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Molecular cloning and nucleotide sequence of the alpha-toxin (phospholipase C) of Clostridium perfringens.

机译:产气荚膜梭菌α-毒素(磷脂酶C)的分子克隆和核苷酸序列。

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摘要

A fragment of DNA containing the gene coding for the phospholipase C (alpha-toxin) of Clostridium perfringens was cloned into Escherichia coli. The cloned DNA appeared to code only for the alpha-toxin and contained both the coding region and its associated gene promoter. The nucleotide sequence of the cloned DNA was determined, and an open reading frame was identified which encoded a protein with a molecular weight of 42,528. By comparison of the gene sequence with the N-terminal amino acid sequence of the protein, a 28-amino-acid signal sequence was identified. The gene promoter showed considerable homology with the E. coli sigma 55 consensus promoter sequences, and this may explain why the gene was expressed by E. coli. The cloned gene product appeared to be virtually identical to the native protein. A 77-amino-acid stretch that was close to the N terminus of the alpha-toxin showed considerable homology with similarly located regions of the Bacillus cereus phosphatidylcholine, preferring phospholipase C and weaker homology with the phospholipase C from Pseudomonas aeruginosa.
机译:将含有编码产气荚膜梭菌磷脂酶C(α-毒素)基因的DNA片段克隆到大肠杆菌中。克隆的DNA似乎仅编码α毒素,并且既包含编码区,又包含其相关的基因启动子。确定克隆的DNA的核苷酸序列,并鉴定出可读框,其编码分子量为42,528的蛋白质。通过将基因序列与蛋白质的N端氨基酸序列进行比较,鉴定出28个氨基酸的信号序列。该基因启动子与大肠杆菌sigma 55共有启动子序列具有相当的同源性,这可以解释为什么该基因由大肠杆菌表达。克隆的基因产物似乎与天然蛋白质几乎相同。接近α-毒素N末端的77个氨基酸段显示与蜡状芽胞杆菌磷脂酰胆碱的相似区域具有相当的同源性,更倾向于磷脂酶C,而与铜绿假单胞菌的磷脂酶C的同源性较弱。

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