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Exploration of intraclonal adaptation mechanisms of Pseudomonas brassicacearum facing cadmium toxicity

机译:铜绿假单胞菌面对镉毒性的克隆内适应机制探讨

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摘要

Pseudomonas brassicacearum forms phenotypic variants in vitro as well as in planta during root colonization under natural conditions, leading to subpopulations (phase I and II cells) that differ in colony morphology and production of exoenzymes/secondary metabolites. The maximal concentration of cadmium allowing both variants growth was 25 μM; however, phase II cells accumulated fivefold higher Cd than phase I cells, even though both variants showed the same growth rate and kinetics, comprising a long stasis period (50 h). The whole transcriptome analysis of both variants in response to Cd was investigated using the home-made DNA microarrays. This analysis revealed completely different adaptation mechanisms developed by each variant to withstand and grow in the presence of the toxic. A re-organization of the cell wall to limit Cd entrance was noticed for phase I cells, as genes encoding levan exopolymers were downregulated at the expense of an upregulation of genes encoding alginate, and an upregulation of transporters such as cadA, and a downregulation of copper transporters. Phase II cells were unable to prevent Cd entrance and recruited genes under the control of oxyR and soxR regulation to face osmotic and oxidant stresses generated by Cd. Putrescine and spermidine metabolism appeared to play a central role in Cd tolerance. Microarray data were validated by biological analyses such as motility, oxidative stress assay, metabolite profiling with ICR-FT/MS and UPLC, capillary electrophoresis analysis of biogenic amines.
机译:黄铜假单胞菌在自然条件下在根部定殖期间在体外以及在植物中形成表型变体,导致亚群(I和II期细胞)的菌落形态和外酶/次级代谢产物的产生不同。允许两个变体生长的最大镉浓度为25μM;然而,尽管两个变体都显示出相同的生长速率和动力学,包括较长的停滞期(50小时),但II期细胞的Cd比I期细胞高五倍。使用自制的DNA微阵列研究了两种变体对Cd的完整转录组分析。这项分析揭示了每种变体开发出的完全不同的适应机制,它们可以在有毒物质存在下耐受和生长。对于I期细胞,注意到细胞壁的重组以限制Cd的进入,因为编码levan exopolymers的基因被下调,但代价是编码藻酸盐的基因上调,转运蛋白如cadA的上调和cadA的下调。铜运输车。 II期细胞无法阻止Cd进入,并在oxyR和soxR调控下募集基因来面对Cd产生的渗透和氧化应激。腐胺和亚精胺的代谢似乎在Cd耐受中起着核心作用。微阵列数据已通过生物学分析(例如运动性,氧化应激测定,ICR-FT / MS和UPLC的代谢产物谱分析,生物胺的毛细管电泳分析)进行了验证。

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