Affiliation:
1. Microbiology, Department of Biology I, University of Munich, D-80638 Munich
2. Department of Protein Chemistry, Max-Planck-Institute of Biochemistry, D-82152 Martinsried, Germany
Abstract
ABSTRACT
The genome of
Methanococcus maripaludis
harbors genes for at least six selenocysteine-containing proteins and also for homologs that contain a cysteine codon in the position of the UGA selenocysteine codon. To investigate the synthesis and function of both the Se and the S forms, a mutant with an inactivated
selB
gene was constructed and analyzed. The mutant was unable to synthesize any of the selenoproteins, thus proving that the gene product is the archaeal translation factor (aSelB) specialized for selenocysteine insertion. The wild-type form of
M. maripaludis
repressed the synthesis of the S forms of selenoproteins, i.e., the selenium-independent alternative system, in selenium-enriched medium, but the mutant did not. We concluded that free selenium is not involved in regulation but rather a successional compound such as selenocysteyl-tRNA or some selenoprotein. Apart from the S forms, several enzymes from the general methanogenic route were affected by selenium supplementation of the wild type or by the
selB
mutation. Although the growth of
M. maripaludis
on H
2
/CO
2
is only marginally affected by the
selB
lesion, the gene is indispensable for growth on formate because
M. maripaludis
possesses only a selenocysteine-containing formate dehydrogenase.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
51 articles.
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