首页> 外文期刊>Advances in Microbiology >The Wheat Pathogenesis Related Protein (TdPR1.2) Ensures Contrasting Behaviors to &i&E. coli&/i& Transformant Cells under Stress Conditions
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The Wheat Pathogenesis Related Protein (TdPR1.2) Ensures Contrasting Behaviors to &i&E. coli&/i& Transformant Cells under Stress Conditions

机译:小麦发病机制相关蛋白质(TDPR1.2)确保对造影行为与& l; e。 Coli& / i& 压力条件下的转化细胞

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The pathogenesis-related proteins 1 (PR-1) gene family play important roles in the plant metabolism in response to biotic and abiotic stresses. The wheat TdPR1.2 has been previously isolated and characterized. Here we showed by bio-informatic analysis that TdPR1.2 contains six cysteine residues that are conserved between all PR-1 proteins tested. Using ScanProsite tool, we found that TdPR1.2 structure has a CRISP family signature 1 and 2 located at the C-terminal part of the protein. Those two domains are conserved in many identified PR1.2 proteins in plants. Moreover, SignalIP-5.0 analysis revealed that TdPR1.2 contains a putative signal peptide formed by 25 amino acids at the N-terminal extremity. The presence of this signal peptide suggested that the mature proteins will be secreted after the cleavage of the signal sequence. Further, we investigate the role of the TdPR1.2 proteins in the growth of Escherichia coli transformants cells under different abiotic stresses. Our results showed that the full-length form of TdPR1.2 enhanced tolerance of E. coli against salt and osmotic stress but not to KCl. Moreover, TdPR1.2 protein confers bacterial tolerance to heavy metals in solid and liquid mediums. Based on these results, we suggest that the TdPR1.2 protein could play an important role in response to abiotic stress conditions.
机译:病因相关蛋白1(PR-1)基因家族在植物代谢中对生物和非生物应激作出重要作用。小麦TDPR1.2已经预先分离和表征。在这里,我们通过生物信息分析表明,TDPR1.2含有六个半胱氨酸残基,这些残留物在所有测试的所有PR-1蛋白之间保守。使用Scanperite工具,我们发现TDPR1.2结构具有位于蛋白质的C末端部分的清晰家族签名1和2。这些两个域在许多鉴定的PR1.2蛋白中保存在植物中。此外,SignaliP-5.0分析显示TDPR1.2含有由N-末端的25个氨基酸形成的推定信号肽。该信号肽的存在表明成熟蛋白在信号序列的切割后将分泌。此外,我们研究了TDPR1.2蛋白在不同的非生物胁迫下在大肠杆菌转化体细胞生长中的作用。我们的研究结果表明,TDPR1.2的全长形式增强了 e的耐受性。大肠杆菌对抗盐和渗透胁迫,但不是kcl。此外,TDPR1.2蛋白在固体和液体培养基中赋予对重金属的细菌耐受性。基于这些结果,我们表明TDPR1.2蛋白可以在反应非生物胁迫条件下发挥重要作用。

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