Kosak H G, Kemper B W
Institut für Genetik der Universität zu Köln, Federal Republic of Germany.
Eur J Biochem. 1990 Dec 27;194(3):779-84. doi: 10.1111/j.1432-1033.1990.tb19469.x.
Endonuclease VII is the product of gene 49 of phage T4 and was the first enzyme shown to resolve Holliday structures in vitro [Mizuuchi, K. et al. (1982) Cell 29, 357-365]. Low amounts of the enzyme were originally purified from phage-infected cells [Kemper, B. & Garabett, M. (1981) Eur. J. Biochem. 115, 123-131]. We now report a purification procedure for milligram amounts of cloned endonuclease VII expressed in Escherichia coli with gene 49 under the control of a temperature-inducible promoter on a plasmid system [Tomaschewski, J. (1988) PhD Thesis, University of Bochum, FRG]. The protein was purified 500-fold from crude extracts in five steps with a recovery of 15%. The steps include (a) poly(ethyleneglycol)/dextran two-phase separation; (b) DEAE-cellulose; (c) single-stranded DNA-agarose; (d) Mono-Q and (e) Mono-S chromatography. The final protein was more than 98% pure as estimated from SDS/PAGE analysis. The protein has an apparent molecular mass of 17.8 kDa on SDS-containing polyacrylamide gels and 36 kDa when determined by gel filtration or sedimentation through sucrose gradients in the presence of high salt (600 mM NaCl). In the absence of additional salt, the enzyme has a tendency to aggregate and products of molecular masses differing in steps of about 18 kDa appear on SDS-containing polyacrylamide gels.
核酸内切酶VII是噬菌体T4基因49的产物,是第一个被证明能在体外解析霍利迪结构的酶[水内, K.等人(1982年)《细胞》29卷, 357 - 365页]。最初从噬菌体感染的细胞中纯化出少量该酶[肯珀, B. & 加拉贝特, M. (1981年)《欧洲生物化学杂志》115卷, 123 - 131页]。我们现在报告一种纯化程序,可从在质粒系统上由温度诱导型启动子控制的带有基因49的大肠杆菌中表达的核酸内切酶VII中纯化出毫克量的该酶[托马舍夫斯基, J. (1988年)博士论文,德国波鸿大学]。该蛋白从粗提物中经五步纯化了500倍,回收率为15%。这些步骤包括:(a)聚乙二醇/葡聚糖双相分离;(b)DEAE - 纤维素;(c)单链DNA - 琼脂糖;(d)Mono - Q和(e)Mono - S层析。根据SDS/PAGE分析估计,最终蛋白纯度超过98%。在含SDS的聚丙烯酰胺凝胶上,该蛋白的表观分子量为17.8 kDa,而在高盐(600 mM NaCl)存在下通过凝胶过滤或蔗糖梯度沉降测定时为36 kDa。在没有额外盐的情况下,该酶有聚集的倾向,在含SDS的聚丙烯酰胺凝胶上会出现分子量以约18 kDa步长变化的产物。