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 AbstractIdentification of Key Root Volatiles Signaling Preference of Tomato over Spinach by the Root Knot Nematode Meloidogyne incognita    Next AbstractBlood brain barrier: A tissue engineered microfluidic chip »

Biochem J


Title:Insights into the unique carboxylation reactions in the metabolism of propylene and acetone
Author(s):Mus F; Wu HH; Alleman AB; Shisler KA; Zadvornyy OA; Bothner B; Dubois JL; Peters JW;
Address:"Institute of Biological Chemistry, Washington State University, Pullman, WA 99164, U.S.A. Department of Chemistry, Washington State University, WA 99164. Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717, U.S.A"
Journal Title:Biochem J
Year:2020
Volume:477
Issue:11
Page Number:2027 - 2038
DOI: 10.1042/BCJ20200174
ISSN/ISBN:1470-8728 (Electronic) 0264-6021 (Linking)
Abstract:"Alkenes and ketones are two classes of ubiquitous, toxic organic compounds in natural environments produced in several biological and anthropogenic processes. In spite of their toxicity, these compounds are utilized as primary carbon and energy sources or are generated as intermediate metabolites in the metabolism of other compounds by many diverse bacteria. The aerobic metabolism of some of the smallest and most volatile of these compounds (propylene, acetone, isopropanol) involves novel carboxylation reactions resulting in a common product acetoacetate. Propylene is metabolized in a four-step pathway involving five enzymes where the penultimate step is a carboxylation reaction catalyzed by a unique disulfide oxidoreductase that couples reductive cleavage of a thioether linkage with carboxylation to produce acetoacetate. The carboxylation of isopropanol begins with conversion to acetone via an alcohol dehydrogenase. Acetone is converted to acetoacetate in a single step by an acetone carboxylase which couples the hydrolysis of MgATP to the activation of both acetone and bicarbonate, generating highly reactive intermediates that are condensed into acetoacetate at a Mn2+ containing the active site. Acetoacetate is then utilized in central metabolism where it is readily converted to acetyl-coenzyme A and subsequently converted into biomass or utilized in energy metabolism via the tricarboxylic acid cycle. This review summarizes recent structural and biochemical findings that have contributed significant insights into the mechanism of these two unique carboxylating enzymes"
Keywords:2-Propanol/metabolism Acetoacetates/metabolism Acetone/*metabolism Acetyl Coenzyme A/metabolism Alkenes/*metabolism Bacteria/*metabolism Bicarbonates/metabolism Catalysis Citric Acid Cycle/physiology 2-kpcc acetone carboxylase alkenes ketones metabolism;
Notes:"MedlineMus, Florence Wu, Hsin-Hua Alleman, Alexander B Shisler, Krista A Zadvornyy, Oleg A Bothner, Brian Dubois, Jennifer L Peters, John W eng Research Support, U.S. Gov't, Non-P.H.S. Review England 2020/06/05 Biochem J. 2020 Jun 12; 477(11):2027-2038. doi: 10.1042/BCJ20200174"

 
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 26-12-2024