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Preparation, purification and regeneration optimizing research of protoplasts from Rhizoctonia solani

机译:茄根丝菌原生质体的制备,纯化及再生优化研究

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The aim of this work was to study the standardization of conditions to obtain and regenerate?protoplasts of?Rhizoctonia solani.?The optimal way of harvesting 1.67 × 109protoplasts per gram from?Rhizoctonia solani?was to deal with 12 h aged mycelium in 0.6 M MgSO4?stabilizer (pH 5.2) combining cellulase and driselase at 35°C for 3 h. Meanwhile, the most suitable condition for protoplast regeneration had been attained. The condition was to deal with 16 h aged mycelium in 0.6 M MgSO4?stabilizer (pH 5.2) combining cellulase with driselase at 35°C for 2.5 h, and incubation at 26°C in the regeneration medium. Furthermore, a two-phase system of 0.6 M sucrose and 0.6 M mannitol was developed for separation and purification of intact protoplasts from broken protoplasts, excellent results were obtained. There was a breakthrough for protoplast technology of?R. solani?and other fungus was recorded in this paper.
机译:这项工作的目的是研究获得和再生茄红根瘤菌原生质体条件的标准化。从茄红根瘤菌中每克收获1.67×109原生质体的最佳方法是处理0.6 M的12 h老化菌丝体在35°C下将纤维素酶和果胶酶合并的MgSO4稳定剂(pH 5.2)3 h。同时,获得了最适合原生质体再生的条件。条件是在35 M的纤维素酶和果胶酶混合的0.6 M MgSO 4稳定剂(pH 5.2)中处理16 h老化的菌丝体,然后在26°C的再生培养基中孵育。此外,开发了0.6 M蔗糖和0.6 M甘露醇的两相系统,用于从破碎的原生质体中分离和纯化完整的原生质体,获得了出色的结果。 R的原生质体技术取得了突破。本文记录了茄尼和其他真菌。

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