| 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 |
| Substrate | Dibutyl-phthalate |
| Gene_locus | acilw-ESTA |
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