华北农学报 ›› 2008, Vol. 23 ›› Issue (5): 131-135. doi: 10.7668/hbnxb.2008.05.029

所属专题: 生物技术

• 论文 • 上一篇    下一篇

苏云金杆菌vip1A/vip2A基因的鉴定及其与cry1基因的联系

申建茹, 郭巍, 张霞, 李晶   

  1. 河北农业大学, 生命科学学院, 河北省农作物病虫害生物防治工程技术中心, 河北, 保定, 071001
  • 收稿日期:2008-06-13 出版日期:2008-10-28
  • 作者简介:申建茹(1981-),女,河北保定人,在读硕士,主要从事生物技术与生防微生物研究。
  • 基金资助:
    国家重点基础研究发展计划(“973”计划)(2003CB114201);河北省自然科学基金项目(C2007000542)

Identification of thevip1A/vip2A Gene from Bacillus thuringiensis Isolates and the Linkage withcry1Gene

SHEN Jian-ru, GUO Wei, ZHANG Xia, LI Jing   

  1. College of Life Science, Biological Control Center of Plant Diseases and Pests of Hebei Province, Agricultural University of Hebei, Baoding 071001, China
  • Received:2008-06-13 Published:2008-10-28

摘要: 利用PCR方法检测vip1A/vip2A基因在野生型Bt菌株中的分布,进行基因片段的克隆和序列分析。结合cry1基因的PCR-RFLP基因型鉴定体系,分析与vip1A/vip2A基因有联系的cry1类基因。结果表明,分离保存的171株野生型Bt菌株中,有20株菌株含有vip1A/vip2A基因,分布率为11.69%。成功克隆了菌株Bt16的vip1A/vip2A基因片段,命名为vip1A/vip2A-16,GenBank 登录号为EU94327.cry1基因的PCR-RFLP鉴定结果表明,该20株菌株均含有cry1Fa基因,说明vip1A/vip2A基因与cry1Fa可能具有某种联系。

关键词: 二元毒素, vip1A/vip2A, vip1A/vip2A-16, PCR-RFLP, cry1Fa

Abstract: A PCR method and a PCR-restriction fragment length polymorphism method were used for identification ofvip1A/vip2A genes andcry1-type genes from Bacillus thuringiensis isolates,respectively.The result showed thatvip1A/vip2A-type genes appeared in 20 of 117 B.thuringiensis isolates.Avip1A/vip2A gene fragment was cloned and sequenced.GenBank accession number is EU594327 Thecry1-type genes were ident ified ascry1Fa.The results indicated that there was some linkage between thevip1A/vip2A andcry1Fa.

Key words: Binary toxin, vip1A /vip2A, vip1A /vip2A-16, PCR-RFLP, cry1Fa

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引用本文

申建茹, 郭巍, 张霞, 李晶. 苏云金杆菌vip1A/vip2A基因的鉴定及其与cry1基因的联系[J]. 华北农学报, 2008, 23(5): 131-135. doi: 10.7668/hbnxb.2008.05.029.

SHEN Jian-ru, GUO Wei, ZHANG Xia, LI Jing. Identification of thevip1A/vip2A Gene from Bacillus thuringiensis Isolates and the Linkage withcry1Gene[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2008, 23(5): 131-135. doi: 10.7668/hbnxb.2008.05.029.