Multiple Formate Dehydrogenase Enzymes in the Facultative Methylotroph Methylobacterium extorquens AM1 Are Dispensable for Growth on Methanol
Open Access
- 1 January 2004
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 186 (1) , 22-28
- https://doi.org/10.1128/jb.186.1.22-28.2004
Abstract
Formate dehydrogenase has traditionally been assumed to play an essential role in energy generation during growth on C 1 compounds. However, this assumption has not yet been experimentally tested in methylotrophic bacteria. In this study, a whole-genome analysis approach was used to identify three different formate dehydrogenase systems in the facultative methylotroph Methylobacterium extorquens AM1 whose expression is affected by either molybdenum or tungsten. A complete set of single, double, and triple mutants was generated, and their phenotypes were analyzed. The growth phenotypes of the mutants suggest that any one of the three formate dehydrogenases is sufficient to sustain growth of M. extorquens AM1 on formate, while surprisingly, none is required for growth on methanol or methylamine. Nuclear magnetic resonance analysis of the fate of [ 13 C]methanol revealed that while cells of wild-type M. extorquens AM1 as well as cells of all the single and the double mutants continuously produced [ 13 C]bicarbonate and 13 CO 2 , cells of the triple mutant accumulated [ 13 C]formate instead. Further studies of the triple mutant showed that formate was not produced quantitatively and was consumed later in growth. These results demonstrated that all three formate dehydrogenase systems must be inactivated in order to disrupt the formate-oxidizing capacity of the organism but that an alternative formate-consuming capacity exists in the triple mutant.Keywords
This publication has 45 references indexed in Scilit:
- Methylotrophy in Methylobacterium extorquens AM1 from a Genomic Point of ViewJournal of Bacteriology, 2003
- Poly-β-Hydroxybutyrate Biosynthesis in the Facultative Methylotroph Methylobacterium extorquens AM1: Identification and Mutation of gap11 , gap20 , and phaRJournal of Bacteriology, 2002
- C 1 Transfer Enzymes and Coenzymes Linking Methylotrophic Bacteria and Methanogenic ArchaeaScience, 1998
- Alternative NAD+-dependent formate dehydrogenases in the facultative methylotroph Mycobacterium vaccae 10FEMS Microbiology Letters, 1991
- Mass transfer characterization of an airlift probe for oxygenating and mixing cell suspensions in an NMR spectrometerBiotechnology & Bioengineering, 1991
- Evidence for the presence of a new NAD+-dependent formate dehydrogenase in Pseudomonas sp. 101 cells grown on a molybdenum-containing mediumFEMS Microbiology Letters, 1989
- Evidence for the presence of a new NAD+-dependent formate dehydrogenase inPseudomonassp. 101 cells grown on a molybdenum-containing mediumFEMS Microbiology Letters, 1989
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983
- A Possible Alternative Mechanism for the Oxidation of Formaldehyde to FormateMicrobiology, 1982
- Methanol Assimilation by Hyphomicrobium sp.Journal of General Microbiology, 1973