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一种纳豆芽孢杆菌的分子鉴定及纳豆激酶基因克隆
引用本文:李建强,石洪凌,肖冬光.一种纳豆芽孢杆菌的分子鉴定及纳豆激酶基因克隆[J].唐山师范学院学报,2013(2):37-40.
作者姓名:李建强  石洪凌  肖冬光
作者单位:天津科技大学生物工程学院;唐山师范学院生命科学系
摘    要:以实验室保藏的一株具有溶解血栓能力的芽孢杆菌(LJQ—NK)为出发菌株,通过形态学分析和16SrRNA比对,对菌株进行鉴定,更进一步利用聚合酶链式反应(PCR)克隆纳豆激酶DNA片段⑤16SrRNA比对。结果表明LJQ-NK与已报道的纳豆激酶16SrRNA序列有99.9%以上的同源性,初步认定为一株纳豆芽孢杆菌。克隆获得1120bp的DNA片段,应用DNAMAN软件分析,与已报道的纳豆激酶编码基因(G129164926)存在两个碱基的差异,编码纳豆激酶开放阅读框区域序列完全相同。

关 键 词:纳豆芽孢杆菌  纳豆激酶  16S  rRNA比对

Molecular Indentification of Bacillus Subtilis Natto and Clone Gene ofNattokinase
LI Jian-qiang,SHI Hong-ling,XIAO Dong-guang.Molecular Indentification of Bacillus Subtilis Natto and Clone Gene ofNattokinase[J].Journal of Tangshan Teachers College,2013(2):37-40.
Authors:LI Jian-qiang  SHI Hong-ling  XIAO Dong-guang
Institution:1(1.College of Biotechnology,Tianjin University of Science and Technology,Tianjin 300000,China;2.Department of Life Science,Tangshan Teachers College,Tangshan 063000,China)
Abstract:LJQ-NK, a strain with ability of fibrinolysis was identified by molecular biology method. Sequence analysis shows that the homology of 16S rRNA between LJQ-NK and Bacillus subtilis natto was exceeded 99. 9%. The putative nattokinase cDNA was cloned from LJQ-NK using RT-PCR and a 1 126 bp cDNA clone was obtained. Result of BLAST-X sequence homology search show that two bases of putative nattokinase cDNA clone were differed from nattokinase and the ORF sequence ofnattokinase between LJQ-NK and Bacillus subtilis natto were identical.
Keywords:Bacillus subtilis natto  Nattokinase  16S rRNA gene alignment
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