Hoheisel J D
Fakultät für Biologie, Universität Konstanz, Germany.
Anal Biochem. 1993 Mar;209(2):238-46. doi: 10.1006/abio.1993.1114.
Exonuclease III (Exo III) of Escherichia coli is a DNA-modifying enzyme very frequently used in molecular biology. The experiments described here were carried out with the aims of reliably controlling exonuclease activity and of learning more about the enzyme's specificities. The dependence of Exo III activity on factors such as temperature (including heat inactivation), the concentrations of Exo III and NaCl, and the concentration and shape of 3' termini was investigated. Double stranded DNA was found to be a competitive inhibitor of the enzyme activity. Some four nucleotide 3' protrusions were shown to be sensitive to Exo III digestion. The synchronism of deletion was also examined. Implications for the proposed mechanism of activity are discussed.
大肠杆菌核酸外切酶III(Exo III)是一种在分子生物学中非常常用的DNA修饰酶。本文所述实验旨在可靠地控制核酸外切酶活性,并进一步了解该酶的特异性。研究了Exo III活性对温度(包括热失活)、Exo III和NaCl浓度以及3'末端浓度和形状等因素的依赖性。发现双链DNA是该酶活性的竞争性抑制剂。结果表明,一些四个核苷酸的3'突出端对Exo III消化敏感。还研究了缺失的同步性。并讨论了对所提出的活性机制的影响。