Voordouw G, Walker J E, Brenner S
Eur J Biochem. 1985 May 2;148(3):509-14. doi: 10.1111/j.1432-1033.1985.tb08868.x.
The gene encoding the hydrogenase from Desulfovibrio vulgaris (Hildenborough) has been cloned in Escherichia coli. D. vulgaris DNA was digested with the restriction endonucleases EcoRI and SalI and ligated into the vector pUC9 [Vieira, J. & Messing, J. (1982) Gene 19, 259-268], which had been cut with these same enzymes. Approximately 9000 recombinant clones were obtained by transformation of E. coli JM 101 followed by growth on rich plates with ampicillin for selection and isopropyl-beta-D-thiogalactoside and 5-bromo-4-chloro-3-indolyl-beta-D-galactopyranoside present for detection of recombinants. The recombinant clones were then screened for production of immunoreactive proteins with rabbit antisera against purified hydrogenase and 125I-labelled protein A. 28 positive clones were found in this initial screening. These were further tested in an immunocompetition experiment, which showed that the protein product from one clone behaved identically to purified hydrogenase. The plasmid pHV15 isolated from this clone has a 4.7 X 10(3)-base-pair SalI/EcoRI insert. Cells of E. coli JM 101 transformed with pHV 15 produce a hydrogenase polypeptide of molecular mass 46 kDa as detected by Western blotting. The mass, as well as the Cleveland mapping pattern of the polypeptide produced by E. coli, are identical with those of the hydrogenase isolated from D. vulgaris (Hildenborough). Southern blotting of restriction-enzyme-digested D. vulgaris DNA, using the nick-translated 4.7 X 10(3)-base-pair SalI/EcoRI fragment as a probe, indicates the presence of a single gene with an internal PstI site. The NH2-terminal sequence of the hydrogenase was determined to be: (sequence in text). This information should allow an unambiguous identification of the hydrogenase gene.
编码普通脱硫弧菌(希登伯勒菌株)氢化酶的基因已在大肠杆菌中克隆出来。用限制性内切酶EcoRI和SalI消化普通脱硫弧菌的DNA,然后将其连接到用相同酶切割过的载体pUC9 [维埃拉,J. 和梅辛,J.(1982年)《基因》19卷,259 - 268页] 中。通过转化大肠杆菌JM 101,然后在含有氨苄青霉素的丰富平板上生长以进行选择,并加入异丙基 - β - D - 硫代半乳糖苷和5 - 溴 - 4 - 氯 - 3 - 吲哚基 - β - D - 吡喃半乳糖苷来检测重组体,获得了大约9000个重组克隆。然后用针对纯化氢化酶的兔抗血清和125I标记的蛋白A对重组克隆进行筛选,以检测免疫反应性蛋白的产生。在初次筛选中发现了28个阳性克隆。对这些克隆在免疫竞争实验中进行了进一步检测,结果表明来自一个克隆的蛋白产物与纯化的氢化酶表现相同。从该克隆中分离出的质粒pHV15有一个4.7×10³碱基对的SalI/EcoRI插入片段。用pHV 15转化的大肠杆菌JM 101细胞产生一种分子量为46 kDa的氢化酶多肽,通过蛋白质印迹法检测到。大肠杆菌产生的多肽的分子量以及克利夫兰图谱模式与从普通脱硫弧菌(希登伯勒菌株)分离出的氢化酶相同。用缺口平移的4.7×10³碱基对的SalI/EcoRI片段作为探针,对用限制性内切酶消化的普通脱硫弧菌DNA进行Southern印迹分析,表明存在一个具有内部PstI位点的单一基因。确定氢化酶的NH₂末端序列为:(文中序列)。这些信息应能明确鉴定氢化酶基因。