Zinkevich V E, Alekseev A M, Taniashin V I
Mol Biol (Mosk). 1986 Nov-Dec;20(6):1638-44.
E. coli hsd genes were subcloned from lambda 642 (ral+) into lambda L47.1 vector (ral-after replacement). The influence of bacteriophage lambda ral gene on the expression efficiency of hsdS kappa, hsdM kappa genes was investigated. It was shown, that its presence in vitro enhanced the synthesis of beta-subunit, hsdM gene product, and the increase of modification in vivo was observed. It is proposed that the increase of modification rate of lambda phage fully unmodified DNA is connected with the appearance of E. coli DNA methylase consisting of beta- and gamma-subunits but lacking alpha-subunit.
大肠杆菌的hsd基因从λ642(ral+)亚克隆到λL47.1载体(替换后ral-)中。研究了噬菌体λral基因对hsdSκ、hsdMκ基因表达效率的影响。结果表明,其在体外的存在增强了β亚基(hsdM基因产物)的合成,并观察到体内修饰的增加。有人提出,λ噬菌体完全未修饰DNA修饰率的增加与由β亚基和γ亚基组成但缺乏α亚基的大肠杆菌DNA甲基化酶的出现有关。