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Cyclic mononucleotide- and Clr-dependent gene regulation in Sinorhizobium meliloti

机译:苜蓿中华根瘤菌的环状单核苷酸和Clr依赖性基因调控

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To identify physiological processes affected by cAMP in the plant-symbiotic nitrogen-fixing α-proteobacterium Sinorhizobium meliloti Rm2011, cAMP levels were artificially increased by overexpression of its cognate adenylate/guanylate cyclase gene cyaJ. This resulted in high accumulation of cAMP in the culture supernatant, decreased swimming motility and increased production of succinoglycan, an exopolysaccharide involved in host invasion. Weaker, similar phenotypic changes were induced by overexpression of cyaB and cyaG1. Effects on swimming motility and succinoglycan production were partially dependent on clr encoding a cyclic AMP receptor-like protein. Transcriptome profiling of an cyaJ-overexpressing strain identified 72 upregulated and 82 downregulated genes. A considerable number of upregulated genes are related to polysaccharide biosynthesis and osmotic stress response. These included succinoglycan biosynthesis genes, genes of the putative polysaccharide synthesis nodP2-exoF3 cluster and feuN, the first gene of the operon encoding the FeuNPQ regulatory system. Downregulated genes were mostly related to respiration, central metabolism and swimming motility. Promoter-probe studies in the presence of externally added cAMP revealed 18 novel Clr-cAMP-regulated genes. Moreover, the addition of cGMP into the growth medium also promoted clr-dependent gene regulation. In vitro binding of Clr-cAMP and Clr-cGMP to the promoter regions of SMc02178, SMb20906,SMc04190, SMc00925, SMc01136 and cyaF2 required the DNA motif (A/C/T)GT(T/C)(T/C/A)C (N4) G(G/A)(T/A)ACA. Furthermore, SMc02178, SMb20906,SMc04190and SMc00653 promoters were activated by Clr-cAMP/cGMP in Escherichia coli as heterologous host. These findings suggest direct activation of these 7 genes by Clr-cAMP/cGMP.
机译:为了鉴定在植物共生固氮α-变形杆菌Sinorhizobium meliloti Rm2011中受cAMP影响的生理过程,通过过度表达其同源腺苷酸/鸟苷酸环化酶基因cyaJ来人工提高cAMP水平。这导致cAMP在培养上清液中大量积累,降低了游泳运动,并增加了琥珀聚糖(一种参与宿主入侵的胞外多糖)的产量。较弱的是,cyaB和cyaG1的过表达诱导了类似的表型变化。对游泳运动和琥珀聚糖生产的影响部分取决于编码环状AMP受体样蛋白的clr。 cyaJ过表达菌株的转录组谱分析鉴定了72个上调的基因和82个下调的基因。大量上调的基因与多糖的生物合成和渗透应激反应有关。这些包括琥珀聚糖生物合成基因,推定的多糖合成nodP2-exoF3簇基因和feuN,操纵子的第一个编码FeuNPQ调节系统的基因。下调的基因主要与呼吸,中枢代谢和游泳运动有关。在外部添加cAMP的情况下进行的启动子探针研究揭示了18个受Clr-cAMP调控的新基因。此外,向生长培养基中添加cGMP也促进了clr依赖性基因调节。 Clr-cAMP和Clr-cGMP与SMc02178,SMb20906,SMc04190,SMc00925,SMc01136和cyaF2的启动子区域的体外结合需要DNA基序(A / C / T)GT(T / C)(T / C / A C(N4)G(G / A)(T / A)ACA。此外,SMc02178,SMb20906,SMc04190和SMc00653启动子在大肠杆菌中被Clr-cAMP / cGMP激活,作为异源宿主。这些发现表明Clr-cAMP / cGMP可直接激活这7个基因。

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