Serveur d'exploration sur la mycorhize

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Hypericin and pseudohypericin concentrations of a valuable medicinal plant Hypericum perforatum L. are enhanced by arbuscular mycorrhizal fungi.

Identifieur interne : 002289 ( Main/Corpus ); précédent : 002288; suivant : 002290

Hypericin and pseudohypericin concentrations of a valuable medicinal plant Hypericum perforatum L. are enhanced by arbuscular mycorrhizal fungi.

Auteurs : Szymon Zubek ; Sebastian Mielcarek ; Katarzyna Turnau

Source :

RBID : pubmed:21626142

English descriptors

Abstract

Hypericum perforatum L. (St. John's-wort, Hypericaceae) is a valuable medicinal plant species cultivated for pharmaceutical purposes. Although the chemical composition and pharmacological activities of H. perforatum have been well studied, no data are available concerning the influence of arbuscular mycorrhizal fungi (AMF) on this important herb. A laboratory experiment was therefore conducted in order to test three AMF inocula on H. perforatum with a view to show whether AMF could influence plant vitality (biomass and photosynthetic activity) and the production of the most valuable secondary metabolites, namely anthraquinone derivatives (hypericin and pseudohypericin) as well as the prenylated phloroglucinol-hyperforin. The following treatments were prepared: (1) control-sterile soil without AMF inoculation, (2) Rhizophagus intraradices (syn. Glomus intraradices), (3) Funneliformis mosseae (syn. Glomus mosseae), and (4) an AMF Mix which contained: Funneliformis constrictum (syn. Glomus constrictum), Funneliformis geosporum (syn. Glomus geosporum), F. mosseae, and R. intraradices. The application of R. intraradices inoculum resulted in the highest mycorrhizal colonization, whereas the lowest values of mycorrhizal parameters were detected in the AMF Mix. There were no statistically significant differences in H. perforatum shoot mass in any of the treatments. However, we found AMF species specificity in the stimulation of H. perforatum photosynthetic activity and the production of secondary metabolites. Inoculation with the AMF Mix resulted in higher photosynthetic performance index (PI(total)) values in comparison to all the other treatments. The plants inoculated with R. intraradices and the AMF Mix were characterized by a higher concentration of hypericin and pseudohypericin in the shoots. However, no differences in the content of these metabolites were detected after the application of F. mosseae. In the case of hyperforin, no significant differences were found between the control plants and those inoculated with any of the AMF applied. The enhanced content of anthraquinone derivatives and, at the same time, better plant vitality suggest that the improved production of these metabolites was a result of the positive effect of the applied AMF strains on H. perforatum. This could be due to improved mineral nutrition or to AMF-induced changes in the phytohormonal balance. Our results are promising from the biotechnological point of view, i.e. the future inoculation of H. perforatum with AMF in order to improve the quality of medicinal plant raw material obtained from cultivation.

DOI: 10.1007/s00572-011-0391-1
PubMed: 21626142
PubMed Central: PMC3261393

Links to Exploration step

pubmed:21626142

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Hypericin and pseudohypericin concentrations of a valuable medicinal plant Hypericum perforatum L. are enhanced by arbuscular mycorrhizal fungi.</title>
<author>
<name sortKey="Zubek, Szymon" sort="Zubek, Szymon" uniqKey="Zubek S" first="Szymon" last="Zubek">Szymon Zubek</name>
<affiliation>
<nlm:affiliation>Laboratory of Mycology, Institute of Botany, Jagiellonian University, Lubicz 46, Kraków, Poland. szymon.zubek@uj.edu.pl</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Mielcarek, Sebastian" sort="Mielcarek, Sebastian" uniqKey="Mielcarek S" first="Sebastian" last="Mielcarek">Sebastian Mielcarek</name>
</author>
<author>
<name sortKey="Turnau, Katarzyna" sort="Turnau, Katarzyna" uniqKey="Turnau K" first="Katarzyna" last="Turnau">Katarzyna Turnau</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2012">2012</date>
<idno type="RBID">pubmed:21626142</idno>
<idno type="pmid">21626142</idno>
<idno type="doi">10.1007/s00572-011-0391-1</idno>
<idno type="pmc">PMC3261393</idno>
<idno type="wicri:Area/Main/Corpus">002289</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">002289</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Hypericin and pseudohypericin concentrations of a valuable medicinal plant Hypericum perforatum L. are enhanced by arbuscular mycorrhizal fungi.</title>
<author>
<name sortKey="Zubek, Szymon" sort="Zubek, Szymon" uniqKey="Zubek S" first="Szymon" last="Zubek">Szymon Zubek</name>
<affiliation>
<nlm:affiliation>Laboratory of Mycology, Institute of Botany, Jagiellonian University, Lubicz 46, Kraków, Poland. szymon.zubek@uj.edu.pl</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Mielcarek, Sebastian" sort="Mielcarek, Sebastian" uniqKey="Mielcarek S" first="Sebastian" last="Mielcarek">Sebastian Mielcarek</name>
</author>
<author>
<name sortKey="Turnau, Katarzyna" sort="Turnau, Katarzyna" uniqKey="Turnau K" first="Katarzyna" last="Turnau">Katarzyna Turnau</name>
</author>
</analytic>
<series>
<title level="j">Mycorrhiza</title>
<idno type="eISSN">1432-1890</idno>
<imprint>
<date when="2012" type="published">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Glomeromycota (physiology)</term>
<term>Hypericum (chemistry)</term>
<term>Hypericum (metabolism)</term>
<term>Hypericum (microbiology)</term>
<term>Mycorrhizae (physiology)</term>
<term>Perylene (analogs & derivatives)</term>
<term>Perylene (analysis)</term>
<term>Perylene (metabolism)</term>
<term>Plants, Medicinal (chemistry)</term>
<term>Plants, Medicinal (metabolism)</term>
<term>Plants, Medicinal (microbiology)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en">
<term>Perylene</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en">
<term>Perylene</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>Hypericum</term>
<term>Plants, Medicinal</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Hypericum</term>
<term>Perylene</term>
<term>Plants, Medicinal</term>
</keywords>
<keywords scheme="MESH" qualifier="microbiology" xml:lang="en">
<term>Hypericum</term>
<term>Plants, Medicinal</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Glomeromycota</term>
<term>Mycorrhizae</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Hypericum perforatum L. (St. John's-wort, Hypericaceae) is a valuable medicinal plant species cultivated for pharmaceutical purposes. Although the chemical composition and pharmacological activities of H. perforatum have been well studied, no data are available concerning the influence of arbuscular mycorrhizal fungi (AMF) on this important herb. A laboratory experiment was therefore conducted in order to test three AMF inocula on H. perforatum with a view to show whether AMF could influence plant vitality (biomass and photosynthetic activity) and the production of the most valuable secondary metabolites, namely anthraquinone derivatives (hypericin and pseudohypericin) as well as the prenylated phloroglucinol-hyperforin. The following treatments were prepared: (1) control-sterile soil without AMF inoculation, (2) Rhizophagus intraradices (syn. Glomus intraradices), (3) Funneliformis mosseae (syn. Glomus mosseae), and (4) an AMF Mix which contained: Funneliformis constrictum (syn. Glomus constrictum), Funneliformis geosporum (syn. Glomus geosporum), F. mosseae, and R. intraradices. The application of R. intraradices inoculum resulted in the highest mycorrhizal colonization, whereas the lowest values of mycorrhizal parameters were detected in the AMF Mix. There were no statistically significant differences in H. perforatum shoot mass in any of the treatments. However, we found AMF species specificity in the stimulation of H. perforatum photosynthetic activity and the production of secondary metabolites. Inoculation with the AMF Mix resulted in higher photosynthetic performance index (PI(total)) values in comparison to all the other treatments. The plants inoculated with R. intraradices and the AMF Mix were characterized by a higher concentration of hypericin and pseudohypericin in the shoots. However, no differences in the content of these metabolites were detected after the application of F. mosseae. In the case of hyperforin, no significant differences were found between the control plants and those inoculated with any of the AMF applied. The enhanced content of anthraquinone derivatives and, at the same time, better plant vitality suggest that the improved production of these metabolites was a result of the positive effect of the applied AMF strains on H. perforatum. This could be due to improved mineral nutrition or to AMF-induced changes in the phytohormonal balance. Our results are promising from the biotechnological point of view, i.e. the future inoculation of H. perforatum with AMF in order to improve the quality of medicinal plant raw material obtained from cultivation.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">21626142</PMID>
<DateCompleted>
<Year>2012</Year>
<Month>05</Month>
<Day>01</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>11</Month>
<Day>13</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1432-1890</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>22</Volume>
<Issue>2</Issue>
<PubDate>
<Year>2012</Year>
<Month>Feb</Month>
</PubDate>
</JournalIssue>
<Title>Mycorrhiza</Title>
<ISOAbbreviation>Mycorrhiza</ISOAbbreviation>
</Journal>
<ArticleTitle>Hypericin and pseudohypericin concentrations of a valuable medicinal plant Hypericum perforatum L. are enhanced by arbuscular mycorrhizal fungi.</ArticleTitle>
<Pagination>
<MedlinePgn>149-56</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s00572-011-0391-1</ELocationID>
<Abstract>
<AbstractText>Hypericum perforatum L. (St. John's-wort, Hypericaceae) is a valuable medicinal plant species cultivated for pharmaceutical purposes. Although the chemical composition and pharmacological activities of H. perforatum have been well studied, no data are available concerning the influence of arbuscular mycorrhizal fungi (AMF) on this important herb. A laboratory experiment was therefore conducted in order to test three AMF inocula on H. perforatum with a view to show whether AMF could influence plant vitality (biomass and photosynthetic activity) and the production of the most valuable secondary metabolites, namely anthraquinone derivatives (hypericin and pseudohypericin) as well as the prenylated phloroglucinol-hyperforin. The following treatments were prepared: (1) control-sterile soil without AMF inoculation, (2) Rhizophagus intraradices (syn. Glomus intraradices), (3) Funneliformis mosseae (syn. Glomus mosseae), and (4) an AMF Mix which contained: Funneliformis constrictum (syn. Glomus constrictum), Funneliformis geosporum (syn. Glomus geosporum), F. mosseae, and R. intraradices. The application of R. intraradices inoculum resulted in the highest mycorrhizal colonization, whereas the lowest values of mycorrhizal parameters were detected in the AMF Mix. There were no statistically significant differences in H. perforatum shoot mass in any of the treatments. However, we found AMF species specificity in the stimulation of H. perforatum photosynthetic activity and the production of secondary metabolites. Inoculation with the AMF Mix resulted in higher photosynthetic performance index (PI(total)) values in comparison to all the other treatments. The plants inoculated with R. intraradices and the AMF Mix were characterized by a higher concentration of hypericin and pseudohypericin in the shoots. However, no differences in the content of these metabolites were detected after the application of F. mosseae. In the case of hyperforin, no significant differences were found between the control plants and those inoculated with any of the AMF applied. The enhanced content of anthraquinone derivatives and, at the same time, better plant vitality suggest that the improved production of these metabolites was a result of the positive effect of the applied AMF strains on H. perforatum. This could be due to improved mineral nutrition or to AMF-induced changes in the phytohormonal balance. Our results are promising from the biotechnological point of view, i.e. the future inoculation of H. perforatum with AMF in order to improve the quality of medicinal plant raw material obtained from cultivation.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Zubek</LastName>
<ForeName>Szymon</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Laboratory of Mycology, Institute of Botany, Jagiellonian University, Lubicz 46, Kraków, Poland. szymon.zubek@uj.edu.pl</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Mielcarek</LastName>
<ForeName>Sebastian</ForeName>
<Initials>S</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Turnau</LastName>
<ForeName>Katarzyna</ForeName>
<Initials>K</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2011</Year>
<Month>05</Month>
<Day>28</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>Germany</Country>
<MedlineTA>Mycorrhiza</MedlineTA>
<NlmUniqueID>100955036</NlmUniqueID>
<ISSNLinking>0940-6360</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>5QD5427UN7</RegistryNumber>
<NameOfSubstance UI="D010569">Perylene</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>7V2F1075HD</RegistryNumber>
<NameOfSubstance UI="C004965">hypericin</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>MQ0U4663ZO</RegistryNumber>
<NameOfSubstance UI="C056602">pseudohypericin</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D055137" MajorTopicYN="N">Glomeromycota</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D020902" MajorTopicYN="N">Hypericum</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D038821" MajorTopicYN="N">Mycorrhizae</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010569" MajorTopicYN="N">Perylene</DescriptorName>
<QualifierName UI="Q000031" MajorTopicYN="Y">analogs & derivatives</QualifierName>
<QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010946" MajorTopicYN="N">Plants, Medicinal</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
<QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2011</Year>
<Month>03</Month>
<Day>10</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2011</Year>
<Month>05</Month>
<Day>15</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2011</Year>
<Month>6</Month>
<Day>1</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2011</Year>
<Month>6</Month>
<Day>1</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2012</Year>
<Month>5</Month>
<Day>2</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">21626142</ArticleId>
<ArticleId IdType="doi">10.1007/s00572-011-0391-1</ArticleId>
<ArticleId IdType="pmc">PMC3261393</ArticleId>
</ArticleIdList>
<ReferenceList>
<Reference>
<Citation>Mycorrhiza. 2007 Oct;17(7):581-7</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">17578608</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Am J Bot. 2002 Feb;89(2):337-45</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">21669742</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Planta. 2002 Nov;216(1):148-54</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">12430024</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2006 Sep;16(6):443-6</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16909287</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Biosci Biotechnol Biochem. 2002 Apr;66(4):762-9</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">12036048</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2010 Nov;20(8):519-30</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">20697748</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2006 Jul;16(5):299-363</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16845554</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2005 Nov;15(8):596-605</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16133256</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2007 Jun;17(4):291-7</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">17273856</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>New Phytol. 2009 Mar;181(4):938-49</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">19140934</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2009 Feb;19(2):113-23</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">19011910</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2010 Oct;20(7):445-57</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">20652364</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2006 Oct;16(7):485-94</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16896796</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2003 Mar;13(1):49-52</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">12634919</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2007 Jun;17(4):349-53</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">17476534</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2009 Aug;19(6):393-402</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">19377892</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2010 Oct;20(7):497-504</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">20177715</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Am J Health Syst Pharm. 2002 Mar 15;59(6):545-7</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">11908248</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>New Phytol. 2008;177(3):779-89</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">18042204</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Mycorrhiza. 2010 Jun;20(5):293-306</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">19838743</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Bois/explor/MycorrhizaeV1/Data/Main/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002289 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd -nk 002289 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Bois
   |area=    MycorrhizaeV1
   |flux=    Main
   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:21626142
   |texte=   Hypericin and pseudohypericin concentrations of a valuable medicinal plant Hypericum perforatum L. are enhanced by arbuscular mycorrhizal fungi.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Corpus/RBID.i   -Sk "pubmed:21626142" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a MycorrhizaeV1 

Wicri

This area was generated with Dilib version V0.6.37.
Data generation: Wed Nov 18 15:34:48 2020. Site generation: Wed Nov 18 15:41:10 2020