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Osmotic stress adaptation in Lactobacillus casei BL23 leads to structural changes in the cell wall polymer lipoteichoic acid

机译:乳酸杆菌BL23中的渗透胁迫适应导致细胞壁聚合物脂酸酸的结构变化

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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乳酸杆菌酪虫Bl23天然与盐胁迫栖息地相反。先前已经报道,含有0.8M NaCl的高盐培养基的生长导致该细菌的细胞包膜中的修饰。在这项研究中,我们报告了L.酪蛋白BL23具有更高的形成生物膜的能力和在高盐条件下结合阳离子。这种行为与涉及噻吩的表面性质的修饰相关,这是重要的细胞壁组分。我们还表明,在这些高盐条件下,L.酪蛋白的BL23产生较少的细胞壁聚合物Lipoteichid酸(LTA),并且该阴离子聚合物具有较短的均线链长和较低水平的D-丙烷 - 取代水平。分析DLTABCS型术的转录物水平,编码将D-丙氨酸掺入阴离子聚合物中所需的酶,表明mRNA水平降低16倍,这与LTA的D-丙氨酸取代的降低一致。此外,针对推定的LTA合成酶编码的基因LCabl_09330,观察到转录水平的13倍降低。为了提供进一步的实验证据,即LCabl_09330是L.酪蛋白BL23中的真实LTA合酶(LTA),克隆酶结构域并在大肠杆菌中表达。纯化的蛋白质能够以预期的LTA合成酶水解膜脂磷脂酰甘油,因此LCABl_09330重命名LTA。纯化的酶显示出Mn 2 +下依赖性活性,其活性通过NaCl浓度的差异调节。在高盐条件下观察到的LTA转录水平和酶活性的降低可能影响LTA主链链的长度。讨论改性LTA结构的推定功能,其与盐胁迫条件下的生长相容,并且在这种应力条件下发生整体包络修饰。

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