Storts D R, Markovitz A
Department of Biochemistry and Molecular Biology, University of Chicago, Illinois 60637.
J Bacteriol. 1988 Apr;170(4):1541-7. doi: 10.1128/jb.170.4.1541-1547.1988.
Plasmid pJMC21 contains Escherichia coli chromosomal DNA encoding Lon protease, HU-beta (HU-1), and an unidentified 67,000-dalton protein. A kanamycin resistance cassette was used in the construction of insertion and deletion mutations in hupB, the gene encoding HU-beta on plasmid pJMC21. The reconstructed plasmids were linearized and used to introduce hupB chromosomal mutations into JC7623 (recBC sbcBC). These mutations, as expected, mapped in the 9.8-min region of the E. coli chromosome by P1 transduction (16% linkage to proC+). Southern blot hybridization of chromosomal fragments verified that hupB+ was replaced by the mutant allele, with no indication of gene duplication. All the mutant strains had growth rates identical to that of wild-type E. coli, were resistant to UV irradiation and nitrofurantoin, and supported the in vivo transposition-replication of bacteriophage Mu, Mu lysogenization, Tn10 transposition from lambda 1098, and lambda replication-lysogenization. The only observable phenotypic variation was a reduced Mu plaque size on the hupB mutant strains; however, the yield of bacteriophage Mu in liquid lysates prepared from the mutant strains was indistinguishable from the yield for the wild type.
质粒pJMC21含有编码Lon蛋白酶、HU-β(HU-1)和一种未鉴定的67000道尔顿蛋白质的大肠杆菌染色体DNA。卡那霉素抗性盒用于在hupB(质粒pJMC21上编码HU-β的基因)中构建插入和缺失突变。将重建的质粒线性化,并用于将hupB染色体突变引入JC7623(recBC sbcBC)。如预期的那样,通过P1转导,这些突变定位于大肠杆菌染色体的9.8分钟区域(与proC+的连锁率为16%)。染色体片段的Southern印迹杂交证实hupB+被突变等位基因取代,没有基因重复的迹象。所有突变菌株的生长速率与野生型大肠杆菌相同,对紫外线照射和呋喃妥因具有抗性,并支持噬菌体Mu的体内转座复制、Mu溶原化、来自λ1098的Tn10转座以及λ复制-溶原化。唯一可观察到的表型变异是hupB突变菌株上Mu噬菌斑大小减小;然而,从突变菌株制备的液体裂解物中噬菌体Mu的产量与野生型的产量没有区别。