Menon N K, Robbins J, Peck H D, Chatelus C Y, Choi E S, Przybyla A E
Department of Biochemistry, School of Chemical Sciences, University of Georgia, Athens 30602.
J Bacteriol. 1990 Apr;172(4):1969-77. doi: 10.1128/jb.172.4.1969-1977.1990.
DNA encompassing the structural genes of an Escherichia coli [NiFe] hydrogenase has been cloned and sequenced. The genes were identified as those encoding the large and small subunits of hydrogenase isozyme 1 based on NH2-terminal sequences of purified subunits (kindly provided by K. Francis and K. T. Shanmugam). The structural genes formed part of a putative operon that contained four additional open reading frames. We have designated the operon hya and the six open reading frames hyaA through F. hyaA and hyaB encode the small and large structural subunits, respectively. The nucleotide-derived amino acid sequence of hyaC has a calculated molecular mass of 27.6 kilodaltons, contains 20% aromatic residues, and has four potential membrane-spanning regions. Open reading frames hyaD through F could encode polypeptides of 21.5, 14.9, and 31.5 kilodaltons, respectively. These putative peptides have no homology to other reported protein sequences, and their functions are unknown.
包含大肠杆菌[NiFe]氢化酶结构基因的DNA已被克隆并测序。根据纯化亚基的NH2末端序列(由K. Francis和K. T. Shanmugam提供),这些基因被鉴定为编码氢化酶同工酶1的大亚基和小亚基的基因。这些结构基因是一个假定操纵子的一部分,该操纵子还包含另外四个开放阅读框。我们将该操纵子命名为hya,六个开放阅读框分别命名为hyaA至F。hyaA和hyaB分别编码小结构亚基和大结构亚基。hyaC的核苷酸推导氨基酸序列计算分子量为27.6千道尔顿,含有20%的芳香族残基,并有四个潜在的跨膜区域。开放阅读框hyaD至F分别可编码分子量为21.5、14.9和31.5千道尔顿的多肽。这些假定的肽与其他已报道的蛋白质序列无同源性,其功能未知。