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A组链球菌荚膜基因区域的分子分析:hasAB基因足以实现荚膜表达。

Molecular analysis of the capsule gene region of group A Streptococcus: the hasAB genes are sufficient for capsule expression.

作者信息

Ashbaugh C D, Albertí S, Wessels M R

机构信息

Channing Laboratory, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.

出版信息

J Bacteriol. 1998 Sep;180(18):4955-9. doi: 10.1128/JB.180.18.4955-4959.1998.

Abstract

Enzymes directing the biosynthesis of the group A streptococcal hyaluronic acid capsule are encoded in the hasABC gene cluster. Inactivation of hasC, encoding UDP-glucose pyrophosphorylase in the heavily encapsulated group A streptococcal strain 87-282, had no effect on capsule production, indicating that hasC is not required for hyaluronic acid synthesis and that an alternative source of UDP-glucose is available for capsule production. Nucleotide sequence and deletion mutation analysis of the 5.5 kb of DNA upstream of hasA revealed that this region is not required for capsule expression. Many (10 of 23) group A streptococcal strains were found to contain insertion element IS1239' approximately 50 nucleotides upstream of the -35 site of the hasA promoter. The presence of IS1239' upstream of hasA did not prevent capsule expression. These results elucidate the molecular architecture of the group A streptococcal chromosomal region upstream of the has operon, indicate that hasABC are the sole components of the capsule gene cluster, and demonstrate that hasAB are sufficient to direct capsule synthesis in group A streptococci.

摘要

指导A群链球菌透明质酸荚膜生物合成的酶由hasABC基因簇编码。在高度荚膜化的A群链球菌菌株87 - 282中,编码UDP - 葡萄糖焦磷酸化酶的hasC失活对荚膜产生没有影响,这表明透明质酸合成不需要hasC,并且存在UDP - 葡萄糖的替代来源用于荚膜产生。对hasA上游5.5 kb DNA的核苷酸序列和缺失突变分析表明,该区域对于荚膜表达不是必需的。发现许多(23株中的10株)A群链球菌菌株在hasA启动子的 - 35位点上游约50个核苷酸处含有插入元件IS1239'。hasA上游存在IS1239'并不妨碍荚膜表达。这些结果阐明了has操纵子上游A群链球菌染色体区域的分子结构,表明hasABC是荚膜基因簇的唯一组成部分,并证明hasAB足以指导A群链球菌中的荚膜合成。

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