Mouches C, Barroso G, Bové J M
J Bacteriol. 1983 Nov;156(2):952-5. doi: 10.1128/jb.156.2.952-955.1983.
Two plasmids, pMH1 with 7 kilobase pairs and pM41 with 8 kilobase pairs, were purified from the plant pathogen Spiroplasma citri and characterized by restriction mapping. Upon in vitro DNA recombination with plasmid pBR328 as a vector, we have cloned pMH1 in Escherichia coli. A radioactive probe obtained upon nick translation of the recombinant plasmid was used to further characterize and compare pMH1 and pM41.
从植物病原体柑橘螺原体中纯化出两个质粒,分别是7千碱基对的pMH1和8千碱基对的pM41,并通过限制性酶切图谱分析对其进行了表征。以质粒pBR328作为载体进行体外DNA重组后,我们已将pMH1克隆到大肠杆菌中。通过对重组质粒进行切口平移获得的放射性探针,用于进一步表征和比较pMH1和pM41。