Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol

ABSTRACT: A correlation has been established between production of specific phenylphenalenones and resistance of various banana and plantain varieties towards certain pathogens. In addition a dihydrotrihydroxyphenylphenalene was isolated from the resistant 'Pelipita' plantain variety in re...

Full description

Autores:
Otálvaro Tamayo, Felipe
Echeverri López, Luis Fernando
Quiñones Fletcher, Winston
Torres, Fernando
Schneider, Bernd
Tipo de recurso:
Article of investigation
Fecha de publicación:
2002
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/23687
Acceso en línea:
http://hdl.handle.net/10495/23687
Palabra clave:
Musa acuminata
Biosíntesis
Biosynthesis
Fitoalexina
Phytoalexins
Organismos patógenos
Pathogens
Resistance
Susceptibility
http://aims.fao.org/aos/agrovoc/c_4994
http://aims.fao.org/aos/agrovoc/c_928
http://aims.fao.org/aos/agrovoc/c_16109
http://aims.fao.org/aos/agrovoc/c_5630
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
id UDEA2_60d903c4c81023873e2dc5ae9e156f40
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/23687
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
title Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
spellingShingle Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
Musa acuminata
Biosíntesis
Biosynthesis
Fitoalexina
Phytoalexins
Organismos patógenos
Pathogens
Resistance
Susceptibility
http://aims.fao.org/aos/agrovoc/c_4994
http://aims.fao.org/aos/agrovoc/c_928
http://aims.fao.org/aos/agrovoc/c_16109
http://aims.fao.org/aos/agrovoc/c_5630
title_short Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
title_full Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
title_fullStr Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
title_full_unstemmed Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
title_sort Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol
dc.creator.fl_str_mv Otálvaro Tamayo, Felipe
Echeverri López, Luis Fernando
Quiñones Fletcher, Winston
Torres, Fernando
Schneider, Bernd
dc.contributor.author.none.fl_str_mv Otálvaro Tamayo, Felipe
Echeverri López, Luis Fernando
Quiñones Fletcher, Winston
Torres, Fernando
Schneider, Bernd
dc.contributor.researchgroup.spa.fl_str_mv Química Orgánica de Productos Naturales
dc.subject.agrovoc.none.fl_str_mv Musa acuminata
Biosíntesis
Biosynthesis
Fitoalexina
Phytoalexins
Organismos patógenos
Pathogens
topic Musa acuminata
Biosíntesis
Biosynthesis
Fitoalexina
Phytoalexins
Organismos patógenos
Pathogens
Resistance
Susceptibility
http://aims.fao.org/aos/agrovoc/c_4994
http://aims.fao.org/aos/agrovoc/c_928
http://aims.fao.org/aos/agrovoc/c_16109
http://aims.fao.org/aos/agrovoc/c_5630
dc.subject.proposal.spa.fl_str_mv Resistance
Susceptibility
dc.subject.agrovocuri.none.fl_str_mv http://aims.fao.org/aos/agrovoc/c_4994
http://aims.fao.org/aos/agrovoc/c_928
http://aims.fao.org/aos/agrovoc/c_16109
http://aims.fao.org/aos/agrovoc/c_5630
description ABSTRACT: A correlation has been established between production of specific phenylphenalenones and resistance of various banana and plantain varieties towards certain pathogens. In addition a dihydrotrihydroxyphenylphenalene was isolated from the resistant 'Pelipita' plantain variety in relatively high concentrations and its structure and relative configuration were assigned on the basis of 1D and 2D NMR and NOE information. This compound is considered a key intermediate in the biosynthesis of phenylphenalenone phytoalexins.
publishDate 2002
dc.date.issued.none.fl_str_mv 2002
dc.date.accessioned.none.fl_str_mv 2021-11-02T13:58:17Z
dc.date.available.none.fl_str_mv 2021-11-02T13:58:17Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.coarversion.spa.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.driver.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.version.spa.fl_str_mv info:eu-repo/semantics/publishedVersion
format http://purl.org/coar/resource_type/c_2df8fbb1
status_str publishedVersion
dc.identifier.citation.spa.fl_str_mv Otálvaro, F., Echeverri, F., Quiñones, W., Torres, F., & Schneider, B. (2002). Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol. Molecules, 7(3), 331–340. Retrieved from http://dx.doi.org/10.3390/70300331
dc.identifier.issn.none.fl_str_mv 1420-3049
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/23687
dc.identifier.doi.none.fl_str_mv 10.3390/70300331
identifier_str_mv Otálvaro, F., Echeverri, F., Quiñones, W., Torres, F., & Schneider, B. (2002). Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol. Molecules, 7(3), 331–340. Retrieved from http://dx.doi.org/10.3390/70300331
1420-3049
10.3390/70300331
url http://hdl.handle.net/10495/23687
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Molecules
dc.relation.citationendpage.spa.fl_str_mv 340
dc.relation.citationissue.spa.fl_str_mv 3
dc.relation.citationstartpage.spa.fl_str_mv 331
dc.relation.citationvolume.spa.fl_str_mv 7
dc.relation.ispartofjournal.spa.fl_str_mv Molecules
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by/2.5/co/
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by/4.0/
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.coar.spa.fl_str_mv http://purl.org/coar/access_right/c_abf2
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/co/
https://creativecommons.org/licenses/by/4.0/
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.extent.spa.fl_str_mv 10
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv MDPI
dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
bitstream.url.fl_str_mv https://bibliotecadigital.udea.edu.co/bitstreams/916042c1-0591-445a-bbd4-4c2b38fe73a1/download
https://bibliotecadigital.udea.edu.co/bitstreams/edbd01d1-de93-456c-893c-c21ee0cc4248/download
https://bibliotecadigital.udea.edu.co/bitstreams/1befae07-18b9-4ec4-b0ff-36ab2e94ba50/download
https://bibliotecadigital.udea.edu.co/bitstreams/8f04c42b-c281-45ab-934b-eb97fd317563/download
https://bibliotecadigital.udea.edu.co/bitstreams/1dd58c81-9d74-47a2-9853-1c140fb1b4cc/download
bitstream.checksum.fl_str_mv e0441425bcfaccad1548fbfdc502369d
1646d1f6b96dbbbc38035efc9239ac9c
8a4605be74aa9ea9d79846c1fba20a33
81cd835abc6d09566ab49a562735462c
c18cb4df1c472dd868020ea7c29b970d
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv Repositorio Institucional de la Universidad de Antioquia
repository.mail.fl_str_mv aplicacionbibliotecadigitalbiblioteca@udea.edu.co
_version_ 1851052234797744128
spelling Otálvaro Tamayo, FelipeEcheverri López, Luis FernandoQuiñones Fletcher, WinstonTorres, FernandoSchneider, BerndQuímica Orgánica de Productos Naturales2021-11-02T13:58:17Z2021-11-02T13:58:17Z2002Otálvaro, F., Echeverri, F., Quiñones, W., Torres, F., & Schneider, B. (2002). Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene Triol. Molecules, 7(3), 331–340. Retrieved from http://dx.doi.org/10.3390/703003311420-3049http://hdl.handle.net/10495/2368710.3390/70300331ABSTRACT: A correlation has been established between production of specific phenylphenalenones and resistance of various banana and plantain varieties towards certain pathogens. In addition a dihydrotrihydroxyphenylphenalene was isolated from the resistant 'Pelipita' plantain variety in relatively high concentrations and its structure and relative configuration were assigned on the basis of 1D and 2D NMR and NOE information. This compound is considered a key intermediate in the biosynthesis of phenylphenalenone phytoalexins.COL001533910application/pdfengMDPIBasilea, Suizahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Correlation between Phenylphenalenone Phytoalexins and Phytopathological Properties in Musa and the Role of a Dihydrophenylphenalene TriolArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionMusa acuminataBiosíntesisBiosynthesisFitoalexinaPhytoalexinsOrganismos patógenosPathogensResistanceSusceptibilityhttp://aims.fao.org/aos/agrovoc/c_4994http://aims.fao.org/aos/agrovoc/c_928http://aims.fao.org/aos/agrovoc/c_16109http://aims.fao.org/aos/agrovoc/c_5630Molecules34033317MoleculesBiosynthesisPublicationORIGINALOtálvaroFelipe_2002_CorrelationPhenylphenalenonePhytoalexins.pdfOtálvaroFelipe_2002_CorrelationPhenylphenalenonePhytoalexins.pdfArtículo de investigaciónapplication/pdf64955https://bibliotecadigital.udea.edu.co/bitstreams/916042c1-0591-445a-bbd4-4c2b38fe73a1/downloade0441425bcfaccad1548fbfdc502369dMD51trueAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/edbd01d1-de93-456c-893c-c21ee0cc4248/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/1befae07-18b9-4ec4-b0ff-36ab2e94ba50/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADTEXTOtálvaroFelipe_2002_CorrelationPhenylphenalenonePhytoalexins.pdf.txtOtálvaroFelipe_2002_CorrelationPhenylphenalenonePhytoalexins.pdf.txtExtracted texttext/plain21152https://bibliotecadigital.udea.edu.co/bitstreams/8f04c42b-c281-45ab-934b-eb97fd317563/download81cd835abc6d09566ab49a562735462cMD54falseAnonymousREADTHUMBNAILOtálvaroFelipe_2002_CorrelationPhenylphenalenonePhytoalexins.pdf.jpgOtálvaroFelipe_2002_CorrelationPhenylphenalenonePhytoalexins.pdf.jpgGenerated Thumbnailimage/jpeg14181https://bibliotecadigital.udea.edu.co/bitstreams/1dd58c81-9d74-47a2-9853-1c140fb1b4cc/downloadc18cb4df1c472dd868020ea7c29b970dMD55falseAnonymousREAD10495/23687oai:bibliotecadigital.udea.edu.co:10495/236872025-03-26 19:03:35.535http://creativecommons.org/licenses/by/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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