sodium;
NADH;
ubiquinone;
electron transport;
flavin;
site-directed mutagenesis;
Vibrio cholerae;
D O I:
10.1016/S0014-5793(01)02224-4
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 [生物化学与分子生物学];
081704 [应用化学];
摘要:
The Na+-translocating NADH:quinone oxidoreductase (Na+-NQR) is present in the membranes of a number of marine bacteria and pathogenic bacteria. Two of the six subunits of the Na+-NQR, NqrB and NqrC, have been previously shown to contain covalently bound flavin adenine mononucleotide (FMN). In the current work, the cloning of nqrC from Vibrio cholerae is reported, The gene has been expressed in V. cholerae and shown to contain one equivalent of covalently bound FMN. In contrast, no covalent flavin was detected when threonine-225 was replaced by leucine, The data show that the FMN attachment does not require assembly of the enzyme and are consistent with the unusual threonine attachment site. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
机构:Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
Kawagishi, I
;
Homma, M
论文数: 0引用数: 0
h-index: 0
机构:
Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, JapanNagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
机构:Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
Kawagishi, I
;
Homma, M
论文数: 0引用数: 0
h-index: 0
机构:
Nagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, JapanNagoya Univ, Grad Sch Sci, Div Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan