为了明确内切葡聚糖酶CgEg1B与杧果炭疽病菌Colletotrichum gloeosporioides致病力的关系,本试验以杧果炭疽病菌DNA为模板,利用同源克隆技术扩增CgEg1B,对其序列特征、蛋白保守结构域进行分析,并借助In-Fusion HD Cloning Kit技术进行敲除载体构建。结果表明,该基因DNA和cDNA全长分别为1 077bp、1 020bp,编码区有内含子(57bp)1个,推测编码339个氨基酸,其分子量约为37.13kDa,等电点PI为5.11。与NCBI网站中已公布的基因进行Blastp比对,发现该序列与鳄梨炭疽菌C.gloeosporioides(EQB54542.1)的内切葡聚糖酶基因相似性为99%;该基因的敲除载体pCgEg1BGH-1构建成功。CgEg1B基因具备真菌内切葡聚糖酶基因家族的序列特征,推测CgEg1B基因可能与杧果炭疽病菌的侵入、定殖和致病性有关。
【英文摘要】
Mango anthracnose was one of the most serious diseases.In order to clarify the relationship between virulence and endoglucanase gene CgEg1 B of C.gloeosporioides,CgEg1 B gene was cloned fromC.gloeosporioides from mango by method of homologous cloning.The sequence characteristics and the conservative structure domains on predicted protein of CgEg1 B gene were analyzed.The knockout vector of CgEg1 B gene was constructed by method of In-Fusion HD Cloning Kit.The results showed that the complete DNA and cDNA se...
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