首页> 美国卫生研究院文献>Journal of Bacteriology >Cloning and nucleotide sequence of the Vibrio cholerae hemagglutinin/protease (HA/protease) gene and construction of an HA/protease-negative strain.
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Cloning and nucleotide sequence of the Vibrio cholerae hemagglutinin/protease (HA/protease) gene and construction of an HA/protease-negative strain.

机译:霍乱弧菌血凝素/蛋白酶(HA /蛋白酶)基因的克隆和核苷酸序列以及HA /蛋白酶阴性菌株的构建。

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摘要

The structural gene hap for the extracellular hemagglutinin/protease (HA/protease) of Vibrio cholerae was cloned and sequenced. The cloned DNA fragment contained a 1,827-bp open reading frame potentially encoding a 609-amino-acid polypeptide. The deduced protein contains a putative signal sequence followed by a large propeptide. The extracellular HA/protease consists of 414 amino acids with a computed molecular weight of 46,700. In the absence of protease inhibitors, this is processed to the 32-kDa form which is usually isolated. The deduced amino acid sequence of the mature HA/protease showed 61.5% identity with the Pseudomonas aeruginosa elastase. The cloned hap gene was inactivated and introduced into the chromosome of V. cholerae by recombination to construct the HA/protease-negative strain HAP-1. The cloned fragment containing the hap gene was then shown to complement the mutant strain.
机译:霍乱弧菌胞外血凝素/蛋白酶(HA /蛋白酶)的结构基因hap被克隆并测序。克隆的DNA片段包含一个1,827-bp的开放阅读框,可能编码609个氨基酸的多肽。推导的蛋白质包含一个推定的信号序列,后接一个大的前肽。细胞外HA /蛋白酶由414个氨基酸组成,计算的分子量为46,700。在不存在蛋白酶抑制剂的情况下,将其加工为通常分离的32 kDa形式。推导的成熟HA /蛋白酶的氨基酸序列与铜绿假单胞菌弹性蛋白酶显示61.5%的同一性。将克隆的hap基因失活,并通过重组将其引入霍乱弧菌的染色体,以构建HA /蛋白酶阴性菌株HAP-1。然后显示了包含hap基因的克隆片段与突变菌株互补。

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