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通过顺序酶切制备质粒DNA。

Preparation of plasmid DNA by sequential enzymatic digestion.

作者信息

Hyman E D

机构信息

Sybtrel Biotechnology, Harahan, LA 70123.

出版信息

Biotechniques. 1992 Oct;13(4):550-4.

PMID:1362068
Abstract

A new method for the preparation of plasmid DNA from Escherichia coli, sequential enzymatic digestion, is described. The method is based on sequential and selective enzymatic digestion of all components of E. coli except for the supercoiled plasmid DNA. The key enzymes are exonuclease I and exonuclease III that specifically hydrolyze linear chromosomal DNA and are unable to attack supercoiled plasmid DNA under controlled conditions. Isolated plasmid DNA can be sequenced and digested with restriction enzymes.

摘要

本文描述了一种从大肠杆菌中制备质粒DNA的新方法——连续酶切法。该方法基于对大肠杆菌所有成分(除超螺旋质粒DNA外)进行连续且选择性的酶切。关键酶是核酸外切酶I和核酸外切酶III,它们能特异性水解线性染色体DNA,且在可控条件下无法作用于超螺旋质粒DNA。分离得到的质粒DNA可进行测序并用限制性内切酶进行酶切。

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