Spano G, Capozzi V, Vernile A, Massa S
Department of Food Science, Foggia University, Foggia, Italy.
J Appl Microbiol. 2004;97(4):774-82. doi: 10.1111/j.1365-2672.2004.02359.x.
Understanding the molecular response to stress tolerance of wine Lactobacillus plantarum.
Two genes codifying for heat shock proteins were cloned from wine L. plantarum. The coding regions of the two heat shock genes are 420 and 444 nucleotides long, and started with an ATG codon suggesting that they were translated. The protein sequences deduced from the isolated genes have a molecular mass of 18.483 and 19.282 kDa, respectively, and were therefore named hsp18.5 and hsp19.3. The expression of small heat shock genes was analysed by RT-PCR analysis. Moreover, the 5' and 3' noncoding regions were cloned and sequenced.
The expression of the heat shock genes was strongly induced by heat, cold and ethanol stress. Analysis of the 5' and 3' flanking regions of hsp18.5 and hsp19.3 genes, revealed the presence of an inverted repeat sequence (TTAGCACTC-N(9)-GAGTGCTAA) homologue to the CIRCE elements found to the upstream regulatory region of heat shock operons, and an inverted sequence that could form a stem and loop structure that it is likely to function as a transcriptional terminator. Based on their structures, the genes were classified as belonging to Class I of heat shock genes according to the B. subtilis nomenclature of heat response genes.
Small heat shock genes isolated from wine L. plantarum might have a role in preventing damage by cold stress.
了解葡萄酒植物乳杆菌对胁迫耐受性的分子反应。
从葡萄酒植物乳杆菌中克隆了两个编码热休克蛋白的基因。这两个热休克基因的编码区分别为420和444个核苷酸长,起始于ATG密码子,表明它们可被翻译。从分离出的基因推导的蛋白质序列分子量分别为18.483和19.282 kDa,因此分别命名为hsp18.5和hsp19.3。通过RT-PCR分析对小热休克基因的表达进行了分析。此外,对5'和3'非编码区进行了克隆和测序。
热休克基因的表达受到热、冷和乙醇胁迫的强烈诱导。对hsp18.5和hsp19.3基因5'和3'侧翼区域的分析显示,存在一个与热休克操纵子上游调控区中发现的CIRCE元件同源的反向重复序列(TTAGCACTC-N(9)-GAGTGCTAA),以及一个可能形成茎环结构并可能作为转录终止子发挥作用的反向序列。根据其结构,按照枯草芽孢杆菌热反应基因的命名法,这些基因被归类为热休克基因的I类。
从葡萄酒植物乳杆菌中分离出的小热休克基因可能在预防冷胁迫造成的损害方面发挥作用。