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Molecular cloning, sequencing, and expression of lytM, a unique autolytic gene of Staphylococcus aureus.

机译:lytM(金黄色葡萄球菌独特的自溶基因)的分子克隆,测序和表达。

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摘要

A gene encoding an autolytic activity was identified in an autolysis-deficient mutant (Lyt-) of Staphylococcus aureus which produces only a single band in autolytic-activity gels (N. Mani, P. Tobin, and R. K. Jayaswal, J. Bacteriol. 175:1493-1499, 1993). An open reading frame, designated lytM, of 948 bp that could encode a polypeptide of 316 amino acid residues was identified. The calculated molecular mass of the lytM gene product (34.4 kDa) corresponded to that of the autolytic activity detected (approximately 36 kDa) in the Lyt- mutant. Results deduced from amino acid sequence analysis and N-terminal amino acid sequencing data suggest that LytM is a secreted protein. The C-terminal region of the putative protein encoded by lytM showed 51% identity with the N-terminal region of the mature lysostaphin from Staphylococcus simulans and 50% identity with the N-terminal region of ALE-1 from Staphylococcus capitis EPK1. Northern blot analysis showed that lytM expresses a transcript of approximately 955 bp, as predicted from the DNA sequence. Escherichia coli clones carrying the lytM gene exhibited autolytic-activity bands of approximately 36 kDa as well as of 19 and 22 kDa in activity gels. The lytM gene was mapped to the SmaI-D fragment on the S. aureus chromosome. Mapping data and results of hybridization experiments with primers generated from gene sequences of known autolytic genes of S. aureus clearly indicate that the lytM gene is distinct from other staphylococcal autolytic genes reported to date.
机译:在金黄色葡萄球菌的自溶缺陷型突变体(Lyt-)中鉴定出一种编码自溶活性的基因,该突变体在自溶活性凝胶中仅产生一条条带(N. Mani,P. Tobin和RK Jayaswal,J. Bacteriol。175)。 :1493-1499,1993)。鉴定了一个948 bp的开放阅读框,称为lytM,其可以编码316个氨基酸残基的多肽。 lytM基因产物的计算分子量(34.4 kDa)与在Lyt突变体中检测到的自溶活性(约36 kDa)相对应。从氨基酸序列分析和N端氨基酸测序数据推导出的结果表明LytM是一种分泌蛋白。 lytM编码的推定蛋白的C末端区域与来自葡萄球菌的成熟溶葡萄球菌素的N末端区域具有51%的一致性,与来自葡萄球菌EPK1的ALE-1的N末端区域具有50%的一致性。 Northern印迹分析表明,根据DNA序列的预测,lytM表达约955 bp的转录本。携带lytM基因的大肠杆菌克隆在活性凝胶中显示出约36 kDa以及19和22 kDa的自溶活性带。 lytM基因被定位到金黄色葡萄球菌染色体上的SmaI-D片段。映射数据和杂交实验结果与从金黄色葡萄球菌已知自溶基因的基因序列产生的引物清楚地表明,lytM基因与迄今报道的其他葡萄球菌自溶基因不同。

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  • 作者

    Ramadurai, L; Jayaswal, R K;

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  • 年度 1997
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