Cloning, sequencing and expression of ribonucleotide reductase R2 from Trypanosoma brucei

被引:19
|
作者
Dormeyer, M
Schoneck, R
Dittmar, GAG
KrauthSiegel, RL
机构
[1] UNIV HEIDELBERG,BIOCHEM ZENTRUM HEIDELBERG,D-69120 HEIDELBERG,GERMANY
[2] DEUTSCH KREBSFORSCHUNGSZENTRUM,ABT BIOCHEM ZELLE,D-69120 HEIDELBERG,GERMANY
关键词
ribonucleotide reductase; drug target; trypanothione; (Trypanosoma brucei);
D O I
10.1016/S0014-5793(97)01036-3
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
Ribonucleotide reductase (RR) is an attractive drug target molecule. The gene of the R2 protein of Trypanosoma brucei RR (nrd B) has been cloned. It encodes a protein of 337 residues which shows about 60% identity with other eukaryotic R2 proteins. All residues which bind the iron center, the tyrosyl radical or are supposed to participate in the radical transfer are conserved in the trypanosomal protein sequence Overexpression of the gene in E. coli resulted in 2-5 mg pure R2 protein from 100 ml bacterial cell culture. Northern blot analysis revealed a transcript of 1.85 kb in bloodstream and procyclic forms of the parasite. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:449 / 453
页数:5
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