In this pathway carbon dioxide is reduced to carbon monoxide (CO) and formic acid (HCOOH) or directly into a formyl group (R−CH=O), the formyl group is reduced to a methyl group (−CH3) and then combined with the carbon monoxide and coenzyme A to produce acetyl-CoA. Two specific enzymes participate on the carbon monoxide side of the pathway: CO dehydrogenase and acetyl-CoA synthase. The former catalyzes the reduction of the CO2 and the latter combines the resulting CO with a methyl group to give acetyl-CoA.[1][2]
Some anaerobic bacteria use the Wood–Ljungdahl pathway in reverse to break down acetate. For example, sulfate-reducing bacteria (SRB) transform acetate completely into CO2 and H2 coupled with the reduction of sulfate to sulfide.[3] When operating in the reverse direction, the acetyl-CoA synthase is sometimes called acetyl-CoA decarbonylase.
It has been proposed that the reductive acetyl-CoA pathway might have begun at deep seaalkalinehydrothermal vents where metal sulfides and transition metalscatalyze the prebiotic reactions of the reductive acetyl-CoA pathway.[7] Recent experiments have tried to replicate this pathway by attempting to reduce CO2, with very little pyruvate observed using native iron (Fe0, zerovalent Fe) as a reducing agent (< 30 μM),[8] and even less so under hydrothermal settings with H2 (10 μM).[9] Joseph Moran and colleagues state that "it has been proposed that either the complete or “horseshoe” forms of the rTCA cycle may have once been united with the acetyl CoA pathway in an ancestral, possibly prebiotic, carbon fixation network".[8]
Last universal common ancestor
A 2016 study of the genomes of a set of bacteria and archaea suggested that the last universal common ancestor (LUCA) of all cells was using an ancient Wood–Ljungdahl pathway in a hydrothermal setting,[10] but more recent work challenges this conclusion as they argued that the previous study had "undersampled protein families, resulting in incomplete phylogenetic trees which do not reflect protein family evolution".[11] However geological evidence and phylogenomic reconstructions of the metabolic network of the common ancestors of archaea and bacteria support that LUCA fixed CO2 and relied on H2.[12][9]
Ljungdahl LG (1986). "The autotrophic pathway of acetate synthesis in acetogenic bacteria". Annual Review of Microbiology. 40 (1): 415–50. doi:10.1146/annurev.micro.40.1.415. PMID3096193.
^ abRagsdale Stephen W (2006). "Metals and Their Scaffolds To Promote Difficult Enzymatic Reactions". Chem. Rev. 106 (8): 3317–3337. doi:10.1021/cr0503153. PMID16895330.
^Paul A. Lindahl "Nickel-Carbon Bonds in Acetyl-Coenzyme A Synthases/Carbon Monoxide Dehydrogenases" Met. Ions Life Sci. 2009, volume 6, pp. 133–150. doi:10.1039/9781847559159-00133
^Spormann, Alfred M.; Thauer, Rudolf K. (1988). "Anaerobic acetate oxidation to CO2 by Desulfotomaculum acetoxidans". Archives of Microbiology. 150 (4): 374–380. doi:10.1007/BF00408310. ISSN0302-8933. S2CID2158253.