Collins J, Hohn B
Proc Natl Acad Sci U S A. 1978 Sep;75(9):4242-6. doi: 10.1073/pnas.75.9.4242.
Evidence is presented that ColE1 hybrid plasmids carrying the cohesive-end site (cos) of lambda can be used as gene cloning vectors in conjunction with the lambda in vitro packaging system of Hohn and Murray [(1977) Proc. Natl. Acad. Sci. USA 74, 3259--3263]. Due to the requirement for a large DNA molecule for efficient packaging, there is a direct selection for hybrids carrying large sections of foreign DNA. The small vector plasmids do not contribute a large background in the transduced population, which is therefore markedly enriched for large hybrid plasmids (over 90%). The efficiency of the in vitro packaging system is on the order of 10(5) hybrid clones per microgram of foreign DNA for hybrids in the 20--30 million dalton range.
有证据表明,携带λ噬菌体粘性末端位点(cos)的ColE1杂种质粒可与霍恩和默里的λ噬菌体体外包装系统[(1977年)《美国国家科学院院刊》74, 3259 - 3263]一起用作基因克隆载体。由于高效包装需要大的DNA分子,因此可直接筛选携带大片段外源DNA的杂种。小载体质粒在转导群体中不会产生大量背景,因此转导群体中显著富集了大型杂种质粒(超过90%)。对于2000万至3000万道尔顿范围内的杂种,体外包装系统的效率约为每微克外源DNA产生10⁵个杂种克隆。