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链格孢菌(Alternaria tenuissima)cDNA酵母表达文库的构建
引用本文:冯飞,梁佳勇,纪春艳,曾洪梅,邱德文.链格孢菌(Alternaria tenuissima)cDNA酵母表达文库的构建[J].中国农学通报,2009,25(12):25-29.
作者姓名:冯飞  梁佳勇  纪春艳  曾洪梅  邱德文
作者单位:1. 仲恺农业工程学院生命科学学院,广州,510225
2. 华南农业大学植物病理学系,广州,510643
3. 中国农业科学院植物保护研究所,蛋白药物工程实验室,北京,100081
基金项目:国家高技术研究发展计划(863计划) 
摘    要:为了解链格孢菌(Alternaria tenuissima)遗传学背景,克隆及研究该菌功能基因,根据Gateway技术构建了既能在酵母细胞中表达外源基因又能在原核细胞大量复制的酵母表达载体pRS-DEST42,构建了细极链格孢菌(A. tenuissima)cDNA酵母表达文库。经检测,该文库的平均滴度为2.44×106(cfu/ml),文库总容量为2.44×107,阳性克性率为100%,平均插入片段约为1.38kb。细极链格孢菌(A. tenuissima)cDNA酵母表达文库是一个质量较高的表达文库,为克隆与分离全长目的基因及其功能奠定了坚实的基础。

关 键 词:山区    山区    植被恢复    进展
收稿时间:2009-02-11
修稿时间:2009-04-03

Construction of cDNA yeast expression library of Alternaria tenuissima
Feng Fei,Liang Jiayong,Ji Chunyan,Zeng Hongmei,Qiu Dewen.Construction of cDNA yeast expression library of Alternaria tenuissima[J].Chinese Agricultural Science Bulletin,2009,25(12):25-29.
Authors:Feng Fei  Liang Jiayong  Ji Chunyan  Zeng Hongmei  Qiu Dewen
Institution:Feng Fei, Liang Jiayong, Ji Chunyan, Zeng Hongmei, Qiu Dewen (1.College of life science, Zhongkai Agriculture & Technology University, Guangzhou 510225; 2.Department of Plant Pathology, South China Agricultural University, Guangzhou 510643; 3.Laboratories of Protein Pesticides, Department of Microbial Pesticides and Molecular Design, Institute of Plant Protection, Chinese Academy of Agricultural Science, Beijing 100081)
Abstract:For further understand genetics background and functional genes of A. tenuissima. A yeast destination vector pRS-DEST42, express foreign genes in a low-copy number in yeast and high-copy in E. coli, was constructed. The entry cDNA library of A. tenuissima was transferred into vector pRS-DEST42 through Gateway system. The cDNA yeast expression library has a higher titer of 2.44×106(cfu/ml) and a total clones of 2.44×107. The rate of positive recombinants clones was 100% and the size of average insert cDNA was 1.38 kb. This provides a basis for isolate and study on functional genes in A. tenuissima.
Keywords:cDNA
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