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. 2014 Apr 1;14(4):308–343. doi: 10.1089/ast.2013.1110

Table 1.

Top-Down Imperatives of Life Compared to Bottom-Up Electrochemical Tensions and Their Likely Expenditures

  References
Top down
Overall, life requires convection (or advection) for delivery of nutrients and removal of waste. Open University Course Team, 1993; Russell and Arndt, 2005
While minimizing internal entropy, cells export entropy to the environment through the use of molecular motors or nanoengines. Leduc, 1911; Westheimer, 1962; Wicken, 1987; Boyer, 1997; Hoffmann, 2012
All life derives from a single ancestor. Woese et al., 1990; Doolittle, 1999; Harris et al., 2003
All independent life-forms are cellular and compartmentalized with “chemiosmotic” membranes housing ATPases. Leduc, 1911; Mitchell, 1979a, 1979b; Kell, 1988; Boyer, 1997; Spitzer and Poole, 2009
Gluconeogenesis predates glycolysis. Say and Fuchs, 2010; Fuchs, 2011
The first bacteria and archaea were autotrophic. Berg et al., 2010; Fuchs, 2011
All autotrophic organisms use a redox gradient within the bounds of ∼180 mV to 1.2 V. Thauer et al., 1977; Ducluzeau et al., 2009
The acetyl coenzyme A pathway is the oldest and simplest known. Fuchs, 1989, 2011; Crabtree, 1997
Redox bifurcation is used to overcome uphill reactions (quinones, flavins, NAD, methanophenazine, Mo and W enzymes). Herrmann et al., 2008; Nitschke and Russell, 2009; Kaster et al., 2011; Buckel and Thauer, 2013
LUCA enzymes comprise ferredoxins, acetyl-CoA synthase (ACS), carbon monoxide dehydrogenase (CODH), [NiFe]-hydrogenase, hydrogenlyase, and Mo-pterins, all assembled from a “redox protein construction kit.” Baymann et al., 2003; Nitschke and Russell, 2009; Schoepp-Cothenet et al., 2012; Nitschke et al., 2013
Alkaline conditions support amine, phosphate, thiol, and sugar chemistries as well as general self-assembly and condensations. ab intra; Mellersh and Smith, 2010; Cafferty et al., 2013
Lost City Methanosarcinales that thrive at pH 9–10 and 70–80°C use H2 and CH4 as fuels and sulfate (or perhaps nitrate) as electron acceptor and produce CO2 and possibly acetate as waste. Brazelton et al., 2011; Lang et al., 2012
Bottom up
The emergence of life is coupled to convection. Baross and Hoffman, 1985; Russell et al., 1989, 1994, 2010; Shock, 1992
Submarine alkaline systems resulting from serpentinization during hydrothermal convection are low entropy and feed H2, CH4, and minor NH3 to the ocean floor. Russell et al., 1989, 1994, 2003, 2013; Nitschke and Russell, 2009, 2013; Simoncini et al., 2011
Submarine alkaline systems produce mounds comprising inorganic compartments. Russell et al., 1989, 1994; Kelley et al., 2005; Mielke et al., 2010, 2011; McGlynn et al., 2012
All the inorganic elements required for life to emerge are supplied from either ocean or spring. Russell and Hall, 1997, 2006; Nitschke and Russell, 2009
Inorganic compartments at the margins of submarine mounds may promote reactions between CO2, NO3-, NO2- and FeIII in the ocean and hydrothermal H2 and CH4 Nitschke and Russell, 2013; Russell et al., 2013
Proton and redox gradients are an inevitable aspect of interfacing an acidulous ocean and alkaline hydrothermal fluid across a spontaneously precipitated inorganic membrane. Russell et al., 1994; Russell and Hall, 1997, 2006
Electrochemical gradient energy availability (redox+pH) at such springs totals up to ∼1 V. Russell and Hall, 1997, 2006; Ducluzeau et al., 2009; Nitschke and Russell, 2009; Barge et al., 2014
Alkaline hydrothermal fluids promote certain reductions, aminations, condensations, and polymerizations. Huber and Wächtershäuser, 1997, 2003
Mo and W presence could enable uphill thermodynamic reactions through redox bifurcation. Nitschke and Russell, 2009, 2011
The structures of mackinawite and greigite are affine with [FeFe]- and [FeNi]-hydrogenase and ACS and CODH, and of fougèrite to methane monooxygenase. Morse and Arakaki, 1993; Russell and Hall, 1997, 2006; McGlynn et al., 2009; Nitschke et al., 2013
Thermal gradients drive a convective polymerase chain reaction and the concentration of charged polymers through thermal diffusion. Braun et al., 2003; Baaske et al., 2007; Mast and Braun, 2010; Mast et al., 2012, 2013
The duration of alkaline springs in steady state is >30,000 years or >1017 μs—presumed time enough to drive disequilibria-driven pathways toward the production of the complex organic molecules required of life's first chemical and mechanical operations? Ludwig et al., 2011