scholarly journals Role of carbon monoxide dehydrogenase in the autotrophic pathway used by acetogenic bacteria.

1984 ◽  
Vol 81 (20) ◽  
pp. 6261-6265 ◽  
Author(s):  
E. Pezacka ◽  
H. G. Wood
2021 ◽  
Author(s):  
Ji-Eun Lee ◽  
Akira Yamaguchi ◽  
Hideshi Ooka ◽  
Tomohiro Kazami ◽  
Masahiro Miyauchi ◽  
...  

In situ electrochemical IR study of the CO2 reduction by inorganic analogues of carbon monoxide dehydrogenase (CODH) reveals the critical role of Ni in the activity and selectivity of Fe sulfides for CO2 reduction.


mBio ◽  
2016 ◽  
Vol 7 (3) ◽  
Author(s):  
Fungmin Liew ◽  
Anne M. Henstra ◽  
Klaus Winzer ◽  
Michael Köpke ◽  
Sean D. Simpson ◽  
...  

ABSTRACTThe future sustainable production of chemicals and fuels from nonpetrochemical resources and reduction of greenhouse gas emissions are two of the greatest societal challenges. Gas fermentation, which utilizes the ability of acetogenic bacteria such asClostridium autoethanogenumto grow and convert CO2and CO into low-carbon fuels and chemicals, could potentially provide solutions to both. Acetogens fix these single-carbon gases via the Wood-Ljungdahl pathway. Two enzyme activities are predicted to be essential to the pathway: carbon monoxide dehydrogenase (CODH), which catalyzes the reversible oxidation of CO to CO2, and acetyl coenzyme A (acetyl-CoA) synthase (ACS), which combines with CODH to form a CODH/ACS complex for acetyl-CoA fixation. Despite their pivotal role in carbon fixation, their functions have not been confirmedin vivo. By genetically manipulating all three CODH isogenes (acsA,cooS1, andcooS2) ofC. autoethanogenum, we highlighted the functional redundancies of CODH by demonstrating thatcooS1andcooS2are dispensable for autotrophy. Unexpectedly, thecooS1inactivation strain showed a significantly reduced lag phase and a higher growth rate than the wild type on H2and CO2. During heterotrophic growth on fructose, theacsAinactivation strain exhibited 61% reduced biomass and the abolishment of acetate production (a hallmark of acetogens), in favor of ethanol, lactate, and 2,3-butanediol production. A translational readthrough event was discovered in the uniquely truncated (compared to those of other acetogens)C. autoethanogenum acsAgene. Insights gained from studying the function of CODH enhance the overall understanding of autotrophy and can be used for optimization of biotechnological production of ethanol and other commodities via gas fermentation.IMPORTANCEGas fermentation is an emerging technology that converts the greenhouse gases CO2and CO in industrial waste gases and gasified biomass into fuels and chemical commodities. Acetogenic bacteria such asClostridium autoethanogenumare central to this bioprocess, but the molecular and genetic characterization of this microorganism is currently lacking. By targeting all three of the isogenes encoding carbon monoxide dehydrogenase (CODH) inC. autoethanogenum, we identified the most important CODH isogene for carbon fixation and demonstrated that genetic inactivation of CODH could improve autotrophic growth. This study shows that disabling of the Wood-Ljungdahl pathway via the inactivation ofacsA(encodes CODH) significantly impairs heterotrophic growth and alters the product profile by abolishing acetate production. Moreover, we discovered a previously undescribed mechanism for controlling the production of this enzyme. This study provides valuable insights into the acetogenic pathway and can be used for the development of more efficient and productive strains for gas fermentation.


2000 ◽  
Vol 381 (9-10) ◽  
Author(s):  
Ortwin Meyer ◽  
Lothar Gremer ◽  
Reinhold Ferner ◽  
Marion Ferner ◽  
Holger Dobbek ◽  
...  

2018 ◽  
Vol 115 (6) ◽  
pp. E1166-E1173 ◽  
Author(s):  
Panagiotis S. Adam ◽  
Guillaume Borrel ◽  
Simonetta Gribaldo

Carbon monoxide dehydrogenase/acetyl-CoA synthase (CODH/ACS) is a five-subunit enzyme complex responsible for the carbonyl branch of the Wood–Ljungdahl (WL) pathway, considered one of the most ancient metabolisms for anaerobic carbon fixation, but its origin and evolutionary history have been unclear. While traditionally associated with methanogens and acetogens, the presence of CODH/ACS homologs has been reported in a large number of uncultured anaerobic lineages. Here, we have carried out an exhaustive phylogenomic study of CODH/ACS in over 6,400 archaeal and bacterial genomes. The identification of complete and likely functional CODH/ACS complexes in these genomes significantly expands its distribution in microbial lineages. The CODH/ACS complex displays astounding conservation and vertical inheritance over geological times. Rare intradomain and interdomain transfer events might tie into important functional transitions, including the acquisition of CODH/ACS in some archaeal methanogens not known to fix carbon, the tinkering of the complex in a clade of model bacterial acetogens, or emergence of archaeal–bacterial hybrid complexes. Once these transfers were clearly identified, our results allowed us to infer the presence of a CODH/ACS complex with at least four subunits in the last universal common ancestor (LUCA). Different scenarios on the possible role of ancestral CODH/ACS are discussed. Despite common assumptions, all are equally compatible with an autotrophic, mixotrophic, or heterotrophic LUCA. Functional characterization of CODH/ACS from a larger spectrum of bacterial and archaeal lineages and detailed evolutionary analysis of the WL methyl branch will help resolve this issue.


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