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Genome-Driven Investigation of Compatible Solute Biosynthesis Pathways of Pseudomonas syringae pv. syringae and Their Contribution to Water Stress Tolerance

机译:丁香假单胞菌PV溶质生物合成途径的基因组驱动研究。丁香科植物及其对水分胁迫耐性的贡献

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The foliar pathogen Pseudomonas syringae pv. syringae exhibits an exceptional ability to survive on asymptomatic plants as an epiphyte. Intermittent wetting events on plants lead to osmotic and matric stresses which must be tolerated for survival as an epiphyte. In this study, we have applied bioinformatic, genetic, and biochemical approaches to address water stress tolerance in P. syringae pv. syringae strain B728a, for which a complete genome sequence is available. P. syringae pv. syringae B728a is able to produce the compatible solutes betaine, ectoine, N -acetylglutaminylglutamine amide (NAGGN), and trehalose. Analysis of osmolyte profiles of P. syringae pv. syringae B728a under a variety of in vitro and in planta conditions reveals that the osmolytes differentially contribute to water stress tolerance in this species and that they interact at the level of transcription to yield a hierarchy of expression. While the interruption of a putative gene cluster coding for NAGGN biosynthesis provided the first experimental evidence of the NAGGN biosynthetic pathway, application of this knockout strain and also a gfp reporter gene fusion strain demonstrated the small contribution of NAGGN to cell survival and desiccation tolerance of P. syringae pv. syringae B728a under in planta conditions. Additionally, detailed investigation of ectC , an orphan of the ectoine cluster (lacking the ectA and ectB homologs), revealed its functionality and that ectoine production could be detected in NaCl-amended cultures of P. syringae pv. syringae B728a to which sterilized leaves of Syringa vulgaris had been added.
机译:叶病原体丁香假单胞菌PV。丁香科植物具有作为附生植物在无症状植物上生存的非凡能力。植物的间歇性润湿事件会导致渗透和基质胁迫,为作为附生植物的生存必须忍受。在这项研究中,我们已应用生物信息学,遗传和生化方法来解决丁香假单胞菌pv中的水分胁迫耐受性。完整的基因组序列的丁香丁香菌株B728a。丁香假单胞菌丁香香脂素B728a能够生产兼容的溶质甜菜碱,ectoine,N-乙酰谷氨酰胺基谷氨酰胺(NAGGN)和海藻糖。丁香假单胞菌渗透压谱的分析。丁香丁香B728a在多种体外和植物条件下揭示,渗透压在该物种中对水分胁迫的耐受性差异很大,并且它们在转录水平上相互作用以产生表达层次。虽然推定的编码NAGGN生物合成的基因簇的打断提供了NAGGN生物合成途径的第一个实验证据,但该敲除菌株以及gfp报告基因融合菌株的应用证明NAGGN对P的细胞存活和耐干燥性的贡献很小。丁香花光伏丁香B728a在植物条件下。此外,对ectC的详细研究(ectoine簇的孤儿(缺少ectA和ectB同源物))揭示了其功能,并且可以在丁香假单胞菌pv的NaCl改良培养物中检测到ectoine的产生。紫丁香B728a,其中已添加了普通丁香叶的灭菌叶。

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