首页> 外文期刊>Research in Microbiology >Molecular characterization of femA from Staphylococcus hominis and Staphylococcus saprophyticus, and femA-based discrimination of staphylococcal species.
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Molecular characterization of femA from Staphylococcus hominis and Staphylococcus saprophyticus, and femA-based discrimination of staphylococcal species.

机译:来自人葡萄球菌和腐生葡萄球菌的femA的分子特征,以及基于femA的葡萄球菌种类的鉴别。

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摘要

The femA gene encodes a protein precursor which plays a role in peptidoglycan biosynthesis in Staphylococcus aureus and is also considered as a factor influencing the level of methicillin resistance. A femA homologous gene was recently characterized in S. epidermidis, entailing the possibility of femA phylogenetic conservation in staphylococcal species. Accordingly, we assessed the presence of femA homologous genes in S. hominis and S. saprophyticus. Strategy for identification relied upon alignment of S. aureus and D. epidermidis femA sequences and upon identification of potentially conserved regions. Amplifications of portions of the femA genes were performed under permissive annealing conditions, by using several sets of primers designed to match the consensus regions. DNA sequencing of overlapping PCR fragments led to the characterization of the entire femA genes of S. hominis and S. saprophyticus, and provided more precise information on the femA start codon for all five species. The genomic organization of all these femA genes appeared highly conserved, with alternance of homologous and variable regions. On this basis, a consensus sequence of the femA gene was defined and interspecies variations were exploited to design strategies for staphylococci species-specific identification, including multiplex PCR amplification and a reverse hybridization assay.
机译:femA基因编码的蛋白质前体在金黄色葡萄球菌的肽聚糖生物合成中起作用,并且也被认为是影响甲氧西林耐药性水平的因素。最近在表皮葡萄球菌中鉴定了femA同源基因,这提示在葡萄球菌物种中femA系统发生保守。因此,我们评估了在人沙门氏菌和腐生链球菌中femA同源基因的存在。鉴定策略依赖于金黄色葡萄球菌和表皮葡萄球菌femA序列的比对以及潜在保守区域的鉴定。 femA基因的部分扩增是在允许的退火条件下进行的,使用了设计用于匹配共有区的几组引物。重叠PCR片段的DNA测序导致表征了S. hominis和S. saprophyticus的整个femA基因,并为所有五个物种的femA起始密码子提供了更精确的信息。所有这些femA基因的基因组组织看起来都是高度保守的,具有同源和可变区的交替。在此基础上,定义了femA基因的共有序列,并利用种间变异设计策略用于葡萄球菌物种特异性鉴定,包括多重PCR扩增和反向杂交测定。

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