Bioenergetic constraints for conversion of syngas to biofuels in acetogenic bacteria

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Abstract

Synthesis gas (syngas) is a gas mixture consisting mainly of H2, CO, and CO2 and can be derived from different sources, including renewable materials like lignocellulose. The fermentation of syngas to certain biofuels, using acetogenic bacteria, has attracted more and more interest over the last years. However, this technology is limited by two things: (1) the lack of complete knowledge of the energy metabolism of acetogenic bacteria, and (2) the lack of sophisticated genetic tools for the modification of acetogens. In this review, we discuss the bioenergetic constraints for the conversion of syngas to different biofuels. We will mainly focus on Acetobacterium woodii, which is the best understood acetogen in terms of energy conservation. Syngas fermentation with Clostridium autoethanogenum will also be discussed, since this organism is well suited to convert syngas to certain products and already used in large-scale industrial processes.

Figures

  • Fig. 1 Enzymology of the Wood–Ljungdahl pathway. One CO2 is reduced to a THF-bound methyl group, a second CO2 is reduced to an enzyme-bound CO group. The methyl and the CO group are condensed by the CODH/ACS and further converted to acetate. [H] reducing equivalent; THF tetrahydrofolate; CoFeS corrinoid–iron-sulfur protein; CODH/ACS carbon monoxide dehydrogenase/acetyl-CoA synthase
  • Fig. 2 Bioenergetics of acetate formation from H2 + CO2 in A. woodii. The reducing equivalents for the reductive steps in the WLP are provided by an H2-oxidizing, electron-bifurcating hydrogenase which reduces Fd and NAD +. Excess Fd2− is oxidized by the Rnf complex which reduces NAD+ and builds up a Na+ gradient. This gradient drives ATP synthesis via the Na+-dependent ATP synthase. In total, 0.3 ATP could be synthesized per acetate produced. THF tetrahydrofolate; CoFeS corrinoid–iron-sulfur protein
  • Fig. 3 Bioenergetics of acetate formation from CO in A. woodii. The reducing equivalents for the reductive steps in the WLP are provided by the CO-oxidizing CODH/ACS which reduces Fd. Excess Fd2− is oxidized by the Rnf complex which reduces NAD+ and builds up a Na+ gradient. This gradient drives ATP synthesis via the Na+-dependent ATP synthase. The electron-bifurcating hydrogenase provides the H2 required for the reduction of CO2 to formate. In total, 1.5 ATP could be synthesized per acetate produced. THF tetrahydrofolate; CoFeS corrinoid–iron-sulfur protein; CODH/ACS carbon monoxide dehydrogenase/acetyl-CoA synthase
  • Table 1 ATP yield for the synthesis of products from acetyl-CoA with H2 or CO as electron donor
  • Fig. 4 Ethanol formation from acetyl-CoA. Acetyl-CoA is synthesized via the Wood–Ljungdahl pathway (WL pathway) and can be reduced to ethanol either by means of acetaldehyde dehydrogenase (AldDH) or by means of aldehyde:ferredoxin oxidoreductase (AOR)
  • Table 2 Potential aldehyde: ferredoxin oxidoreductases (AORs) in acetogens
  • Fig. 5 Butanol formation from acetyl-CoA. Acetyl-CoA is synthesized via the Wood–Ljungdahl pathway (WL pathway) and 2 acetyl-CoA can be reduced to butanol either by means of butyraldehyde dehydrogenase or by means of aldehyde:ferredoxin oxidoreductase (AOR). The butyryl-CoA dehydrogenase (Bcd) uses NADH as electron donor, if the Bcd is electron-bifurcating it reduces ferredoxin simultaneously with crotonyl-CoA

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APA

Bertsch, J., & Müller, V. (2015, December 10). Bioenergetic constraints for conversion of syngas to biofuels in acetogenic bacteria. Biotechnology for Biofuels. BioMed Central Ltd. https://doi.org/10.1186/s13068-015-0393-x

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