Growth of Dehalococcoides mccartyi strain CBDB1 by reductive dehalogenation of brominated benzenes to benzene

Wagner, A; Cooper, M; Ferdi, S; Seifert, J; Adrian, L

HERO ID

1646072

Reference Type

Journal Article

Year

2012

Language

English

PMID

22800291

HERO ID 1646072
In Press No
Year 2012
Title Growth of Dehalococcoides mccartyi strain CBDB1 by reductive dehalogenation of brominated benzenes to benzene
Authors Wagner, A; Cooper, M; Ferdi, S; Seifert, J; Adrian, L
Journal Environmental Science & Technology
Volume 46
Issue 16
Page Numbers 8960-8968
Abstract Brominated aromatics are used in many different applications but occur also naturally. Here, we demonstrate organohalide respiration and growth of Dehalococcoides mccartyi strain CBDB1 with 1,2,4-tribromobenzene, all three dibrominated benzene congeners and monobromobenzene. All bromobenzenes were fully dehalogenated to benzene. Growth yields were between 1.8 × 10(14) and 2.8 × 10(14) cells per mol of bromide released. Furthermore, a newly designed high-throughput methyl viologen-based photometric microtiter plate assay was established to determine the activity of the reductive dehalogenases in resting cell assays of strain CBDB1 with brominated aromatics as electron acceptors. Activities of 2.8-13.2 nkat per mg total cell protein (0.16-0.8 units per mg total cell protein) were calculated after cultivation of strain CBDB1 on 1,2,4-tribromobenzene. Mass spectrometric analyses and activity assays with whole cell extracts of strain CBDB1 gave strong evidence that four to six reductive dehalogenases were involved in the dehalogenation of all tested brominated benzenes, including the reductive dehalogenases CbdbA80 and CbrA.
Doi 10.1021/es3003519
Pmid 22800291
Wosid WOS:000307697700052
Url <Go to ISI>://WOS:000307697700052
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000307697700052
Is Public Yes
Language Text English