HIGH-LEVEL EXPRESSION IN ESCHERICHIA-COLI AND PURIFICATION OF YEAST TRANSCRIPTION FACTOR IIIA

被引:11
|
作者
OTTONELLO, S
BALLABENI, A
SONCINI, C
DIECI, G
机构
[1] Institute of Biochemical Sciences, University of Parma
关键词
D O I
10.1006/bbrc.1994.2312
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Saccharomyces cerevisiae transcription factor IIIA, a sequence-specific DNA binding protein that is required for transcription of 5S rRNA genes by RNA polymerase III, has been expressed in Escherichia coli in a full length, native form. High level expression was achieved through the combined use of a T7 RNA polymerase expression system and of a multicopy plasmid carrying an E.coli gene, argU, which codes for a minor Arg(AGA/AGG) tRNA species. Recombinant yeast transcription factor IIIA was purified to 95% homogeneity, at a final yield of 8 mg/liter of bacterial culture, by three chromatographic steps, and it was shown to be at least 55% active by quantitative in vitro transcription assays. (C) 1994 Academic Press, Inc.
引用
收藏
页码:1217 / 1223
页数:7
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