bioelectrical signals make invisible processes visible through artworks that translate ecological data into aesthetic experience (You et al. 2022; Armstrong and Hughes 2023). The sensory richness of the wetland: the sight of flowing water, the sound of trickling, the smell of damp earth, and the humidity transforms the space into a green reception area, countering the sterility of purely mechanical systems. The pattern operates at three social scales that mirror the metabolic framework. For the individual, the visible wetland and its bioelectrical display create a restorative environment, with real‐time biosignals displayed as changing LED colours or patterns that provide immediate feedback on water quality and transform an invisible ecological process into a tangible personal experience of stewardship and agency. Within households, weekly plant tending and water quality monitoring become shared rituals that embed ecological awareness in domestic care. At the community scale, the wetland's biosignals can be shared as public data art or educational displays, while polished greywater can irrigate shared green spaces, positioning the pattern as a visible demonstration of circular water management.

10. Common Principles

The patterns described above share a common principle: the bioelectrochemical function is intrinsic to the metabolic transformation of waste streams into resources. Although BES are not yet commercially available at scale, their significance lies in the connecting logic they provide for bioreactor networking, which enables the grouping and sequencing of bioreactors through electrical signals, coordinating metabolic work with the temporal rhythms of daily life. The architectural affordances that emerge from this coordination make these systems socially relevant. Moving beyond individual bioreactors requires this spatial networked dimension, which is the foundation of the metabolic design patterns as an architectural proposition. The patterns are a design vocabulary for staging this networked logic rather than engineering blueprints, allowing different families, climates, and waste streams to produce equally valid instantiations of the same underlying ontology (Tables 2 and 3).

TABLE 2.

Bioelectrical platforms and their potential roles in a regenerative home.

Platform Direction Input Output Role in living home
Microbial Fuel Cell (MFC) Biological → Electrical Organic waste (urine, greywater, food scraps) Low‐voltage DC power (0.5–1.0 V per cell), clean water, biofertilizer Power generation, sanitation, biosensing
PEE POWER (12‐module MFC stack) Biological → Electrical Undiluted human urine ~150 mW continuous (12 modules), extrapolated to 1–2 W/24–48 Wh/day for 1000‐unit stack Field‐validated urinal lighting, emergency 5G Wi‐Fi, pathogen suppression
Microbial Electrolysis Cell (MEC) Electrical → Biological Organic waste + small voltage (0.2–0.8 V) Hydrogen, organic compounds (e.g., methane acetate), biosurfactants Chemical synthesis, waste upgrading
Living Algal Photovoltaic (LSP) Biological → Electrical (indirect) CO2, light, nutrients Current (via respiratory breakdown of stored carbon) Continuous (24 h) power, carbon capture
Hybrid PV + LSP Both Light, CO2, wastewater Electricity (PV) + current (algae) + hot water Combined power, water heating, microbial feedstock
Electroactive Biofilm (EAB) Both Organic substrate + optional bias Current, redox potential, chemical products Sensor, logic gate, memory storage, power source

TABLE 3.

Summary of the three metabolic design patterns across their technical, spatial, and social dimensions.

Pattern Primary input Primary output Bioreactor type Key microbes Spatial logic Social programme Maintenance
Toilet as Hearth Urine, faeces Power (12V DC), treated effluent, fertiliser MFC stack

Geobacter,

Shewanella

Visible, central, culturally integrated Community hub, agency, education Weekly cleaning, monitoring
Kitchen Garden Food waste, CO2 Fermented foods, probiotics, O2 MEC + fermenters

Lactobacillus,

Saccharomyces

Social heart of the home Culinary ritual, gut‐brain axis, cultural expression Daily feeding, weekly harvesting
Greywater Wetland Greywater Treated water, biosignals Constructed wetland + MFC sensors Diverse biofilm community Edge/transition space Sensory connection, ecological education Weekly plant tending, monitoring

11. The Building Anatomy: A Roadmap for Staged Retrofit

The transition from metabolic design pattern concept to implementation may initially appear challenging, as bioreactors are not part of the standard infrastructure of contemporary buildings. However, the proposed metabolic design patterns do not require wholesale renovation or extensive construction. By leveraging the Building Anatomy framework, a staged retrofit roadmap can respect the building's existing systems while progressively introducing metabolic infrastructure according to the capacity and ambition of the homeowner (Maia et al. 2021; Lally et al. 2026). People can choose which patterns work for their household and install them incrementally as their circumstances allow (Maia et al. 2021).

The roadmap proceeds through three stages, each building on the last. Stage 1, foundational sensing, establishes the informatic baseline at minimal cost and disruption. Millivolt signals from a pilot MFC provide data on water quality and, indirectly, indoor air quality by detecting changes in microbial metabolism caused by airborne contaminants that dissolve into the liquid phase (Jiang et al. 2018). At this point, the first affordances emerge. By selecting and cultivating electroactive microbial communities, inhabitants can begin to read the metabolic health of their home, identify resource savings, and potentially engage in standalone bioprocesses, such as composting or making cheese, that they find economically and practically useful.

Stage 2, local processing, introduces novel physical metabolic infrastructure, including the 12 V DC bus, while leaving the building's core systems intact (Dulout et al. 2017). Bypassing existing plumbing to treat greywater locally, this stage networks bioreactors into the home's existing infrastructure, supplementing the existing building systems with a living metabolic layer that can be expanded over time. With networked bioreactors in place, more complex affordances emerge, and a metabolic economy begins to form where the outputs of one bioreactor become the inputs for another. These strategic exchanges establish resource savings, reduce reliance on external inputs, and make the metabolic potential of the space more visible and effective.

Stage 3, neighbourhood metabolic exchange, scales the pattern beyond the individual home to provide recognisable affordances and community assets. Biosurfactants, fertiliser, or treated water can be shared among neighbouring households (Maia et al. 2021). While Stage 2 establishes a metabolic economy within an individual home, Stage 3 extends this logic outward to a neighbourhood trading space, enabling a microeconomy based on the exchange of physical commodities. A home with surplus electricity can store that energy in local batteries or supercapacitors; a home with a productive microbial electrolysis cell can supply detergents, biosurfactants, or platform chemicals to neighbouring households (Gaur et al. 2026; Poda and Botte 2026); a home with excess biofertiliser can share it with a neighbour's hydroponic garden. These exchanges need not be monetised; they can be governed through reciprocity or shared infrastructure according to neighbourhood community principles. Macroscale affordances also invite specific social practices, transforming isolated metabolic functions into shared community rituals. As the number of networked bioreactors grows, so too does the sophistication of the social affordances they enable. New patterns begin to emerge from this complexity through the configuration of bioreactors and the metabolic relationships they establish within the home. For example, the coordination of fermentation, hydroponic cultivation, and waste processing may give rise to a hybrid space that functions as both a kitchen and a pantry, blurring the boundaries between food preparation, preservation, composting, and production.

Through this staged logic, the metabolic design patterns evolve from conceptual frameworks into a design framework for implemented reality. Each stage introduces new capabilities without requiring what came before to be replaced or demolished. The home thus grows in metabolic complexity over time, becoming a dynamic participant in resource flows: a regenerative oikos that increases in capability and value as it matures.

This evolution also revalues domestic work in ways that directly address social inequalities. Individuals not engaged in wage labour, including infants, the elderly, and disabled people, become valuable contributors through their metabolic presence. Biological functionality becomes a unit of domestic worth, challenging a century of economic logic that has devalued care work and excluded those outside formal labour markets from being counted as economically productive members of society (Schumacher and de Vylder 2024).

Alongside these social dimensions, practical operational challenges must be considered. The intense interdependency of actors within the holobiont framework means that periods when inhabitants are away must be accounted for. System viability during low‐occupancy intervals requires further investigation. As noted earlier, the dormancy and reactivation capacity of electroactive biofilms provides a biological buffer (Hentati et al. 2025; Saheb‐Alam et al. 2019), but additional mitigation strategies, including metabolic buffers, supplementary carbon sources, hibernation modes, and community‐scale sharing, merit further investigation.

A practical challenge is the electrical infrastructure. Conventional domestic appliances are designed for 230 V AC and consume hundreds of watts. A 12‐V DC system delivering 1–2 watts continuously cannot power them under the existing paradigm. However, this need not be an innovation bottleneck but an active selection strategy for catalysing the advent of low‐power electronics. Ultrasonic cleaning can operate efficiently at low power (Kimmel et al. 2023). Slow fermentation for food preparation is a culturally embedded practice that can be integrated without significant electrical power (Blanchet et al. 2025). The 12‐V constraint catalyses innovation in low‐power domestic technologies, liberating the home from the legacy of twentieth‐century appliance design (EcoFlow 2025).

Table 4 provides a comparative analysis of appliance power requirements and the potential for low‐voltage alternatives.

TABLE 4.

Comparative analysis of appliance power requirements and the potential for low‐voltage alternatives.

Appliance type Conventional power (230V AC) Low‐voltage alternative Estimated power (12V DC) Status
Washing machine 500–2000 W Ultrasonic cleaning 5–50 W Research stage (Kimmel et al. 2023)
Refrigerator 100–400 W Thermoelectric cooling 50–150 W Low efficiency, research stage (Klinar et al. 2024)
Lighting 5–50 W LED 3–10 W Commercially available
Cooking 1000–3000 W Induction (12 V) 100–500 W Research stage
Communication 3–10 W 5G Wi‐Fi 3–10 W Commercially available
Sensors/Controls 0.5–5 W Microcontrollers 0.1–2 W Commercially available

12. Limitations of the Study

The framework's practical viability depends on several interdependent factors that deserve acknowledgment. These limitations are invitations for innovation rather than barriers to entry, and they are inseparable from the institutional barriers addressed in the following section.

The most immediate limitation concerns the practical energy balance for individual households. Changing the analytical lens from community infrastructure to individual households, the energy balance for a three‐person household using the current state of the art MFC falls below performance requirements for a conventional home and is shown in Table 5. Current field‐validated PEE POWER data indicates 150 milliwatts from 12 modules. In contrast to the community‐scale theoretical extrapolation discussed previously (1000 units; 115–300 L; 24–48 Wh/day), the household‐scale estimate relies on directly measured field data rather than projected scaling laws. A proposed household stack of 50 urine‐fed and 100 greywater‐fed units is estimated to produce 0.25–0.5 watts continuous, equivalent to 6–12 watt‐hours per day. Interestingly, despite the non‐linear scaling challenges noted earlier, this household estimate actually exceeds a linear down‐scaling of the community projection, suggesting that modular architectures remain robust even at reduced unit counts. This is attributable to several factors: volumetric efficiency at smaller stack volumes, lower internal resistance from shorter current paths, improved biofilm homogeneity across fewer units, the inherent benefits of modular architectures, and more concentrated substrate concentrations at household scale. This output covers approximately 20 to 35% of low‐power needs, with a supply–demand deficit of 22–28 watt‐hours per day. Rather than a fatal flaw, this deficit is a design invitation: the energy gap provides clear specifications for what low‐power technologies need to achieve, catalysing innovation in low‐power 12‐V appliances such as ultrasonic cleaners for textiles and thermoelectric coolers for small‐scale refrigeration (Kimmel et al. 2023; Klinar et al. 2024).

TABLE 5.

Practical energy balance for a 3‐person household.

Parameter Value Notes
Daily urine production 4.5 L 1.5 L/person/day
Daily greywater ~150 L Showers, washing, kitchen
Daily food waste ~1.5 kg Kitchen scraps
Current PEE POWER data 12 modules, 19.2 L, 150 mW Field‐validated
Proposed household stack 50‐unit MFC (urine) + 100‐unit MFC (greywater) Scaled down
Estimated output 0.25–0.5 W continuous (6–12 Wh/day) Conservative estimate
Load demand 34 Wh/day LED lighting (10 Wh), sensors (12 Wh), Wi‐Fi (12 Wh)
Supply–demand gap 22–28 Wh/day deficit Bioelectrical covers ~20%–35% of low‐power needs

This energy deficit has direct implications for water quality and effluent standards. Reuse applications currently fall short of autonomous operation requirements and are presented in Table 6. Current MFC performance achieves 60%–90% chemical oxygen demand removal and 1–3 log pathogen reduction, as detailed in Table 7. While MFC treatment alone is sufficient for non‐potable applications, meeting drinking water standards requires additional treatments such as UV disinfection and membrane filtration.

TABLE 6.

Water quality and effluent standards.

Parameter Target level (WHO/EU) Reuse application
COD < 30 mg/L Irrigation, toilet flushing
BOD < 10 mg/L Irrigation, toilet flushing
Total Nitrogen < 15 mg/L Hydroponic fertiliser
Total Phosphorus < 2 mg/L Hydroponic fertiliser
E. coli < 100 CFU/100 mL Irrigation (not food contact)
E. coli < 10 CFU/100 mL Hydroponic nutrient solution
Heavy metals Below drinking water standards EU 98/83/EC

TABLE 7.

Safety profile of MFC.

Pathogen/indicator Log reduction Notes
E. coli 1–2 log (90%–99% removal)
Enterococci 1–2 log (90%–99% removal)
Salmonella 2–3 log (99%–99.9% removal) under optimal conditions
Hepatitis B virus Insufficient data No reliable claim possible

A further, closely related limitation is health and safety. The pathogen reduction data in Table 6 provides empirical grounding for the sanitation claims made in the paper. For example, E. coli reduction is in the range of 1–2 log (90%–99% removal), Enterococci at 1–2 log, and Salmonella at 2–3 log under optimal conditions (Ieropoulos et al. 2017; Xu et al. 2022). Hepatitis B virus data remains insufficient, meaning no reliable claim can be made for viral pathogen reduction. MFC‐based sanitation systems therefore function as a secondary treatment stage and do not yet operate as standalone systems (Tsekouras et al. 2022).

Beyond these technical performance limitations, significant economic barriers remain. Owing to the bespoke availability of BES implementation, the capital cost of MFC components remains high. The cathode catalyst and membrane alone can represent more than 80% of the total cost (Abdallah et al. 2019). Life cycle assessments indicate that the embodied environmental footprint of building an MFC infrastructure, using energy‐intensive metals and plastics, can create a ‘large environmental debt’ that low‐power yields struggle to repay (Jafary et al. 2026). Consequently, the economic case for a thousand‐unit stack rests less on energy production and more on the value of decentralised wastewater treatment with reduced external energy input, combined with niche applications in off‐grid and remote settings where alternatives are even more costly or logistically challenging. Comprehensive life cycle assessment accounting for carbon, water, critical raw materials, and end‐of‐life e‐waste is urgently needed to quantify these trade‐offs and guide material selection.

A final limitation concerns system viability during low‐occupancy periods. As noted earlier, the dormancy and reactivation capacity of electroactive biofilms provides a biological buffer, but the effectiveness of additional mitigation strategies, including metabolic buffers, supplementary carbon sources, hibernation modes, and community‐scale sharing, requires further investigation.

Taken together, these limitations define current boundaries of empirical support and set priorities for future research. They also point directly to the institutional barriers that compound them, which are addressed in the following section.

13. Policy and Institutional Barriers to Transformation

Behavioural and institutional barriers must be addressed alongside the technical challenges. Yet the greatest obstacle to implementing metabolic design patterns may not be technological at all, but rather the regulatory, economic, and cultural frameworks that currently govern our built environment. These barriers are deeply interconnected, and each one compounds the others.

The most fundamental hurdle is regulatory. The Waste Directive 2008/98/EC and EU Biosafety Standards exclusively regard indoor microbes as contaminants to be eliminated. This creates a paradox: no legal category currently exists for a beneficial indoor microbe or for an MFC biofilm integral to a building's bioremediating function. Standards for beneficial indoor microbes do not currently exist, and the legal distinction between pathogenic contamination and productive microbial colonisation remains unresolved. Until legislation distinguishes between these two fundamentally different forms of microbial presence, the metabolic design pattern framework will remain confined to demonstration projects.

This regulatory blindspot is reinforced by economic disincentives. Centralised wastewater treatment receives substantial public subsidy while distributed MFC systems receive no such support. This misalignment perpetuates the very infrastructural lock‐in that the framework seeks to overcome. Yet financial support could stimulate the transition: subsidies for zero e‐waste living electronics and tax breaks for retrofits that include MFC stacks would address cost barriers directly. Without this assistance, however, the economic challenges will persist and the regulatory framework will remain unchallenged.

Cultural constructs compound both the regulatory and economic barriers. Attitudes toward discarded organic materials and effluents are negatively framed in contemporary culture, leading to their avoidance and concealment rather than revaluation. Reimagining metabolically rich wastes like urine and faeces as productive nodes, comparable to a hearth around which the community gathers, as discussed in the Toilet as Hearth pattern, requires technical demonstration, architecture, and cultural work in equal measure. Institutional inertia in building codes and professional training privileges the 230‐V electrical energy paradigm, reinforcing the very infrastructure that the framework seeks to transform. Functional demonstrators that provide implementable operational templates are essential, as they can alter both cultural perceptions and institutional practices simultaneously.

These overlapping barriers also generate risks that must be acknowledged and managed, as summarised in Table 8. Operational risks can be mitigated through modular design and redundancy. Health risks can be managed with standard operating procedures and disinfection protocols. Environmental risks can be limited through biocontainment strategies. Economic risks can be addressed through staged deployment and government incentives. Regulatory risks can be mitigated through early engagement with regulators. Significantly, the staged retrofit pathway outlined in the Building Anatomy framework provides a mechanism for managing these risks incrementally, enabling technical and institutional dimensions to evolve together, each stage introducing new capabilities while allowing for adaptation and learning, and reducing the potential for catastrophic failure.

TABLE 8.

Risk categories.

Risk category Specific risks Mitigation strategies
Operational System failure, biofilm instability, substrate depletion Modular design, redundancy, continuous bioelectrical monitoring, metabolic buffers
Health Pathogen exposure during maintenance Standard operating procedures, PPE, robust disinfection protocols; additional treatment (UV, membrane) for potable water
Environmental Unintended biofilm release Biocontainment (auxotrophic strains), compliance with biosafety regulations
Economic High capital costs, uncertain lifecycle Staged deployment, techno‐economic analysis, government incentives, LCA
Regulatory No permitting pathways Engagement with regulators, safety data generation, policy development

The correspondence between each technical limitation and its associated institutional barrier forms the basis for a strategic alignment between the framework and the Sustainable Development Goals (SDGs). Aligning these interventions with the SDG framework strengthens the policy case for reform with tangible impacts. SDG 6 targets (6.1, 6.3, 6.4) require innovation in water quality monitoring and treatment, functions that MFC biosensors and constructed wetlands directly provide. SDG 7 targets (7.1, 7.2, 7.a) call for affordable, clean energy access and technology transfer, areas where 12‐V bioelectrical systems can contribute to off‐grid and distributed solutions. SDG 9 targets (9.4, 9.5, 9.a) demand infrastructure modernisation and technological innovation, both addressed through the Building Anatomy staged retrofit model. SDG 11 targets (11.6, 11.b) require reducing the environmental impact of cities and implementing integrated policies; the framework's neighbourhood metabolic exchange stage directly advances these. SDG 12 targets (12.2, 12.5) mandate sustainable resource management and waste reduction through circularity, the core logic of all three metabolic design patterns.

The Building Anatomy framework's contribution lies in making these connections explicit and providing a staged logic for addressing them in parallel, ensuring that technical advances and regulatory reform advance in concert rather than in isolation. Without this integrated approach, the technical promise of metabolic design patterns will remain unrealised, confined, as noted earlier, to demonstration projects rather than becoming a lived reality in our homes and communities.

14. Conclusion: Regenerative Rituals of Habitation

The transition from homes that consume resources to homes that regenerate them is the central challenge of sustainable architecture. Meeting this challenge requires a step‐change in how we imagine the home itself. Moving beyond the formal qualities of our living spaces, the geometries and materials, it is imperative to address the metabolic systems that sustain them. The twentieth‐century home was designed around fossil fuels; the regenerative home must be weaned from them entirely.

Metabolic design patterns offer a strategy for this transformation, drawing on the insights and technologies of the Age of Biology to bring nature directly into our living spaces. In doing so, the framework provides a concrete architectural pathway toward SDGs 6, 7, 9, 11 and 12, goals that are often addressed in policy but rarely operationalised in building design. The Greywater Wetland and Toilet as Hearth patterns advance SDG 6 through biosensing, treatment, and sanitation. The 12‐V bioelectrical platform addresses SDG 7 via energy recovery from waste. The staged retrofit model and living electronic components serve SDG 9. SDG 11 is advanced through regenerative urban housing and community‐scale resource exchange, while SDG 12 is embedded in every pattern through closed‐loop resource processing.

The three scales of the framework link the foundational work of microbes with the daily rituals of occupants. At the microscale, microbial metabolisms form the living bridge between consumption and regeneration, using biochemistry and redox gradients to transform molecules from a “waste” product into something of value within the domestic realm. Metabolic design patterns shape the context for this work by networking bioreactors, which offer affordances that reposition the home as a metabolic participant that enables occupants to perform “housework.” By orchestrating metabolic flows, human inhabitation and daily rituals become intertwined into recognisable programmes of habitation such as kitchen and toilet. They also facilitate the emergence of new types of spaces that reflect the metabolic nature of the regenerative oikos.

The networking of bioreactors and AI that advises on system performance catalyses a new kind of sustainability narrative. The home becomes a site of continuous feedback, where inhabitants can visualise, interpret, and act upon the metabolic flows that sustain them. What we do consciously now, aided by future AI, will become as seamless as the transformations within our soils, requiring as little attention as we give to those natural processes.

The patterns presented here: Toilet as Hearth, Kitchen Garden, and Greywater Wetland are examples of how intimate domestic rituals can become acts of stewardship that redefine the “sense of home” beyond spatial composition and material assembly. At the heart of this framework is symbiosis, where humans and microbes are partners in shared metabolic activities, which positions human designers as embracing collaborative co‐evolution with microbes as the strategy for domestic regeneration (Timmis and Hallsworth 2021).

Beyond good ecological citizenship, the metabolic design patterns value individuals for their biological activity. The metabolic presence of an inhabitant in a domestic space challenges a century of economic logic that has devalued care work and employment outside formal labour markets. Inhabitants become active contributors to local microeconomies through their innate biological existence, establishing viable interdependencies with nature that enrich both domestic life and the broader community.

While this vision is still some years away, staged retrofit provides the first steps toward implementation. Standalone appliances such as composters and fermenters offer an entry point at TRL 9, while bioelectrical systems remain essential but aspirational informatic backbones at TRL 4–6. Accommodated through the Building Anatomy framework, the metabolic capabilities of a living space can evolve as technologies mature, while architectural design sets out a vision for reaching these regenerative possibilities, thereby driving investment in scientific advancement alongside the anticipation of technological readiness.

Challenges remain. Current BES power yields are modest, component costs remain high, regulatory pathways require development, and cultural taboos around sanitation persist. However, these limitations are invitations for innovation. The deficit between supply and demand invites low‐power appliance design, economic barriers stimulate material innovation and economies of scale, and regulatory gaps demand policy development. Design itself generates momentum for realisation, even when conditions are imperfect.

Perhaps the most pressing motivation, however, is the climate tipping point we are already approaching. In a world of stable resources, the need for advanced self‐sufficiency may seem remote. Once those resources falter, the homes we have built that are designed for abundance and oblivious to their own metabolic dependencies will be exposed as fragile. The metabolic design patterns proposed here are a small step toward a more resilient future: a preparation for self‐sufficiency that does not require abandoning comfort or convenience, but rather reimagining them.

A regenerative living home that participates in metabolic flows through the bodies of microbes is within reach. By placing microbial metabolism at the heart of domestic space, the framework invites a rethinking of what a home can be, how we value the microbial realm, and what it means to dwell well within the living world. Each step on this pathway builds on the last, integrating technical, cultural, and institutional dimensions into a seamless, regenerative oikos. Homes can then contribute positively to the health of the planet rather than depleting its resources.

The pathway from concept to implementation is a staged journey through networked bioreactors, staged retrofits, and inhabitants who become metabolic participants. As we edge closer to a world where homes are living systems, inhabitants can begin to participate in the cycles of life rather than extracting from them.

Author Contributions

Rachel Armstrong: conceptualization, methodology, writing – original draft, funding acquisition, visualization, writing – review and editing, project administration, validation. Pablo Carbonell: conceptualization, writing – review and editing. Deshendran Moodley: conceptualization, writing – review and editing, formal analysis. Ioannis Ieropoulos: conceptualization, writing – review and editing, formal analysis. Jorge Barriuso: conceptualization, writing – review and editing, formal analysis.

Funding

This work was supported by HORIZON EUROPE European Innovation Council, 101114746.

Ethics Statement

The authors have nothing to report.

Consent

The authors have nothing to report.

Conflicts of Interest

The authors declare no conflicts of intertest.

Acknowledgements

This work was supported by the EIC Pathfinder Challenges Portfolio ‘Carbon Dioxide and Nitrogen Valorisation and Management’ through the Microbial Hydroponics (Mi‐Hy) project under grant agreement 101114746. Declaration of AI‐assisted technology: During the preparation of this work, the authors used AI‐assisted tools (specifically, grammar and spell‐checking software) solely for the purpose of language refinement and copy‐editing. No generative AI was used to write, conceptualise, or generate the scientific content, arguments, data analysis, or original text. All intellectual contributions, conceptual framing, literature interpretation, and critical revisions were performed entirely by the human authors. The authors have reviewed and verified the final manuscript in its entirety and take full responsibility for its accuracy and originality.

Data Availability Statement

The data that support the findings of this study are available in UWE Research Bristol at https://uwe‐repository.worktribe.com/. These data were derived from the following resources available in the public domain: https://uwe‐repository.worktribe.com/output/864494/pee‐power‐urinal‐ii‐urinal‐scale‐up‐with‐microbial‐fuel‐cell‐scale‐down‐for‐improved‐lighting; https://uwe‐repository.worktribe.com/output/884148/electrifying‐bacteria‐the‐power‐of‐pee; https://uwe‐repository.worktribe.com/output/915491/pee‐power‐urinal‐microbial‐fuel‐cell‐technology‐field‐trials‐in‐the‐context‐of‐sanitation; https://uwe‐repository.worktribe.com/output/5803554/multidimensional‐benefits‐of‐improved‐sanitation‐evaluating‐pee‐power‐in‐kisoro‐uganda.

References

  1. Abdallah, M. , Feroz S., Alani S., Sayed E. T., and Shanableh A.. 2019. “Continuous and Scalable Applications of Microbial Fuel Cells: A Critical Review.” Reviews in Environmental Science and Biotechnology 18: 543–578. 10.1007/s11157-019-09508-x. [DOI] [Google Scholar]
  2. Aguirre‐Sierra, A. , Bacchetti‐De Gregoris T., Berná A., Salas J. J., Aragón C., and Esteve‐Núñez A.. 2016. “Microbial Electrochemical Systems Outperform Fixed‐Bed Biofilters in Cleaning Up Urban Wastewater.” Environmental Science: Water Research & Technology 2: 984–993. 10.1039/c6ew00172f. [DOI] [Google Scholar]
  3. Alexander, C. , Ishikawa S., and Silverstein M.. 1977. A Pattern Language. Oxford University Press. [Google Scholar]
  4. Amselem, I. 2025. Winners of Toronto's TO the Loo Competition Prove Public Restrooms Can be Beautiful Too. Architect's Newspaper. https://www.archpaper.com/2025/08/toronto‐to‐the‐loo‐competition‐public‐restrooms/. [Google Scholar]
  5. Andersen, S. J. , Hennebel T., Gildemyn S., et al. 2014. “Electrolytic Membrane Extraction Enables Production of Fine Chemicals From Biorefinery Sidestreams.” Environmental Science & Technology 48: 7135–7142. 10.1021/es500483w. [DOI] [PubMed] [Google Scholar]
  6. Andrews, S. S. , Wiley H. S., and Sauro H. M.. 2024. “Design Patterns of Biological Cells.” BioEssays 46, no. 3: e2300188. 10.1002/bies.202300188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Aouf, R. S. 2021. Introducing AirBubble: The New Environmentally‐Friendly Playground. World Economic Forum. https://www.weforum.org/stories/urban‐transformation/introducing‐airbubble‐the‐new‐environmentally‐friendly‐playground/. [Google Scholar]
  8. Apollon, W. , Kumar V., Rusyn I., et al. 2026. “Living Circuits: Sustainable Bioelectrochemical Interfaces for Clean Energy and Environmental Sensing.” Journal of Chemical Technology and Biotechnology 101: 1117–1125. 10.1002/jctb.70173. [DOI] [Google Scholar]
  9. Armstrong, R. 2023. “Towards the Microbial Home: An Overview of Developments in Next Generation Sustainable Architecture.” Microbial Biotechnology 16: 1112–1130. 10.1111/1751-7915.14256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Armstrong, R. 2025. “Monstrous Matter: The Microbial Foundations for a Living Planet.” Filozofija i Drustvo 36: 955–984. [Google Scholar]
  11. Armstrong, R. , and Moodley D.. 2026. “A Hybrid Ontology for Metabolic Architecture and Human‐Centred AI: An Explainable New Vision for the Home.” AI & Society. 10.1007/s00146-026-03301-5. [DOI] [Google Scholar]
  12. Armstrong, R. , and Hughes R.. 2023. Towards the 3rd Architectural Digital Turn. Vol. 67. EAAE Annual Conference Proceedings. 10.51588/eaaeacp.141. [DOI] [Google Scholar]
  13. Atkinson, J. T. , Chavez M. S., Niman C. M., and El‐Naggar M. Y.. 2022. “Living Electronics: A Catalogue of Engineered Living Electronic Components.” Microbial Biotechnology 16: 507–533. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Barouni, K. , Ghribi N. E., and Acevedo‐De‐los‐Ríos A.. 2026. “Toward an Ontology of Life: A Systemic Reading of Christopher Alexander's Trajectory.” In Systems Thinking in Architecture and Urbanism, 1–21. Springer. [Google Scholar]
  15. Bartczak, A. , Budziński W., Chilton S., McDonald R., and Nielsen J. S.. 2021. “Altruism and Efficient Allocations in Three‐Generation Households.” Journal of Risk and Uncertainty 62: 113–135. 10.1007/s11166-021-09350-z. [DOI] [Google Scholar]
  16. Bennetto, P. H. 1987. “Microbes Come to Power.” New Scientist 114: 36–40. [Google Scholar]
  17. Bhattacharyya, A. , Mavrodi O., Bhowmik N., Weller D., Thomashow L., and Mavrodi D.. 2023. “Bacterial Biofilms as an Essential Component of Rhizosphere Plant‐Microbe Interactions.” Methods in Microbiology 53: 3–48. 10.1016/bs.mim.2023.05.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Blanchet, M. , Perez‐Cueto F. J. A., and Michaud M.. 2025. “Fermenting Is Not About the Cooking. The Social Practice of Fermenting Foods at Home.” International Journal of Gastronomy and Food Science 40: 101169. 10.1016/j.ijgfs.2025.101169. [DOI] [Google Scholar]
  19. Bond, D. R. , and Lovley D. R.. 2003. “Electricity Production by Geobacter sulfurreducens Attached to Electrodes.” Applied and Environmental Microbiology 69: 1548–1555. 10.1128/AEM.69.3.1548-1555.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Budania, Y. , Chauhan M., Mishra S., and Singh S.. 2024. “N/NiO‐Ornated Graphitic Fiber‐Engrained Micro‐Carbon Beads: Innovative Packed Bed Type Capacitive Electrodes for Microbial Fuel Cells.” Chemical Engineering Journal 499: 156018. 10.1016/j.cej.2024.156018. [DOI] [Google Scholar]
  21. Cantin, R. 2026. “Social and Environmental Impacts of Digitalization: Building Habitat Complexity.” In LNNS, vol. 1869, 268–284. Springer. [Google Scholar]
  22. Carbelim . 2026. Algae Oxygen Generators: The New Bio‐Tech Solution That Removes CO2 and Improves Air Quality. https://carbelim.io/algae‐oxygen‐generators‐the‐new‐bio‐tech‐solution‐that‐removes‐co2‐and‐improves‐air‐quality/.
  23. Carbonell, P. , Armstrong R., Barriuso J., and Ieropoulos I.. 2026. “Living Buildings With Living Electronics: Towards Biologically Intelligent Biohybrids.” Trends in Biotechnology. 10.1016/j.tibtech.2026.05.015. [DOI] [PubMed] [Google Scholar]
  24. Chan, E. W. C. , Wong S. K., and Chan H. T.. 2021. “Natto and Miso: An Overview on Their Preparation, Bioactive Components and Health‐Promoting Effects.” Food Research 5: 446–452. 10.26656/fr.2017.5(3).587. [DOI] [Google Scholar]
  25. Chao, Y. 2025. “Microbial Fuel Cells as a Strategy for Biomass Waste Utilization and Low Carbon Energy Generation.” MATEC Web Conf 410: 01032. 10.1051/matecconf/202541001032. [DOI] [Google Scholar]
  26. Corazao, T. , and Zauscher S.. 2026. “Living Actuators: Harnessing the Power of Microbes for Active Devices.” Current Opinion in Colloid & Interface Science 81: 101592. 10.1016/j.cocis.2026.101592. [DOI] [Google Scholar]
  27. de Gerlache, J. 2026. Comparing the Role of Individual and Collective Boundaries in Complex Dissipative Systems. Vol. 1869, 420–435. LNNS. [Google Scholar]
  28. de Rosset, A. , Tyszkiewicz N., Wiśniewski J., et al. 2024. “Bioelectrochemical Synthesis of Rhamnolipids and Energy Production and Its Correlation With Nitrogen in Air‐Cathode Microbial Fuel Cells.” Journal of Environmental Management 365: 121514. 10.1016/j.jenvman.2024.121514. [DOI] [PubMed] [Google Scholar]
  29. Dulout, J. , Alonso C., Séguier L., and Jammes B.. 2017. Development of a Photovoltaic Low Voltage DC Microgrid for Buildings With Energy Storage Systems, 6p. hal‐01526247. ELECTRIMACS 2017. [Google Scholar]
  30. EcoFlow . 2025. Will Our Future Power be DC? The Rise of the Home Microgrid. https://www.ecoflow.com/us/blog/home‐microgrid‐dc‐power‐guide.
  31. Elsayed, A. , Abdelrahman A. M., al Saleh M., et al. 2026. “Alternative Configurations for the Intensification of the Anaerobic Digestion Process: A Comprehensive Review.” PRO 14: 695. 10.3390/pr14030695. [DOI] [Google Scholar]
  32. Fang, Z. , Hu J., Xu M.‐Y., et al. 2024. “A Biocompatible Electrode/Exoelectrogens Interface Augments Bidirectional Electron Transfer and Bioelectrochemical Reactions.” Bioelectrochemistry 158: 108723. 10.1016/j.bioelechem.2024.108723. [DOI] [PubMed] [Google Scholar]
  33. Feng, Y. , Barr W., and Harper W. F. Jr. 2013. “Neural Network Processing of Microbial Fuel Cell Signals for the Identification of Chemicals Present in Water.” Journal of Environmental Management 120: 84–92. 10.1016/j.jenvman.2013.01.018. [DOI] [PubMed] [Google Scholar]
  34. Feng, Y. , Kayode O., and Harper W. F. Jr. 2013. “Using Microbial Fuel Cell Output Metrics and Nonlinear Modeling Techniques for Smart Biosensing.” Sci Total Environ 449: 223–228. 10.1016/j.scitotenv.2013.01.004. [DOI] [PubMed] [Google Scholar]
  35. Ferdeș, M. , Zăbavă B. S., Paraschiv G., Ionescu M., Dincă M. N., and Moiceanu G.. 2022. “Food Waste Management for Biogas Production in the Context of Sustainable Development.” Energies 15: 6268. 10.3390/en15176268. [DOI] [Google Scholar]
  36. Fernandes, M. , Gama M., Douardo F., and Souto A. P.. 2019. “Development of Novel Bacterial Cellulose Composites for the Textile and Shoe Industry.” Microbial Biotechnology 12: 650–661. 10.1111/1751-7915.13387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Gadkari, S. 2022. “Artificial Intelligence Methods for BES.” In Scaling up of Microbial Electrochemical Systems, 437–455. Elsevier. 10.1016/B978-0-323-90765-1.00023-X. [DOI] [Google Scholar]
  38. Gagnaire, V. , Jardin J., Rabah H., Briard‐Bion V., and Jan G.. 2015. “Emmental Cheese Environment Enhances Propionibacterium freudenreichii Stress Tolerance.” PLoS One 10: e0135780. 10.1371/journal.pone.0135780. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Gajda, I. , You J., Santoro C., Greenman J., and Ieropoulos I. A.. 2020. “A New Method for Urine Electrofiltration and Long Term Power Enhancement Using Surface Modified Anodes With Activated Carbon in Ceramic Microbial Fuel Cells.” Electrochimica Acta 353: 136388. 10.1016/j.electacta.2020.136388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Garbini, G. , Barra Caracciolo A., and Grenni P.. 2023. “Electroactive Bacteria in Natural Ecosystems and Their Applications in Microbial Fuel Cells for Bioremediation: A Review.” Microorganisms 11: 1255. 10.3390/microorganisms11051255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Gaur, P. K. , Bisht P. R., Verma K. K., et al. 2026. “Functional Roles of Microbial Biosurfactants in Pharmaceutical Formulation and Targeted Drug Delivery.” Journal of Surfactants and Detergents 29: 419–433. 10.1002/jsde.70030. [DOI] [Google Scholar]
  42. Gauthier, O. , Bernillon S., Khireddine R., et al. 2025. “Use of Penicillium roqueforti in Plant‐Based Veined‐Blue Cheese: A Source of Mycotoxin Hazards?” Food Control 171: 111130. 10.1016/j.foodcont.2024.111130. [DOI] [Google Scholar]
  43. Geerlings, N. M. J. , Karman C., Trashin S., et al. 2020. “Division of Labor and Growth During Electrical Cooperation in Multicellular Cable Bacteria.” Proceedings of the National Academy of Sciences of the United States of America 117: 5478–5485. 10.1073/pnas.1916244117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Gong, Z. , Yu H., Zhang J., Li F., and Song H.. 2020. “Microbial Electro‐Fermentation for Synthesis of Chemicals and Biofuels Driven by Bi‐Directional Extracellular Electron Transfer.” Synthetic and Systems Biotechnology 5: 304–313. 10.1016/j.synbio.2020.08.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Gorby, Y. A. , Yanina S., McLean J. S., et al. 2006. “Electrically Conductive Bacterial Nanowires Produced by Shewanella oneidensis Strain MR‐1 and Other Microorganisms.” Proceedings of the National Academy of Sciences of the United States of America 103: 11358–11363. 10.1073/pnas.0604517103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Greenman, J. , and Ieropoulos I. A.. 2017. “Allometric Scaling of Microbial Fuel Cells and Stacks: The Lifeform Case for Scale‐Up.” Journal of Power Sources 356: 365–370. 10.1016/j.jpowsour.2017.04.033. [DOI] [Google Scholar]
  47. Greenman, J. , Thorn R., Willey N., and Ieropoulos I.. 2024. “Energy Harvesting From Plants Using Hybrid Microbial Fuel Cells; Potential Applications and Future Exploitation.” Frontiers in Bioengineering and Biotechnology 12: 1276176. 10.3389/fbioe.2024.1276176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Gupta, R. B. , and Basile A.. 2020. Hydrogen Production: By Electrochemical, Photochemical, and Biological Processes. Elsevier. [Google Scholar]
  49. Gupta, S. , Patro A., Mittal Y., et al. 2023. “The Race Between Classical Microbial Fuel Cells, Sediment‐Microbial Fuel Cells, Plant‐Microbial Fuel Cells, and Constructed Wetlands‐Microbial Fuel Cells: Applications and Technology Readiness Level.” Sci Total Environ 879: 162757. 10.1016/j.scitotenv.2023.162757. [DOI] [PubMed] [Google Scholar]
  50. Habibi, S. , Pons Valladares O., and Peña D. M.. 2022. “Sustainability Performance by Ten Representative Intelligent Façade Technologies: A Systematic Review.” Sustainable Energy Technologies and Assessments 52: 102001. 10.1016/j.seta.2022.102001. [DOI] [Google Scholar]
  51. Han, W. , Wayposts C., Kwok R., Baniasadi M., and de Lorenzo V.. 2022. “Biologically Engineered Microbes for Bioremediation of Electronic Waste: Wayposts.” Engineering Biology 6: 1–10. 10.1049/enb2.12018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Hanum, L. , Newcombe P., and Scott T.. 2024. “A Systematic Review of Intergenerational Co‐Residence Between Older People and Adult Children.” Journal of Family Studies 30: 968–987. 10.1080/13229400.2024.2361694. [DOI] [Google Scholar]
  53. Hentati, E. , Buttay C., and Haddour N.. 2025. Development of Microbial Fuel Cell‐Based Sensor for In‐Situ Water Monitoring. Proceedings of the International MEEP Symposium. [Google Scholar]
  54. Hockfield, S. 2019. The Age of Living Machines: How Biology Will Build the Next Technology Revolution. WW Norton & Company. [Google Scholar]
  55. Ieropoulos, I. A. , and Moreno D. Z.. 2025. “Microbial Fuel Cells Powering Robots and Beyond: Historical Perspective and Future Directions.” Bioelectrochemistry 166: 109010. 10.1016/j.bioelechem.2025.109010. [DOI] [PubMed] [Google Scholar]
  56. Ieropoulos, I. , Pasternak G., and Greenman J.. 2017. “Urine Disinfection and In Situ Pathogen Killing Using a Microbial Fuel Cell Cascade System.” PLoS One 12: e0176475. 10.1371/journal.pone.0176475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Ieropoulos, I. A. , Singh A., Moreno D. Z., and Greenman J.. 2024. “Bioelectrochemical Systems and Their Readiness for Commercialisation.” Current Opinion in Electrochemistry 46: 101540. 10.1016/j.coelec.2024.101540. [DOI] [Google Scholar]
  58. Ieropoulos, I. , Winfield J., and Greenman J.. 2010. “Effects of Flow Rate, Inoculum and Time on the Internal Resistance of Microbial Fuel Cells.” Bioresource Technology 101: 3520–3525. 10.1016/j.biortech.2009.12.108. [DOI] [PubMed] [Google Scholar]
  59. Jadhav, D. A. , Chendake A. D., Vinayak V., Atabani A., Abdelkareem M. A., and Chae K.‐J.. 2022. “Scale‐Up of the Bioelectrochemical System: Strategic Perspectives and Normalization of Performance Indices.” Bioresource Technology 363: 127935. 10.1016/j.biortech.2022.127935. [DOI] [PubMed] [Google Scholar]
  60. Jafary, T. , Mousavi A., Yeneneh A. M., Al‐Kalbani M. S., and Al‐Wahaibi B. M.. 2026. “Recent Advances in Scaling up Microbial Fuel Cell Systems for Wastewater Treatment, Energy Recovery, and Environmental Sustainability.” Sustainability 18: 638. 10.3390/su18020638. [DOI] [Google Scholar]
  61. Jiang, Y. , Liang P., Huang X., and Ren Z. J.. 2018. “A Novel Microbial Fuel Cell Sensor With a Gas Diffusion Biocathode Sensing Element for Water and Air Quality Monitoring.” Chemosphere 203: 21–25. 10.1016/j.chemosphere.2018.03.169. [DOI] [PubMed] [Google Scholar]
  62. Joonhwan, Y. 2023. ecoLogicStudio Grows Air‐Purifying Architecture With Algae. Metropolis Magazine. https://metropolismag.com/profiles/ecologicstudio‐grows‐air‐purifying‐architecture‐with‐algae/. [Google Scholar]
  63. Joshi, A. 2019. “Working Principle and Interconnectivity of Microbial Fuel Cells for Bioelectricity Generation.” International Journal of Innovation and Research in Technology 6: 243–248. [Google Scholar]
  64. Jung, J. Y. , Lee S. H., Kim J. M., et al. 2011. “Metagenomic Analysis of Kimchi, a Traditional Korean Fermented Food.” Applied and Environmental Microbiology 77: 2264–2274. 10.1128/AEM.02157-10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Kadier, A. , Simayi Y., Abdeshahian P., Azman N. F., Chandrasekhar K., and Kalil M. S.. 2016. “A Comprehensive Review of Microbial Electrolysis Cells (MEC) Reactor Designs and Configurations for Sustainable Hydrogen Gas Production.” Alexandria Engineering Journal 55: 427–443. 10.1016/j.aej.2015.10.008. [DOI] [Google Scholar]
  66. Kato, S. 2015. “Biotechnological Aspects of Microbial Extracellular Electron Transfer.” Microbes and Environments 30: 133–139. 10.1264/jsme2.ME15028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Kembel, S. W. , Jones E., Kline J., et al. 2012. “Architectural Design Influences the Diversity and Structure of the Built Environment Microbiome.” ISME Journal 6: 1469–1479. 10.1038/ismej.2011.211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Kimmel, T. , Kunkel C., Ait Sghir M., and Kessler A.. 2023. “Potential of Ultrasonics for Energy Saving in the Household Washing Process.” Energy Efficiency 16: 33. 10.1007/s12053-023-10115-7. [DOI] [Google Scholar]
  69. Klinar, K. , Law J. Y., Franco V., Moya X., and Kitanovski A.. 2024. “Perspectives and Energy Applications of Magnetocaloric, Pyromagnetic, Electrocaloric, and Pyroelectric Materials.” Advanced Energy Materials 14: 2401739. 10.1002/aenm.202401739. [DOI] [Google Scholar]
  70. Konig, A. , Nacinovic M., Prest T., and Gruden M.. 2015. “A Review of the Application of Microbial Fuel Cells in Wastewater Treatment.” Water Science and Technology 72: 1016–1024. [Google Scholar]
  71. Kumar, J. S. , Venkata Subbiah K., and Prasada Rao P. V. V.. 2011. “Management of Municipal Solid Waste by Vermicompost A Case.” In Sustainable Solid Waste Management, edited by Unnisa S. A. and Rav S. B., 47–56. Apple Academic Press. [Google Scholar]
  72. Lally, P. , Little J., Rebow M., and Ahern C.. 2026. “Dynamic Life Cycle Assessment of Staged Energy Retrofits: Evaluating Time‐Variant Carbon Emissions in Decarbonising Pathways – A Use Case in Ireland.” Energy and Buildings 352: 116872. 10.1016/j.enbuild.2025.116872. [DOI] [Google Scholar]
  73. Lederberg, J. , and McCray A. T.. 2001. “Ome Sweet Omics: A Genealogical Treasury of Words.” Scientist 15: 8. [Google Scholar]
  74. Lee, J. , Ryu E., Kim J. Y., Lee J. H., and Yun M. H.. 2025. “A Simulation Approach to Validating Optimized Kitchen Layouts: Reassessing the Work Triangle Through Real Apartment Floor Plan Analysis.” Work 80: 1838–1853. 10.1177/10519815241300413. [DOI] [PubMed] [Google Scholar]
  75. Leech, J. A. , Nelson W. C., Burnett R. T., Aaron S., and Raizenne M. E.. 2002. “It's About Time: A Comparison of Canadian and American Time‐Activity Patterns.” Journal of Exposure Analysis and Environmental Epidemiology 12: 427–432. [DOI] [PubMed] [Google Scholar]
  76. Lehmann, S. 2011. “Optimizing Urban Material Flows and Waste Streams in Urban Development Through Principles of Zero Waste and Sustainable Consumption.” In Sustainable Solid Waste Management, edited by Unnisa S. A. and Rav S. B., 103–132. Apple Academic Press. [Google Scholar]
  77. Leshem, D. 2016. “Retrospectives: What Did the Ancient Greeks Mean by Oikonomia?” Journal of Economic Perspectives 30: 225–238. [Google Scholar]
  78. Liu, H. , Chen T., and Li J.. 2024. “Exogenous Electric Field as a Biochemical Driving Factor for Extracellular Electron Transfer: Increasing Power Output of Microbial Fuel Cell.” Energy Conversion and Management 301: 118050. 10.1016/j.enconman.2023.118050. [DOI] [Google Scholar]
  79. Liu, Y. , Dai Z., Wang D., Ma Y., and Guo P.. 2025. “Root Surface Microbial Biofilms in Phytoremediation: Formation Processes, Regulatory Mechanisms, Influencing Factors and Roles.” Environmental Technology and Innovation 40: 104406. 10.1016/j.eti.2025.104406. [DOI] [Google Scholar]
  80. Logan, B. E. 2010. “Scaling Up Microbial Fuel Cells and Other Bioelectrochemical Systems.” Applied Microbiology and Biotechnology 85: 1665–1671. 10.1007/s00253-009-2378-9. [DOI] [PubMed] [Google Scholar]
  81. Logan, B. E. , and Rabaey K.. 2012. “Conversion of Wastes Into Bioelectricity and Chemicals by Using Microbial Electrochemical Technologies.” Science 337: 686–690. 10.1126/science.1217412. [DOI] [PubMed] [Google Scholar]
  82. Luo, S. , Sun H., Ping Q., Jin R., and He Z.. 2016. “A Review of Modeling Bioelectrochemical Systems: Engineering and Statistical Aspects.” Energies 9: 111. 10.3390/en09020111. [DOI] [Google Scholar]
  83. Maia, I. , Kranzl L., and Müller A.. 2021. “New Step‐By‐Step Retrofitting Model for Delivering Optimum Timing.” Applied Energy 290: 116714. 10.1016/j.apenergy.2021.116714. [DOI] [Google Scholar]
  84. Manolakelli, A. 2025. Gibson's Affordance Theory in Architecture: Understanding the Design of Possibility. ArchPsych. https://www.archpsych.co.uk/post/gibson‐affordance‐theory‐in‐architecture‐understanding‐the‐design‐of‐possibility. [Google Scholar]
  85. Meah, A. 2016. “Extending the Contested Spaces of the Modern Kitchen.” Geography Compass 10: 41–55. 10.1111/gec3.12252. [DOI] [Google Scholar]
  86. Memon, M. A. 2011. “Integrated Solid Waste Management Based on the 3R Approach.” In Sustainable Solid Waste Management, edited by Unnisa S. A. and Rav S. B., 133–150. Apple Academic Press. [Google Scholar]
  87. Merck, K. 2026. Best Kitchen Composters and Food Recyclers. Wired. https://www.wired.com/story/home‐composters‐buying‐guide/. [Google Scholar]
  88. Merino‐Jiménez, I. , Walter X. A., Greenman J., and Ieropoulos I.. 2021. “Bioelectrochemical Systems for Building Integrated Applications.” Journal of Power Sources 500: 229965. [Google Scholar]
  89. Meyer, A. R. , Gettemans T., Tan J. P., et al. 2026. “Rising Together: Exploring Sourdough Fermentation Diversity Through Co‐Design in the HealthFerm Citizen Science Initiative.” npj Science of Food 10: 76. 10.1038/s41538-026-00725-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  90. Mittal, R. , Debs L. H., Patel A. P., et al. 2017. “Neurotransmitters: The Critical Modulators Regulating Gut–Brain Axis.” Journal of Cellular Physiology 232: 2359–2372. 10.1002/jcp.25518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. Modesto, L. , Ogun Ramalhete E., Ravasi S., et al. 2026. “A Modular Microbial–Hydroponic System for Circular Urban Plant Cultivation.” Frontiers in Horticulture 5: 1799169. 10.3389/fhort.2026.1799169. [DOI] [Google Scholar]
  92. Mohajerani, A. , Ukwatta A., Jeffrey‐Bailey T., et al. 2019. “A Proposal for Recycling the World's Unused Stockpiles of Treated Wastewater Sludge (Biosolids) in Fired‐Clay Bricks.” Buildings 9: 14. 10.3390/buildings9010014. [DOI] [Google Scholar]
  93. Mukherjee, A. , Patel V., Shah M. T., et al. 2022. “Effective Power Management System in Stacked Microbial Fuel Cells for Onsite Applications.” Journal of Power Sources 517: 230684. 10.1016/j.jpowsour.2021.230684. [DOI] [Google Scholar]
  94. Nassikas, N. J. , McCormack M. C., Ewart G., et al. 2024. “Indoor Air Sources of Outdoor Air Pollution: Health Consequences, Policy, and Recommendations: An Official American Thoracic Society Workshop Report.” Annals of the American Thoracic Society 21: 365–376. 10.1513/AnnalsATS.202312-1067ST. [DOI] [PMC free article] [PubMed] [Google Scholar]
  95. Nastro, R. A. , Kuppam C., Toscanesi M., et al. 2025. “Bio‐Electrosynthesis of Polyhydroxybutyrate and Surfactants in Microbial Fuel Cells: A Preliminary Study.” Frontiers in Microbiology 16: 1372302. 10.3389/fmicb.2025.1372302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  96. Nath, D. , and Ieropoulos I. A.. 2025. “Electricity and Fertilizer Production Using Microbial Fuel Cell Stacks for Possible Integration With Hydroponics.” Journal of Power Sources 652: 237546. 10.1016/j.jpowsour.2025.237546. [DOI] [Google Scholar]
  97. National Association of REALTORS . 2025. “2025 Home Buyers and Sellers Generational Trends Report.” https://cms.nar.realtor/sites/default/files/2025‐03/2025‐home‐buyers‐and‐sellers‐generational‐trends‐report‐04‐01‐2025.pdf.
  98. Ollár, A. , Granath K., Femenías P., and Rahe U.. 2022. “Is There a Need for New Kitchen Design? Assessing the Adaptative Capacity of Space to Enable Circularity in Multiresidential Buildings.” Frontiers of Architectural Research 11: 891–916. 10.1016/j.foar.2022.03.009. [DOI] [Google Scholar]
  99. Onwuemezie, L. , and Gohari Darabkhani H.. 2024. “Biohydrogen Production From Solar and Wind Assisted AF‐MEC Coupled With MFC, PEM Electrolysis of H2O and H2 Fuel Cell for Small‐Scale Applications.” Renewable Energy 224: 120160. 10.1016/j.renene.2024.120160. [DOI] [Google Scholar]
  100. Pan, P. , and Bhattacharyya N.. 2025. “Advanced Strategies for Storing Electricity Generated by MFCs With Enhanced Mathematical Modeling for Real‐World Applications. SSRN Preprint SSRN:5399771.” 10.2139/ssrn.5399771. [DOI]
  101. Park, Y. , and Newman G. D.. 2017. “A Framework for Place‐Making Using Alexander's Patterns.” Urban Design International 22: 349–362. 10.1057/s41289-017-0040-1. [DOI] [Google Scholar]
  102. Pasternak, G. , Greenman J., and Ieropoulos I.. 2018. “Self‐Powered, Autonomous Biological Oxygen Demand Biosensor for Water Quality Monitoring.” Biosensors & Bioelectronics 112: 123–131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  103. Poda, S. , and Botte G.. 2026. “Electrochemical Valorization of Biosolids: A Comprehensive Review of Resource Recovery and High‐Value Product Generation.” Annals of Environmental Science and Toxicology 10: 1–24. 10.17352/aest.000092. [DOI] [Google Scholar]
  104. Potter, M. C. 1911. “Electrical Effects Accompanying the Decomposition of Organic Compounds.” Proceedings of the Royal Society B 84: 260–276. [Google Scholar]
  105. Prasad, J. , and Tripathi R. K.. 2021. “Effect of Sediment Microbial Fuel Cell Stacks on 9 V/12 V DC Power Supply.” International Journal of Hydrogen Energy 46: 14628–14638. 10.1016/j.ijhydene.2020.07.187. [DOI] [Google Scholar]
  106. Rahman, M. M. , Khan M. M. H., Ullah M. A., Zhang X., and Kumar A.. 2016. “A Hybrid Renewable Energy System for a North American Off‐Grid Community.” Energy 97: 151–160. 10.1016/j.energy.2015.12.105. [DOI] [Google Scholar]
  107. Randall, D. G. , and Naidoo V.. 2018. “Urine: The Next Generation Fertilizer.” Science of the Total Environment 645: 1438–1455. [Google Scholar]
  108. Rohwer, F. , and Kelley S.. 2004. “Culture‐Independent Analyses of Coral‐Associated Microbes.” In Coral Health and Disease, edited by Rosenberg E. and Loya Y., 265–277. Springer. [Google Scholar]
  109. Rohwer, F. , Seguritan V., Azam F., and Knowlton N.. 2002. “Diversity and Distribution of Coral‐Associated Bacteria.” Marine Ecology Progress Series 243: 1–10. 10.3354/meps243001. [DOI] [Google Scholar]
  110. Romero Mejía, A. A. , Vásquez J. A., and Lugo González A.. 2012. “Bacterias, Fuente de Energía Para el Futuro (Bacteria, Source of Energy for the Future).” Tecnura 16, no. 32: 118–143. [Google Scholar]
  111. Rosenberg, E. , Koren O., Reshef L., Efrony R., and Zilber‐Rosenberg I.. 2007. “The Role of Microorganisms in Coral Health, Disease and Evolution.” Nature Reviews. Microbiology 5: 355–362. 10.1038/nrmicro1635. [DOI] [PubMed] [Google Scholar]
  112. Saheb‐Alam, S. , Persson F., Wilén B. M., Hermansson M., and Modin O.. 2019. “Response to Starvation and Microbial Community Composition in Microbial Fuel Cells Enriched on Different Electron Donors.” Microbial Biotechnology 12: 962–975. 10.1111/1751-7915.13449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  113. Sahoo, N. C. , Mohapatro S., Sahu A. K., and Mohapatro B. S.. 2017. Loss and Cost Evaluation of Typical DC Distribution for Residential House. IEEE Xplore/School of Electrical Sciences. [Google Scholar]
  114. Salgado, C. A. 2009. “Microbial Fuel Cells Powered by Geobacter sulfurreducens .” Basic Biotechnology 5: 96–101. [Google Scholar]
  115. Sato, C. , Apollon W., Luna‐Maldonado A. I., Paucar N. E., Hibbert M., and Dudgeon J.. 2023. “Integrating Microbial Fuel Cell and Hydroponic Technologies Using a Ceramic Membrane Separator to Develop an Energy–Water–Food Supply System.” Membranes 13: 803. 10.3390/membranes13090803. [DOI] [PMC free article] [PubMed] [Google Scholar]
  116. Savenije, D. 2013. Bill Gates' Foundation Invests in Urine Fueled Electricity. Utility Dive. https://www.utilitydive.com/news/bill‐gates‐foundation‐invests‐in‐urine‐fueled‐electricity/195513/. [Google Scholar]
  117. Schumacher, L. , and de Vylder J.. 2024. “The Metabolic Kitchen: Blurring the Boundaries of Architectural Domesticity Through Bioprocessing.” Journal of Architectural Research and Design 19: 112–126. [Google Scholar]
  118. Soemarie, Y. B. , Abdullah A., and Setyawan M.. 2021. Application of Microbial Fuel Cell (MFC) for Wastewater Treatment: A Review. Vol. 782, 032089. IOP Conference Series: Earth and Environmental Science. [Google Scholar]
  119. Sönmez, M. , and Özçelik N. E.. 2025. “Building Anatomy: Rethinking Internal and External Dynamics in Architecture.” Buildings 15: 3461. [Google Scholar]
  120. Tan, W. H. , Chong S., Fang H.‐W., et al. 2021. “Microbial Fuel Cell Technology—A Critical Review on Scale‐Up Issues.” PRO 9: 985. 10.3390/pr9060985. [DOI] [Google Scholar]
  121. Telhan, O. 2025. “Bioreactors as Additive Manufacturing Environments.” 3D Printing and Additive Manufacturing 12, no. 2: 169–180. 10.1089/3dp.2024.0023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  122. Terraviva . 2026. Urban Toilets, Architecture Competition. https://www.terravivacompetitions.com/urban‐toilets‐competition‐2026.
  123. Timmis, K. , and Hallsworth J. E.. 2021. “The Darkest Microbiome—A Post‐Human Biosphere.” Microbial Biotechnology 15: 176–185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  124. Tsekouras, G. J. , Deligianni P. M., Kanellos F. D., et al. 2022. “Microbial Fuel Cell for Wastewater Treatment as Power Plant in Smart Grids: Utopia or Reality?” Frontiers in Energy Research 10: 843768. 10.3389/fenrg.2022.843768. [DOI] [Google Scholar]
  125. Volume Zero Competitions . 2025. Little Big Loo 2025, Architecture Competition, Edition #2. https://volumezerocompetitions.com/little‐big‐loo‐2025.
  126. Walter, X. A. , Merino‐Jiménez I., Greenman J., and Ieropoulos I.. 2018. “PEE POWER Urinal II – Urinal Scale‐Up With Microbial Fuel Cell Scale‐Down for Improved Lighting.” Journal of Power Sources 392: 150–158. 10.1016/j.jpowsour.2018.02.047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  127. Whipps, J. M. , Lewis K., and Cooke R. C.. 1988. “Mycoparasitism and Plant Disease Control.” In Fungi in Biological Control Systems, edited by Burge N. M., 161–187. Manchester University Press. [Google Scholar]
  128. World Green Building Council . 2019. Bringing Embodied Carbon Upfront: Coordinated Action for the Building and Construction Sector to Tackle Embodied Carbon. https://worldgbc.org/climate‐action/embodied‐carbon/.
  129. Wouterszoon Jansen, B. , Duijghuisen J.‐A., van Bortel G., and Gruis V.. 2023. “Comparing Circular Kitchens: A Study of the Dutch Housing Sector.” Buildings 13: 1698. 10.3390/buildings13071698. [DOI] [Google Scholar]
  130. Xiao, L. , Ge Z., Kelly P., Zhang F., and He Z.. 2014. “Evaluation of Normalized Energy Recovery (NER) in Microbial Fuel Cells Affected by Reactor Dimensions and Substrates.” Bioresource Technology 157: 77–83. 10.1016/j.biortech.2014.01.086. [DOI] [PubMed] [Google Scholar]
  131. Xu, K. , Lu J., Hu L., et al. 2022. “Pathogens Inactivation in Nutrient Recovery From Urine: A Review.” Frontiers in Environmental Science 10: 1056019. 10.3389/fenvs.2022.1056019. [DOI] [Google Scholar]
  132. You, J. , Mendis A., Greenman J., et al. 2022. “Development of a Bio‐Digital Interface Powered by Microbial Fuel Cells.” Sustainability 14: 1735. 10.3390/su14031735. [DOI] [Google Scholar]
  133. Zacharoff, L. A. , and El‐Naggar M. Y.. 2017. “Redox Conduction in Biofilms: From Respiration to Living Electronics.” Curr Opin Electrochem 4: 182–189. 10.1016/j.coelec.2017.09.003. [DOI] [Google Scholar]
  134. Zaman, A. U. 2011. “Comparative Study of Municipal Solid Waste Treatment Technologies Using Life Cycle Assessment Method.” In Sustainable Solid Waste Management, edited by Unnisa S. A. and Rav S. B., 1–14. Apple Academic Press. [Google Scholar]
  135. Zhou, T. , Han H., Liu P., Xiong J., Tian F., and Li X.. 2017. “Microbial Fuel Cell Based Biosensor for Toxicity Detection: A Review.” Sensors 17: 2230. 10.3390/s17102230. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data that support the findings of this study are available in UWE Research Bristol at https://uwe‐repository.worktribe.com/. These data were derived from the following resources available in the public domain: https://uwe‐repository.worktribe.com/output/864494/pee‐power‐urinal‐ii‐urinal‐scale‐up‐with‐microbial‐fuel‐cell‐scale‐down‐for‐improved‐lighting; https://uwe‐repository.worktribe.com/output/884148/electrifying‐bacteria‐the‐power‐of‐pee; https://uwe‐repository.worktribe.com/output/915491/pee‐power‐urinal‐microbial‐fuel‐cell‐technology‐field‐trials‐in‐the‐context‐of‐sanitation; https://uwe‐repository.worktribe.com/output/5803554/multidimensional‐benefits‐of‐improved‐sanitation‐evaluating‐pee‐power‐in‐kisoro‐uganda.


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