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Molecular cloning and expression of the spsB gene encoding an essential type I signal peptidase from Staphylococcus aureus.

机译:编码金黄色葡萄球菌必不可少的I型信号肽酶的spsB基因的分子克隆和表达。

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摘要

The gene, spsB, encoding a type I signal peptidase has been cloned from the gram-positive eubacterium Staphylococcus aureus. The gene encodes a protein of 191 amino acid residues with a calculated molecular mass of 21,692 Da. Comparison of the protein sequence with those of known type I signal peptidases indicates conservation of amino acid residues known to be important or essential for catalytic activity. The enzyme has been expressed to high levels in Escherichia coli and has been demonstrated to possess enzymatic activity against E. coli preproteins in vivo. Experiments whereby the spsB gene was transferred to a plasmid that is temperature sensitive for replication indicate that spsB is an essential gene. We identified an open reading frame immediately upstream of the spsB gene which encodes a type I signal peptidase homolog of 174 amino acid residues with a calculated molecular mass of 20,146 Da that is predicted to be devoid of catalytic activity.
机译:已从革兰氏阳性真细菌金黄色葡萄球菌克隆了编码I型信号肽酶的基因spsB。该基因编码一个191个氨基酸残基的蛋白质,计算的分子量为21692 Da。蛋白质序列与已知的I型信号肽酶序列的比较表明,保守的氨基酸残基对于催化活性是重要的或必不可少的。该酶已在大肠杆菌中高水平表达,并已证明在体内具有针对大肠杆菌前蛋白的酶活性。将spsB基因转移到对复制敏感的质粒上的实验表明spsB是必需基因。我们确定了紧邻spsB基因上游的开放阅读框,该框架编码174个氨基酸残基的I型信号肽酶同源物,其计算分子量为20,146 Da,预计没有催化活性。

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