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盐生杜氏藻cbr基因的克隆
Molecular Cloning of cbr Gene in Dunaliella.Salina
【摘要】 首先对其他物种cbr/elip基因的同源序列进行相似性分析,设计一对简并引物,利用TR PCR技术获得一250bp的片段,经克隆测序分析发现其同D.bardwail的cbr基因有67.0%的同源性,然后再以此片段为模板设计引物,通过RACE技术构建盐生杜氏藻cbr基因的全长序列.
【Abstract】 At first, the degenerate primers were designed based on the homologous gene of cbr/elip in other organisms. Then, using RTPCR technique, the authors obtained a cDNA fragment of 250bp from D.salina. After cloning and DNA sequencing, the result indicated that 67.0% of the sequence of the fragment was homologous to the cbr in D.bardwail. Based on this sequence, the authors newly designed a pairs of primers. By the RACE technique, the fulllength cDNA of cbr was successfully constructed in D.salina.
【关键词】 同源克隆;
简并引物;
cbr;
RACE;
【Key words】 homologous cloning; degenerate primer; cbr(carotene biosynthesis related); RACE(rapid amplification of cDNA end);
【Key words】 homologous cloning; degenerate primer; cbr(carotene biosynthesis related); RACE(rapid amplification of cDNA end);
【基金】 国家转基因植物与产业化及"863"项目基金
- 【文献出处】 四川大学学报(自然科学版) ,Journal of Sichuan University (Natural Science Edition) , 编辑部邮箱 ,2003年03期
- 【分类号】Q943.2
- 【被引频次】10
- 【下载频次】168