Lehrstuhl für Biochemie der Pflanzen, Biologisches Institut II, Universität Freiburg, Schänzlestrasse 1, W-7800, Freiburg, FRG.
Planta. 1992 Nov;188(4):498-505. doi: 10.1007/BF00197041.
An in-vitro culture system allowing the simultaneous germination of cysts was used to study the early host-independent release of phytoalexin elicitors by Phytophthora megasperma f. sp. glycinea, a soybean pathogen. Significant elicitor activity could be detected in the culture medium as early as 2 h after germination of P.m. f. sp. glycinea, race 1, cysts. The phytoalexin elicitor was heat-stable and heterogeneous in size. The apparent molecular mass ranged from 3 to 80 kDa. Anion exchange and lectin-affinity chromatography followed by sugar analysis confirmed that the elicitor activity resided primarily in glucans. The time course of elicitor release could then be accurately monitored by means of a competitive radioligand-displacement assay using the β-glucan elicitor-binding sites of soybean (Glycine max (L.) Merr.) membranes. Linkage-composition analysis of the glucan elicitors showed that they were primarily (1 → 3)β-linked with (1 → 6)-β-branches, a composition similar to that of glucans obtained by heat release from mature mycelium but different from that of elicitors obtained by acid hydrolysis or from spontaneous autohydrolytic release by senescent cultures. The naturally released elicitors displayed a biological activity in soybean cotyledon bioassays higher than purified acid-hydrolysed glucan elicitor or than the hepta-(1 → 3, 1 → 6)-β-glucoside, the smallest known carbohydrate elicitor for soybean. The present results demonstrate that elicitor release from the pathogen and perception by the potential host can take place in this system as early as during germ-tube formation and independent of the presence of host-produced endoglucanases.
一种允许同时萌发胞囊的体外培养系统被用于研究大豆病原菌大豆疫霉(Phytophthora megasperma f. sp. glycinea)在宿主独立阶段早期释放的植物抗毒素激发子。早在 1 号生理小种大豆疫霉胞囊萌发后 2 小时,就可以在培养介质中检测到显著的激发子活性。该植物抗毒素激发子具有热稳定性,且大小不均一。表观分子量范围为 3 至 80 kDa。阴离子交换和凝集素亲和层析,随后进行糖分析,证实该激发子活性主要存在于葡聚糖中。通过使用大豆(Glycine max (L.) Merr.)细胞膜上的β-葡聚糖激发子结合位点的竞争性放射性配体置换测定法,可以准确监测激发子释放的时间进程。葡聚糖激发子的连接组成分析表明,它们主要是(1 → 3)β-连接,带有(1 → 6)-β-支链,其组成与从成熟菌丝体热释放得到的葡聚糖相似,但与酸水解得到的激发子或来自衰老培养物自发自水解释放的激发子不同。天然释放的激发子在大豆子叶生物测定中的生物活性高于纯化的酸水解葡聚糖激发子或比最小的已知的大豆碳水化合物激发子七-(1 → 3, 1 → 6)-β-葡糖苷高。这些结果表明,在该系统中,病原体的激发子释放和潜在宿主的感知可以在萌发管形成期间发生,且与宿主产生的内切葡聚糖酶无关。