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海洋聚磷菌中核苷二磷酸激酶基因的克隆及序列分析
引用本文:任世英,肖天.海洋聚磷菌中核苷二磷酸激酶基因的克隆及序列分析[J].海洋科学,2008,32(9):61-63.
作者姓名:任世英  肖天
作者单位:1. 中国科学院,海洋研究所,山东,青岛,266071;中国科学院,研究生院,北京,100049
2. 中国科学院,海洋研究所,山东,青岛,266071
基金项目:国家重点基础研究发展计划项目(2006CB400604); 国家自然科学基金资助项目(40376048)
摘    要:以海洋聚磷菌Halomonas YSR-3的总DNA为模板,用PCR法扩增核苷二磷酸激酶基因,将扩增片段克隆到pGM.T载体,转化Escherichia coli TOP10菌株,经蓝白斑筛选、菌落PCR得到阳性克隆,测序后对序列进行Blast比对分析。得到的基因序列长度为420bp,翻译后的序列与Loktanella vestfoldensis SKA53,Jannaschia sp.CCS1,Roseobacter sp.CCS2的核苷二磷酸激酶蛋白序列相似性分别为89%,86%,85%。

关 键 词:盐单胞菌属  聚磷菌  核苷二磷酸激酶(NDPK)
收稿时间:2008/2/28 0:00:00
修稿时间:2008/5/10 0:00:00

Cloning and analyse of nucleoside diphosphate kinase gene sequence from marine polyphosphate-accumulating bacterium, Halomonas YSR-3
REN Shi-ying,XIAO Tian.Cloning and analyse of nucleoside diphosphate kinase gene sequence from marine polyphosphate-accumulating bacterium, Halomonas YSR-3[J].Marine Sciences,2008,32(9):61-63.
Authors:REN Shi-ying  XIAO Tian
Abstract:Nucleoside diphosphate kinase(NDPK) gene was amplified from marine polyphosphate-accumula- ting bacterium Halomonas YSR-3 by PCR and molecular clone techniques and inserted into a pGM-T vector.The recombinant plasmid was transformed into an Escherichia coli TOP10 strain.The positive transformants with NDPK gene were obtained by blue-white selection and clony PCR method,then the positive ones were sequenced. The sequenced fragment concluded 420 pairs of bases and was analyzed by NCBI database.The similaritie...
Keywords:Halomonas  polyphosphate-accumulating bacterium  nucleoside diphosphate kinase(NDPK)  
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