[目的]建立一套快捷、安全、有效的丝核菌菌株DNA提取方法。[方法]采用Chelex-100法提取丝核菌菌株DNA,作为5.8S r DNA-ITS序列的PCR扩增模板,评价提取的DNA质量。[结果]采用Chelex-100法提取丝核菌DNA能够在15 min之内完成,提取的DNA...[目的]建立一套快捷、安全、有效的丝核菌菌株DNA提取方法。[方法]采用Chelex-100法提取丝核菌菌株DNA,作为5.8S r DNA-ITS序列的PCR扩增模板,评价提取的DNA质量。[结果]采用Chelex-100法提取丝核菌DNA能够在15 min之内完成,提取的DNA可以直接作为PCR扩增模板,PCR产物经电泳检测,条带整齐、清晰、明亮,产量大,符合常规测序要求,测序结果准确。[结论]该方法具有快速简便、省时省力、经济高效的特点,是一种较为理想的丝核菌基因组DNA提取方法,适用于丝核菌菌株的分类鉴定。展开更多
From over 800 fungal strains of Tri-choderma Spp. , 6 strains were foundto greatly inhibit the growing of Rhi-zocotonia solani, the pathogen of ricesheath blight in dual culture. Amongthem, strain T3 was the best anta...From over 800 fungal strains of Tri-choderma Spp. , 6 strains were foundto greatly inhibit the growing of Rhi-zocotonia solani, the pathogen of ricesheath blight in dual culture. Amongthem, strain T3 was the best antago-nist, which reduced the growing ofthe pathogen by 52.54% (Table 1).展开更多
文摘[目的]建立一套快捷、安全、有效的丝核菌菌株DNA提取方法。[方法]采用Chelex-100法提取丝核菌菌株DNA,作为5.8S r DNA-ITS序列的PCR扩增模板,评价提取的DNA质量。[结果]采用Chelex-100法提取丝核菌DNA能够在15 min之内完成,提取的DNA可以直接作为PCR扩增模板,PCR产物经电泳检测,条带整齐、清晰、明亮,产量大,符合常规测序要求,测序结果准确。[结论]该方法具有快速简便、省时省力、经济高效的特点,是一种较为理想的丝核菌基因组DNA提取方法,适用于丝核菌菌株的分类鉴定。
文摘From over 800 fungal strains of Tri-choderma Spp. , 6 strains were foundto greatly inhibit the growing of Rhi-zocotonia solani, the pathogen of ricesheath blight in dual culture. Amongthem, strain T3 was the best antago-nist, which reduced the growing ofthe pathogen by 52.54% (Table 1).
