» Articles » PMID: 16348226

Anaerobic Oxidation of Toluene, Phenol, and P-Cresol by the Dissimilatory Iron-Reducing Organism, GS-15

Overview
Date 1990 Jun 1
PMID 16348226
Citations 98
Authors
Affiliations
Soon will be listed here.
Abstract

The dissimilatory Fe(III) reducer, GS-15, is the first microorganism known to couple the oxidation of aromatic compounds to the reduction of Fe(III) and the first example of a pure culture of any kind known to anaerobically oxidize an aromatic hydrocarbon, toluene. In this study, the metabolism of toluene, phenol, and p-cresol by GS-15 was investigated in more detail. GS-15 grew in an anaerobic medium with toluene as the sole electron donor and Fe(III) oxide as the electron acceptor. Growth coincided with Fe(III) reduction. [ring-C]toluene was oxidized to CO(2), and the stoichiometry of CO(2) production and Fe(III) reduction indicated that GS-15 completely oxidized toluene to carbon dioxide with Fe(III) as the electron acceptor. Magnetite was the primary iron end product during toluene oxidation. Phenol and p-cresol were also completely oxidized to carbon dioxide with Fe(III) as the sole electron acceptor, and GS-15 could obtain energy to support growth by oxidizing either of these compounds as the sole electron donor. p-Hydroxybenzoate was a transitory extracellular intermediate of phenol and p-cresol metabolism but not of toluene metabolism. GS-15 oxidized potential aromatic intermediates in the oxidation of toluene (benzylalcohol and benzaldehyde) and p-cresol (p-hydroxybenzylalcohol and p-hydroxybenzaldehyde). The metabolism described here provides a model for how aromatic hydrocarbons and phenols may be oxidized with the reduction of Fe(III) in contaminated aquifers and petroleum-containing sediments.

Citing Articles

Differential degradation of petroleum hydrocarbons by under aerobic and anaerobic conditions.

Li Y, Liu Y, Guo D, Dong H Front Microbiol. 2024; 15:1389954.

PMID: 38659987 PMC: 11040095. DOI: 10.3389/fmicb.2024.1389954.


Biocatalyst developed with recovered iron-rich minerals enhances the biotransformation of SARS-CoV-2 antiviral drugs in anaerobic bioreactors.

Mares-Carbajal F, Espinosa-Arzate M, Ramirez-Montoya L, Pat-Espadas A, Ramirez J, Rangel-Mendez J J Water Process Eng. 2022; 50:103337.

PMID: 36407934 PMC: 9663753. DOI: 10.1016/j.jwpe.2022.103337.


Iron Compounds in Anaerobic Degradation of Petroleum Hydrocarbons: A Review.

Castro A, Martins G, Salvador A, Cavaleiro A Microorganisms. 2022; 10(11).

PMID: 36363734 PMC: 9695802. DOI: 10.3390/microorganisms10112142.


Significance of Species for the Phytoavailability and Toxicity of Arsenic-A Review.

Darma A, Yang J, Zandi P, Liu J, Mozdzen K, Xia X Biology (Basel). 2022; 11(3).

PMID: 35336844 PMC: 8944983. DOI: 10.3390/biology11030472.


The Effect of an Adsorbent Matrix on Recovery of Microorganisms from Hydrocarbon-Contaminated Groundwater.

Taylor N, Toth C, Collins V, Mussone P, Gieg L Microorganisms. 2021; 9(1).

PMID: 33401442 PMC: 7823327. DOI: 10.3390/microorganisms9010090.


References
1.
Thauer R, Jungermann K, Decker K . Energy conservation in chemotrophic anaerobic bacteria. Bacteriol Rev. 1977; 41(1):100-80. PMC: 413997. DOI: 10.1128/br.41.1.100-180.1977. View

2.
Bossert I, Whited G, Gibson D, Young L . Anaerobic oxidation of p-cresol mediated by a partially purified methylhydroxylase from a denitrifying bacterium. J Bacteriol. 1989; 171(6):2956-62. PMC: 210000. DOI: 10.1128/jb.171.6.2956-2962.1989. View

3.
Evans W, Fuchs G . Anaerobic degradation of aromatic compounds. Annu Rev Microbiol. 1988; 42:289-317. DOI: 10.1146/annurev.mi.42.100188.001445. View

4.
Grbic-Galic D, Vogel T . Transformation of toluene and benzene by mixed methanogenic cultures. Appl Environ Microbiol. 1987; 53(2):254-60. PMC: 203647. DOI: 10.1128/aem.53.2.254-260.1987. View

5.
Kuhn E, Zeyer J, Eicher P, Schwarzenbach R . Anaerobic degradation of alkylated benzenes in denitrifying laboratory aquifer columns. Appl Environ Microbiol. 1988; 54(2):490-6. PMC: 202478. DOI: 10.1128/aem.54.2.490-496.1988. View