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一种由T4 DNA连接酶催化的新型DNA连接活性。

A novel DNA joining activity catalyzed by T4 DNA ligase.

作者信息

Western L M, Rose S J

机构信息

Research Department, Syva Company, Palo Alto, CA 94304.

出版信息

Nucleic Acids Res. 1991 Feb 25;19(4):809-13. doi: 10.1093/nar/19.4.809.

Abstract

The use of T4 and E. coli DNA ligases in genetic engineering technology is usually associated with nick-closing activity in double stranded DNA or ligation of 'sticky-ends' to produce recombinant DNA molecules. We describe in this communication the ability of T4 DNA ligase to catalyze intramolecular loop formation between annealed oligodeoxyribonucleotides wherein Watson-Crick base pairing is absent on one side of the ligation site. Enzyme concentration, loop size, substrate specificity, and base composition were explored in an effort to maximize yield. Amounts of T4 DNA ligase in large molar excess to DNA template and ligated product are necessary to achieve high yields.

摘要

在基因工程技术中,T4和大肠杆菌DNA连接酶的使用通常与双链DNA中的切口封闭活性或“粘性末端”的连接相关,以产生重组DNA分子。在本通讯中,我们描述了T4 DNA连接酶催化退火寡脱氧核糖核苷酸之间分子内环形成的能力,其中在连接位点的一侧不存在沃森-克里克碱基配对。为了使产量最大化,我们研究了酶浓度、环大小、底物特异性和碱基组成。为了获得高产,需要大量摩尔过量的T4 DNA连接酶相对于DNA模板和连接产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0a3/333715/db79f309d45d/nar00240-0116-a.jpg

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