PURIFICATION METHODS FOR RECOMBINANT LACTOBACILLUS-CASEI THYMIDYLATE SYNTHASE AND MUTANTS - A GENERAL, AUTOMATED PROCEDURE

被引:32
作者
KEALEY, JT
SANTI, DV
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94143
[2] UNIV CALIF SAN FRANCISCO,DEPT PHARMACEUT CHEM,SAN FRANCISCO,CA 94143
关键词
D O I
10.1016/S1046-5928(05)80039-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
General procedures for the rapid, large-scale purification of recombinantLactobacillus casei thymidylate synthase and its mutants have been established. An effective method employs sequential phosphocellulose and hydroxylapatite chromatography. Crude cell extracts are directly applied to phosphocellulose, and the enzyme is obtained in a nearly pure state by stepwise elution with KCI. The eluate is directly applied to hydroxylapatite, and the homogeneous enzyme is eluted with a gradient of potassium phosphate. The method has been successful for the purification of recombinant wild-type enzyme and all mutants thus far examined. The entire purification procedure has been automated using a commonly available FPLC system and can be performed in several hours with minimal operator time. © 1992 Academic Press, Inc.
引用
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页码:380 / 385
页数:6
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