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从葡萄酒植物乳杆菌中分离出的小热休克基因家族新成员hsp 18.55基因的克隆与特性分析

Cloning and characterization of the hsp 18.55 gene, a new member of the small heat shock gene family isolated from wine Lactobacillus plantarum.

作者信息

Spano G, Beneduce L, Perrotta C, Massa S

机构信息

Department of Food Science, Foggia University, via Napoli 25, 71100 Foggia, Italy.

出版信息

Res Microbiol. 2005 Mar;156(2):219-24. doi: 10.1016/j.resmic.2004.09.014. Epub 2004 Dec 15.

Abstract

Using a molecular approach based on PCR, RT-PCR and northern blot analysis, a new member of the small heat shock family of wine, Lactobacillus plantarum, was cloned and characterized. The protein sequence deduced from the isolated gene had a calculated molecular mass of 18.548 kDa and was therefore named HSP 18.55. The gene codes for a protein homologous to the previously characterized HSP 19.3 and HSP 18.5 and is co-transcribed with an upstream gene of unknown function. Analysis of the 5' flanking region of the hsp 18.55 gene revealed the presence of putative cis elements able to bind alternative sigma factor sigma(B). Based on its structure, the gene was classified as belonging to class II of the heat shock genes according to Bacillus subtilis nomenclature for shock-responsive genes. Expression of the newly identified small heat shock gene, analyzed by RT-PCR and northern blot analysis, was induced by a wide range of abiotic stresses including heat, cold and ethanol, suggesting that the small family of heat shock genes is probably involved in the general stress response in wine L. plantarum. Moreover, the expression of hsp 18.5, hsp 18.55 and hsp 19.3 genes, analyzed over a complete culture cycle, revealed that early growing cells contained substantial amounts of hsp 18.5, hsp 18.55 and hsp 19.3 mRNAs, which rapidly declined upon entry into stationary phase.

摘要

利用基于PCR、RT-PCR和Northern印迹分析的分子方法,克隆并鉴定了葡萄酒中植物乳杆菌小热休克家族的一个新成员。从分离基因推导的蛋白质序列计算分子量为18.548 kDa,因此命名为HSP 18.55。该基因编码一种与先前鉴定的HSP 19.3和HSP 18.5同源的蛋白质,并与一个功能未知的上游基因共转录。对hsp 18.55基因5'侧翼区域的分析揭示了能够结合替代sigma因子sigma(B)的假定顺式元件的存在。根据枯草芽孢杆菌应激反应基因的命名法,基于其结构,该基因被归类为热休克基因的II类。通过RT-PCR和Northern印迹分析对新鉴定的小热休克基因的表达进行分析,结果表明,包括热、冷和乙醇在内的多种非生物胁迫均可诱导其表达,这表明热休克基因小家族可能参与了葡萄酒植物乳杆菌的一般应激反应。此外,在整个培养周期中对hsp 18.5、hsp 18.55和hsp 19.3基因的表达进行分析,结果显示,早期生长的细胞含有大量的hsp 18.5、hsp 18.55和hsp 19.3 mRNA,进入稳定期后这些mRNA迅速下降。

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