Hugouvieux-Cotte-Pattat Nicole
Unité de Microbiologie et Génétique-Composante INSA, UMR CNRS-INSA-UCB 5122, bat Lwoff, 10 rue Dubois, Domaine Scientifique de la Doua, 69622 Villeurbanne Cedex, France.
Mol Microbiol. 2004 Mar;51(5):1361-74. doi: 10.1046/j.1365-2958.2003.03908.x.
Erwinia chrysanthemi causes soft-rot diseases of various plants by enzymatic degradation of the pectin in plant cell walls. The linear regions of pectin are composed of an acidic sugar, D-galacturonic acid. The ramified regions of pectin also include neutral sugars, and are rich in L-rhamnose residues. E. chrysanthemi is able to degrade these polysaccharides, polygalacturonate and rhamnogalacturonate. In E. chrysanthemi, the production of pectinases acting on linear regions is induced in the presence of polygalacturonate by a mechanism involving the repressor KdgR. The induction of the two adjacent E. chrysanthemi genes, designated rhiT and rhiN, is maximal after the simultaneous addition of both polygalacturonate and L-rhamnose. The rhiT product is homologous to the oligogalacturonide transporter TogT of E. chrysanthemi. The rhiN product is homologous to various proteins of unknown function, including a protein encoded by the plant-inducible locus picA of Agrobacterium tumefaciens. Both rhiT and rhiN are highly induced during plant infection. Various data suggest that RhiT and RhiN are involved in rhamnogalacturonate catabolism. RhiN is able to degrade the oligomers liberated by the rhamnogalacturonate lyase RhiE. The induction of the rhiTN operon in the presence of polygalacturonate results from control by the repressor KdgR. The additional induction of these genes by rhamnose is directly mediated by RhaS, a protein homologous to the activator of rhamnose catabolism in Escherichia coli. The virulence of an E. chrysanthemi rhaS mutant towards different host plants was clearly reduced. In this phytopathogenic bacterial species, RhaS positively regulates the transcription of the rhaBAD operon, involved in rhamnose catabolism, of the rhiE gene and of the rhiTN operon. The regulator RhaS plays a larger role in E. chrysanthemi than in other enterobacteria. Indeed, the RhaS control is not restricted to the catabolism of rhamnose but is extended to the degradation of plant polysaccharides that contain this sugar.
菊欧文氏菌通过酶解植物细胞壁中的果胶引发多种植物的软腐病。果胶的线性区域由酸性糖D - 半乳糖醛酸组成。果胶的分支区域还包括中性糖,且富含L - 鼠李糖残基。菊欧文氏菌能够降解这些多糖,即聚半乳糖醛酸和鼠李糖半乳糖醛酸。在菊欧文氏菌中,在聚半乳糖醛酸存在的情况下,通过一种涉及阻遏物KdgR的机制诱导作用于线性区域的果胶酶的产生。同时添加聚半乳糖醛酸和L - 鼠李糖后,菊欧文氏菌中两个相邻基因rhiT和rhiN的诱导作用达到最大值。rhiT产物与菊欧文氏菌的低聚半乳糖醛酸转运蛋白TogT同源。rhiN产物与多种功能未知的蛋白质同源,包括根癌土壤杆菌植物诱导型基因座picA编码的一种蛋白质。rhiT和rhiN在植物感染期间均被高度诱导。各种数据表明,RhiT和RhiN参与鼠李糖半乳糖醛酸的分解代谢。RhiN能够降解由鼠李糖半乳糖醛酸裂解酶RhiE释放的寡聚物。在聚半乳糖醛酸存在的情况下,rhiTN操纵子的诱导是由阻遏物KdgR控制的。鼠李糖对这些基因的额外诱导是由RhaS直接介导的,RhaS是一种与大肠杆菌中鼠李糖分解代谢激活剂同源的蛋白质。菊欧文氏菌rhaS突变体对不同寄主植物的毒力明显降低。在这种植物致病细菌中,RhaS正向调节参与鼠李糖分解代谢的rhaBAD操纵子、rhiE基因和rhiTN操纵子的转录。调节因子RhaS在菊欧文氏菌中比在其他肠杆菌中发挥更大的作用。实际上,RhaS的调控并不局限于鼠李糖的分解代谢,而是扩展到含有这种糖的植物多糖的降解。