Stintzi A, Heitz T, Prasad V, Wiedemann-Merdinoglu S, Kauffmann S, Geoffroy P, Legrand M, Fritig B
Institut de Biologie Moléculaire des Plantes du CNRS, Université Louis Pasteur, Strasbourg, France.
Biochimie. 1993;75(8):687-706. doi: 10.1016/0300-9084(93)90100-7.
The hypersensitive reaction to a pathogen is one of the most efficient defense mechanisms in nature and leads to the induction of numerous plant genes encoding defense proteins. These proteins include: 1) structural proteins that are incorporated into the extracellular matrix and participate in the confinement of the pathogen; 2) enzymes of secondary metabolism, for instance those of the biosynthesis of plant antibiotics; 3) pathogenesis-related (PR) proteins which represent major quantitative changes in soluble protein during the defense response. The PRs have typical physicochemical properties that enable them to resist to acidic pH and proteolytic cleavage and thus survive in the harsh environments where they occur: vacuolar compartment or cell wall or intercellular spaces. Since the discovery of the first PRs in tobacco many other similar proteins have been isolated from tobacco but also from other plant species, including dicots and monocots, the widest range being characterized from hypersensitively reacting tobacco. Based first on serological properties and later on sequence data, the tobacco PRs have been classified in five major groups. Group PR-1 contains the first discovered PRs of 15-17 kDa molecular mass, whose biological activity is still unknown, but some members have been shown recently to have antifungal activity. Group PR-2 contains three structurally distinct classes of 1,3-beta-glucanases, with acidic and basic counterparts, with dramatically different specific activity towards linear 1,3-beta-glucans and with different substrate specificity. Group PR-3 consists of various chitinases-lysozymes that belong to three distinct classes, are vacuolar or extracellular, and exhibit differential chitinase and lysozyme activities. Some of them, either alone or in combination with 1,3-beta-glucanases, have been shown to be antifungal in vitro and in vivo (transgenic plants), probably by hydrolysing their substrates as structural components in the fungal cell wall. Group PR-4 is the less studied, and in tobacco contains four members of 13-14.5 kDa of unknown activity and function. Group PR-5 contains acidic-neutral and very basic members with extracellular and vacuolar localization, respectively, and all members show sequence similarity to the sweet-tasting protein thaumatin. Several members of the PR-5 group from tobacco and other plant species were shown to display significant in vitro activity of inhibiting hyphal growth or spore germination of various fungi probably by a membrane permeabilizing mechanism.(ABSTRACT TRUNCATED AT 400 WORDS)
对病原体的过敏反应是自然界中最有效的防御机制之一,会诱导许多编码防御蛋白的植物基因表达。这些蛋白质包括:1)整合到细胞外基质中并参与限制病原体的结构蛋白;2)次生代谢酶,例如植物抗生素生物合成的酶;3)病程相关(PR)蛋白,它们是防御反应期间可溶性蛋白的主要定量变化。PR蛋白具有典型的物理化学性质,使其能够抵抗酸性pH和蛋白水解切割,从而在它们所处的恶劣环境(液泡区室、细胞壁或细胞间隙)中存活。自从在烟草中发现首批PR蛋白以来,许多其他类似蛋白不仅从烟草中,也从其他植物物种中分离出来,包括双子叶植物和单子叶植物,其中研究最广泛的是过敏反应的烟草。首先基于血清学特性,后来基于序列数据,烟草PR蛋白被分为五大类。PR-1组包含最早发现的分子量为15-17 kDa的PR蛋白,其生物学活性仍然未知,但最近一些成员已被证明具有抗真菌活性。PR-2组包含三类结构不同的1,3-β-葡聚糖酶,有酸性和碱性对应物,对线性1,3-β-葡聚糖的比活性差异很大,底物特异性也不同。PR-3组由属于三个不同类别的各种几丁质酶-溶菌酶组成,存在于液泡或细胞外,几丁质酶和溶菌酶活性不同。其中一些单独或与1,3-β-葡聚糖酶联合使用,已被证明在体外和体内(转基因植物)具有抗真菌作用,可能是通过水解真菌细胞壁中的结构成分底物。PR-4组研究较少,在烟草中包含四个分子量为13-14.5 kDa、活性和功能未知的成员。PR-5组包含酸性-中性和非常碱性的成员,分别定位于细胞外和液泡,所有成员与甜味蛋白thaumatin序列相似。烟草和其他植物物种的PR-5组中的几个成员被证明在体外具有显著的抑制各种真菌菌丝生长或孢子萌发的活性,可能是通过膜通透机制。(摘要截断于400字)