Cloning of a dibutyl phthalate hydrolase gene from Acinetobacter sp. strain M673 and functional analysis of its expression product in Escherichia coli

Wu, J; Liao, X; Yu, F; Wei, Z; Yang, L

HERO ID

1332542

Reference Type

Journal Article

Year

2013

Language

English

PMID

22729233

HERO ID 1332542
In Press No
Year 2013
Title Cloning of a dibutyl phthalate hydrolase gene from Acinetobacter sp. strain M673 and functional analysis of its expression product in Escherichia coli
Authors Wu, J; Liao, X; Yu, F; Wei, Z; Yang, L
Journal Applied Microbiology and Biotechnology
Volume 97
Issue 6
Page Numbers 2483-2491
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.
Doi 10.1007/s00253-012-4232-8
Pmid 22729233
Wosid WOS:000315650100018
Url https://search.proquest.com/docview/1469194629?accountid=171501
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword article; Acinetobacter; Carboxylic Ester Hydrolases; Cloning, Molecular; DNA, Bacterial; Dibutyl Phthalate; Escherichia coli; Kinetics; Molecular Sequence Data; Sequence Analysis, DNA; Substrate Specificity; bacteria; cell suspension culture; genomic libraries; open reading frames