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产气荚膜梭菌磷脂酶C基因的克隆与测序

Cloning and sequencing of a phospholipase C gene of Clostridium perfringens.

作者信息

Okabe A, Shimizu T, Hayashi H

机构信息

Department of Microbiology, Kagawa Medical School, Japan.

出版信息

Biochem Biophys Res Commun. 1989 Apr 14;160(1):33-9. doi: 10.1016/0006-291x(89)91616-1.

Abstract

The gene encoding phospholipase C (alpha-toxin) of Clostridium perfringens was cloned into lambda gt10. The maximal size of the coding region was 1.4 kb and the minimum was 1.1 kb as determined by subcloning into the vector pBR322 and testing for activity. The nucleotide sequence of this region contained a single open reading frame of 1194 bp corresponding to a protein of Mr 45473 with a possible N-terminal signal sequence of 28 amino acids which when removed, would give a mature protein of Mr 42521. This is in good agreement with the reported size of 43 kDa. The coding region has a dG + dC content of 33.7%, and the codon usage displays a pronounced preference for codons with the lowest dG + dC content.

摘要

产气荚膜梭菌编码磷脂酶C(α毒素)的基因被克隆到λgt10中。通过亚克隆到载体pBR322并检测活性,确定编码区的最大长度为1.4 kb,最小长度为1.1 kb。该区域的核苷酸序列包含一个1194 bp的单一开放阅读框,对应于一个分子量为45473的蛋白质,其可能的N端信号序列为28个氨基酸,去除该信号序列后,将产生一个分子量为42521的成熟蛋白质。这与报道的43 kDa大小非常吻合。编码区的dG + dC含量为33.7%,密码子使用情况显示出对dG + dC含量最低的密码子有明显偏好。

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