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DNA聚合酶I的5'至3'核酸外切酶活性对肺炎链球菌至关重要。

The 5' to 3' exonuclease activity of DNA polymerase I is essential for Streptococcus pneumoniae.

作者信息

Díaz A, Lacks S A, López P

机构信息

Centro de Investigaciones Biológicas, CSIC, Madrid, Spain.

出版信息

Mol Microbiol. 1992 Oct;6(20):3009-19. doi: 10.1111/j.1365-2958.1992.tb01759.x.

Abstract

Three different mutations were introduced in the polA gene of Streptococcus pneumoniae by chromosomal transformation. One mutant gene encodes a truncated protein that possesses 5' to 3' exonuclease but has lost polymerase activity. This mutation does not affect cell viability. Other mutated forms of polA that encode proteins with only polymerase activity or with no enzymatic activity could not substitute for the wild-type polA gene in the chromosome unless the 5' to 3' exonuclease domain was encoded elsewhere in the chromosome. Thus, it appears that the 5' to 3' exonuclease activity of the DNA polymerase I is essential for cell viability in S. pneumoniae. Absence of the polymerase domain of DNA polymerase I slightly diminished the ability of S. pneumoniae to repair DNA lesions after ultraviolet irradiation. However, the polymerase domain of the pneumococcal DNA polymerase I gave almost complete complementation of the polA5 mutation in Escherichia coli with respect to resistance to ultraviolet irradiation.

摘要

通过染色体转化,在肺炎链球菌的polA基因中引入了三种不同的突变。一种突变基因编码一种截短的蛋白质,该蛋白质具有5'至3'外切核酸酶活性,但已丧失聚合酶活性。这种突变不影响细胞活力。polA的其他突变形式编码仅具有聚合酶活性或无酶活性的蛋白质,除非5'至3'外切核酸酶结构域在染色体的其他位置编码,否则它们不能替代染色体中的野生型polA基因。因此,似乎DNA聚合酶I的5'至3'外切核酸酶活性对于肺炎链球菌的细胞活力至关重要。DNA聚合酶I的聚合酶结构域缺失会略微降低肺炎链球菌在紫外线照射后修复DNA损伤的能力。然而,肺炎球菌DNA聚合酶I的聚合酶结构域在抗紫外线照射方面几乎完全互补了大肠杆菌中的polA5突变。

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