Genetics Department, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran.
Genetics Department, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran.
Microbiol Res. 2014 Feb-Mar;169(2-3):232-8. doi: 10.1016/j.micres.2013.06.010. Epub 2013 Aug 3.
Streptomyces strain C-2012 is a salt tolerant biocontrol PGPR that has been isolated from Iranian soil. The main aim of current study was finding strain C-2012 taxonomic position and to find the genes which are potentially involved in salt tolerance phenotype. Strain C-2012 chemotaxonomic, morphological and molecular characteristics indicate that this strain is a member of the genus Streptomyces. Phylogenetic analyses based on an almost complete 16S rRNA gene sequence revealed that this strain is closely related to Streptomyces rimosus JCM 4667(T). Also, DNA-DNA hybridization test estimated 74% relatedness between two strains and confirmed that C-2012 is a strain of S. rimosus. In order to find novel genes that are differentially expressed in response to the salt treatment, cDNA-AFLP was carried out. One of the selected expressed sequence tags (TDF-1) was found to be homologous to lon gene which produces a bacterial ATP-dependent proteases (proteases LA). Lon gene expression was induced following 450 mM salt (NaCl) treatment and its expression level was further (5.2-fold) increased in response to salt when ectoine was added to the medium. These results suggest that two protein protection systems including ectoine and ATP-dependent proteases synergistically are related. NaCl stress also caused an enhancement in the activity of extracellular protease.
C-2012 链霉菌是一种耐盐生物防治 PGPR,它是从伊朗土壤中分离出来的。本研究的主要目的是确定菌株 C-2012 的分类地位,并找到可能与耐盐表型相关的基因。菌株 C-2012 的化学生态、形态和分子特征表明,该菌株是链霉菌属的一员。基于近乎完整的 16S rRNA 基因序列的系统发育分析表明,该菌株与棘孢小单孢菌 JCM 4667(T)密切相关。此外,DNA-DNA 杂交试验估计两株之间的相关性为 74%,证实 C-2012 是棘孢小单孢菌的一个菌株。为了找到在盐处理下差异表达的新基因,进行了 cDNA-AFLP 分析。所选表达序列标签(TDF-1)之一与 lon 基因同源,lon 基因产生一种细菌 ATP 依赖性蛋白酶(蛋白酶 LA)。Lon 基因在 450mM 盐(NaCl)处理后被诱导表达,当向培养基中添加 1,4-丁二醇时,其表达水平进一步(5.2 倍)增加。这些结果表明,包括 1,4-丁二醇和 ATP 依赖性蛋白酶在内的两种蛋白质保护系统协同相关。NaCl 胁迫还导致细胞外蛋白酶活性增强。