» Articles » PMID: 16348548

Effects of Sulfuroxy Anions on Degradation of Pentachlorophenol by a Methanogenic Enrichment Culture

Overview
Date 1991 Sep 1
PMID 16348548
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

We studied the degradation of pentachlorophenol (PCP) under methanogenic and sulfate-reducing conditions with an anaerobic mixed culture derived from sewage sludge. The consortium degraded PCP via 2,3,4,5-tetrachlorophenol, 3,4,5-trichlorophenol, and 3,5-dichlorophenol and eventually accumulated 3-chlorophenol. Dechlorination of PCP and metabolites was inhibited in the presence of sulfate, thiosulfate, and sulfite. A decrease in the rate of PCP transformation was noted when the endogenous dissolved H(2) was depleted below 0.11 muM in sulfate-reducing cultures. The effect on dechlorination observed with sulfate could be relieved by addition of molybdate, a competitive inhibitor of sulfate reduction. Addition of H(2) reduced the inhibition observed with sulfuroxy anions. The inhibitory effect of sulfuroxy anions may be due to a competition for H(2) between sulfate reduction and dechlorination. When cultured under methanogenic conditions, the consortium degraded several chlorinated and brominated phenols.

Citing Articles

Function and Evolution of the Sox Multienzyme Complex in the Marine Gammaproteobacterium Congregibacter litoralis.

Spring S ISRN Microbiol. 2014; 2014:597418.

PMID: 25006520 PMC: 4003848. DOI: 10.1155/2014/597418.


Reductive dehalogenation and mineralization of 3-chlorobenzoate in the presence of sulfate by microorganisms from a methanogenic aquifer.

Townsend G, Ramanand K, Suflita J Appl Environ Microbiol. 1997; 63(7):2785-91.

PMID: 16535650 PMC: 1389205. DOI: 10.1128/aem.63.7.2785-2791.1997.


[H]thymidine incorporation to estimate growth rates of anaerobic bacterial strains.

Winding A Appl Environ Microbiol. 1992; 58(8):2660-2.

PMID: 16348755 PMC: 195835. DOI: 10.1128/aem.58.8.2660-2662.1992.


Dehalogenation and biodegradation of brominated phenols and benzoic acids under iron-reducing, sulfidogenic, and methanogenic conditions.

Monserrate E, Haggblom M Appl Environ Microbiol. 1998; 63(10):3911-5.

PMID: 9480645 PMC: 168701. DOI: 10.1128/aem.63.10.3911-3915.1997.


Physiological characterization of a bacterial consortium reductively dechlorinating 1,2,3- and 1,2,4-trichlorobenzene.

Adrian L, Manz W, Szewzyk U, Gorisch H Appl Environ Microbiol. 1998; 64(2):496-503.

PMID: 9464384 PMC: 106072. DOI: 10.1128/AEM.64.2.496-503.1998.


References
1.
Linkfield T, Tiedje J . Characterization of the requirements and substrates for reductive dehalogenation by strain DCB-1. J Ind Microbiol. 1990; 5(1):9-15. DOI: 10.1007/BF01569601. View

2.
Haggblom M, Young L . Chlorophenol degradation coupled to sulfate reduction. Appl Environ Microbiol. 1990; 56(11):3255-60. PMC: 184938. DOI: 10.1128/aem.56.11.3255-3260.1990. View

3.
Zhang X, Wiegel J . Sequential anaerobic degradation of 2,4-dichlorophenol in freshwater sediments. Appl Environ Microbiol. 1990; 56(4):1119-27. PMC: 184352. DOI: 10.1128/aem.56.4.1119-1127.1990. View

4.
Kohring G, Zhang X, Wiegel J . Anaerobic dechlorination of 2,4-dichlorophenol in freshwater sediments in the presence of sulfate. Appl Environ Microbiol. 1989; 55(10):2735-7. PMC: 203155. DOI: 10.1128/aem.55.10.2735-2737.1989. View

5.
King G . Dehalogenation in marine sediments containing natural sources of halophenols. Appl Environ Microbiol. 1988; 54(12):3079-85. PMC: 204430. DOI: 10.1128/aem.54.12.3079-3085.1988. View