Pissavin C, Robert-Baudouy J, Hugouvieux-Cotte-Pattat N
Laboratoire de Génétique Moléculaire des Microorganismes et des Interactions Cellulaires, UMR 5577, INSA, Villeurbanne, France.
J Bacteriol. 1996 Dec;178(24):7187-96. doi: 10.1128/jb.178.24.7187-7196.1996.
The phytopathogenic enterobacterium Erwinia chrysanthemi 3937 produces five major and several secondary endo-pectate lyases encoded by the pel genes. Most of these genes are arranged in clusters on the bacterial chromosome. The genomic region surrounding the pelB-pelC cluster was supposed to be involved in the regulation of PelB and PelC synthesis. We demonstrated that the variation of pelB expression resulted from the titration of a regulatory protein by the gene adjacent to pelC. This gene was renamed pelZ since it encodes a protein of 420 amino acids with an endo-pectate lyase activity. Regulation of pelZ expression was investigated by using transcriptional fusions and a study of mRNA synthesis. Its transcription depends on different environmental conditions. It is induced in planta and in the presence of pectic catabolite products. This induction seems to be partially mediated by the KdgR protein but does not result from a direct interaction of KdgR with the pelZ 5' region. The transcription of pelZ leads to the synthesis of a monocistronic mRNA. However, the synthesis of a polycistronic mRNA from the pelC promoter, regulated by KdgR, is responsible for increased production of PelZ under inducing conditions. pelZ transcription is also controlled by pecT, which regulates some other pel genes, but it is independent of the pecS regulatory locus. The pelZ gene appears to be widespread in different strains of E. chrysanthemi. Moreover, a gene homologous to pelZ exists in Erwinia carotovora subsp. atroseptica adjacent to the cluster containing the pectate lyase-encoding genes pel1, pel2, and pel3. This conservation could reflect a significant role of PelZ in the pectinolytic system of Erwiniae. We showed pelZ is not a predominant virulence factor of E. chrysanthemi but is involved in host specificity.
植物致病肠道细菌菊欧文氏菌3937产生五种主要的和几种次要的内切果胶裂解酶,这些酶由pel基因编码。这些基因大多成簇排列在细菌染色体上。pelB - pelC基因簇周围的基因组区域被认为参与PelB和PelC合成的调控。我们证明pelB表达的变化是由于与pelC相邻的基因对一种调控蛋白的滴定作用所致。该基因被重新命名为pelZ,因为它编码一种具有内切果胶裂解酶活性的420个氨基酸的蛋白质。通过使用转录融合和mRNA合成研究对pelZ表达的调控进行了研究。其转录取决于不同的环境条件。它在植物体内以及存在果胶分解代谢产物时被诱导。这种诱导似乎部分由KdgR蛋白介导,但并非源于KdgR与pelZ 5'区域的直接相互作用。pelZ的转录导致单顺反子mRNA的合成。然而,在诱导条件下,由KdgR调控的从pelC启动子合成的多顺反子mRNA负责PelZ产量的增加。pelZ转录也受pecT控制,pecT调控其他一些pel基因,但它独立于pecS调控位点。pelZ基因似乎在菊欧文氏菌的不同菌株中广泛存在。此外,在胡萝卜软腐欧文氏菌黑腐亚种中,与pelZ同源的一个基因存在于包含果胶裂解酶编码基因pel1、pel2和pel3的基因簇附近。这种保守性可能反映了PelZ在欧文氏菌果胶分解系统中的重要作用。我们表明pelZ不是菊欧文氏菌的主要毒力因子,但参与宿主特异性。