An extracellular [NiFe] hydrogenase mediating iron corrosion is encoded in a genetically unstable genomic island in Methanococcus maripaludis

在沼泽甲烷球菌(Methanococcus maripaludis)中,一个介导铁腐蚀的胞外[NiFe]氢化酶编码于一个遗传不稳定的基因组岛中。

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Abstract

Certain methanogens deteriorate steel surfaces through a process called microbiologically influenced corrosion (MIC). However, the mechanisms of MIC, whereby methanogens oxidize zerovalent iron (Fe(0)), are largely unknown. In this study, Fe(0)-corroding Methanococcus maripaludis strain OS7 and its derivative (strain OS7mut1) defective in Fe(0)-corroding activity were isolated. Genomic analysis of these strains demonstrated that the strain OS7mut1 contained a 12-kb chromosomal deletion. The deleted region, termed "MIC island", encoded the genes for the large and small subunits of a [NiFe] hydrogenase, the TatA/TatC genes necessary for the secretion of the [NiFe] hydrogenase, and a gene for the hydrogenase maturation protease. Thus, the [NiFe] hydrogenase may be secreted outside the cytoplasmic membrane, where the [NiFe] hydrogenase can make direct contact with Fe(0), and oxidize it, generating hydrogen gas: Fe(0) + 2 H(+) → Fe(2+) + H(2). Comparative analysis of extracellular and intracellular proteomes of strain OS7 supported this hypothesis. The identification of the MIC genes enables the development of molecular tools to monitor epidemiology, and to perform surveillance and risk assessment of MIC-inducing M. maripaludis.

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