Toggle Main Menu Toggle Search

Open Access padlockePrints

Acetate as a source of reducing equivalents in the reductive dechlorination of 2,5-dichlorobenzoate

Lookup NU author(s): Dr Jan DolfingORCiD


Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Desulfomonile tiedjei is the key dechlorinating organism in a three-tiered bacterial consortium that grows on the methanogenic degradation of 3-chlorobenzoate. 2,5-Dichlorobenzoate, however, is only converted to 2-chlorobenzoate and is not a methanogenic substrate for the consortium. The dechlorinator uses hydrogen produced from benzoate by the benzoate degrading member of consortium as its source of reducing equivalents for the dechlorination reaction. Incubation of 3-chlorobenzoate grown consortium cells with 2,5-dichlorobenzoate resulted in the consumption of acetate concurrent with the formation of 2-chlorobenzoate indicating that acetate can serve as an alternative source of reducing equivalents for reductive dechlorination. This interpretation was confirmed by the finding that the formation of (CO2)-C-14 from 2-C-14-labeled acetate was stoichiometric. The addition of hydrogen to 2,5-dichlorobenzoate metabolizing cells resulted in (i) an 2.7-fold increase in the rate of dechlorination, and (ii) a drop in the amount of label recovered as CO2 + CH4 from methyl C-14-labeled acetate, indicating that hydrogen was the preferred source of reducing equivalents for reductive dechlorination. Benzoate, an indirect source of H2 in the consortium, also inhibited the oxidation of acetate, while glucose, methanol, and butyrate did not affect labeled gas production and therefore were not suitable electron donors. Concomittant to dechlorination of 2,5-dichlorobenzoate 3- and 4-methoxybenzoate were converted to 3- and 4-hydroxybenzoate respectively. These conversions stimulated the rate of dechlorination 2-fold. Demethylation of 4-methoxybenzoate stimulated, but demethylation of 3-methoxybenzoate inhibited the oxidation of benzoate during the dechlorination of 2,5-dichlorobenzoate, suggesting that these isomers are metabolized through different pathways. Experiments with benzoate, 3-chlorobenzoate and 2,5-dichlorobenzoate metabolizing cells amended with (CO2)-C-14 showed that actively dechlorinating cells catalyzed an exchange reaction between CO2 and acetate.

Publication metadata

Author(s): Dolfing J, Tiedje JM

Publication type: Article

Publication status: Published

Journal: Archives of Microbiology

Year: 1991

Volume: 156

Issue: 5

Pages: 356-361

Print publication date: 01/10/1991

ISSN (print): 0302-8933

ISSN (electronic): 1432-072X

Publisher: Springer Berlin


DOI: 10.1007/BF00248710

Notes: Times Cited: 10 Cited Reference Count: 16 English Article ARCH MICROBIOL GL209


Altmetrics provided by Altmetric