Formation of di-isodityrosine and loss of isodityrosine in the cell walls of tomato cell-suspension cultures treated with fungal elicitors or H2O2

About 84% of the hydroxyproline residues in a cell culture of tomato (Lycopersicon esculentum X Lycopersicon peruvianum) were present in phenol-inextractable (i.e. covalently wall-bound) material. Treatment of the cells with any of three fungal elicitors (wall fragments from Phytophthora megasperma...

Full description

Saved in:
Bibliographic Details
Published inPlant physiology (Bethesda) Vol. 115; no. 1; pp. 87 - 92
Main Authors Brady, J.D, Fry, S.C
Format Journal Article
LanguageEnglish
Published Rockville, MD American Society of Plant Physiologists 01.09.1997
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:About 84% of the hydroxyproline residues in a cell culture of tomato (Lycopersicon esculentum X Lycopersicon peruvianum) were present in phenol-inextractable (i.e. covalently wall-bound) material. Treatment of the cells with any of three fungal elicitors (wall fragments from Phytophthora megasperma and Pythium aphanidermatum and xylanase from Aureobasidium pullulans) or with 1 mM H2O2 had little effect on the quantity of phenol-inextractable hydroxyproline per milligram of freeze-dried cells. However, each treatment induced a decrease in the content of phenol-inextractable isodityrosine (Idt) residues. Each treatment, except with the P. megasperma fragments, also induced an increase in phenol-inextractable di- (Di-Idt). The increase in Di-Idt partly accounted for the loss of Idt. We conclude that the elicitors and H2O2 acted to reinforce the existing cross-linking of cell wall (glyco) proteins by evoking oxidative coupling reactions to convert Idt to Di-Idt plus unidentified products. The promotion of cross-linking by elicitor treatment is proposed to be a defensive response that restricts the penetration of pathogens
Bibliography:F60
1997063168
H20
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0032-0889
1532-2548
DOI:10.1104/pp.115.1.87