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Genetic Confirmation of the Role of Sulfopyruvate Decarboxylase in Coenzyme M Biosynthesis inMethanococcus maripaludis
Author(s) -
Felipe Sarmiento,
Courtney K. Ellison,
William B. Whitman
Publication year - 2013
Publication title -
archaea
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.8
H-Index - 40
eISSN - 1472-3654
pISSN - 1472-3646
DOI - 10.1155/2013/185250
Subject(s) - complementation , auxotrophy , mutant , cofactor , transposon mutagenesis , biosynthesis , biology , methanogenesis , coenzyme a , biochemistry , mutagenesis , gene , genetics , enzyme , transposable element , reductase , bacteria
Coenzyme M is an essential coenzyme for methanogenesis. The proposed biosynthetic pathway consists of five steps, of which the fourth step is catalyzed by sulfopyruvate decarboxylase (ComDE). Disruption of the gene comE by transposon mutagenesis resulted in a partial coenzyme M auxotroph, which grew poorly in the absence of coenzyme M and retained less than 3% of the wild type level of coenzyme M biosynthesis. Upon coenzyme M addition, normal growth of the mutant was restored. Moreover, complementation of the mutation with the wild type comE gene in trans restored full growth in the absence of coenzyme M. These results confirm that ComE plays an important role in coenzyme M biosynthesis. The inability to yield a complete CoM auxotroph suggests that either the transposon insertion failed to completely inactivate the gene or M. maripaludis possesses a promiscuous activity that partially complemented the mutation.

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