» Articles » PMID: 16346807

Dissimilation of Carbon Monoxide to Acetic Acid by Glucose-Limited Cultures of Clostridium Thermoaceticum

Overview
Date 1985 Jun 1
PMID 16346807
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Clostridium thermoaceticum was cultivated in glucose-limited media, and the dissimilation of CO to acetic acid was evaluated. We found that cultures catalyzed the rapid dissimilation of CO to acetic acid and CO(2), with the stoichiometry obtained for conversion approximating that predicted from the following reaction: 4CO + 2H(2)O --> CH(3)CO(2)H + 2CO(2). Growing cultures formed approximately 50 mmol (3 g) of CO-derived acetic acid per liter of culture, with the rate of maximal consumption approximating 9.1 mmol of CO consumed/h per liter of culture. In contrast, resting cells were found not to dissimilate CO to acetic acid. CO was incorporated, with equal distribution between the carboxyl and methyl carbons of acetic acid when the initial cultivation gas phase was 100% CO, whereas CO(2) preferentially entered the carboxyl carbon when the initial gas phase was 100% CO(2). Significantly, in the presence of saturating levels of CO, CO(2) preferentially entered the methyl carbon, whereas saturating levels of CO(2) yielded CO-derived labeling predominantly in the carboxyl carbon. These findings are discussed in relation to the path of carbon flow to acetic acid.

Citing Articles

Formate-Dependent Acetogenic Utilization of Glucose by the Fecal Acetogen .

Yao Y, Fu B, Han D, Zhang Y, Liu H Appl Environ Microbiol. 2020; 86(23).

PMID: 32948524 PMC: 7657615. DOI: 10.1128/AEM.01870-20.


Production of acetic acid by Clostridium thermoaceticum in electrodialysis culture using a fermenter equipped with an electrodialyser.

Nomura Y, Iwahara M, Hongo M World J Microbiol Biotechnol. 2014; 10(4):427-32.

PMID: 24421091 DOI: 10.1007/BF00144466.


Competing formate- and carbon dioxide-utilizing prokaryotes in an anoxic methane-emitting fen soil.

Hunger S, Schmidt O, Hilgarth M, Horn M, Kolb S, Conrad R Appl Environ Microbiol. 2011; 77(11):3773-85.

PMID: 21478308 PMC: 3127604. DOI: 10.1128/AEM.00282-11.


Anaerobic biodegradation of methyl esters by Acetobacterium woodii and Eubacterium limosum.

Liu S, Suflita J J Ind Microbiol. 1994; 13(5):321-7.

PMID: 7765371 DOI: 10.1007/BF01569735.


Source of carbon and hydrogen in methane produced from formate by Methanococcus thermolithotrophicus.

Sparling R, Daniels L J Bacteriol. 1986; 168(3):1402-7.

PMID: 3782041 PMC: 213652. DOI: 10.1128/jb.168.3.1402-1407.1986.


References
1.
Diekert G, Thauer R . Carbon monoxide oxidation by Clostridium thermoaceticum and Clostridium formicoaceticum. J Bacteriol. 1978; 136(2):597-606. PMC: 218584. DOI: 10.1128/jb.136.2.597-606.1978. View

2.
Wang G, Wang D . Elucidation of Growth Inhibition and Acetic Acid Production by Clostridium thermoaceticum. Appl Environ Microbiol. 1984; 47(2):294-8. PMC: 239662. DOI: 10.1128/aem.47.2.294-298.1984. View

3.
SCHULMAN M, Ghambeer R, Ljungdahl L, Wood H . Total synthesis of acetate from CO2. VII. Evidence with Clostridium thermoaceticum that the carboxyl of acetate is derived from the carboxyl of pyruvate by transcarboxylation and not by fixation of CO2. J Biol Chem. 1973; 248(18):6255-61. View

4.
Ljungdahl L . Total synthesis of acetate from CO2 by heterotrophic bacteria. Annu Rev Microbiol. 1969; 23:515-38. DOI: 10.1146/annurev.mi.23.100169.002503. View

5.
Zeikus J . Metabolism of one-carbon compounds by chemotrophic anaerobes. Adv Microb Physiol. 1983; 24:215-99. DOI: 10.1016/s0065-2911(08)60387-2. View