摘要
对紫云英根瘤菌7653R基因文库的5个重组质粒,即pNR102,pNR103,pNR108,pNR203,pNR213进行各种内切酶的酶切分析。结果证实它们均含有1.7kb的EcoRⅠ-Bg1Ⅱ双酶切片段和1.9kb的EcoRⅠ-SacⅠ双酶切片段,而pNR213的外源片段最大,包含有其余质粒所具有的各种片段。以pNR108的外源片段作探针,进行DIG杂交,发现探针与其余4个重组质粒的外源片段有强的同源杂交;与7653R的内源质粒杂交还表明,pNR108的外源片段来源于共生质粒pRa7-2。
The recombinant plasmids, pNR102, pNR103, pNR108, pNR203,and pNR213, from Rhizobium huakuii strain 7653R (field type), were digested with differrent endonucleases. The cleavage mapping showed that they all contained 1.7 kb and 1.9 kb fragments. The probe was prepared with the foreign fragment of plasmid pNR108.Its DIG hybridization showed that the probe had extensive homologization with other foreign fragments of the recombinant plasmids. It also showed that the foreign fragment of plasmid pNR108 came from the symbiotic plasmid of strain 7653R.
出处
《华中农业大学学报》
CAS
CSCD
北大核心
1994年第6期531-537,共7页
Journal of Huazhong Agricultural University
基金
国家自然科学基金
关键词
重组质粒
紫云英
根瘤菌
互补结瘤菌株
recombinant plasmid
restriction endonuclease
DIG hybridization