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Stress responses of Synechocystis sp. strain PCC 6803 mutants impaired in genes encoding putative alternative sigma factors

机译:SyneChocystis SP的应力反应。菌株PCC 6803突变体在编码推定的替代Σ因素的基因中受损

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In the complete genome sequence of the cyanobacterium Synechocystis sp. strain PCC 6803 [Kaneko et al. (1996R19). DNA Res 3, 109–136] genes were identified encoding putative group 3?σ-factors SigH (Sll-0856), SigG (Slr-1545) and SigF (Slr-1564) and the regulatory protein RsbU (Slr-2031). Mutations in these genes were generated by interposon mutagenesis to study their importance in stress acclimation. For the genes sigH, sigF and rsbU, the loci segregated completely. However, attempts to mutagenize the sigG locus resulted in merodiploids. Under standard growth conditions only minor differences were detected between the mutants and wild-type. However, cells of the RsbU mutant showed a clear defect in regenerating growth after a nitrogen- and sulphur-starvation-induced stationary phase. After applying salt, heat and high-light shocks, stress protein synthesis was analysed by means of one- and two-dimensional electrophoresis. Cells of the SigF mutant showed a severe defect in the induction of salt stress proteins. Although the acclimation to moderate salt stress up to 684?mM NaCl was not significantly changed in this mutant, its ability to acclimate to higher concentrations of NaCl was reduced. Northern blot experiments showed a constitutive expression of the rsbU and sigF genes. The expression of the sigH gene was found to be stress-stimulated, particularly in heat-shocked cells, whilst that of sigG was transiently decreased under stress conditions. Possible functions of these regulatory proteins in stress acclimation of Synechocystis cells are discussed.
机译:在Cyanobacterium snechocystis sp的完整基因组序列中。菌株PCC 6803 [Kaneko等人。 (1996R19)。鉴定DNA Res 3,109-136]基因被鉴定了编码推定群3〜σ-因子静脉(SLL-0856),SIGG(SLR-1545)和SIGF(SLR-1564)和调节蛋白RSBU(SLR-2031)。这些基因中的突变被颞膜诱变产生,以研究其在应激适应方面的重要性。对于叹气,Sigf和RSBU的基因,基因座完全分离。然而,尝试诱变Sigg轨迹导致使用商品倍数。在标准生长条件下,突变体和野生型之间只检测到微细差异。然而,RSBU突变体的细胞在氮气和硫饥饿诱导的固定相后,在再生生长中显示出透明的缺陷。在施加盐,热和高光冲击后,通过单向和二维电泳分析应激蛋白质合成。 SigF突变体的细胞在盐胁迫蛋白诱导中显示出严重的缺陷。虽然在该突变体中适应到684毫升的适度盐胁迫不显着变化,但其适应更高浓度的NaCl的能力。 Northern印迹实验表明RSBu和Sigf基因的组成型表达。发现静态基因的表达被刺激,特别是在热震动的细胞中,同时在应力条件下Sigg的瞬时降低。讨论了这些调节蛋白在综合症细胞应激驯化中的可能功能。

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