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Effect of culture medium, light and air circulation on sporulation of Neonectria ditissima

机译:培养基,光气流循环对Neonectria Ditissima的孢子

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In culture, most isolates of Neonectria ditissima, the causal organism of European canker, do not produce conidia. Those that do, often produce single-celled conidia rather than the typical multi-celled conidia that are found in nature. A series of experiments was conducted to determine the conditions needed for conidium production. Four culture media (malt extract agar, modified Matsushima's medium (MM), apple sap amended water agar (ASAWA) and water agar), five light regimes, including darkness, near ultra violet (NUV) light and white fluorescent light, and three plate sealing patterns were tested. Subculturing onto MM in sealed plates, exposed to NUV light at 20°C for 3 weeks, resulted in 100% of isolates producing large numbers of viable conidia, of which 71% produced multi-celled conidia. Similarly, under a white fluorescent light/darkness regime, all isolates produced viable conidia on MM and ASAWA, and 100% and 97% of the isolates produced multi-celled conidia, respectively.
机译:在培养中,大多数欧洲溃疡的NeoNectria Ditissima的孤立株,欧洲溃疡的因果生物,不产生分类。那些做的人通常会产生单细胞分类而不是本质上发现的典型的多种细胞分枝蛋白。进行了一系列实验以确定植物生产所需的条件。四种培养基(麦芽提取物琼脂,修饰的Matsushima培养基(mm),苹果汁修正的水琼脂(Asawa)和水琼脂),五个灯制度,包括黑暗,近紫外线(Nuv)光和白色荧光灯,以及三板测试密封图案。在密封板中推进mm,暴露于20℃的Nuv光3周,导致100%的分离物产生大量可行的分析蛋白,其中71%产生多纤维的分类。类似地,在白色荧光灯/暗度状态下,所有分离物都会产生可行的Catidia,分别产生100%和97%的分离物产生多纤维的分类。

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