Zenno S, Saigo K
Department of Biophysics and Biochemistry, School of Science, University of Tokyo, Japan.
J Bacteriol. 1994 Jun;176(12):3544-51. doi: 10.1128/jb.176.12.3544-3551.1994.
Genes encoding NAD(P)H-flavin oxidoreductases (flavin reductases) similar in both size and sequence to Fre, the most abundant flavin reductase in Escherichia coli, were identified in four species of luminous bacteria, Photorhabdus luminescens (ATCC 29999), Vibrio fischeri (ATCC 7744), Vibrio harveyi (ATCC 33843), and Vibrio orientalis (ATCC 33934). Nucleotide sequence analysis showed Fre-like flavin reductases in P. luminescens and V. fischeri to consist of 233 and 236 amino acids, respectively. As in E. coli Fre, Fre-like enzymes in luminous bacteria preferably used riboflavin as an electron acceptor when NADPH was used as an electron donor. These enzymes also were good suppliers of reduced flavin mononucleotide (FMNH2) to the bioluminescence reaction. In V. fischeri, the Fre-like enzyme is a minor flavin reductase representing < 10% of the total FMN reductase. That the V. fischeri Fre-like enzyme has no appreciable homology in amino acid sequence to the major flavin reductase in V. fischeri, FRase I, indicates that at least two different types of flavin reductases supply FMNH2 to the luminescence system in V. fischeri. Although Fre-like flavin reductases are highly similar in sequence to luxG gene products (LuxGs), Fre-like flavin reductases and LuxGs appear to constitute two separate groups of flavin-associated proteins.
在四种发光细菌中鉴定出了编码与大肠杆菌中最丰富的黄素还原酶Fre在大小和序列上相似的NAD(P)H-黄素氧化还原酶(黄素还原酶)的基因,这四种发光细菌分别是发光光杆状菌(ATCC 29999)、费氏弧菌(ATCC 7744)、哈氏弧菌(ATCC 33843)和东方弧菌(ATCC 33934)。核苷酸序列分析表明,发光光杆状菌和费氏弧菌中的类Fre黄素还原酶分别由233和236个氨基酸组成。与大肠杆菌Fre一样,发光细菌中的类Fre酶在以NADPH作为电子供体时,优选使用核黄素作为电子受体。这些酶也是生物发光反应中还原黄素单核苷酸(FMNH2)的良好供应者。在费氏弧菌中,类Fre酶是一种次要的黄素还原酶,占总FMN还原酶的比例不到10%。费氏弧菌的类Fre酶在氨基酸序列上与费氏弧菌中的主要黄素还原酶FRase I没有明显的同源性,这表明至少有两种不同类型的黄素还原酶为费氏弧菌的发光系统提供FMNH2。尽管类Fre黄素还原酶在序列上与luxG基因产物(LuxGs)高度相似,但类Fre黄素还原酶和LuxGs似乎构成了两组不同的黄素相关蛋白。