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极端嗜热厌氧纤维素分解菌基因文库的构建及其内切葡聚糖酶基因片段的克隆

Construction Genomic Library of Extremely Thermophilic Anaerobic Bacterium BANG 2 and Cloning of Endoglucanase Gene Fragments

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【作者】 洪芳田宇徐恒邓宇胡国全张辉

【Author】 HONG Fang~(1),TIAN Yu~(1),XU Heng~(1),DENG Yu~(2), HU Guo-quan~(2),ZHANG Hui~(2) (1.College of Life Science,Sichuan University,Chengdu 610064,China;2.Biogas Institute of the Ministry of Agriculture,Chengdu 610041,China)

【机构】 四川大学生命科学学院农业部沼气科学研究所农业部沼气科学研究所 成都610064成都610064成都610041成都610041

【摘要】 以从云南邦拿掌温泉中分离、纯化的高温厌氧纤维素分解菌邦2菌(Cadicellulosiruptor)为材料,制备其总DNA,经限制性核酸内切酶EcoRⅠ部分酶切后,在T4DNA连接酶的作用下与经EcoRⅠ完全酶切、去磷酸化的质粒载体pUC18连接,然后转化E.coliJM109,建立了邦2的基因文库,经筛选鉴定得到6.3×103个重组子;重组子经刚果红平板验证:约有23.5%菌落呈现透明圈;重组子经EcoRⅠ酶切验证显示:重组质粒均含有外源DNA插入片段.结果表明已克隆到邦2菌纤维素酶系中的内切葡聚糖酶基因(ED基因)片段.

【Abstract】 An extremely thermophilic anaerobic bacterium was isolated from Bangnazhang hotspring in Yunnan province, named Bang2. The strain Bang2 was initially identified as Cadicellulo siruptor.Genomic DNA of Bang2 was extracted and was partially digested by restriction enzyme EcoRⅠ,and ligated with plasmid pUC18 by T4DNA ligase. After transformation E.coli JM109,the genomic library was constructed and 6.3×103recombinants was obtained.The ratio of the recombinants which formed transparent zones on the Congo Red plates was 23.5%. The results after digested by restriction enzyme EcoRⅠrevealed that the recombinants which had been picked out contained foreign DNA fragments. The results showed that the endoglucanase gene has been cloned.

【基金】 2002年四川省科技厅重点科技项目(02SG022 022)
  • 【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06期
  • 【分类号】Q933
  • 【被引频次】20
  • 【下载频次】432
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