Wu_2013_Appl.Microbiol.Biotechnol_97_2483

Reference

Title : Cloning of a dibutyl phthalate hydrolase gene from Acinetobacter sp. strain M673 and functional analysis of its expression product in Escherichia coli - Wu_2013_Appl.Microbiol.Biotechnol_97_2483
Author(s) : Wu J , Liao X , Yu F , Wei Z , Yang L
Ref : Applied Microbiology & Biotechnology , 97 :2483 , 2013
Abstract :

A dibutyl phthalate (DBP) transforming bacterium, strain M673, was isolated and identified as Acinetobacter sp. This strain could not grow on dialkyl phthalates, including dimethyl, diethyl, dipropyl, dibutyl, dipentyl, dihexyl, di(2-ethylhexyl), di-n-octyl, and dinonyl phthalate, but suspensions of cells could transform these compounds to phthalate via corresponding monoalkyl phthalates. During growth in Luria-Bertani medium, M673 produced the high amounts of non-DBP-induced intracellular hydrolase in the stationary phase. One DBP hydrolase gene containing an open reading frame of 1,095 bp was screened from a genomic library, and its expression product hydrolyzed various dialkyl phthalates to the corresponding monoalkyl phthalates.

PubMedSearch : Wu_2013_Appl.Microbiol.Biotechnol_97_2483
PubMedID: 22729233
Gene_locus related to this paper: acilw-ESTA

Related information

Substrate Dibutyl-phthalate
Gene_locus acilw-ESTA

Citations formats

Wu J, Liao X, Yu F, Wei Z, Yang L (2013)
Cloning of a dibutyl phthalate hydrolase gene from Acinetobacter sp. strain M673 and functional analysis of its expression product in Escherichia coli
Applied Microbiology & Biotechnology 97 :2483

Wu J, Liao X, Yu F, Wei Z, Yang L (2013)
Applied Microbiology & Biotechnology 97 :2483