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作 者:WANG CHANG-LIN 王常霖(Institute of Plant Physiology,Academia Sinica,Shanghai 200032,PRC)
机构地区:[1]Institute of Plant Physiology,Academia Sinica,Shanghai 200032,PRC
出 处:《Science China Chemistry》1991年第4期429-437,共9页中国科学(化学英文版)
基 金:Project supported by the National Postdoctoral Science Foundation of China.
摘 要:A recombinant transposon Tn5-GmSp,produced by replacing the central BglⅡfragmentwith a BamHⅠone of R1033,was utilized to detect Tn5 transposition inhibition in Rhizo-bium leguminosarum.Two types of suicide plasmids(pXS102 and pCW3/pCW30)were con-structed for Tn5-GmSp transposition.The frequency of transposition in both constructs wasgreatly reduced in the Rhizobium strains where a resident Tn5 was already present.WhenpXS102 was transferred into a Tn5-containing Rhizobium strain,the transconjugants retainedthe deleted forms of pXS102,indicating that the failure of transposition was due to the lossof the unstable prophage Mu element.In the case of pCW3/pCW30,vectors were not ob-served in the transconjugants although most of them retained the antibiotic resistant markers.This result suggested the integration of Tn5-GmSp into the rhizobial host genome through recombination.
关 键 词:R.leguminosarum recombinant Tn5-CmSp transposition inhibition Tn5 in situ replacement
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