Table 1.
Application of microbial electrosynthesis for bioproduction.
| Microorganism | EET Mode | Key engineering strategy | Substrate | Product | Key Findings | Ref |
|---|---|---|---|---|---|---|
| Shewanella oneidensis | DET | Two-stage electro-fermentation; electro-regulated CRISPRi for pathway suppression | Lactate | Isobutanol | Two-stage electro-fermentation process, using different voltages for growth and biosynthesis, enhanced isobutanol production. Directing reducing equivalents using NADH biosensor and suppressing byproduct pathways via CRISPRi led to an isobutanol titre of 1321.5 mg/L (94.9 % of theoretical yield). | 28 |
| Shewanella oneidensis | DET | Engineered glycerol utilization and (R)-acetoin biosynthesis pathway | Glycerol | (R)-Acetoin | Expanded substrate range of S. oneidensis to glycerol. (R)-acetoin production reached 313.61 mg/L. | 29 |
| Escherichia coli | DET | Expressed heterologous S. oneidensis electron transfer proteins and biosynthesis pathways for isobutanol and 3-methylbutanol | Glycerol | Isobutanol, 3-methylbutanol | Enhanced anoxic glycerol utilization. Total isobutanol and 3-methylbutanol production reached 232 mg/L, 25 % higher than using glucose | 30 |
| Escherichia coli | IET (Neutral red- and 2-hydroxy-1,4-naphthoquinone mediated) | Engineered glycerol reductive pathways to produce 1,3-propanediol (1,3-PDO) and 3-hydroxypropionic acid (3-HP) | Glycerol | 1,3-PDO, 3-HP | Increased 1,3-PDO titre by 2.5-fold–15.5 mM with negative potential. Enable 3-HP production at 10.9 mM with positive potential. | 33 |
| Rhodopseudomonas palustris | DET | Engineered n-butanol biosynthesis pathway; deleted nitrogenases | CO2 | n-Butanol | Produced 0.91 mg/L of n-butanol using CO2, electricity, and light. Demonstrated first solar panel-powered microbial electrosynthesis platform for n-butanol production. | 39 |
| Rhodopseudomonas palustris | DET | Overexpressed RuBisCO form I and II to increase CO2 fixation | CO2 | Polyhydroxyalkanoate | Overexpression of RuBisCO increased polyhydroxyalkanoate production up to five-fold; engineered RuBisCO strains increased electron uptake under non-nitrogen-fixing conditions | 40 |
| Yarrowia lipolytica | IET (Neutral red-mediated) | Expressed AckA and Pta to increase acetyl-CoA; expressed pathway genes to produce fatty alcohols, lupeol and betulinic acid | Acetate, glucose | Fatty alcohols, lupeol, betulinic acid | Enhanced NADPH regeneration by MES drove acetate utilization, resulting in 6.17-fold increase in fatty alcohol production; demonstrated first MES application in Y. lipolytica | 32 |
| Synechocystis sp. PCC 6803 | DET | Inactivated photosystem II; expressed heterologous ethylene-forming enzyme | CO2, HCO3− | Acetate, ethylene | External electrons and light enabled CO2 fixation at 9.3 % energy conversion efficiency; achieved acetate and ethylene production from CO2. | 25 |
| Cupriavidus necator | IET (H2-mediated) | Expressed heterologous mevalonate pathway and α-humulene synthase | H2, CO2 | α-Humulene | Produced 10.8 mg/L α-humulene by MES; first example of electroautotrophic terpene production from CO2 | 37 |
| Cupriavidus necator | IET (H2-mediated) | Expressed lycopene pathway | H2, CO2 | Lycopene | Produced 1.73 mg/L lycopene from CO2 from power plant exhaust gas | 38 |
| Cupriavidus necator | DET and IET (flavin-mediated) | Expressed heterologous S. oneidensis MtrCAB electron conduit proteins and Gloeobacter violaceus rhodopsin; overexpressed native carbonic anhydrase | CO2 | Biomass | Created an artificial photoelectrochemical microbial system that directs CO2 into the central metabolism | 41 |