Chatterton Syama, Punja Zamir K
Department of Biological Sciences, Simon Fraser University, 8888 University Drive, Burnaby, BC V5A 1S6, Canada.
Can J Microbiol. 2009 Apr;55(4):356-67. doi: 10.1139/w08-156.
Clonostachys rosea f. catenulata (syn. Gliocladium catenulatum) is an effective fungal biological agent against Fusarium root and stem rot and Pythium damping-off diseases on cucumber plants. Both chitinase and beta-1,3-glucanase enzymes were produced when C. rosea was grown on a synthetic medium containing chitin or laminarin as a sole carbon source, respectively. Chitinase production was also induced by Fusarium cell walls, while beta-1,3-glucanase activity was induced by both Fusarium and Pythium cell walls, as well as by growth on homogenized cucumber roots and on low-carbon media. Mycelial growth of Fusarium and Pythium, when exposed to C. rosea culture filtrates that contain glucanase activity, was significantly reduced compared with the controls, and cell walls of both pathogens were degraded. On excised cucumber roots, hyphae of C. rosea formed appressorium-like structures and coiled around hyphae of Pythium. In culture, C. rosea caused localized degradation of Fusarium hyphae. Cucumber root tissues colonized by C. rosea showed higher levels of beta-1,3-glucanase activity at 7 days post-application compared with untreated controls. To determine if this activity was derived from C. rosea, glucanase isoforms were separated on activity gels. Fungal culture filtrates and root extracts contained the same predominant 20 kDa isoform. Reverse-transcription polymerase chain reaction (RT-PCR) using primers designed to amplify a beta-1,3-glucanase gene in C. rosea confirmed glucanase expression on roots. These results show that C. rosea produces beta-1,3-glucanase in situ, which can degrade hyphae of Fusarium and Pythium and contribute to biological control efficacy.
粉红粘帚霉链状变种(同义词:链状粘帚霉)是一种有效的真菌生物制剂,可防治黄瓜植株上的镰刀菌根腐病和茎腐病以及瓜果腐霉菌猝倒病。当粉红粘帚霉分别在以几丁质或海带多糖作为唯一碳源的合成培养基上生长时,会产生几丁质酶和β-1,3-葡聚糖酶。镰刀菌细胞壁也可诱导几丁质酶的产生,而β-1,3-葡聚糖酶的活性可由镰刀菌和瓜果腐霉菌的细胞壁诱导产生,同时在匀浆的黄瓜根上生长以及在低碳培养基上生长也可诱导其产生。与对照相比,当镰刀菌和瓜果腐霉菌暴露于含有葡聚糖酶活性的粉红粘帚霉培养滤液时,其菌丝生长显著减少,并且两种病原菌的细胞壁均被降解。在离体黄瓜根上,粉红粘帚霉的菌丝形成附着胞样结构,并缠绕在瓜果腐霉菌的菌丝周围。在培养过程中,粉红粘帚霉可导致镰刀菌菌丝的局部降解。与未处理的对照相比,接种粉红粘帚霉的黄瓜根组织在接种后7天显示出更高水平的β-1,3-葡聚糖酶活性。为了确定这种活性是否源自粉红粘帚霉,在活性凝胶上分离了葡聚糖酶同工型。真菌培养滤液和根提取物含有相同的主要20 kDa同工型。使用设计用于扩增粉红粘帚霉中β-一,3-葡聚糖酶基因的引物进行逆转录聚合酶链反应(RT-PCR),证实了根上葡聚糖酶的表达。这些结果表明,粉红粘帚霉在原位产生β-1,3-葡聚糖酶,该酶可降解镰刀菌和瓜果腐霉菌的菌丝,并有助于提高生物防治效果。