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作 者:洪青[1] 徐剑宏[1] 王云端[1] 武俊[1] 张晓舟[1] 李顺鹏[1]
机构地区:[1]南京农业大学生命科学学院/农业部农业环境微生物工程重点开放实验室
出 处:《应用与环境生物学报》2006年第3期375-378,共4页Chinese Journal of Applied and Environmental Biology
基 金:国家自然基金项目(No.30400013);江苏省科技厅项目(BG2005322);南京农业大学SRT项目(0506A10)资助~~
摘 要:通过固体亚硝基胍诱变获得了Halom onassp.BYS-1的盐敏感突变株BYS-1M.以pBBR1MCS-2为载体在E.coliDH5α中构建了BYS-1的基因文库.以文库菌E.coliDH5α(pBBR-X)为供体菌、E.coliWD803(pRK2013)为辅助菌、BYS-1M为受体菌进行三亲接合,筛选到了恢复耐盐性能的接合子HR-23,提取接合子HR-23的重组质粒pHR23,酶切确定其插入的耐盐相关DNA片段大小分为5.4 kb.该片段为Halom onassp.BYS-1耐盐相关基因的克隆奠定了基础.A salt-sensitive mutant BYS-1M of strain Halomonas sp. BYS-1 was obtained by nitriguanidine mutagenesis. The gene library of BYS-1 was constructed in E. coli OHSα with pBBR1MCS-2 as the vector by the method of shotgun cloning. Triparental conjucation was conducted with BYS-1M as recipient, the library strain E. coil DHSα (pBBR-X) as donors and E. coil WD803 (pRK2013) as helper, In this way, the gene library of BYS-1 was transferred into BYS-1M to look for the complementation of the mutant, One hybrid named HR-23, which had recovered the same salt-tolerance characteristics as the original strain BYS-1 was obtained, The recombinant plasmid pHR-23 was extracted from the HR-23 and subjected to restriction analysis; the results showed that the length of inserted salt-tolerance related DNA fragment in pHR-23 was 5.4 kb. This fragment laid the foundation for the cloning of salt-related gene of Halomonas sp, BYS-1. Fig 5, Tab 1, Ref 14
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