» Articles » PMID: 3223770

Dehalogenation in Marine Sediments Containing Natural Sources of Halophenols

Overview
Date 1988 Dec 1
PMID 3223770
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Halophenols such as 2,4-dibromophenol (DBP) occur naturally in some marine sediments, as a consequence of various animal and algal activities. In an earlier study, DBP was observed in the burrow microenvironment of the hemichordate Saccoglossus kowalewskii. At the concentrations found in the burrow lining, aerobic respiration appeared to be inhibited significantly relative to anaerobic catabolism. This effect, as well as factors contributing to the degradation of DBP, has been documented further here. Results from the addition of radiolabeled DBP to oxic and anoxic sediment slurries and growth experiments with aerobic and anaerobic enrichments suggested that aerobes did not significantly metabolize DBP and that concentrations likely to be encountered on the inner surfaces of the burrow wall were inhibitory. In contrast, only minimal inhibition of growth occurred for anaerobes exposed to 1 mM DBP; in addition, DBP was substantially degraded in both enrichments and sediments under anaerobic conditions. Dehalogenation with the consequent production of phenol appeared to initiate anaerobic degradation. Sulfate-reducing bacteria did not dehalogenate DBP but appeared to degrade phenol. Decreased bacterial numbers and marked differences in the concentration and chemical speciation of iron in sediments from S. kowalewskii burrows may be attributed to toxic effects of DBP on aerobic bacteria.

Citing Articles

Construction of Aerobic/Anaerobic-Substrate-Induced Gene Expression Procedure for Exploration of Metagenomes From Subseafloor Sediments.

Wakamatsu T, Mizobuchi S, Mori F, Futagami T, Terada T, Morono Y Front Microbiol. 2022; 12:726024.

PMID: 35095779 PMC: 8793675. DOI: 10.3389/fmicb.2021.726024.


Microbiomes of the Enteropneust, , and Associated Marine Intertidal Sediments of Cod Cove, Maine.

King G Front Microbiol. 2019; 9:3066.

PMID: 30631312 PMC: 6315191. DOI: 10.3389/fmicb.2018.03066.


A Review of "Polychaeta" Chemicals and their Possible Ecological Role.

Coutinho M, Teixeira V, Santos C J Chem Ecol. 2017; 44(1):72-94.

PMID: 29273953 DOI: 10.1007/s10886-017-0915-z.


Distribution of dehalogenation activity in subseafloor sediments of the Nankai Trough subduction zone.

Futagami T, Morono Y, Terada T, Kaksonen A, Inagaki F Philos Trans R Soc Lond B Biol Sci. 2013; 368(1616):20120249.

PMID: 23479745 PMC: 3638456. DOI: 10.1098/rstb.2012.0249.


Acetogenesis in the energy-starved deep biosphere - a paradox?.

Lever M Front Microbiol. 2012; 2:284.

PMID: 22347874 PMC: 3276360. DOI: 10.3389/fmicb.2011.00284.


References
1.
Stockdale M, Selwyn M . Influence of ring substituents on the action of phenols on some dehydrogenases, phospholinases and the soluble ATPase from mitochondria. Eur J Biochem. 1971; 21(3):416-23. DOI: 10.1111/j.1432-1033.1971.tb01486.x. View

2.
Sheikh Y . 2,6-Dibromophenol and 2,4,6-tribromophenols. Antiseptic secondary metabolites of Phoronopsis viridis. Experientia. 1975; 31(3):265-6. DOI: 10.1007/BF01922529. View

3.
Stockdale M, Selwyn M . Effects of ring substituents on the activity of phenols as inhibitors and uncouplers of mitochondrial respiration. Eur J Biochem. 1971; 21(4):565-74. DOI: 10.1111/j.1432-1033.1971.tb01502.x. View

4.
Ghosal D, You I, Chatterjee D, Chakrabarty A . Microbial degradation of halogenated compounds. Science. 1985; 228(4696):135-42. DOI: 10.1126/science.228.4696.135. View

5.
van den Tweel W, Kok J, de Bont J . Reductive dechlorination of 2,4-dichlorobenzoate to 4-chlorobenzoate and hydrolytic dehalogenation of 4-chloro-, 4-bromo-, and 4-iodobenzoate by Alcaligenes denitrificans NTB-1. Appl Environ Microbiol. 1987; 53(4):810-5. PMC: 203761. DOI: 10.1128/aem.53.4.810-815.1987. View