首页 | 本学科首页   官方微博 | 高级检索  
     检索      

核酸酶BN基因的克隆及序列分析
引用本文:邵寒霜,李继红.核酸酶BN基因的克隆及序列分析[J].热带作物学报,1997,18(1):46-49.
作者姓名:邵寒霜  李继红
作者单位:中国热带农业科学院热带作物生物技术国家重点实验室
摘    要:从解淀粉芽孢杆菌中提取染色体DNA,经过PCR扩增得到Bamase(核酸酶BN)基因,然后克隆到质粒P^GEM-72f(+)的Smal位点上并进行序列分析。结果表明,核酸酶BN基因的核苷酸序列与已报道的序列相比具有99.7%的同源性,长度为336bp,根据核苷酸序列推断的氨基酸序列则完全一致。该工作为以后利用核酸酶的特异表达来获得雄性不育植物打下了基础。

关 键 词:核酸酶BN基因  克隆  序列分析

Cloning and Sequencing of the Ribonuclease (Barnase) Gene
Shao Hanshuang, Li Jihong, Chen Shoucai, Zheng Xueqin.Cloning and Sequencing of the Ribonuclease (Barnase) Gene[J].Chinese Journal of Tropical Crops,1997,18(1):46-49.
Authors:Shao Hanshuang  Li Jihong  Chen Shoucai  Zheng Xueqin
Abstract:Chromosomal DNA was isolated from the Bacillus amyloliquefaciens, and Barnase gene was amplified by PCR, then cloned and sequenced at the SmaI site of plasmid PGEM- 7zf(+ ). The result found that the nucleotide sequence with 336 bp in length had a homology of 99 - 7 % as com-pared with the reported sequence. Amino acid sequence was produced according to the nucleotide sequence. Our study makes a future contribution to producing male sterile transgenic plants by using Barnas gene.
Keywords:Barnase gene  cloning  sequencing  
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号