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 AbstractCharacterization of Different Si- and Al-based Catalysts with Pd Modification and Their Use for Catalytic Dehydration of Ethanol    Next AbstractFoliage inoculation by Burkholderia vietnamiensis CBMB40 antagonizes methyl jasmonate-mediated stress in Eucalyptus grandis »

Biochem J


Title:The conformational state of polyphenol oxidase from field bean (Dolichos lablab) upon SDS and acid-pH activation
Author(s):Kanade SR; Paul B; Rao AG; Gowda LR;
Address:"Department of Protein Chemistry and Technology, Central Food Technological Research Institute (CFTRI), Mysore-570 020, India"
Journal Title:Biochem J
Year:2006
Volume:395
Issue:3
Page Number:551 - 562
DOI: 10.1042/BJ20051509
ISSN/ISBN:1470-8728 (Electronic) 0264-6021 (Print) 0264-6021 (Linking)
Abstract:"Field bean (Dolichos lablab) contains a single isoform of PPO (polyphenol oxidase)--a type III copper protein that catalyses the o-hydroxylation of monophenols and oxidation of o-diphenols using molecular oxygen--and is a homotetramer with a molecular mass of 120 kDa. The enzyme is activated manyfold either in the presence of the anionic detergent SDS below its critical micellar concentration or on exposure to acid-pH. The enhancement of kcat upon activation is accompanied by a marked shift in the pH optimum for the oxidation of t-butyl catechol from 4.5 to 6.0, an increased sensitivity to tropolone, altered susceptibility to proteolytic degradation and decreased thermostability. The Stokes radius of the native enzyme is found to increase from 49.1+/-2 to 75.9+/-0.6 A (1 A=0.1 nm). The activation by SDS and acid-pH results in a localized conformational change that is anchored around the catalytic site of PPO that alters the microenvironment of an essential glutamic residue. Chemical modification of field bean and sweet potato PPO with 1-ethyl-3-(3-dimethylaminopropyl)carbodi-imide followed by kinetic analysis leads to the conclusion that both the enzymes possess a core carboxylate essential to activity. This enhanced catalytic efficiency of PPO, considered as an inducible defence oxidative enzyme, is vital to the physiological defence strategy adapted by plants to insect herbivory and pathogen attack"
Keywords:"Acids Amino Acid Sequence Carboxylic Acids/pharmacology Catechol Oxidase/*chemistry/*metabolism Chromatography, High Pressure Liquid Circular Dichroism Dimerization Dolichos/*enzymology Enzyme Activation/drug effects Enzyme Stability Hydrogen-Ion Concentr;"
Notes:"MedlineKanade, Santosh R Paul, Beena Rao, A G Appu Gowda, Lalitha R eng Research Support, Non-U.S. Gov't England 2006/01/06 Biochem J. 2006 May 1; 395(3):551-62. doi: 10.1042/BJ20051509"

 
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 21-09-2024