Wegrzyn G
Department of Molecular Biology, University of Gdańsk, Poland.
J Biotechnol. 1995 Dec 1;43(2):139-43. doi: 10.1016/0168-1656(95)00132-5.
It was previously demonstrated that, contrary to wild-type stringent (rel+) strains of Escherichia coli, in amino acid-starved relaxed (relA) mutants the replication of lambda plasmid proceeds for several hours. The replication leads to amplification of lambda plasmid DNA. Here, the conditions for this amplification have been optimized. The amplification efficiency depends on the temperature as well as on the nature of amino acid starvation, but it is only little or totally not dependent on the pH value of the medium in a range from 6.0 to 8.0. It seems that the most efficient amplification can be achieved by overnight cultivation of E. coli relA arg strain harbouring lambda plasmid at 36-39 degrees C in minimal medium containing Casamino acids. Under these conditions, the copy number of lambda plasmid increases from about 40 to about 300 per cell giving greater than 7-fold amplification.
先前已证明,与野生型严格(rel +)大肠杆菌菌株相反,在氨基酸饥饿的松弛(relA)突变体中,λ质粒的复制会持续数小时。这种复制导致λ质粒DNA的扩增。在此,已对这种扩增的条件进行了优化。扩增效率取决于温度以及氨基酸饥饿的性质,但在6.0至8.0的范围内,它仅很少或完全不依赖于培养基的pH值。似乎通过在含有酪蛋白氨基酸的基本培养基中于36 - 39℃过夜培养携带λ质粒的大肠杆菌relA arg菌株,可以实现最有效的扩增。在这些条件下,λ质粒的拷贝数从每个细胞约40增加到约300,实现了大于7倍的扩增。