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Cloning of the Streptococcus mutans Gene Encoding Glucan Binding Protein B and Analysis of Genetic Diversity and Protein Production in Clinical Isolates

机译:葡聚糖结合蛋白B变异链球菌基因的克隆及临床分离株的遗传多样性和蛋白质生产分析

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摘要

Streptococcus mutans, the primary etiological agent of dental caries, produces several activities that promote its accumulation within the dental biofilm. These include glucosyltransferases, their glucan products, and proteins that bind glucan. At least three glucan binding proteins have been identified, and GbpB, the protein characterized in this study, appears to be novel. The gbpB gene was cloned and the predicted protein sequence contained several unusual features and shared extensive homology with a putative peptidoglycan hydrolase from group B streptococcus. Examination of gbpB genes from clinical isolates of S. mutans revealed that DNA polymorphisms, and hence amino acid changes, were limited to the central region of the gene, suggesting functional conservation within the amino and carboxy termini of the protein. The GbpB produced by clinical isolates and laboratory strains showed various distributions between cells and culture medium, and amounts of protein produced by individual strains correlated positively with their ability to grow as biofilms in an in vitro assay.
机译:变形链球菌是龋齿的主要病因,它产生几种促进其在牙齿生物膜内积累的活动。这些包括葡糖基转移酶,其葡聚糖产物和结合葡聚糖的蛋白质。已经鉴定出至少三种葡聚糖结合蛋白,并且该研究中表征的蛋白GbpB似乎是新颖的。克隆了gbpB基因,预测的蛋白质序列包含一些异常特征,并与B组链球菌的假定肽聚糖水解酶具有广泛的同源性。从变形链球菌的临床分离物中检测gbpB基因发现,DNA多态性以及氨基酸变化仅限于基因的中心区域,表明该蛋白质的氨基和羧基末端具有功能保守性。临床分离株和实验室菌株产生的GbpB在细胞和培养基之间显示出各种分布,单个菌株产生的蛋白质量与其在体外测定中作为生物膜的生长能力呈正相关。

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