» Articles » PMID: 6769418

Oxidation of Biphenyl by the Cyanobacterium, Oscillatoria Sp., Strain JCM

Overview
Journal Arch Microbiol
Specialty Microbiology
Date 1980 Apr 1
PMID 6769418
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

The oxidation of biphenyl by Cyanobacterium, Oscillatoria sp., strain JCM was studied. The organism grown photoautotrophically in the presence of biphenyl oxidized biphenyl to form 4-hydroxybiphenyl. The structure of the metabolite was elucidated by ultraviolet and mass spectra and shown to be identical to authentic 4-hydroxybiphenyl. In addition this metabolite had properties identical to 4-hydroxybiphenyl when analyzed by thin-layer and high-pressure liquid chromatography. Experiments with [14C]-biphenyl showed that over a 24 h period the organism oxidized 2.9% of the added biphenyl to ethyl acetate-soluble products.

Citing Articles

Potential Toxicity Risk Assessment and Priority Control Strategy for PAHs Metabolism and Transformation Behaviors in the Environment.

Zhao L, Zhou M, Zhao Y, Yang J, Pu Q, Yang H Int J Environ Res Public Health. 2022; 19(17).

PMID: 36078713 PMC: 9517862. DOI: 10.3390/ijerph191710972.


Bacteria, Fungi and Microalgae for the Bioremediation of Marine Sediments Contaminated by Petroleum Hydrocarbons in the Omics Era.

Dell Anno F, Rastelli E, Sansone C, Brunet C, Ianora A, Dell Anno A Microorganisms. 2021; 9(8).

PMID: 34442774 PMC: 8400010. DOI: 10.3390/microorganisms9081695.


Metabolic relation of cyanobacteria to aromatic compounds.

Zyszka-Haberecht B, Niemczyk E, Lipok J Appl Microbiol Biotechnol. 2018; 103(3):1167-1178.

PMID: 30580382 PMC: 6394484. DOI: 10.1007/s00253-018-9568-2.


Investigation of the removal mechanism of antibiotic ceftazidime by green algae and subsequent microbic impact assessment.

Yu Y, Zhou Y, Wang Z, Torres O, Guo R, Chen J Sci Rep. 2017; 7(1):4168.

PMID: 28646154 PMC: 5482816. DOI: 10.1038/s41598-017-04128-3.


Cyanobacteria: A Precious Bio-resource in Agriculture, Ecosystem, and Environmental Sustainability.

Singh J, Kumar A, Rai A, Singh D Front Microbiol. 2016; 7:529.

PMID: 27148218 PMC: 4838734. DOI: 10.3389/fmicb.2016.00529.


References
1.
Raig P, AMMON R . [Gas chromatographic analysis of phenolic metabolic products of biphenyl]. Arzneimittelforschung. 1970; 20(9):1266-9. View

2.
Dodge R, Cerniglia C, Gibson D . Fungal metabolism of biphenyl. Biochem J. 1979; 178(1):223-30. PMC: 1186500. DOI: 10.1042/bj1780223. View

3.
Meyer T, SCHELINE R . The metabolism of biphenyl. II. Phenolic metabolites in the rat. Acta Pharmacol Toxicol (Copenh). 1976; 39(4):419-32. DOI: 10.1111/j.1600-0773.1976.tb03193.x. View

4.
Wiebkin P, Fry J, Jones C, Lowing R, Bridges J . The metabolism of biphenyl by isolated viable rat hepatocytes. Xenobiotica. 1976; 6(12):725-43. DOI: 10.3109/00498257609151390. View

5.
Ahmed M, Focht D . Degradation of polychlorinated biphenyls by two species of Achromobacter. Can J Microbiol. 1973; 19(1):47-52. DOI: 10.1139/m73-007. View