Bourson C, Favey S, Reverchon S, Robert-Baudouy J
INSA 406 Laboratoire Génétique Moléculaire des Microorganismes LGMM, Villeurbanne, France.
J Gen Microbiol. 1993 Jan;139(1):1-9. doi: 10.1099/00221287-139-1-1.
The phytopathogenicity of Erwinia chrysanthemi is chiefly supported by the production of pectate lyase isoenzymes, encoded by the pel genes. One of these enzymes, PelA, encoded by the pelA gene, seems to represent only a small part of the total pectate lyase activity, but is required for full bacterial pathogenicity. To study the regulation of pelA gene expression, a pelA::uidA gene fusion was constructed. Expression of this fusion was analysed under various growth conditions and in various genetic backgrounds. Whatever the culture conditions, the pelA gene was weakly expressed. Moreover, pelA expression seems not to be regulated by the pecS gene product, but essentially by the kdgR gene product. In many plant-associated bacteria, genes involved in pathogenicity are induced by certain plant compounds. In this work, we demonstrate that E. chrysanthemi pel genes are induced in the presence of plant extracts, but only in synergy with known pectate lyase inducers (KDG: 2-keto-3-deoxygluconate; DKII: 2,5-diketo-3-deoxygluconate). However, different pel genes did not exhibit the same sensitivity to plant signal molecules. Partial purification of inducing plant compounds suggested that plant extracts contain at least one molecule involved in pectate lyase induction. This compound is thermoresistant, and has a low molecular mass and a very hydrophilic behaviour.
菊欧文氏菌的植物致病性主要由果胶酸裂解酶同工酶的产生所支撑,这些同工酶由pel基因编码。其中一种酶PelA由pelA基因编码,似乎仅占果胶酸裂解酶总活性的一小部分,但却是细菌完全致病所必需的。为了研究pelA基因表达的调控,构建了一个pelA::uidA基因融合体。在各种生长条件下和各种遗传背景下分析了该融合体的表达。无论培养条件如何,pelA基因的表达都很弱。此外,pelA的表达似乎不受pecS基因产物的调控,而主要受kdgR基因产物的调控。在许多与植物相关的细菌中,参与致病性的基因由某些植物化合物诱导。在这项工作中,我们证明菊欧文氏菌的pel基因在植物提取物存在的情况下被诱导,但仅与已知的果胶酸裂解酶诱导剂(KDG:2-酮-3-脱氧葡萄糖酸;DKII:2,5-二酮-3-脱氧葡萄糖酸)协同作用。然而,不同的pel基因对植物信号分子的敏感性不同。对诱导性植物化合物的部分纯化表明,植物提取物中至少含有一种参与果胶酸裂解酶诱导的分子。这种化合物耐热,分子量低,具有很强的亲水性。