Reprogramming the metabolism of an acetogenic bacterium to homoformatogenesis

• Published in: The ISME Journal Vol. 17; no. 7; pp. 984 - 992
• Main Authors: Moon, Jimyung, Schubert, Anja, Waschinger, Lara M., Müller, Volker
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01-07-2023; Nature Publishing Group
• Subjects: 45/29; 45/70; 45/77; 631/158/855; 631/208/737; 631/326; 631/326/171; 631/443/319; Acetates - metabolism; Acetic acid; Acetobacterium - genetics; Acetobacterium - metabolism; Acetogenesis; Bacteria; Bacteria - metabolism; Biomedical and Life Sciences; Biotechnology; Carbon; Carbon dioxide; Carbon Dioxide - metabolism; Carbon monoxide; Carbon sources; Carboxyl group; Ecology; Electron transfer; Electrons; Energy sources; Enzymes; Evolutionary Biology; Formates - metabolism; Glycine; Glycine betaine; Life Sciences; Microbial Ecology; Microbial Genetics and Genomics; Microbiology; Microorganisms; Mutants; Oxidation; Oxidation-Reduction
• ISSN: 1751-7362; 1751-7370
• DOI: 10.1038/s41396-023-01411-2

Methyl groups are abundant in anoxic environments and their utilization as carbon and energy sources by microorganisms involves oxidation of the methyl groups to CO
2
, followed by transfer of the electrons to an acceptor. In acetogenic bacteria, the electron acceptor is CO
2
that is reduced to enzyme bound carbon monoxide, the precursor of the carboxyl group in acetate. Here, we describe the generation of a mutant of the acetogen
Acetobacterium woodii
in which the last step in methyl group oxidation, formate oxidation to CO
2
catalyzed by the HDCR enzyme, has been genetically deleted. The mutant grew on glycine betaine as methyl group donor, and in contrast to the wild type, formed formate alongside acetate, in a 1:2 ratio, demonstrating that methyl group oxidation stopped at the level of formate and reduced electron carriers were reoxidized by CO
2
reduction to acetate. In the presence of the alternative electron acceptor caffeate, CO
2
was no longer reduced to acetate, formate was the only product and all the carbon went to formate. Apparently, acetogenesis was not required to sustain formatogenic growth. This is the first demonstration of a genetic reprogramming of an acetogen into a formatogen that grows by homoformatogenesis from methyl groups. Formate production from methyl groups is not only of biotechnological interest but also for the mechanism of electron transfer in syntrophic interactions in anoxic environments.