Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins

New isolates Mayfair 2 and Laird 2 of the blackleg fungus [<i>Phoma lingam</i>, perfect stage <i>Leptosphaeria maculans</i> (Desm.) Ces. et de Not.] cause blackleg on the traditionally resistant brown mustard (<i>Brassica juncea</i>). Mayfair 2/Laird 2 isolates of...

Full description

Bibliographic Details
Main Author: Chumala, Paulos Barbe
Other Authors: Majewski, Marek
Format: Others
Language:en
Published: University of Saskatchewan 2008
Online Access:http://library.usask.ca/theses/available/etd-09182008-080157/
id ndltd-USASK-oai-usask.ca-etd-09182008-080157
record_format oai_dc
spelling ndltd-USASK-oai-usask.ca-etd-09182008-0801572013-01-08T16:33:34Z Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins Chumala, Paulos Barbe New isolates Mayfair 2 and Laird 2 of the blackleg fungus [<i>Phoma lingam</i>, perfect stage <i>Leptosphaeria maculans</i> (Desm.) Ces. et de Not.] cause blackleg on the traditionally resistant brown mustard (<i>Brassica juncea</i>). Mayfair 2/Laird 2 isolates of the blackleg fungus produce a diverse array of secondary metabolites in liquid cultures in minimal media. The isolation (FCC, RP-FCC, prep TLC) and characterization (NMR, MS, X-ray) of these metabolites resulted in the identification of four groups of compounds: polanrazines, sesquiterpenes, phomapyrones, and depsilairdin, where eleven of them were new. Phytotoxic assays conducted with these metabolites on <i>B. napus</i> (resistant),<i> B. juncea</i> (susceptible), and S. alba (resistant) indicated depsilairdin (<b>122</b>) to be a host-selective toxin. Studies on the biosynthetic origin of phomapyrone A suggested phomapyrones to be of polyketide origin.<p> Sixteen Thlaspi isolates of blackleg fungus originating from Saskatchewan were characterized on the basis of their secondary metabolite profiles, and it was determined that two of them were Polish type isolates and the remaining fourteen were weakly virulent type isolates.<p> The investigation of <i>Thlaspi arvense</i> (stinkweed) for phytoalexins led to the isolation of two phytoalexins: arvelexin (<b>142</b>) and wasalexin A (<b>38</b>). The structures of these phytoalexins as well as that of isovitexin, a secondary metabolite of <i>T. arvense</i>, were established based on spectroscopic methods and by synthesis. Arvelexin, as a phytoalexin, was reported for the first time here, but wasalexin A was previously reported from wasabi (<i>Wasabia japonica</i>, syn. <i>Eutrema wasabi</i>). Arvelexin (<b>142</b>) exhibited similar antifungal activity as indole-3-acetonitrile against <i>L. maculans/P. lingam</i>.<p> The secondary metabolites potentially involved in mediating the interactions between <i>Brassica</i> species and the new blackleg isolates Mayfair 2 and Laird 2 were analysed in infected plant tissues by HPLC. The host-selective toxins phomalairdenone A (<b>55</b>) and depsilairdin (<b>122</b>), and phytoalexins, brassinin (<b>35</b>), rutalexin (<b>137</b>) and spirobrassinin (<b>138</b>) were detected in B. napus, whereas brassilexin (<b>139</b>) and sinalexin <b>(140</b>) were detected in <i>S. alba</i>, and brassilexin (<b>139</b>) was detected in <i>B. juncea</i>. Majewski, Marek Kraatz, Heinz-Bernhard Harrison, Paul Dimmock, Jonathan R. Pedras, M. Soledade C. University of Saskatchewan 2008-10-06 text application/pdf http://library.usask.ca/theses/available/etd-09182008-080157/ http://library.usask.ca/theses/available/etd-09182008-080157/ en unrestricted I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Saskatchewan or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.
collection NDLTD
language en
format Others
sources NDLTD
description New isolates Mayfair 2 and Laird 2 of the blackleg fungus [<i>Phoma lingam</i>, perfect stage <i>Leptosphaeria maculans</i> (Desm.) Ces. et de Not.] cause blackleg on the traditionally resistant brown mustard (<i>Brassica juncea</i>). Mayfair 2/Laird 2 isolates of the blackleg fungus produce a diverse array of secondary metabolites in liquid cultures in minimal media. The isolation (FCC, RP-FCC, prep TLC) and characterization (NMR, MS, X-ray) of these metabolites resulted in the identification of four groups of compounds: polanrazines, sesquiterpenes, phomapyrones, and depsilairdin, where eleven of them were new. Phytotoxic assays conducted with these metabolites on <i>B. napus</i> (resistant),<i> B. juncea</i> (susceptible), and S. alba (resistant) indicated depsilairdin (<b>122</b>) to be a host-selective toxin. Studies on the biosynthetic origin of phomapyrone A suggested phomapyrones to be of polyketide origin.<p> Sixteen Thlaspi isolates of blackleg fungus originating from Saskatchewan were characterized on the basis of their secondary metabolite profiles, and it was determined that two of them were Polish type isolates and the remaining fourteen were weakly virulent type isolates.<p> The investigation of <i>Thlaspi arvense</i> (stinkweed) for phytoalexins led to the isolation of two phytoalexins: arvelexin (<b>142</b>) and wasalexin A (<b>38</b>). The structures of these phytoalexins as well as that of isovitexin, a secondary metabolite of <i>T. arvense</i>, were established based on spectroscopic methods and by synthesis. Arvelexin, as a phytoalexin, was reported for the first time here, but wasalexin A was previously reported from wasabi (<i>Wasabia japonica</i>, syn. <i>Eutrema wasabi</i>). Arvelexin (<b>142</b>) exhibited similar antifungal activity as indole-3-acetonitrile against <i>L. maculans/P. lingam</i>.<p> The secondary metabolites potentially involved in mediating the interactions between <i>Brassica</i> species and the new blackleg isolates Mayfair 2 and Laird 2 were analysed in infected plant tissues by HPLC. The host-selective toxins phomalairdenone A (<b>55</b>) and depsilairdin (<b>122</b>), and phytoalexins, brassinin (<b>35</b>), rutalexin (<b>137</b>) and spirobrassinin (<b>138</b>) were detected in B. napus, whereas brassilexin (<b>139</b>) and sinalexin <b>(140</b>) were detected in <i>S. alba</i>, and brassilexin (<b>139</b>) was detected in <i>B. juncea</i>.
author2 Majewski, Marek
author_facet Majewski, Marek
Chumala, Paulos Barbe
author Chumala, Paulos Barbe
spellingShingle Chumala, Paulos Barbe
Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
author_sort Chumala, Paulos Barbe
title Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
title_short Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
title_full Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
title_fullStr Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
title_full_unstemmed Chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
title_sort chemical study of the blackleg fungus : metabolites, phytotoxins and phytoalexins
publisher University of Saskatchewan
publishDate 2008
url http://library.usask.ca/theses/available/etd-09182008-080157/
work_keys_str_mv AT chumalapaulosbarbe chemicalstudyoftheblacklegfungusmetabolitesphytotoxinsandphytoalexins
_version_ 1716532505962610688