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Induction of Extracellular Matrix Glycoproteins in Brassica Petioles by Wounding and in Response to Xanthomonas campestris

机译:伤口和对油菜黄单胞菌的诱导诱导芸苔叶柄中细胞外基质糖蛋白的表达

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A panel of monoclonal antibodies that recognize plant extracellular matrix glycoproteins previously implicated in plant-microbe interactions was used to study the effects of pathogen inoculation and wounding on glycoproteins in petioles of Brassica campestris . The panel of monoclonals comprised two sets: JIM11, JIM12, and JIM20 recognize epitopes carried on hydroxyproline-rich glycoproteins (HRGPs) (M. Smallwood, A. Beven, N. Donovan, S. J. Neill, J. Peart, K. Roberts, and J. P. Knox, Plant J. 5:237–246, 1994); MAC204 and MAC265 recognize glycoproteins of the Rhizobium infection thread (K. A. VandenBosch, D. J. Bradley, S. Perotto, G. W. Butcher, and N. J. Brewin, EMBO J. 8:335–342, 1989). Wounding or inoculation of petioles with avirulent strains of pathovars of Xanthomonas campestris induced the synthesis of two new groups of antigens: gp160 ran as a smear on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) with apparent molecular mass from 120 to 200 kDa and was recognized by JIM20 and MAC204; gpS remained in the stacking gel on SDS-PAGE and was recognized by JIM11, JIM20, and MAC204. The response to virulent strains of pathovars of X. campestris was either less pronounced or absent. gpS comprised several components that were resolved by cation-exchange chromatography. Some of these components were characterized as extensin-like HRGPs. The level of induction of the gpS group of antigens by virulent strains was not altered by mutation of a number of genes required for basic pathogenicity or by heat-killing the bacteria.
机译:一组识别先前与植物-微生物相互作用有关的植物细胞外基质糖蛋白的单克隆抗体被用于研究病原体接种和创伤对油菜叶柄中糖蛋白的影响。一组单克隆抗体包括两套:JIM11,JIM12和JIM20识别富含羟脯氨酸的糖蛋白(HRGP)携带的表位(M. Smallwood,A。Beven,N。Donovan,SJ Neill,J。Peart,K。Roberts和JP Knox,Plant J. 5:237-246,1994); MAC204和MAC265识别根瘤菌感染线的糖蛋白(K. A. VandenBosch,D。J. Bradley,S。Perotto,G。W. Butcher,和N. J. Brewin,EMBO J. 8:335-342,1989)。用无毒力的油菜黄单胞菌的致病菌株对叶柄进行伤口或接种诱导了两组新的抗原的合成:gp160在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)上涂片,其表观分子量为120至200 kDa并被JIM20和MAC204认可; gpS保留在SDS-PAGE上的堆积凝胶中,并被JIM11,JIM20和MAC204识别。对野油菜(X. campestris)病原菌的毒力菌株的反应较不明显或不存在。 gpS包含通过阳离子交换色谱分离的几种组分。这些成分中的一些被表征为类似延伸蛋白的HRGP。致病菌株对gpS基团抗原的诱导水平不会因基本致病性所需的许多基因突变或通过热杀死细菌而改变。

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