Granston A E, Alessi D M, Eades L J, Friedman D I
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor 48109.
Mol Gen Genet. 1988 Apr;212(1):149-56. doi: 10.1007/BF00322458.
A mutant of lambda was isolated that grows in the Escherichia coli himA delta/gyrB-him320(Ts) double mutant at 42 degrees C; conditions which are non-permissive for wild-type lambda growth. The responsible mutation, ohm1, alters the 40th codon of the Nul reading frame. The Nul and A gene products comprise the terminase protein which cleaves concatameric DNA into unit-length phage genomes during DNA packaging. The Nul-ohm1 gene product acts in trans to support lambda growth in the double himA/gyrB mutant, and lambda cos154 growth in the single himA mutant. The observation that an alteration in Nul suppresses the inhibition of growth in the double himA/gyrB mutant implicates DNA gyrase, as well as integration host factor, in the DNA:protein interactions that occur at the initiation of packaging.
分离出一种λ噬菌体突变体,它能在大肠杆菌himA缺失/gyrB-him320(Ts)双突变体中于42℃生长;而在这些条件下野生型λ噬菌体无法生长。导致该现象的突变ohm1改变了Nul阅读框的第40个密码子。Nul和A基因产物构成了末端酶蛋白,该蛋白在DNA包装过程中将串联体DNA切割成单位长度的噬菌体基因组。Nul-ohm1基因产物以反式作用支持λ噬菌体在双himA/gyrB突变体中的生长,以及λ噬菌体cos154在单himA突变体中的生长。Nul的改变能抑制双himA/gyrB突变体中生长抑制的这一观察结果表明,DNA回旋酶以及整合宿主因子参与了包装起始时发生的DNA:蛋白质相互作用。