Biosynthesis and Secretion of Indole-3-Acetic Acid and Its Morphological Effects on Tricholoma vaccinum-Spruce Ectomycorrhiza.
Identifieur interne : 001380 ( Main/Corpus ); précédent : 001379; suivant : 001381Biosynthesis and Secretion of Indole-3-Acetic Acid and Its Morphological Effects on Tricholoma vaccinum-Spruce Ectomycorrhiza.
Auteurs : Katrin Krause ; Catarina Henke ; Theodore Asiimwe ; Andrea Ulbricht ; Sandra Klemmer ; Doreen Schachtschabel ; Wilhelm Boland ; Erika KotheSource :
- Applied and environmental microbiology [ 1098-5336 ] ; 2015.
English descriptors
- KwdEn :
- DNA, Fungal (chemistry), DNA, Fungal (genetics), Indoleacetic Acids (metabolism), Metabolic Networks and Pathways (genetics), Molecular Sequence Data (MeSH), Mycorrhizae (cytology), Mycorrhizae (drug effects), Mycorrhizae (growth & development), Picea (microbiology), Schizophyllum (cytology), Schizophyllum (drug effects), Sequence Analysis, DNA (MeSH), Tricholoma (genetics), Tricholoma (metabolism).
- MESH :
- chemical , chemistry : DNA, Fungal.
- chemical , genetics : DNA, Fungal.
- chemical , metabolism : Indoleacetic Acids.
- cytology : Mycorrhizae, Schizophyllum.
- drug effects : Mycorrhizae, Schizophyllum.
- genetics : Metabolic Networks and Pathways, Tricholoma.
- growth & development : Mycorrhizae.
- metabolism : Tricholoma.
- microbiology : Picea.
- Molecular Sequence Data, Sequence Analysis, DNA.
Abstract
Fungus-derived indole-3-acetic acid (IAA), which is involved in development of ectomycorrhiza, affects both partners, i.e., the tree and the fungus. The biosynthesis pathway, excretion from fungal hyphae, the induction of branching in fungal cultures, and enhanced Hartig net formation in mycorrhiza were shown. Gene expression studies, incorporation of labeled compounds into IAA, heterologous expression of a transporter, and bioinformatics were applied to study the effect of IAA on fungal morphogenesis and on ectomycorrhiza. Tricholoma vaccinum produces IAA from tryptophan via indole-3-pyruvate, with the last step of this biosynthetic pathway being catalyzed by an aldehyde dehydrogenase. The gene ald1 was found to be highly expressed in ectomycorrhiza and induced by indole-3-acetaldehyde. The export of IAA from fungal cells is supported by the multidrug and toxic extrusion (MATE) transporter Mte1 found in T. vaccinum. The addition of IAA and its precursors induced elongated cells and hyphal ramification of mycorrhizal fungi; in contrast, in saprobic fungi such as Schizophyllum commune, IAA did not induce morphogenetic changes. Mycorrhiza responded by increasing its Hartig net formation. The IAA of fungal origin acts as a diffusible signal, influencing root colonization and increasing Hartig net formation in ectomycorrhiza.
DOI: 10.1128/AEM.01991-15
PubMed: 26231639
PubMed Central: PMC4579454
Links to Exploration step
pubmed:26231639Le document en format XML
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Asiimwe</name><affiliation><nlm:affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Ulbricht, Andrea" sort="Ulbricht, Andrea" uniqKey="Ulbricht A" first="Andrea" last="Ulbricht">Andrea Ulbricht</name><affiliation><nlm:affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Klemmer, Sandra" sort="Klemmer, Sandra" uniqKey="Klemmer S" first="Sandra" last="Klemmer">Sandra Klemmer</name><affiliation><nlm:affiliation>Max Planck Institute for Chemical Ecology, Jena, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Schachtschabel, Doreen" sort="Schachtschabel, Doreen" uniqKey="Schachtschabel D" first="Doreen" last="Schachtschabel">Doreen Schachtschabel</name><affiliation><nlm:affiliation>Max Planck Institute for Chemical Ecology, Jena, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Boland, Wilhelm" sort="Boland, Wilhelm" uniqKey="Boland W" first="Wilhelm" last="Boland">Wilhelm Boland</name><affiliation><nlm:affiliation>Max Planck Institute for Chemical Ecology, Jena, Germany.</nlm:affiliation></affiliation></author><author><name sortKey="Kothe, Erika" sort="Kothe, Erika" uniqKey="Kothe E" first="Erika" last="Kothe">Erika Kothe</name><affiliation><nlm:affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany erika.kothe@uni-jena.de.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Applied and environmental microbiology</title><idno type="eISSN">1098-5336</idno><imprint><date when="2015" type="published">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>DNA, Fungal (chemistry)</term><term>DNA, Fungal (genetics)</term><term>Indoleacetic Acids (metabolism)</term><term>Metabolic Networks and Pathways (genetics)</term><term>Molecular Sequence Data (MeSH)</term><term>Mycorrhizae (cytology)</term><term>Mycorrhizae (drug effects)</term><term>Mycorrhizae (growth & development)</term><term>Picea (microbiology)</term><term>Schizophyllum (cytology)</term><term>Schizophyllum (drug effects)</term><term>Sequence Analysis, DNA (MeSH)</term><term>Tricholoma (genetics)</term><term>Tricholoma (metabolism)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>DNA, Fungal</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>DNA, Fungal</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Indoleacetic Acids</term></keywords><keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Mycorrhizae</term><term>Schizophyllum</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Mycorrhizae</term><term>Schizophyllum</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Metabolic Networks and Pathways</term><term>Tricholoma</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Mycorrhizae</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Tricholoma</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Picea</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Molecular Sequence Data</term><term>Sequence Analysis, DNA</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Fungus-derived indole-3-acetic acid (IAA), which is involved in development of ectomycorrhiza, affects both partners, i.e., the tree and the fungus. The biosynthesis pathway, excretion from fungal hyphae, the induction of branching in fungal cultures, and enhanced Hartig net formation in mycorrhiza were shown. Gene expression studies, incorporation of labeled compounds into IAA, heterologous expression of a transporter, and bioinformatics were applied to study the effect of IAA on fungal morphogenesis and on ectomycorrhiza. Tricholoma vaccinum produces IAA from tryptophan via indole-3-pyruvate, with the last step of this biosynthetic pathway being catalyzed by an aldehyde dehydrogenase. The gene ald1 was found to be highly expressed in ectomycorrhiza and induced by indole-3-acetaldehyde. The export of IAA from fungal cells is supported by the multidrug and toxic extrusion (MATE) transporter Mte1 found in T. vaccinum. The addition of IAA and its precursors induced elongated cells and hyphal ramification of mycorrhizal fungi; in contrast, in saprobic fungi such as Schizophyllum commune, IAA did not induce morphogenetic changes. Mycorrhiza responded by increasing its Hartig net formation. The IAA of fungal origin acts as a diffusible signal, influencing root colonization and increasing Hartig net formation in ectomycorrhiza. </div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26231639</PMID><DateCompleted><Year>2016</Year><Month>06</Month><Day>13</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1098-5336</ISSN><JournalIssue CitedMedium="Internet"><Volume>81</Volume><Issue>20</Issue><PubDate><Year>2015</Year><Month>Oct</Month></PubDate></JournalIssue><Title>Applied and environmental microbiology</Title><ISOAbbreviation>Appl Environ Microbiol</ISOAbbreviation></Journal><ArticleTitle>Biosynthesis and Secretion of Indole-3-Acetic Acid and Its Morphological Effects on Tricholoma vaccinum-Spruce Ectomycorrhiza.</ArticleTitle><Pagination><MedlinePgn>7003-11</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1128/AEM.01991-15</ELocationID><Abstract><AbstractText>Fungus-derived indole-3-acetic acid (IAA), which is involved in development of ectomycorrhiza, affects both partners, i.e., the tree and the fungus. The biosynthesis pathway, excretion from fungal hyphae, the induction of branching in fungal cultures, and enhanced Hartig net formation in mycorrhiza were shown. Gene expression studies, incorporation of labeled compounds into IAA, heterologous expression of a transporter, and bioinformatics were applied to study the effect of IAA on fungal morphogenesis and on ectomycorrhiza. Tricholoma vaccinum produces IAA from tryptophan via indole-3-pyruvate, with the last step of this biosynthetic pathway being catalyzed by an aldehyde dehydrogenase. The gene ald1 was found to be highly expressed in ectomycorrhiza and induced by indole-3-acetaldehyde. The export of IAA from fungal cells is supported by the multidrug and toxic extrusion (MATE) transporter Mte1 found in T. vaccinum. The addition of IAA and its precursors induced elongated cells and hyphal ramification of mycorrhizal fungi; in contrast, in saprobic fungi such as Schizophyllum commune, IAA did not induce morphogenetic changes. Mycorrhiza responded by increasing its Hartig net formation. The IAA of fungal origin acts as a diffusible signal, influencing root colonization and increasing Hartig net formation in ectomycorrhiza. </AbstractText><CopyrightInformation>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Krause</LastName><ForeName>Katrin</ForeName><Initials>K</Initials><AffiliationInfo><Affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Henke</LastName><ForeName>Catarina</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Asiimwe</LastName><ForeName>Theodore</ForeName><Initials>T</Initials><AffiliationInfo><Affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ulbricht</LastName><ForeName>Andrea</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Klemmer</LastName><ForeName>Sandra</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Schachtschabel</LastName><ForeName>Doreen</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Boland</LastName><ForeName>Wilhelm</ForeName><Initials>W</Initials><Identifier Source="ORCID">http://orcid.org/0000-0001-6784-2534</Identifier><AffiliationInfo><Affiliation>Max Planck Institute for Chemical Ecology, Jena, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kothe</LastName><ForeName>Erika</ForeName><Initials>E</Initials><AffiliationInfo><Affiliation>Friedrich Schiller University, Institute of Microbiology, Microbial Communication, Jena, Germany erika.kothe@uni-jena.de.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><DataBankList CompleteYN="Y"><DataBank><DataBankName>GENBANK</DataBankName><AccessionNumberList><AccessionNumber>KP096350</AccessionNumber><AccessionNumber>KP096351</AccessionNumber><AccessionNumber>KP096352</AccessionNumber></AccessionNumberList></DataBank></DataBankList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>07</Month><Day>31</Day></ArticleDate></Article><MedlineJournalInfo><Country>United 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