Description : 
Jeremy D. Semrau, Sheeja Jagadevan, Alan A. DiSpirito, Ashraf Khalifa, Julie Scanlan, Brandt H. Bergman, Brittani C. Freemeier, Bipin S. Baral, Nathan L. Bandow, Alexey Vorobev, Daniel H. Haft, Stéphane Vuilleumier and J. Colin Murrell
Biological oxidation of methane to methanol by aerobic bacteria is catalysed by two different enzymes, the cytoplasmic or soluble methane monooxygenase (sMMO) and the membrane-bound or particulate methane monooxygenase (pMMO). Expression of MMOs is controlled by a ‘copperswitch’, i.e. sMMO is only expressed at very low copper : biomass ratios, while pMMO expression increases as this ratio increases. Methanotrophs synthesize a chalkophore, methanobactin, for the binding and import of copper. Previous work suggested that methanobactin was formed from a polypeptide precursor. Here we report that deletion of the gene suspected to encode for this precursor, mbnA, in Methylosinus trichosporium OB3b, abolishes methanobactin production. Further, gene expression assays indicate that methanobactin, together with another polypeptide of previously unknown function, MmoD, play key roles in regulating expression of MMOs. Based on these data, we propose a general model explaining how expression of the MMO operons is regulated by copper, methanobactin and MmoD. The basis of the ‘copperswitch’ is MmoD, and methanobactin amplifies the magnitude of the switch. Bioinformatic analysis of bacterial genomes indicates that the production of methanobactin-like compounds is not confined to methanotrophs, suggesting that its use as a metalbinding agent and/or role in gene regulation may be widespread in nature.
Methanobactin and MmoD work in concert to act as the ‘copper-switch’ in methanotrophs