An unusually cold active nitroreductase for prodrug activations

被引:38
作者
Celik, Ayhan [1 ]
Yetis, Gulden [1 ]
机构
[1] Gebze Inst Technol, Dept Chem, TR-41400 Gebze, Turkey
关键词
Nitroreductase; Cold active enzyme; Prodrug activation; CB1954; Staphylococcus saprophyticus; Nitrofurazone; OXYGEN-INSENSITIVE NITROREDUCTASES; FMN-DEPENDENT NITROREDUCTASE; MAJOR FLAVIN REDUCTASE; CROSS-LINKING AGENT; ESCHERICHIA-COLI; VIBRIO-HARVEYI; 5-(AZIRIDIN-1-YL)-2,4-DINITROBENZAMIDE CB-1954; BIOCHEMICAL-CHARACTERIZATION; STRUCTURAL-CHARACTERIZATION; SALMONELLA-TYPHIMURIUM;
D O I
10.1016/j.bmc.2012.04.004
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
A set of PCR primers based on the genome sequence were used to clone a gene encoding a hypothetical nitroreductases (named as Ssap-NtrB) from uropathogenic staphylococcus, Staphylococcus saprophyticus strain ATCC 15305, an oxygen insensitive flavoenzyme. Activity studies of the translation product revealed that the nitroreductase catalyses two electron reduction of a nitroaromatic drug of nitrofurazone (NFZ), cancer prodrugs of CB1954 and SN23862 at optimum temperature of 20 degrees C together with retaining its maximum activity considerably at 3 degrees C. The required electrons for such reduction could be supplied by either NADH or NADPH with a small preference for the latter. The gene was engineered for heterologous expression in Escherichia coli, and conditions were found in which the enzyme was produced in a mostly soluble form. The recombinant enzyme was purified to homogeneity and physical, spectral and catalytical properties were determined. The findings lead us to propose that Ssap-NtrB represents a novel nitro reductase with an unusual cold active property, which has not been described previously for prodrug activating enzymes of nitroreductases. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3540 / 3550
页数:11
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