Host plant stimulates hypaphorine accumulation in Pisolithus tinctorius hyphae during ectomycorrhizal infection while excreted fungal hypaphorine controls root hair development
The hypaphorine concentration in Pisolithus tinctorius Coker & Couch hyphae colonizing Eucalyptus roots was 3 to 5 times higher than in adjacent parts of the fungal colony. This phenomenon, observed 24 h after inoculation, was also recorded in several-month-old, well-established ectomycorrhizas....
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Veröffentlicht in: | The New phytologist 1997-07, Vol.136 (3), p.525-532 |
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creator | BÉGUIRISTAIN, THIERRY LAPEYRIE, FRÉDÉRIC |
description | The hypaphorine concentration in Pisolithus tinctorius
Coker & Couch hyphae colonizing Eucalyptus roots was 3
to 5 times higher than in adjacent parts of the fungal colony. This phenomenon,
observed 24 h after inoculation,
was also recorded in several-month-old, well-established ectomycorrhizas.
Accumulation was controlled by
specific root-derived diffusible molecules: it can be induced through a
membrane, but not by non-host plants. In
pure culture, high hypaphorine concentration was found only in the youngest
mycelium, i.e. the outer 2 mm of
the colony. Fungal hypaphorine had no IAA-like activity on Eucalyptus
root development and therefore could not
be considered as an auxin analogue; instead, a strong reduction of root hair
elongation was recorded. |
doi_str_mv | 10.1046/j.1469-8137.1997.00753.x |
format | Article |
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Coker & Couch hyphae colonizing Eucalyptus roots was 3
to 5 times higher than in adjacent parts of the fungal colony. This phenomenon,
observed 24 h after inoculation,
was also recorded in several-month-old, well-established ectomycorrhizas.
Accumulation was controlled by
specific root-derived diffusible molecules: it can be induced through a
membrane, but not by non-host plants. In
pure culture, high hypaphorine concentration was found only in the youngest
mycelium, i.e. the outer 2 mm of
the colony. Fungal hypaphorine had no IAA-like activity on Eucalyptus
root development and therefore could not
be considered as an auxin analogue; instead, a strong reduction of root hair
elongation was recorded.</description><identifier>ISSN: 0028-646X</identifier><identifier>EISSN: 1469-8137</identifier><identifier>DOI: 10.1046/j.1469-8137.1997.00753.x</identifier><identifier>PMID: 33863009</identifier><identifier>CODEN: NEPHAV</identifier><language>eng</language><publisher>Oxford, UK: Cambridge University Press</publisher><subject>Agronomy. Soil science and plant productions ; Auxins ; Biological and medical sciences ; Colonies ; Economic plant physiology ; ectomycorrhiza ; Ectomycorrhizas ; Eucalyptus globulus ; Fundamental and applied biological sciences. Psychology ; Hypaphorine ; Hyphae ; IAA ; Inoculation ; Parasitism and symbiosis ; Pisolithus tinctorius ; Plant physiology and development ; Plant roots ; Plants ; Root hairs ; Seedlings ; Symbiosis ; Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...) ; Tap roots</subject><ispartof>The New phytologist, 1997-07, Vol.136 (3), p.525-532</ispartof><rights>Trustees of the New Phytologist 1997</rights><rights>Copyright 1997 Trustees of The New Phytologist</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4985-7eae7127fe2ecd7c401e55dc3d67a31316e4e002d824c28fefd96a22d1470b913</citedby><cites>FETCH-LOGICAL-c4985-7eae7127fe2ecd7c401e55dc3d67a31316e4e002d824c28fefd96a22d1470b913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2558956$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2558956$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,1411,1427,27901,27902,45550,45551,46384,46808,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2761055$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33863009$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>BÉGUIRISTAIN, THIERRY</creatorcontrib><creatorcontrib>LAPEYRIE, FRÉDÉRIC</creatorcontrib><title>Host plant stimulates hypaphorine accumulation in Pisolithus tinctorius hyphae during ectomycorrhizal infection while excreted fungal hypaphorine controls root hair development</title><title>The New phytologist</title><addtitle>New Phytol</addtitle><description>The hypaphorine concentration in Pisolithus tinctorius
Coker & Couch hyphae colonizing Eucalyptus roots was 3
to 5 times higher than in adjacent parts of the fungal colony. This phenomenon,
observed 24 h after inoculation,
was also recorded in several-month-old, well-established ectomycorrhizas.
Accumulation was controlled by
specific root-derived diffusible molecules: it can be induced through a
membrane, but not by non-host plants. In
pure culture, high hypaphorine concentration was found only in the youngest
mycelium, i.e. the outer 2 mm of
the colony. Fungal hypaphorine had no IAA-like activity on Eucalyptus
root development and therefore could not
be considered as an auxin analogue; instead, a strong reduction of root hair
elongation was recorded.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Auxins</subject><subject>Biological and medical sciences</subject><subject>Colonies</subject><subject>Economic plant physiology</subject><subject>ectomycorrhiza</subject><subject>Ectomycorrhizas</subject><subject>Eucalyptus globulus</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hypaphorine</subject><subject>Hyphae</subject><subject>IAA</subject><subject>Inoculation</subject><subject>Parasitism and symbiosis</subject><subject>Pisolithus tinctorius</subject><subject>Plant physiology and development</subject><subject>Plant roots</subject><subject>Plants</subject><subject>Root hairs</subject><subject>Seedlings</subject><subject>Symbiosis</subject><subject>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</subject><subject>Tap roots</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqNks2O0zAUhSMEYsrAGyDkBUJsUvwTOwlig0ZAkUYwC5DYWa5907hK4mA7TMtT8Yg4bSmsgJXle885V76fswwRvCS4EC-2S1KIOq8IK5ekrsslxiVny92dbHFu3M0WGNMqF4X4cpE9CGGLMa65oPezC8YqwdJtkf1YuRDR2KkhohBtP3UqQkDtflRj67wdACmtp0PdugHZAd3Y4Dob2ymgaAcdk2o6OFoFyEzJs0GQyv1eO-9b-111ydak0hxw29oOEOy0hwgGNdOwSf0_52k3RO-6gLxzEbXKemTgG3Ru7GGID7N7jeoCPDqdl9nnt28-Xa3y64_v3l-9vs51UVc8L0FBSWjZAAVtSl1gApwbzYwoFSOMCCgg7cdUtNC0aqAxtVCUGlKUeF0Tdpk9P-aO3n2dIETZ26ChS5sCNwVJedo0ZkJUSfrsr1IiGC0ZmzOro1B7F4KHRo7e9srvJcFyBiu3cuYnZ35yBisPYOUuWZ-cZkzrHszZ-ItkEjw9CVTQqmu8GrQNZx0tBcGcJ9mro-w2Ydj_93z54WbF6Wx_fLRvQ-L-O53zKn2t1H55eqDq196aDcitm_yQQP37iT8BWP3gVw</recordid><startdate>199707</startdate><enddate>199707</enddate><creator>BÉGUIRISTAIN, THIERRY</creator><creator>LAPEYRIE, FRÉDÉRIC</creator><general>Cambridge University Press</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>199707</creationdate><title>Host plant stimulates hypaphorine accumulation in Pisolithus tinctorius hyphae during ectomycorrhizal infection while excreted fungal hypaphorine controls root hair development</title><author>BÉGUIRISTAIN, THIERRY ; LAPEYRIE, FRÉDÉRIC</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4985-7eae7127fe2ecd7c401e55dc3d67a31316e4e002d824c28fefd96a22d1470b913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Agronomy. Soil science and plant productions</topic><topic>Auxins</topic><topic>Biological and medical sciences</topic><topic>Colonies</topic><topic>Economic plant physiology</topic><topic>ectomycorrhiza</topic><topic>Ectomycorrhizas</topic><topic>Eucalyptus globulus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hypaphorine</topic><topic>Hyphae</topic><topic>IAA</topic><topic>Inoculation</topic><topic>Parasitism and symbiosis</topic><topic>Pisolithus tinctorius</topic><topic>Plant physiology and development</topic><topic>Plant roots</topic><topic>Plants</topic><topic>Root hairs</topic><topic>Seedlings</topic><topic>Symbiosis</topic><topic>Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...)</topic><topic>Tap roots</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BÉGUIRISTAIN, THIERRY</creatorcontrib><creatorcontrib>LAPEYRIE, FRÉDÉRIC</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The New phytologist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BÉGUIRISTAIN, THIERRY</au><au>LAPEYRIE, FRÉDÉRIC</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Host plant stimulates hypaphorine accumulation in Pisolithus tinctorius hyphae during ectomycorrhizal infection while excreted fungal hypaphorine controls root hair development</atitle><jtitle>The New phytologist</jtitle><addtitle>New Phytol</addtitle><date>1997-07</date><risdate>1997</risdate><volume>136</volume><issue>3</issue><spage>525</spage><epage>532</epage><pages>525-532</pages><issn>0028-646X</issn><eissn>1469-8137</eissn><coden>NEPHAV</coden><abstract>The hypaphorine concentration in Pisolithus tinctorius
Coker & Couch hyphae colonizing Eucalyptus roots was 3
to 5 times higher than in adjacent parts of the fungal colony. This phenomenon,
observed 24 h after inoculation,
was also recorded in several-month-old, well-established ectomycorrhizas.
Accumulation was controlled by
specific root-derived diffusible molecules: it can be induced through a
membrane, but not by non-host plants. In
pure culture, high hypaphorine concentration was found only in the youngest
mycelium, i.e. the outer 2 mm of
the colony. Fungal hypaphorine had no IAA-like activity on Eucalyptus
root development and therefore could not
be considered as an auxin analogue; instead, a strong reduction of root hair
elongation was recorded.</abstract><cop>Oxford, UK</cop><pub>Cambridge University Press</pub><pmid>33863009</pmid><doi>10.1046/j.1469-8137.1997.00753.x</doi><tpages>8</tpages></addata></record> |
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source | Jstor Complete Legacy; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content; EZB-FREE-00999 freely available EZB journals |
subjects | Agronomy. Soil science and plant productions Auxins Biological and medical sciences Colonies Economic plant physiology ectomycorrhiza Ectomycorrhizas Eucalyptus globulus Fundamental and applied biological sciences. Psychology Hypaphorine Hyphae IAA Inoculation Parasitism and symbiosis Pisolithus tinctorius Plant physiology and development Plant roots Plants Root hairs Seedlings Symbiosis Symbiosis (nodules, symbiotic nitrogen fixation, mycorrhiza...) Tap roots |
title | Host plant stimulates hypaphorine accumulation in Pisolithus tinctorius hyphae during ectomycorrhizal infection while excreted fungal hypaphorine controls root hair development |
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