Shibusawa Yoichi, Takeuchi Naoko, Sugawara Kazusa, Yanagida Akio, Shindo Heisaburo, Ito Yoichiro
Division of Structural Biology and Analytical Science, School of Pharmacy, Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Dec 5;844(2):217-22. doi: 10.1016/j.jchromb.2006.07.028. Epub 2006 Aug 7.
New aqueous-aqueous two-phase systems composed of relatively low molecular weight polymers such as polyethylene glycol (PEG) (Mr: 1000-4000) and dextran (Mr: 10,000 and 40,000) were evaluated for purification of proteins by counter-current chromatography (CCC). The compositions of aqueous two-phase systems were optimized by measuring parameters such as viscosity and volume ratio between the two phases. CCC purification of a glucosyltransferase (GTF) from Streptococcus mutans (SM) cell-lysate was successfully demonstrated with a 7.5% PEG 3350-10% dextran T40 system containing 10mM potassium phosphate buffer at pH 9.0. After CCC purification, both PEG and dextran contained in the CCC fractions were easily removed by ultrafiltration in a short period of time. The fractionated column contents containing GTF were analyzed by enzymatic activity as well as sodium dodecyl sulfate (SDS) polyacrylamide gel electrophoresis. The recovery of the enzyme from CCC fraction was over 95% as estimated by enzymatic activities.
对由相对低分子量聚合物(如聚乙二醇(PEG)(分子量:1000 - 4000)和葡聚糖(分子量:10,000和40,000))组成的新型水-水两相系统进行了逆流色谱法(CCC)纯化蛋白质的评估。通过测量诸如两相之间的粘度和体积比等参数,对水两相系统的组成进行了优化。在含有10mM磷酸钾缓冲液(pH 9.0)的7.5% PEG 3350 - 10%葡聚糖T40系统中,成功证明了从变形链球菌(SM)细胞裂解物中逆流色谱法纯化葡糖基转移酶(GTF)。在逆流色谱法纯化后,通过超滤在短时间内很容易去除CCC级分中所含的PEG和葡聚糖。通过酶活性以及十二烷基硫酸钠(SDS)聚丙烯酰胺凝胶电泳对含有GTF的分级柱内容物进行了分析。根据酶活性估计,从CCC级分中回收的酶超过95%。