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Lipoteichoic acid (LTA) modifications during osmotic stress adaptation in Lactobacillus casei BL23.

机译:干酪乳杆菌BL23在渗透胁迫适应过程中的脂磷壁酸(LTA)修饰。

摘要

The probiotic Gram-positive bacterium Lactobacillus casei BL23 is naturally confronted with salt- stress habitats. It has been previously reported that growth in high-salt medium, containing 0.8 M NaCl, leads to modifications in the cell envelope of this bacterium. In this study, we report that L. casei BL23 has an increased ability to form biofilms and to bind cations in high-salt conditions. This behaviour correlated with modifications of surface properties involving teichoic acids, which are important cell wall components. We also showed that, in these high-salt conditions, L. casei BL23 produces less of the cell wall polymer lipoteichoic acid (LTA), and that this anionic polymer has a shorter mean chain length and a lower level of D-alanyl-substitution. Analysis of the transcript levels of the dltABCD operon, encoding the enzymes required for the incorporation of D-alanine into anionic polymers, showed a 16-fold reduction in mRNA levels, which is consistent with a decrease in D-alanine substitutions on LTA. Furthermore, a 13-fold reduction in the transcript levels was observed for the gene LCABL_09330 coding for a putative LTA synthase. To provide further experimental evidence that LCABL_09330 is a true LTA synthase (LtaS) in L. casei BL23, the enzymic domain was cloned and expressed in E. coli. The purified protein was able to hydrolyse the membrane lipid phosphatidylglycerol as expected for an LTA synthase enzyme, and hence LCABL_09330 was renamed LtaS. The purified enzyme showed Mn2+-ion dependent activity, and its activity was modulated by differences in NaCl concentration. The decrease in both ltaS transcript levels and enzyme activity observed in high-salt conditions might influence the length of the LTA backbone chain. A putative function of the modified LTA structure is discussed that is compatible with the growth under salt-stress conditions and with the overall envelope modifications taking place during this stress condition.
机译:益生菌革兰氏阳性细菌干酪乳杆菌BL23自然面对盐胁迫的栖息地。以前已经报道过,在含有0.8M NaCl的高盐培养基中的生长导致该细菌的细胞包膜的修饰。在这项研究中,我们报告了干酪乳杆菌BL23在高盐条件下具有更高的形成生物膜和结合阳离子的能力。这种行为与涉及到作为细胞壁重要成分的磷壁酸的表面性质的改变有关。我们还表明,在这些高盐条件下,干酪乳杆菌BL23产生较少的细胞壁聚合物脂磷壁酸(LTA),并且该阴离子聚合物的平均链长较短且D-丙氨酰取代水平较低。分析dltABCD操纵子的转录水平,该转录水平编码将D-丙氨酸掺入阴离子聚合物所需的酶,表明mRNA水平降低了16倍,这与LTA上D-丙氨酸取代的减少是一致的。此外,观察到编码假定的LTA合酶的基因LCABL_09330的转录水平降低了13倍。为了提供进一步的实验证据,表明LCABL_09330是干酪乳杆菌BL23中的真正LTA合酶(LtaS),该酶域被克隆并在大肠杆菌中表达。纯化的蛋白质能够如LTA合酶所预期的那样水解膜脂质磷脂酰甘油,因此LCABL_09330被重命名为LtaS。纯化的酶显示出Mn2 +离子依赖性活性,其活性受NaCl浓度差异的调节。在高盐条件下观察到的ltaS转录水平和酶活性的下降都可能影响LTA主链的长度。讨论了修饰的LTA结构的推定功能,该功能与盐胁迫条件下的生长以及在该胁迫条件下发生的总体包膜修饰兼容。

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