Ponstein A S, Bres-Vloemans S A, Sela-Buurlage M B, van den Elzen P J, Melchers L S, Cornelissen B J
MOGEN International NV, Leiden, The Netherlands.
Plant Physiol. 1994 Jan;104(1):109-18. doi: 10.1104/pp.104.1.109.
A novel pathogen- and wound-inducible antifungal protein of 20 kD was purified from tobacco (Nicotiana tabacum) Samsun NN leaves inoculated with tobacco mosaic virus (TMV). The protein, designated CBP20, was purified by chitin-affinity chromatography and gel filtration. In vitro assays demonstrated that CBP20 exhibits antifungal activity toward Trichoderma viride and Fusarium solani by causing lysis of the germ tubes and/or growth inhibition. In addition it was shown that CBP20 acts synergistically with a tobacco class I chitinase against F. solani and with a tobacco class I beta-1,3-glucanase against F. solani and Alternaria radicina. Analysis of the protein and corresponding cDNAs revealed that CBP20 contains an N-terminal chitin-binding domain that is present also in the class I chitinases of tobacco, the putative wound-induced (WIN) proteins of potato, WIN1 and WIN2, and several plant lectins. The C-terminal domain of CBP20 showed high identity with tobacco pathogenesis-related (PR) proteins, PR-4a and PR-4b, tomato PR-P2, and potato WIN1 and WIN2. CBP20 is synthesized as a preproprotein, which is processed into the mature protein by the removal of an N-terminal signal peptide and a C-terminal propeptide, most likely involved in the vacuolar targeting of the protein. The intracellular localization of CBP20 and its induction upon TMV infection and wounding indicate that CBP20 is the first class I PR-4 type protein purified.
从接种烟草花叶病毒(TMV)的烟草(Nicotiana tabacum)Samsun NN叶片中纯化出一种新型的、由病原体和伤口诱导的20 kD抗真菌蛋白。该蛋白命名为CBP20,通过几丁质亲和层析和凝胶过滤进行纯化。体外试验表明,CBP20通过导致芽管裂解和/或生长抑制,对绿色木霉和茄类镰刀菌表现出抗真菌活性。此外,还表明CBP20与烟草I类几丁质酶协同作用对抗茄类镰刀菌,与烟草I类β-1,3-葡聚糖酶协同作用对抗茄类镰刀菌和萝卜链格孢。对该蛋白及其相应cDNA的分析表明,CBP20含有一个N端几丁质结合结构域,该结构域也存在于烟草的I类几丁质酶、马铃薯的假定伤口诱导(WIN)蛋白WIN1和WIN2以及几种植物凝集素中。CBP20的C端结构域与烟草病程相关(PR)蛋白PR-4a和PR-4b、番茄PR-P2以及马铃薯WIN1和WIN2具有高度同源性。CBP20以前原蛋白形式合成,通过去除N端信号肽和C端前肽加工成成熟蛋白,这很可能参与了该蛋白的液泡靶向定位。CBP20的细胞内定位及其在TMV感染和伤口处理后的诱导表明,CBP20是首个纯化的I类PR-4型蛋白。