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苏云金芽孢杆菌新菌株S249 cry2Ad2的克隆及特征分析
引用本文:冯纪年,李陇梅,张 兴.苏云金芽孢杆菌新菌株S249 cry2Ad2的克隆及特征分析[J].西北农林科技大学学报(社会科学版),2006,34(5):93-96.
作者姓名:冯纪年  李陇梅  张 兴
作者单位:1. 西北农林科技大学植保资源与病虫害防治教育部重点实验室,陕西,杨凌,712100
2. 西北农林科技大学无公害农药研究服务中心,陕西,杨凌,712100
基金项目:国家科技攻关项目;西北农林科技大学校科研和教改项目
摘    要:根据GenBank中cry2Ad基因序列设计1对特异性引物,以苏云金芽孢杆菌新菌株S249质粒 DNA为模板,应用PCR扩增技术得到了1条大小约为2.0 kb的DNA片段(cry2Ad2)。通过引物步行法测定该片段长1919 bp,其中开放阅读框(ORF)长1902 bp,编码633个氨基酸;经DNASTAR软件分析,预测其蛋白分子量为70.72 ku,等电点pI=8.26。序列比较结果表明,该基因与cry2Ad类基因高度同源(同源性达99%)。该基因已在GenBank中登录,登录号为DQ219823,并被Bt δ-内毒素基因国际命名委员会正式命名为cry2Ad2。

关 键 词:苏云金芽孢杆菌  cry2Ad2  微生物杀虫剂  PCR  克隆  序列分析
文章编号:1671-9387(2006)05-0093-04
收稿时间:2005-09-26
修稿时间:2005年9月26日

Cloning and characteristic analysis of cry2Ad2 gene from Novel Strain S249 of Bacillus thuringiensis
FENG Ji-nian,LI Long-mei,ZHANG Xing.Cloning and characteristic analysis of cry2Ad2 gene from Novel Strain S249 of Bacillus thuringiensis[J].Journal of Northwest Sci-Tech Univ of Agr and,2006,34(5):93-96.
Authors:FENG Ji-nian  LI Long-mei  ZHANG Xing
Institution:( Key Laboratory of Plant Protection Resources and Pest Management,Ministry of Education, Research and Development Center of Biorational Pesticide, Northwest A & F University,Yangling,Shaanxi 712100, China)
Abstract:cry2Ad2 gene was cloned by PCR procedure from Novel Strain S249 of Bacillus thuringiensis plasmid with the primers designed according to the cry2Ad sequence in the GenBank. Sequencing was done to the fragments by using primer walking method and its length was 1 919 bp. cry2Ad2 contained 1 902 bp ORF that predicted a protein of 633 amino acid with Mr=70. 72 ku and pI =8. 26. The amino acid sequence of cry2Ad2 gene showed 99% identity to other cry2Ad,and the sequence was registered in GenBank (Accession Number is DQ219823) which was designated cry2Ad2 gene as a novel gene by Bt delta-endotoxin nomenclature committee.
Keywords:cry2Ad2  PCR
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