Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractQuantification of organic acids in particulate matter by coupling of thermally assisted hydrolysis and methylation with thermodesorption-gas chromatography-mass spectrometry    Next AbstractVaried response of Spodoptera littoralis against Arabidopsis thaliana with metabolically engineered glucosinolate profiles »

Biochemistry


Title:Synthesis of brominated heptanones and bromoform by a bromoperoxidase of marine origin
Author(s):Beissner RS; Guilford WJ; Coates RM; Hager LP;
Address:
Journal Title:Biochemistry
Year:1981
Volume:20
Issue:13
Page Number:3724 - 3731
DOI: 10.1021/bi00516a009
ISSN/ISBN:0006-2960 (Print) 0006-2960 (Linking)
Abstract:"The presence of naturally occurring volatile halohydrocarbons in marine organisms, seawater, and the upper atmosphere has prompted a serach for their biosynthetic origin. An earlier report documented the preparation of an enzyme extract from a marine algae which catalyzed the formation of dibromomethane, tribromomethane, and 1-bromopentane from 3-oxooctanoic acid. This report did not establish a pathway nor did it examine potential intermediates involved in the synthesis of the halometabolites (Theiler, R., Cook, J., Hager, L., & Siuda, J. (1978) Science (Washington, D.C.) 202, 1094-1096). This paper shows that an extract of the green marine algae, Penicillus capitatus, which contains a potent bromoperoxidase activity, is capable of catalyzing the incorporation of bromide ion into organic combination in the presence of 3-oxooctanoic acid. By use of gas chromatography and mass spectroscopy, it has been possible to identify tribromomethane, 1-bromo-2-heptanone, 1,1-dibromo-2-heptanone, and 1,1,1-tribromo-2-heptanone as products of this reaction. The properties of the enzymatically synthesized products have been compared to authentic compounds and found to be identical. The mono- and dibromoheptanones can be utilized as precursors for the enzymatic formation of tribromoheptanone, but the final hydrolysis of the tribromoheptanone to bromoform appears to be a nonenzymatic reaction with the P. capitatus extracts"
Keywords:"Chlorophyta/*enzymology Gas Chromatography-Mass Spectrometry Hydrocarbons, Brominated/*biosynthesis/*metabolism Ketones/*metabolism Peroxidases/*metabolism Trihalomethanes;"
Notes:"MedlineBeissner, R S Guilford, W J Coates, R M Hager, L P eng GM 13956/GM/NIGMS NIH HHS/ Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 1981/06/23 Biochemistry. 1981 Jun 23; 20(13):3724-31. doi: 10.1021/bi00516a009"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024