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褐球固氮菌氢化酶基因簇:四个辅助基因hupA、hupB、hupY和hupC的序列及遗传分析

The Azotobacter chroococcum hydrogenase gene cluster: sequences and genetic analysis of four accessory genes, hupA, hupB, hupY and hupC.

作者信息

Tibelius K H, Du L, Tito D, Stejskal F

机构信息

Department of Microbiology, McGill University, Ste. Anne de Bellevue, Québec, Canada.

出版信息

Gene. 1993 May 15;127(1):53-61. doi: 10.1016/0378-1119(93)90616-b.

Abstract

The Azotobacter chroococcum chromosome contains a region spanning about 14 kb associated with hydrogen-uptake (Hup) activity. The small and large subunits of the hydrogenase are encoded by the structural genes hupS and hupL. Two other genes, hupD and hupE, are located 8.9 kb downstream from hupL and are required for the formation of a catalytically active hydrogenase. In this study, we determined the nucleotide sequence of a 3.8-kb region immediately upstream from hupD. This revealed four additional closely linked ORFs which we designated hupA, hupB, hupY and hupC; these genes potentially encode polypeptides with predicted masses of 12.6, 33.3, 80.4 and 9.0 kDa, respectively. This cluster of genes was shown to be essential for hydrogenase activity by insertion mutagenesis using antibiotic-resistance gene cassettes and a Tn5 derivative carrying a promoterless lacZ gene. A 10.5-kb fragment of DNA beginning 3.4 kb downstream from hupL, and including the sequenced region, was able to complement hupA and hupY mutants, supporting earlier evidence for a promoter downstream from hupSL. The deduced amino acid sequences of hupA, hupB and hupC are homologous to the Escherichia coli hypA, hypB and hypC gene products, respectively. Of particular interest is the fact that there is no homologue of the hupY gene product in the E. coli hyp operon. Mutations in hupY or hupB had little effect on beta-galactosidase activity in a strain also carrying a hupL::lacZ fusion, showing that hupY and hupB are not major factors in regulating the transcription of the hydrogenase structural genes.

摘要

褐球固氮菌染色体含有一个跨度约14 kb的区域,与吸氢(Hup)活性相关。氢化酶的小亚基和大亚基由结构基因hupS和hupL编码。另外两个基因hupD和hupE位于hupL下游8.9 kb处,是形成具有催化活性的氢化酶所必需的。在本研究中,我们测定了hupD上游紧邻的一个3.8 kb区域的核苷酸序列。这揭示了另外四个紧密连锁的开放阅读框,我们将其命名为hupA、hupB、hupY和hupC;这些基因可能分别编码预测分子量为12.6、33.3、80.4和9.0 kDa的多肽。通过使用抗生素抗性基因盒和携带无启动子lacZ基因的Tn5衍生物进行插入诱变,表明这一组基因对于氢化酶活性是必需的。从hupL下游3.4 kb开始并包括测序区域的一个10.5 kb DNA片段能够互补hupA和hupY突变体,支持了hupSL下游存在启动子的早期证据。hupA、hupB和hupC推导的氨基酸序列分别与大肠杆菌hypA、hypB和hypC基因产物同源。特别有趣的是,在大肠杆菌hyp操纵子中没有hupY基因产物的同源物。在同时携带hupL::lacZ融合的菌株中,hupY或hupB的突变对β-半乳糖苷酶活性影响很小,表明hupY和hupB不是调节氢化酶结构基因转录的主要因素。

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