Halopicolinic acids, novel products arising through the degradation of chloro- and bromobiphenyl by Sphingomonas paucimobilis BPSI-3

Annette D. Davison; Peter Karuso; Daniel R. Jardine; Duncan A. Veal

doi:10.1139/m96-009

Halopicolinic acids, novel products arising through the degradation of chloro- and bromobiphenyl by Sphingomonas paucimobilis BPSI-3

Annette D. Davison^*, Peter Karuso, Daniel R. Jardine, Duncan A. Veal

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

13 Citations (Scopus)

Abstract

Sphingomonas paucimobilis BPSI-3 was previously isolated from a mixed microbial consortium growing on biphenyl as the sole source of carbon and energy. Transformation of 4-chlorobiphenyl (4CBP) was demonstrated by this strain, although little or no growth was observed. In minimal salts medium supplemented with 4CBP or bromobiphenyl and dextrose, yellow coloured product(s) were rapidly formed. Gas chromatography-mass spectrometry (GC-MS) revealed single ring N-heterocyclic compounds that were identified as halopicolinic acids. We believe this to be the first report of such compounds being formed via biological transformation of halobiphenyls. A mechanism is proposed for their formation.

Original language	English
Pages (from-to)	66-71
Number of pages	6
Journal	Canadian Journal of Microbiology
Volume	42
Issue number	1
DOIs	https://doi.org/10.1139/m96-009
Publication status	Published - 1996

Keywords

bioremediation
halobiphenyl degradation
halopicolinic acid
Sphingomonas paucimobilis BPSI-3

Access to Document

10.1139/m96-009

Cite this

@article{9d7b05dbd2dd46d685a11bc6c9f4a7d6,

title = "Halopicolinic acids, novel products arising through the degradation of chloro- and bromobiphenyl by Sphingomonas paucimobilis BPSI-3",

abstract = "Sphingomonas paucimobilis BPSI-3 was previously isolated from a mixed microbial consortium growing on biphenyl as the sole source of carbon and energy. Transformation of 4-chlorobiphenyl (4CBP) was demonstrated by this strain, although little or no growth was observed. In minimal salts medium supplemented with 4CBP or bromobiphenyl and dextrose, yellow coloured product(s) were rapidly formed. Gas chromatography-mass spectrometry (GC-MS) revealed single ring N-heterocyclic compounds that were identified as halopicolinic acids. We believe this to be the first report of such compounds being formed via biological transformation of halobiphenyls. A mechanism is proposed for their formation.",

keywords = "bioremediation, halobiphenyl degradation, halopicolinic acid, Sphingomonas paucimobilis BPSI-3",

author = "Davison, {Annette D.} and Peter Karuso and Jardine, {Daniel R.} and Veal, {Duncan A.}",

year = "1996",

doi = "10.1139/m96-009",

language = "English",

volume = "42",

pages = "66--71",

journal = "Canadian Journal of Microbiology",

issn = "0008-4166",

publisher = "National Research Council of Canada",

number = "1",

}

TY - JOUR

T1 - Halopicolinic acids, novel products arising through the degradation of chloro- and bromobiphenyl by Sphingomonas paucimobilis BPSI-3

AU - Davison, Annette D.

AU - Karuso, Peter

AU - Jardine, Daniel R.

AU - Veal, Duncan A.

PY - 1996

Y1 - 1996

N2 - Sphingomonas paucimobilis BPSI-3 was previously isolated from a mixed microbial consortium growing on biphenyl as the sole source of carbon and energy. Transformation of 4-chlorobiphenyl (4CBP) was demonstrated by this strain, although little or no growth was observed. In minimal salts medium supplemented with 4CBP or bromobiphenyl and dextrose, yellow coloured product(s) were rapidly formed. Gas chromatography-mass spectrometry (GC-MS) revealed single ring N-heterocyclic compounds that were identified as halopicolinic acids. We believe this to be the first report of such compounds being formed via biological transformation of halobiphenyls. A mechanism is proposed for their formation.

AB - Sphingomonas paucimobilis BPSI-3 was previously isolated from a mixed microbial consortium growing on biphenyl as the sole source of carbon and energy. Transformation of 4-chlorobiphenyl (4CBP) was demonstrated by this strain, although little or no growth was observed. In minimal salts medium supplemented with 4CBP or bromobiphenyl and dextrose, yellow coloured product(s) were rapidly formed. Gas chromatography-mass spectrometry (GC-MS) revealed single ring N-heterocyclic compounds that were identified as halopicolinic acids. We believe this to be the first report of such compounds being formed via biological transformation of halobiphenyls. A mechanism is proposed for their formation.

KW - bioremediation

KW - halobiphenyl degradation

KW - halopicolinic acid

KW - Sphingomonas paucimobilis BPSI-3

UR - http://www.scopus.com/inward/record.url?scp=0029915777&partnerID=8YFLogxK

U2 - 10.1139/m96-009

DO - 10.1139/m96-009

M3 - Article

C2 - 8595598

AN - SCOPUS:0029915777

SN - 0008-4166

VL - 42

SP - 66

EP - 71

JO - Canadian Journal of Microbiology

JF - Canadian Journal of Microbiology

IS - 1

ER -

Halopicolinic acids, novel products arising through the degradation of chloro- and bromobiphenyl by Sphingomonas paucimobilis BPSI-3

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this