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化脓性链菌素:一种由马链球菌兽疫亚种产生的新型、质粒编码的抗菌蛋白(细菌素)。

Dysgalacticin: a novel, plasmid-encoded antimicrobial protein (bacteriocin) produced by Streptococcus dysgalactiae subsp. equisimilis.

作者信息

Heng Nicholas C K, Ragland Nancy L, Swe Pearl M, Baird Hayley J, Inglis Megan A, Tagg John R, Jack Ralph W

机构信息

Department of Microbiology and Immunology, University of Otago, PO Box 56, Dunedin, New Zealand.

出版信息

Microbiology (Reading). 2006 Jul;152(Pt 7):1991-2001. doi: 10.1099/mic.0.28823-0.

Abstract

Dysgalacticin is a novel bacteriocin produced by Streptococcus dysgalactiae subsp. equisimilis strain W2580 that has a narrow spectrum of antimicrobial activity directed primarily against the principal human streptococcal pathogen Streptococcus pyogenes. Unlike many previously described bacteriocins of Gram-positive bacteria, dysgalacticin is a heat-labile 21.5 kDa anionic protein that kills its target without inducing lysis. The N-terminal amino acid sequence of dysgalacticin [Asn-Glu-Thr-Asn-Asn-Phe-Ala-Glu-Thr-Gln-Lys-Glu-Ile-Thr-Thr-Asn-(Asn)-Glu-Ala] has no known homologue in publicly available sequence databases. The dysgalacticin structural gene, dysA, is located on the indigenous plasmid pW2580 of strain W2580 and encodes a 220 aa preprotein which is probably exported via a Sec-dependent transport system. Natural dysA variants containing conservative amino acid substitutions were also detected by sequence analyses of dysA elements from S. dysgalactiae strains displaying W2580-like inhibitory profiles. Production of recombinant dysgalacticin by Escherichia coli confirmed that this protein is solely responsible for the inhibitory activity exhibited by strain W2580. A combination of in silico secondary structure prediction and reductive alkylation was employed to demonstrate that dysgalacticin has a novel structure containing a disulphide bond essential for its biological activity. Moreover, dysgalacticin displays similarity in predicted secondary structure (but not primary amino acid sequence or inhibitory spectrum) with another plasmid-encoded streptococcal bacteriocin, streptococcin A-M57 from S. pyogenes, indicating that dysgalacticin represents a prototype of a new class of antimicrobial proteins.

摘要

乳腺炎性链球菌素是由乳房炎链球菌马链球菌亚种W2580菌株产生的一种新型细菌素,其抗菌活性谱较窄,主要针对主要的人类链球菌病原体化脓性链球菌。与许多先前描述的革兰氏阳性菌细菌素不同,乳腺炎性链球菌素是一种热不稳定的21.5 kDa阴离子蛋白,它能杀死靶标而不诱导裂解。乳腺炎性链球菌素的N端氨基酸序列[天冬酰胺-谷氨酸-苏氨酸-天冬酰胺-天冬酰胺-苯丙氨酸-丙氨酸-谷氨酸-苏氨酸-谷氨酰胺-赖氨酸-谷氨酸-异亮氨酸-苏氨酸-苏氨酸-天冬酰胺-(天冬酰胺)-谷氨酸-丙氨酸]在公开可用的序列数据库中没有已知的同源物。乳腺炎性链球菌素结构基因dysA位于W2580菌株的内源质粒pW2580上,编码一个220个氨基酸的前体蛋白,该蛋白可能通过Sec依赖性转运系统输出。通过对显示W2580样抑制谱的乳房炎链球菌菌株的dysA元件进行序列分析也检测到了含有保守氨基酸取代的天然dysA变体。大肠杆菌产生重组乳腺炎性链球菌素证实该蛋白是W258菌株所表现出的抑制活性的唯一原因。通过计算机辅助二级结构预测和还原烷基化相结合的方法证明,乳腺炎性链球菌素具有一种新的结构,该结构包含一个对其生物活性至关重要的二硫键。此外,乳腺炎性链球菌素在预测的二级结构(但不是一级氨基酸序列或抑制谱)上与另一种质粒编码的链球菌细菌素——化脓性链球菌的链球菌素A-M57相似,这表明乳腺炎性链球菌素代表了一类新型抗菌蛋白的原型。

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