Abstract
The nucleotide sequences encoding the [NiFe] hydrogenase from Desulfovibrio gigas and the [NiFeSe] hydrogenase from Desulfovibrio baculatus (N.K. Menon, H.D. Peck, Jr., J. LeGall, and A.E. Przybyla, J. Bacteriol. 169:5401-5407, 1987; C. Li, H.D. Peck, Jr., J. LeGall, and A.E. Przybyla, DNA 6:539-551, 1987) were analyzed by the codon usage method of Staden and McLachlan. The reported reading frames were found to contain regions of low codon probability which are matched by more probable sequences in other frames. Renewed nucleotide sequencing showed the probable frames to be correct. The corrected sequences of the two small and large subunits share a significant degree of sequence homology. The small subunit, which contains 10 conserved cysteine residues, is likely to coordinate at least 2 iron-sulfur clusters, while the finding of a selenocysteine codon (TGA) near the 3' end of the [NiFeSe] large-subunit gene matched by a regular cysteine codon (TGC) in the [NiFe] large-subunit gene indicates the presence of some of the ligands to the active-site nickel in the large subunit.
MeSH Terms
Amino Acid Sequence
Codon
DNA, Bacterial/genetics
Desulfovibrio/genetics
Genes, Bacterial
Hydrogenase/genetics
Iron
Metalloproteins/genetics
Molecular Sequence Data
Nickel
Selenium
Sequence Homology, Nucleic Acid
Chemicals
Codon
DNA, Bacterial
Metalloproteins
Nickel
Iron
Hydrogenase
Selenium
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Voordouw G
Department of Biological Sciences, University of Calgary, Alberta, Canada.
Menon N K
LeGall J
Choi E S
Peck H D
Przybyla A E
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