Yamamoto I, Wada N, Ujiiye T, Tachibana M, Matsuzaki M, Kajiwara H, Watanabe Y, Hirano H, Okubo A, Satoh T
Department of Biological Sciences, Faculty of Science, Hiroshima University, Japan.
Biosci Biotechnol Biochem. 1995 Oct;59(10):1850-5. doi: 10.1271/bbb.59.1850.
The gene encoding dimethyl sulfoxide (DMSO) reductase, which contains a molybdenum cofactor, of the phototrophic bacterium Rhodobacter sphaeroides f. sp. denitrificans was isolated using an oligonucleotide probe, which was synthesized based on a internal amino acid sequence of the purified enzyme. The DMSO reductase gene coded for 822 amino acids (2466 base pairs, M(r) = 89,206) as a precursor form having a signal peptide of 42 amino acids. The deduced amino acid sequence had high homology with those of some enzymes containing a molybdenum cofactor: trimethyl amine N-oxide reductase (48%), biotin sulfoxide reductase (44%), and DMSO reductase (29%) of Escherichia coli.
利用基于纯化酶内部氨基酸序列合成的寡核苷酸探针,分离出了光合细菌球形红杆菌反硝化亚种中编码含钼辅因子的二甲基亚砜(DMSO)还原酶的基因。DMSO还原酶基因编码822个氨基酸(2466个碱基对,M(r)=89206),为具有42个氨基酸信号肽的前体形式。推导的氨基酸序列与一些含钼辅因子的酶具有高度同源性:大肠杆菌的三甲胺N-氧化物还原酶(48%)、生物素亚砜还原酶(44%)和DMSO还原酶(29%)。