Section of Microbiology and MRC Centre for Molecular Bacteriology and Infection, Imperial College London, South Kensington Campus, London, UK.
Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, IQUIBICEN-CONICET, Ciudad Universitaria, C1428EGA Buenos Aires, Argentina.
Microbiology (Reading). 2013 Nov;159(Pt 11):2416-2426. doi: 10.1099/mic.0.070607-0. Epub 2013 Sep 6.
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 Mn(2+)-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.
产酸乳杆菌 BL23 是一种革兰氏阳性益生菌,其天然生存在盐胁迫的环境中。先前的研究表明,在含有 0.8 M NaCl 的高盐培养基中生长会导致该细菌的细胞包膜发生变化。在本研究中,我们报告称,在高盐条件下,L. casei BL23 具有更强的形成生物膜和结合阳离子的能力。这种行为与涉及到壁磷壁酸的表面性质的变化有关,而壁磷壁酸是细胞壁的重要组成部分。我们还表明,在这些高盐条件下,L. casei BL23 产生的细胞壁聚合物脂磷壁酸(LTA)较少,并且这种阴离子聚合物的平均链长较短,D-丙氨酸取代程度较低。对编码将 D-丙氨酸掺入阴离子聚合物所需酶的 dltABCD 操纵子的转录水平进行分析表明,mRNA 水平降低了 16 倍,这与 LTA 上 D-丙氨酸取代减少一致。此外,LCABL_09330 基因(编码推定的 LTA 合酶)的转录水平也观察到了 13 倍的降低。为了提供进一步的实验证据表明 LCABL_09330 是 L. casei BL23 中真正的 LTA 合酶(LtaS),对其酶结构域进行了克隆和在大肠杆菌中的表达。纯化的蛋白能够水解膜脂质磷脂酰甘油,如 LTA 合酶酶所预期的那样,因此 LCABL_09330 被重新命名为 LtaS。纯化的酶显示 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降低可能会影响 LTA 主链的长度。讨论了修饰后的 LTA 结构的一种可能功能,该功能与在盐胁迫条件下的生长以及在这种胁迫条件下发生的整个包膜变化兼容。