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 AbstractThe ATP-binding cassette multidrug transporter Snq2 of Saccharomyces cerevisiae: a novel target for the transcription factors Pdr1 and Pdr3    Next Abstract"Biogenic secondary organic aerosol formation in an urban area of eastern central India: Seasonal variation, size distribution and source characterization" »

Environ Sci Technol


Title:"Identification of the intermediates of in vivo oxidation of 1 ,4-dioxane by monooxygenase-containing bacteria"
Author(s):Mahendra S; Petzold CJ; Baidoo EE; Keasling JD; Alvarez-Cohen L;
Address:"Department of Civil and Environmental Engineering, University of California, Berkeley, California 94720, USA. mahendras@rice.edu"
Journal Title:Environ Sci Technol
Year:2007
Volume:41
Issue:21
Page Number:7330 - 7336
DOI: 10.1021/es0705745
ISSN/ISBN:0013-936X (Print) 0013-936X (Linking)
Abstract:"1,4-dioxane is a probable human carcinogen and an emerging water contaminant. Monooxygenase-expressing bacteria have been shown to degrade dioxane via growth-supporting as well as cometabolic mechanisms. In this study, the intermediates of dioxane degradation by monooxygenase-expressing bacteria were determined by triple quadrupole-mass spectrometry and Fourier transform ion cyclotron resonance-mass spectrometry. The major intermediates were identified as 2-hydroxyethoxyacetic acid (HEAA), ethylene glycol, glycolate, and oxalate. Studies with uniformly labeled 14C dioxane showed that over 50% of the dioxane was mineralized to CO2 by CB1190, while 5% became biomass-associated after 48 h. Volatile organic acids and non-volatiles, respectively, accounted for 20 and 11% of the radiolabeled carbon. Although strains cometabolizing dioxane exhibited limited transformation capacities, nearly half of the initial dioxane was recovered as CO2. On the basis of these analytical results, we propose a pathway for dioxane oxidation by monooxygenase-expressing cells in which dioxane is first converted to 2-hydroxy-1,4-dioxane, which is spontaneously oxidized to HEAA. During a second monooxygenation step, HEAA is further hydroxylated, resulting in a mixture of dihydroxyethoxyacetic acids with a hydroxyl group at the ortho or para position. After cleavage of the second ether bond, small organic molecules such as ethylene glycol, glycolate, glyoxalate, and oxalate are progressively formed, which are then mineralized to CO2 via common cellular metabolic pathways. Bioremediation of dioxane via this pathway is not expected to cause an accumulation of toxic compounds in the environment"
Keywords:"Acetates/metabolism Bacteria, Aerobic/*metabolism Biodegradation, Environmental Carbon Dioxide/metabolism Dioxanes/*metabolism Environmental Pollutants/*metabolism Mixed Function Oxygenases/metabolism Oxidation-Reduction;"
Notes:"MedlineMahendra, Shaily Petzold, Christopher J Baidoo, Edward E Keasling, Jay D Alvarez-Cohen, Lisa eng Research Support, Non-U.S. Gov't 2007/11/30 Environ Sci Technol. 2007 Nov 1; 41(21):7330-6. doi: 10.1021/es0705745"

 
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