首页> 外文期刊>Molecular Plant-Microbe Interactions >Analysis of the LacI family regulators of Erwinia chrysanthemi 3937, involvement in the bacterial phytopathogenicity.
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Analysis of the LacI family regulators of Erwinia chrysanthemi 3937, involvement in the bacterial phytopathogenicity.

机译:菊花欧文氏菌3937的LacI家族调节物的分析,涉及细菌的致病性。

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Analysis of the regulators of the LacI family was performed in order to identify those potentially involved in pathogenicity of Erwinia chrysanthemi (Dickeya dadantii). Among the 18 members of the LacI family, the function of 11 members is either known or predicted and only 7 members have, as yet, no proposed function. Inactivation of these seven genes, called lfaR, lfbR, lfcR, lfdR, lfeR, lffR, and lfgR, demonstrated that four of them are important for plant infection. The lfaR and lfcR mutants showed a reduced virulence on chicory, Saintpaulia sp., and Arabidopsis. The lfeR mutant showed a reduced virulence on Arabidopsis. The lfdR mutant was more efficient than the wild-type strain in initiating maceration on Saintpaulia sp. The genetic environment of each regulator was examined to detect adjacent genes potentially involved in a common function. Construction of transcriptional fusions in these neighboring genes demonstrated that five regulators, LfaR, LfcR, LfeR, LffR, and LfgR, act as repressors of adjacent genes. Analysis of these fusions also indicated that the genes controlled by LfaR, LfcR, LfgR, and LffR are expressed during plant infection. Moreover, addition of crude plant extracts to culture medium demonstrated that the expression of the LfaR- and LfgR-controlled genes is specifically induced by plant components.
机译:对LacI家族的调节因子进行了分析,以鉴定可能与菊花欧文氏菌(Dickeya dadantii)致病性有关的因子。在LacI家族的18个成员中,有11个成员的功能是已知的或预测的,到目前为止,只有7个成员没有提议的功能。这七个基因的失活称为lfaR,lfbR,lfcR,lfdR,lfeR,lffR和lfgR,表明其中四个对植物感染很重要。 lfaR和lfcR突变体对菊苣,非洲堇和拟南芥显示出降低的毒力。 lfeR突变体在拟南芥上显示出降低的毒力。 lfdR突变体比非洲野生株更有效地启动对非洲堇的浸渍。检查每个调节子的遗传环境,以检测可能参与共同功能的相邻基因。这些邻近基因中转录融合体的构建表明,五个调节子LfaR,LfcR,LfeR,LffR和LfgR充当邻近基因的阻遏物。对这些融合的分析还表明,在植物感染期间表达了受LfaR,LfcR,LfgR和LffR控制的基因。此外,将粗植物提取物添加至培养基证明了LfaR和LfgR控制的基因的表达是由植物成分特异性诱导的。

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