影响炭疽菌高效转化的因素

Regina S. Redman, Rusty J. Rodriguez
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引用次数: 51

摘要

雷德曼,r.s.和罗德里格斯,r.j. 1994。影响炭疽菌有效转化的因素。真菌学通报,2018,33(2):444 - 444。采用增强原生质体、限制性内切酶介导整合(REMI)或电穿孔介导的方法对4种炭疽菌的12株分离物进行转化。增强原生质体转化方案使炭疽菌(Colletotrichum lindemuthianum)和C. magna的转化效率分别提高了100倍和50倍。REMI转化涉及使用HindIII和与HindIII线性化的载体DNA来增加真菌基因组中整合事件和潜在基因破坏的数量。将增强的原生质体与REMI方案相结合,导致C. lindemuthanum耐湿霉素/制氨抑素突变体的数量增加了22倍。对4种炭疽菌菌丝片段和孢子进行了电穿孔介导转化,转化效率高达1000个/μ DNA。具有潮霉素抗性的pHA1.3载体含有来自尖孢镰刀菌的端粒序列,通过自主复制和基因组整合进行转化,是提高转化效率(100 - 10000个/μg DNA)的必要条件。在细菌扩增和真菌转化过程中,pHA1.3发生了修饰,导致质粒能够显著提高C. lindemuthianum的转化效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Affecting the Efficient Transformation of Colletotrichum Species

Redman, R. S., and Rodriguez, R. J. 1994. Factors affecting the efficient transformation of Colletotrichum species. Experimental Mycology, 18, 230-246. Twelve isolates representing four species of Colletotrichum were transformed either by enhanced protoplast, restriction enzyme-mediated integration (REMI), or electroporation-mediated protocols. The enhanced protoplast transformation protocol resulted in 100- and 50-fold increases in the transformation efficiencies of Colletotrichum lindemuthianum and C. magna , respectively. REMI transformation involved the use of Hin dIII and vector DNA linearized with HindIII to increase the number of integration events and potential gene disruptions in the fungal genome. Combining the enhanced protoplast and the REMI protocols resulted in a 22-fold increase in the number of hygromycin/nystatin-resistant mutants in C. lindemuthianum . Electroporation-mediated transformation was performed on mycelial fragments and spores of four Colletotrichum species, resulting in efficiencies of up to 1000 transformants/μg DNA. The pHA1.3 vector which confers hygromycin resistance contains telomeric sequences from Fusarium oxysporum , transforms by autonomous replication and genomic integration, and was essential for elevated transformation efficiencies of 100 to 10,000 transformants/μg DNA. Modifications of pHA1.3 occurred during bacterial amplification and post fungal transformation resulting in plasmids capable of significantly elevated transformation efficiencies in C. lindemuthianum.

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