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Expression,purification and substrate specificities of 3-nitrotoluene dioxygenase from Diaphorobacter sp. strain DS2
Authors:Deepak Singh  Archana Kumari  S. Ramaswamy  Gurunath Ramanathan
Affiliation:1. Department of Chemistry, Indian Institute of Technology, Kanpur 208016, India;2. Institute of Stem Cell Biology and Regenerative Medicine, Bangalore, India
Abstract:3-Nitotoluene dioxygenase (3-NTDO) is the first enzyme in the degradation pathway of 3-nitrotoluene (3-NT) by Diaphorobacter sp. strain DS2. The complete gene sequences of 3-NTDO were PCR amplified from genomic DNA of Diaphorobacter sp., cloned, sequenced and expressed. The 3-NTDO gene revealed a multi component structure having a reductase, a ferredoxin and two oxygenase subunits. Clones expressing the different subunits were constructed in pET21a expression vector system and overexpressed in E. coli BL21(DE3) host. Each subunit was individually purified separately to homogeneity. The active recombinant enzyme was reconstituted in vitro by mixing all three purified subunits. The reconstituted recombinant enzyme could catalyse biotransformations on a variety of organic aromatics.
Keywords:Diaphorobacter   Nitrotoluene (NT)   3-Nitotoluene dioxygenase (3-NTDO)   Biodegradation   Rieske dioxygenase
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