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作 者:农广[1] 张忠明[1] 胡福荣[1] 陈华癸[1]
机构地区:[1]华中农业大学农业微生物重点开放实验室,武汉430070
出 处:《微生物学报》1998年第3期225-228,共4页Acta Microbiologica Sinica
基 金:国家攀登计划;国家自然科学基金
摘 要:The large plasmids of strain 7653R were digested with restriction enzyme EcoRI. Their DNA fragments were cloned into the expression vector pMP220 to construct a lacZ fusion pool, which were transferred into the recipient strain 7653R Tri-transconjugants were selected onto plates containing X-gal and seed extract Five blue colonies were assayed of their β-galactosidase activity after incubation with or without seed extract. A positive induced strain HN18 was obtained. Hybridization of nodDABC probe on the recombinant plasmid pHN18 showed a 1.7kb positive band.The evidence makes a deduction that the pHN18 containes a promoter of nod operon.The large plasmids of strain 7653R were digested with restriction enzyme EcoRI. Their DNA fragments were cloned into the expression vector pMP220 to construct a lacZ fusion pool, which were transferred into the recipient strain 7653R Tri-transconjugants were selected onto plates containing X-gal and seed extract Five blue colonies were assayed of their β-galactosidase activity after incubation with or without seed extract. A positive induced strain HN18 was obtained. Hybridization of nodDABC probe on the recombinant plasmid pHN18 showed a 1.7kb positive band.The evidence makes a deduction that the pHN18 containes a promoter of nod operon.
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