Benzoate Fermentation by the Anaerobic Bacterium Syntrophus aciditrophicus in the Absence of Hydrogen-Using Microorganisms
Open Access
- 1 December 2001
- journal article
- Published by American Society for Microbiology in Applied and Environmental Microbiology
- Vol. 67 (12) , 5520-5525
- https://doi.org/10.1128/aem.67.12.5520-5525.2001
Abstract
The anaerobic bacterium Syntrophus aciditrophicus metabolized benzoate in pure culture in the absence of hydrogen-utilizing partners or terminal electron acceptors. The pure culture of S. aciditrophicus produced approximately 0.5 mol of cyclohexane carboxylate and 1.5 mol of acetate per mol of benzoate, while a coculture of S . aciditrophicus with the hydrogen-using methanogen Methanospirillum hungatei produced 3 mol of acetate and 0.75 mol of methane per mol of benzoate. The growth yield of the S. aciditrophicus pure culture was 6.9 g (dry weight) per mol of benzoate metabolized, whereas the growth yield of the S. aciditrophicus-M. hungatei coculture was 11.8 g (dry weight) per mol of benzoate. Cyclohexane carboxylate was metabolized by S. aciditrophicus only in a coculture with a hydrogen user and was not metabolized by S. aciditrophicus pure cultures. Cyclohex-1-ene carboxylate was incompletely degraded by S. aciditrophicus pure cultures until a free energy change (Δ G ′) of −9.2 kJ/mol was reached (−4.7 kJ/mol for the hydrogen-producing reaction). Cyclohex-1-ene carboxylate, pimelate, and glutarate transiently accumulated at micromolar levels during growth of an S. aciditrophicus pure culture with benzoate. High hydrogen (10.1 kPa) and acetate (60 mM) levels inhibited benzoate metabolism by S. aciditrophicus pure cultures. These results suggest that benzoate fermentation by S. aciditrophicus in the absence of hydrogen users proceeds via a dismutation reaction in which the reducing equivalents produced during oxidation of one benzoate molecule to acetate and carbon dioxide are used to reduce another benzoate molecule to cyclohexane carboxylate, which is not metabolized further. Benzoate fermentation to acetate, CO 2 , and cyclohexane carboxylate is thermodynamically favorable and can proceed at free energy values more positive than −20 kJ/mol, the postulated minimum free energy value for substrate metabolism.Keywords
This publication has 29 references indexed in Scilit:
- Metabolism of Benzoate, Cyclohex-1-ene Carboxylate, and Cyclohexane Carboxylate by “ Syntrophus aciditrophicus ” Strain SB in Syntrophic Association with H 2 -Using MicroorganismsApplied and Environmental Microbiology, 2001
- Syntrophothermus lipocalidus gen. nov., sp. nov., a novel thermophilic, syntrophic, fatty-acid-oxidizing anaerobe which utilizes isobutyrate.International Journal of Systematic and Evolutionary Microbiology, 2000
- Energetics of product formation during anaerobic degradation of phthalate isomers and benzoateFEMS Microbiology Ecology, 1999
- Syntrophobacter fumaroxidans sp. nov., a syntrophic propionate-degrading sulfate-reducing bacteriumInternational Journal of Systematic and Evolutionary Microbiology, 1998
- Energetics of methanogenic benzoate degradation by Syntrophus gentianae in syntrophic cocultureMicrobiology, 1997
- Thermosyntropha lipolytica gen. nov., sp. nov., a Lipolytic, Anaerobic, Alkalitolerant, Thermophilic Bacterium Utilizing Short- and Long-Chain Fatty Acids in Syntrophic Coculture with a Methanogenic ArchaeumInternational Journal of Systematic and Evolutionary Microbiology, 1996
- Pure Culture of Syntrophus buswellii, Definition of its Phylogenetic Status, and Description of Syntrophus gentianae sp. nov.Systematic and Applied Microbiology, 1995
- Fermentation of primary alcohols and diols and pure culture of syntrophically alcohol-oxidizing anaerobesArchiv für Mikrobiologie, 1985
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976