Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications
Identifieur interne : 000422 ( Pmc/Curation ); précédent : 000421; suivant : 000423Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications
Auteurs : Tina Ilc ; Claire Parage ; Benoît Boachon ; Nicolas Navrot ; Danièle Werck-ReichhartSource :
- Frontiers in Plant Science [ 1664-462X ] ; 2016.
Abstract
Plants use monoterpenols as precursors for the production of functionally and structurally diverse molecules, which are key players in interactions with other organisms such as pollinators, flower visitors, herbivores, fungal, or microbial pathogens. For humans, many of these monoterpenol derivatives are economically important because of their pharmaceutical, nutraceutical, flavor, or fragrance applications. The biosynthesis of these derivatives is to a large extent catalyzed by enzymes from the cytochrome P450 superfamily. Here we review the knowledge on monoterpenol oxidative metabolism in plants with special focus on recent elucidations of oxidation steps leading to diverse linalool and geraniol derivatives. We evaluate the common features between oxidation pathways of these two monoterpenols, such as involvement of the CYP76 family, and highlight the differences. Finally, we discuss the missing steps and other open questions in the biosynthesis of oxygenated monoterpenol derivatives.
Url:
DOI: 10.3389/fpls.2016.00509
PubMed: 27200002
PubMed Central: 4844611
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications</title><author><name sortKey="Ilc, Tina" sort="Ilc, Tina" uniqKey="Ilc T" first="Tina" last="Ilc">Tina Ilc</name></author><author><name sortKey="Parage, Claire" sort="Parage, Claire" uniqKey="Parage C" first="Claire" last="Parage">Claire Parage</name></author><author><name sortKey="Boachon, Benoit" sort="Boachon, Benoit" uniqKey="Boachon B" first="Benoît" last="Boachon">Benoît Boachon</name></author><author><name sortKey="Navrot, Nicolas" sort="Navrot, Nicolas" uniqKey="Navrot N" first="Nicolas" last="Navrot">Nicolas Navrot</name></author><author><name sortKey="Werck Reichhart, Daniele" sort="Werck Reichhart, Daniele" uniqKey="Werck Reichhart D" first="Danièle" last="Werck-Reichhart">Danièle Werck-Reichhart</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">27200002</idno><idno type="pmc">4844611</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844611</idno><idno type="RBID">PMC:4844611</idno><idno type="doi">10.3389/fpls.2016.00509</idno><date when="2016">2016</date><idno type="wicri:Area/Pmc/Corpus">000423</idno><idno type="wicri:Area/Pmc/Curation">000422</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications</title><author><name sortKey="Ilc, Tina" sort="Ilc, Tina" uniqKey="Ilc T" first="Tina" last="Ilc">Tina Ilc</name></author><author><name sortKey="Parage, Claire" sort="Parage, Claire" uniqKey="Parage C" first="Claire" last="Parage">Claire Parage</name></author><author><name sortKey="Boachon, Benoit" sort="Boachon, Benoit" uniqKey="Boachon B" first="Benoît" last="Boachon">Benoît Boachon</name></author><author><name sortKey="Navrot, Nicolas" sort="Navrot, Nicolas" uniqKey="Navrot N" first="Nicolas" last="Navrot">Nicolas Navrot</name></author><author><name sortKey="Werck Reichhart, Daniele" sort="Werck Reichhart, Daniele" uniqKey="Werck Reichhart D" first="Danièle" last="Werck-Reichhart">Danièle Werck-Reichhart</name></author></analytic><series><title level="j">Frontiers in Plant Science</title><idno type="eISSN">1664-462X</idno><imprint><date when="2016">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Plants use monoterpenols as precursors for the production of functionally and structurally diverse molecules, which are key players in interactions with other organisms such as pollinators, flower visitors, herbivores, fungal, or microbial pathogens. For humans, many of these monoterpenol derivatives are economically important because of their pharmaceutical, nutraceutical, flavor, or fragrance applications. The biosynthesis of these derivatives is to a large extent catalyzed by enzymes from the cytochrome P450 superfamily. Here we review the knowledge on monoterpenol oxidative metabolism in plants with special focus on recent elucidations of oxidation steps leading to diverse linalool and geraniol derivatives. We evaluate the common features between oxidation pathways of these two monoterpenols, such as involvement of the CYP76 family, and highlight the differences. Finally, we discuss the missing steps and other open questions in the biosynthesis of oxygenated monoterpenol derivatives.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Aharoni, A" uniqKey="Aharoni A">A. Aharoni</name></author><author><name sortKey="Giri, A P" uniqKey="Giri A">A. P. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Front Plant Sci</journal-id><journal-id journal-id-type="iso-abbrev">Front Plant Sci</journal-id><journal-id journal-id-type="publisher-id">Front. Plant Sci.</journal-id><journal-title-group><journal-title>Frontiers in Plant Science</journal-title></journal-title-group><issn pub-type="epub">1664-462X</issn><publisher><publisher-name>Frontiers Media S.A.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">27200002</article-id><article-id pub-id-type="pmc">4844611</article-id><article-id pub-id-type="doi">10.3389/fpls.2016.00509</article-id><article-categories><subj-group subj-group-type="heading"><subject>Plant Science</subject><subj-group><subject>Review</subject></subj-group></subj-group></article-categories><title-group><article-title>Monoterpenol Oxidative Metabolism: Role in Plant Adaptation and Potential Applications</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Ilc</surname><given-names>Tina</given-names></name><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/329890/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Parage</surname><given-names>Claire</given-names></name><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/340507/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Boachon</surname><given-names>Benoît</given-names></name><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/332026/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Navrot</surname><given-names>Nicolas</given-names></name><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/86480/overview"></uri></contrib><contrib contrib-type="author"><name><surname>Werck-Reichhart</surname><given-names>Danièle</given-names></name><xref ref-type="author-notes" rid="fn001"><sup>*</sup></xref><uri xlink:type="simple" xlink:href="http://loop.frontiersin.org/people/218087/overview"></uri></contrib></contrib-group><aff id="aff1"><institution>Institut de Biologie Moléculaire des Plantes, Centre National de la Recherche Scientifique, Université de Strasbourg</institution><country>Strasbourg, France</country></aff><author-notes><fn fn-type="edited-by"><p>Edited by: <italic>Kevin Davies, The New Zealand Institute for Plant & Food Research Ltd, New Zealand</italic></p></fn><fn fn-type="edited-by"><p>Reviewed by: <italic>Reuben Peters, Iowa State University, USA; Fernando Geu-Flores, John Innes Centre, UK</italic></p></fn><corresp id="fn001">*Correspondence: <italic>Danièle Werck-Reichhart, <email xlink:type="simple">werck@unistra.fr</email></italic></corresp><fn fn-type="other" id="fn002"><p>This article was submitted to Plant Metabolism and Chemodiversity, a section of the journal Frontiers in Plant Science</p></fn></author-notes><pub-date pub-type="epub"><day>26</day><month>4</month><year>2016</year></pub-date><pub-date pub-type="collection"><year>2016</year></pub-date><volume>7</volume><elocation-id>509</elocation-id><history><date date-type="received"><day>25</day><month>1</month><year>2016</year></date><date date-type="accepted"><day>31</day><month>3</month><year>2016</year></date></history><permissions><copyright-statement>Copyright © 2016 Ilc, Parage, Boachon, Navrot and Werck-Reichhart.</copyright-statement><copyright-year>2016</copyright-year><copyright-holder>Ilc, Parage, Boachon, Navrot and Werck-Reichhart</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p></license></permissions><abstract><p>Plants use monoterpenols as precursors for the production of functionally and structurally diverse molecules, which are key players in interactions with other organisms such as pollinators, flower visitors, herbivores, fungal, or microbial pathogens. For humans, many of these monoterpenol derivatives are economically important because of their pharmaceutical, nutraceutical, flavor, or fragrance applications. The biosynthesis of these derivatives is to a large extent catalyzed by enzymes from the cytochrome P450 superfamily. Here we review the knowledge on monoterpenol oxidative metabolism in plants with special focus on recent elucidations of oxidation steps leading to diverse linalool and geraniol derivatives. We evaluate the common features between oxidation pathways of these two monoterpenols, such as involvement of the CYP76 family, and highlight the differences. Finally, we discuss the missing steps and other open questions in the biosynthesis of oxygenated monoterpenol derivatives.</p></abstract><kwd-group><kwd>geraniol</kwd><kwd>linalool</kwd><kwd>cytochrome P450</kwd><kwd>oxidation</kwd><kwd>monoterpene indole alkaloids</kwd><kwd>iridoids</kwd><kwd>lilac aldehydes</kwd><kwd>aroma and fragrance</kwd></kwd-group><funding-group><award-group><funding-source id="cn001">Seventh Framework Programme<named-content content-type="fundref-id">10.13039/501100004963</named-content></funding-source></award-group><award-group><funding-source id="cn002">European Cooperation in Science and Technology<named-content content-type="fundref-id">10.13039/501100000921</named-content></funding-source></award-group><award-group><funding-source id="cn003">Agence Nationale de la Recherche<named-content content-type="fundref-id">10.13039/501100001665</named-content></funding-source></award-group></funding-group><counts><fig-count count="6"></fig-count><table-count count="1"></table-count><equation-count count="0"></equation-count><ref-count count="171"></ref-count><page-count count="16"></page-count><word-count count="0"></word-count></counts></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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