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PnrA, a new nitroreductase‐family enzyme in the TNT‐degrading strain Pseudomonas putida JLR11
Author(s) -
Caballero Antonio,
Lázaro Juan J.,
Ramos Juan L.,
EsteveNúñez Abraham
Publication year - 2005
Publication title -
environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.954
H-Index - 188
eISSN - 1462-2920
pISSN - 1462-2912
DOI - 10.1111/j.1462-2920.2005.00801.x
Subject(s) - nitroreductase , pseudomonas putida , biology , enzyme , flavoprotein , biochemistry , escherichia coli , pseudomonas , hydroxylamine , bacteria , microbiology and biotechnology , strain (injury) , gene , genetics , anatomy
Summary Nitroreductases are a group of proteins that catalyse pyridine nucleotide‐dependent reduction of nitroaromatics compounds, showing significant human health and environmental implications. In this study we have identified the nitroreductase‐family enzymes PnrA and PnrB from the TNT‐degrading strain Pseudomonas putida . The enzyme encoded by the pnrA gene was expressed in Escherichia coli , purified to homogeneity and shown to be a flavoprotein that used 2 mol of NADPH to reduce 1 mol of 2,4,6‐trinitrotoluene (TNT) to 4‐hydroxylamine‐2,6‐dinitrotoluene, using a ping‐pong bi‐bi mechanism. The PnrA enzyme also recognized as substrates as a number of other nitroaromatic compounds, i.e. 2,4‐dinitrotoluene, 3‐nitrotoluene, 3‐ and 4‐nitrobenzoate, 3,5‐dinitrobenzamide and 3,5‐dinitroaniline expanding the substrates profile from previously described nitroreductases. However, TNT resulted to be the most efficient substrate examined according to the V max /K m parameter. Expression analysis of pnrA ‐ and pnrB ‐mRNA isolated from cells growing on different nitrogen sources suggested that expression of both genes was constitutive and that its level of expression was relatively constant regardless of the growth substrate. This is in agreement with enzyme‐specific activity determined with cells growing with different N‐sources.