Arif_2012_Appl.Environ.Microbiol_78_6128

Reference

Title : Novel dehalogenase mechanism for 2,3-dichloro-1-propanol utilization in Pseudomonas putida strain MC4 - Arif_2012_Appl.Environ.Microbiol_78_6128
Author(s) : Arif MI , Samin G , van Leeuwen JG , Oppentocht J , Janssen DB
Ref : Applied Environmental Microbiology , 78 :6128 , 2012
Abstract :

A Pseudomonas putida strain (MC4) that can utilize 2,3-dichloro-1-propanol (DCP) and several aliphatic haloacids and haloalcohols as sole carbon and energy source for growth was isolated from contaminated soil. Degradation of DCP was found to start with oxidation and concomitant dehalogenation catalyzed by a 72-kDa monomeric protein (DppA) that was isolated from cell lysate. The dppA gene was cloned from a cosmid library and appeared to encode a protein equipped with a signal peptide and that possessed high similarity to quinohemoprotein alcohol dehydrogenases (ADHs), particularly ADH IIB and ADH IIG from Pseudomonas putida HK. This novel dehalogenating dehydrogenase has a broad substrate range, encompassing a number of nonhalogenated alcohols and haloalcohols. With DCP, DppA exhibited a k(cat) of 17 s(-1). (1)H nuclear magnetic resonance experiments indicated that DCP oxidation by DppA in the presence of 2,6-dichlorophenolindophenol (DCPIP) and potassium ferricyanide [K(3)Fe(CN)(6)] yielded 2-chloroacrolein, which was oxidized to 2-chloroacrylic acid.

PubMedSearch : Arif_2012_Appl.Environ.Microbiol_78_6128
PubMedID: 22752160
Gene_locus related to this paper: psepu-a0a083utf1 , psepu-a0a083uhh3

Related information

Citations formats

Arif MI, Samin G, van Leeuwen JG, Oppentocht J, Janssen DB (2012)
Novel dehalogenase mechanism for 2,3-dichloro-1-propanol utilization in Pseudomonas putida strain MC4
Applied Environmental Microbiology 78 :6128

Arif MI, Samin G, van Leeuwen JG, Oppentocht J, Janssen DB (2012)
Applied Environmental Microbiology 78 :6128