Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2009:63:477-99.
doi: 10.1146/annurev.micro.091208.073600.

The expanding world of methylotrophic metabolism

Affiliations
Review

The expanding world of methylotrophic metabolism

Ludmila Chistoserdova et al. Annu Rev Microbiol. 2009.

Abstract

In the past few years, the field of methylotrophy has undergone a significant transformation in terms of discovery of novel types of methylotrophs, novel modes of methylotrophy, and novel metabolic pathways. This time has also been marked by the resolution of long-standing questions regarding methylotrophy and the challenge of long-standing dogmas. This chapter is not intended to provide a comprehensive review of metabolism of methylotrophic bacteria. Instead we focus on significant recent discoveries that are both refining and transforming the current understanding of methylotrophy as a metabolic phenomenon. We also review new directions in methylotroph ecology that improve our understanding of the role of methylotrophy in global biogeochemical processes, along with an outlook for the future challenges in the field.

PubMed Disclaimer

Figures

Figure 1
Figure 1
The proposed roles of N-methylglutamate synthase (NMGS), γ-glutamylmethylamide synthase (GMAS), and N-methylglutamate dehydrogenase (NMGD) in the oxidation of methylamine and gene clusters encoding enzymes involved in this pathway.
Figure 2
Figure 2
Distinct roles of enzymes catalyzing H4F-linked C1 transfer reactions. (a) FtfL, Fch, and MtdA are involved in assimilatory metabolism in Methylobacterium species during growth on methanol or methylamine. (b) MetF, FolD, and PurU are involved in dissimilatory metabolism of methylated compounds such as chloromethane.
Figure 3
Figure 3
The refined scheme of the glyoxylate regeneration cycle, now termed ethylmalonyl-CoA pathway (right), and its connection to the serine cycle (left). Gene names are shown in blue. Each of these genes has been mutated in Methylobacterium extorquens AM1 and the mutant phenotypes analyzed. The gene for succinyl-CoA hydrolase remains unknown.

References

    1. Alber BE, Spanheimer R, Ebenau-Jehle C, Fuchs G. Study of an alternate glyoxylate cycle for acetate assimilation by Rhodobacter sphaeroides. Mol Microbiol. 2006;61:297–309. - PubMed
    1. Anthony C. The Biochemistry of Methylotrophs. London: Academic; 1982.
    1. Anthony C. The quinoprotein dehydrogenases for methanol and glucose. Arch Biochem Biophys. 2004;428:2–9. - PubMed
    1. Baani M, Liesack W. Two isozymes of particulate methane monooxygenase with different methane oxidation kinetics are found in Methylocystis sp. strain SC2. Proc Natl Acad Sci USA. 2008;105:10203–8. Shows that an organism of the Methylocystis genus is capable of low-affinity methane oxidation. - PMC - PubMed
    1. Baker SC, Ferguson SJ, Ludwig B, Page MD, Richter OM, van Spanning RJ. Molecular genetics of the genus Paracoccus: metabolically versatile bacteria with bioenergetic flexibility. Microbiol Mol Biol Rev. 1998;62:1046–1078. - PMC - PubMed

LinkOut - more resources