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Cloning of type 8 capsule genes and analysis of gene clusters for the production of different capsular polysaccharides in Staphylococcus aureus.

机译:金黄色葡萄球菌中8种荚膜基因的克隆和基因簇的分析,以产生不同的荚膜多糖。

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摘要

Eleven serotypes of capsular polysaccharide from Staphylococcus aureus have been reported. We have previously cloned a cluster of type 1 capsule (cap1) genes responsible for type 1 capsular polysaccharide biosynthesis in S. aureus M. To clone the type 8 capsule (cap8) genes, a plasmid library of type 8 strain Becker was screened with a labelled DNA fragment containing the cap1 genes under low-stringency conditions. One recombinant plasmid containing a 14-kb insert was chosen for further study and found to complement 14 of the 18 type 8 capsule-negative (Cap8-) mutants used in the study. Additional library screening, subcloning, and complementation experiments showed that all of the 18 Cap8- mutants were complemented by DNA fragments derived from a 20.5-kb contiguous region of the Becker chromosome. The mutants were mapped into six complementation groups, indicating that the cap8 genes are clustered. By Southern hybridization analyses under high-stringency conditions, we found that DNA fragments containing the cap8 gene cluster show extensive homology with all 17 strains tested, including type 1 strains. By further Southern analyses and cloning of the cap8-related homolog from strain M, we show that strain M carries an additional capsule gene cluster different from the cap1 gene cluster. In addition, by using DNA fragments containing different regions of the cap8 gene cluster as probes to hybridize DNA from different strains, we found that the central region of the cap8 gene cluster hybridizes only to DNAs from certain strains tested whereas the flanking regions hybridize to DNAs of all strains tested. Thus, the cap8 gene clusters and its closely related homologs are likely to have organizations similar to those of the encapsulation genes of other bacterial systems.
机译:已经报道了来自金黄色葡萄球菌的荚膜多糖的11种血清型。我们以前已经克隆了负责金黄色葡萄球菌M中1型荚膜多糖生物合成的1型荚膜(cap1)基因簇。要克隆8型荚膜(cap8)基因,用8型菌株Becker筛选质粒。低严格条件下含有cap1基因的标记DNA片段。选择了一种包含14kb插入片段的重组质粒进行进一步研究,发现该质粒与研究中使用的18种8型胶囊阴性(Cap8-)突变体中的14种互补。额外的文库筛选,亚克隆和互补实验表明,所有18个Cap8-突变体均被衍生自Becker染色体20.5-kb连续区域的DNA片段所互补。突变体被映射到六个互补组,表明cap8基因是群集的。通过在高严格条件下的Southern杂交分析,我们发现含有cap8基因簇的DNA片段与所有17个菌株(包括1型菌株)均显示出广泛的同源性。通过进一步的Southern分析和菌株M的cap8相关同源物的克隆,我们显示菌株M携带了一个与cap1基因簇不同的附加胶囊基因簇。此外,通过使用包含cap8基因簇不同区域的DNA片段作为探针来杂交来自不同菌株的DNA,我们发现cap8基因簇的中心区域仅与来自某些测试菌株的DNA杂交,而侧翼区域则与DNA杂交。所有测试的菌株。因此,cap8基因簇及其密切相关的同源物可能具有与其他细菌系统的包封基因相似的组织。

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    Sau, S; Lee, C Y;

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  • 年度 1996
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  • 正文语种 en
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