Genetic Engineering Research Center, College of Bioengineering, Chongqing University, Chongqing, China.
Appl Microbiol Biotechnol. 2010 Jul;87(3):1151-6. doi: 10.1007/s00253-010-2636-x. Epub 2010 May 7.
Beauveria bassiana is a filamentous ascomycete that is pathogenic towards a broad host range of insect targets and is increasingly serving as a model for examining fungal development and host-pathogen interactions. B. bassiana displays a prohibitive level of resistance against many current fungal and/or yeast selection markers including hygromycin, neomycin, and zeocin. A genetic transformation system for B. bassiana based upon the use of a sulfonylurea resistance cassette derived from the Magnaporthe grisea, acetolactate synthase gene (sur) was developed. The transformation frequency ranged from 100-150 transformants per microgram DNA/10(8) cells and Southern blot analysis indicated that the plasmid vector was randomly integrated into the genome of B. bassiana. In addition, a construct bearing the sur gene and the enhanced green fluorescent protein gene egfp as a visual marker was used to successfully transform B. bassiana. Over 95% of the transformants retained the sulfonylurea resistance phenotype under non-selective conditions. The described transformation method increases opportunities for the genetic manipulation of B. bassiana.
球孢白僵菌是一种丝状子囊菌,对广泛的昆虫靶标具有致病性,并且越来越多地被用作研究真菌发育和宿主-病原体相互作用的模型。球孢白僵菌对许多当前的真菌和/或酵母选择标记物表现出极强的抗性,包括潮霉素、新霉素和博来霉素。基于从稻瘟病菌中获得的乙酰乳酸合成酶基因(sur)的磺酰脲类抗性盒,开发了一种用于球孢白僵菌的遗传转化系统。转化频率范围为每微克 DNA/10^8 个细胞 100-150 个转化体,Southern blot 分析表明质粒载体随机整合到球孢白僵菌的基因组中。此外,带有 sur 基因和增强型绿色荧光蛋白基因 egfp 作为可视化标记的构建体被成功地转化为球孢白僵菌。超过 95%的转化体在非选择性条件下保留了磺酰脲类抗性表型。所描述的转化方法增加了对球孢白僵菌遗传操作的机会。