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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Biosynthesis of the Halogenated Auxin, 4-Chloroindole-3-Acetic Acid<xref ref-type="author-notes" rid="fn1"><sup>1</sup></xref><xref ref-type="author-notes" rid="fn2"><sup>[W]</sup></xref><xref ref-type="author-notes" rid="fn3"><sup>[OA]</sup></xref></title><author><name sortKey="Tivendale, Nathan D" sort="Tivendale, Nathan D" uniqKey="Tivendale N" first="Nathan D." last="Tivendale">Nathan D. Tivendale</name></author><author><name sortKey="Davidson, Sandra E" sort="Davidson, Sandra E" uniqKey="Davidson S" first="Sandra E." last="Davidson">Sandra E. Davidson</name></author><author><name sortKey="Davies, Noel W" sort="Davies, Noel W" uniqKey="Davies N" first="Noel W." last="Davies">Noel W. Davies</name></author><author><name sortKey="Smith, Jason A" sort="Smith, Jason A" uniqKey="Smith J" first="Jason A." last="Smith">Jason A. Smith</name></author><author><name sortKey="Dalmais, Marion" sort="Dalmais, Marion" uniqKey="Dalmais M" first="Marion" last="Dalmais">Marion Dalmais</name></author><author><name sortKey="Bendahmane, Abdelhafid I" sort="Bendahmane, Abdelhafid I" uniqKey="Bendahmane A" first="Abdelhafid I." last="Bendahmane">Abdelhafid I. Bendahmane</name></author><author><name sortKey="Quittenden, Laura J" sort="Quittenden, Laura J" uniqKey="Quittenden L" first="Laura J." last="Quittenden">Laura J. Quittenden</name></author><author><name sortKey="Sutton, Lily" sort="Sutton, Lily" uniqKey="Sutton L" first="Lily" last="Sutton">Lily Sutton</name></author><author><name sortKey="Bala, Raj K" sort="Bala, Raj K" uniqKey="Bala R" first="Raj K." last="Bala">Raj K. Bala</name></author><author><name sortKey="Le Signor, Christine" sort="Le Signor, Christine" uniqKey="Le Signor C" first="Christine" last="Le Signor">Christine Le Signor</name></author><author><name sortKey="Thompson, Richard" sort="Thompson, Richard" uniqKey="Thompson R" first="Richard" last="Thompson">Richard Thompson</name></author><author><name sortKey="Horne, James" sort="Horne, James" uniqKey="Horne J" first="James" last="Horne">James Horne</name></author><author><name sortKey="Reid, James B" sort="Reid, James B" uniqKey="Reid J" first="James B." last="Reid">James B. Reid</name></author><author><name sortKey="Ross, John J" sort="Ross, John J" uniqKey="Ross J" first="John J." last="Ross">John J. Ross</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">22573801</idno><idno type="pmc">3387693</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387693</idno><idno type="RBID">PMC:3387693</idno><idno type="doi">10.1104/pp.112.198457</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">001A73</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001A73</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Biosynthesis of the Halogenated Auxin, 4-Chloroindole-3-Acetic Acid<xref ref-type="author-notes" rid="fn1"><sup>1</sup></xref><xref ref-type="author-notes" rid="fn2"><sup>[W]</sup></xref><xref ref-type="author-notes" rid="fn3"><sup>[OA]</sup></xref></title><author><name sortKey="Tivendale, Nathan D" sort="Tivendale, Nathan D" uniqKey="Tivendale N" first="Nathan D." last="Tivendale">Nathan D. Tivendale</name></author><author><name sortKey="Davidson, Sandra E" sort="Davidson, Sandra E" uniqKey="Davidson S" first="Sandra E." last="Davidson">Sandra E. Davidson</name></author><author><name sortKey="Davies, Noel W" sort="Davies, Noel W" uniqKey="Davies N" first="Noel W." last="Davies">Noel W. Davies</name></author><author><name sortKey="Smith, Jason A" sort="Smith, Jason A" uniqKey="Smith J" first="Jason A." last="Smith">Jason A. Smith</name></author><author><name sortKey="Dalmais, Marion" sort="Dalmais, Marion" uniqKey="Dalmais M" first="Marion" last="Dalmais">Marion Dalmais</name></author><author><name sortKey="Bendahmane, Abdelhafid I" sort="Bendahmane, Abdelhafid I" uniqKey="Bendahmane A" first="Abdelhafid I." last="Bendahmane">Abdelhafid I. Bendahmane</name></author><author><name sortKey="Quittenden, Laura J" sort="Quittenden, Laura J" uniqKey="Quittenden L" first="Laura J." last="Quittenden">Laura J. Quittenden</name></author><author><name sortKey="Sutton, Lily" sort="Sutton, Lily" uniqKey="Sutton L" first="Lily" last="Sutton">Lily Sutton</name></author><author><name sortKey="Bala, Raj K" sort="Bala, Raj K" uniqKey="Bala R" first="Raj K." last="Bala">Raj K. Bala</name></author><author><name sortKey="Le Signor, Christine" sort="Le Signor, Christine" uniqKey="Le Signor C" first="Christine" last="Le Signor">Christine Le Signor</name></author><author><name sortKey="Thompson, Richard" sort="Thompson, Richard" uniqKey="Thompson R" first="Richard" last="Thompson">Richard Thompson</name></author><author><name sortKey="Horne, James" sort="Horne, James" uniqKey="Horne J" first="James" last="Horne">James Horne</name></author><author><name sortKey="Reid, James B" sort="Reid, James B" uniqKey="Reid J" first="James B." last="Reid">James B. Reid</name></author><author><name sortKey="Ross, John J" sort="Ross, John J" uniqKey="Ross J" first="John J." last="Ross">John J. Ross</name></author></analytic><series><title level="j">Plant Physiology</title><idno type="ISSN">0032-0889</idno><idno type="eISSN">1532-2548</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Seeds of several agriculturally important legumes are rich sources of the only halogenated plant hormone, 4-chloroindole-3-acetic acid. However, the biosynthesis of this auxin is poorly understood. Here, we show that in pea (<italic>Pisum sativum</italic>) seeds, 4-chloroindole-3-acetic acid is synthesized via the novel intermediate 4-chloroindole-3-pyruvic acid, which is produced from 4-chlorotryptophan by two aminotransferases, TRYPTOPHAN AMINOTRANSFERASE RELATED1 and TRYPTOPHAN AMINOTRANSFERASE RELATED2. We characterize a <italic>tar2</italic> mutant, obtained by Targeting Induced Local Lesions in Genomes, the seeds of which contain dramatically reduced 4-chloroindole-3-acetic acid levels as they mature. We also show that the widespread auxin, indole-3-acetic acid, is synthesized by a parallel pathway in pea.</p></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Plant Physiol</journal-id><journal-id journal-id-type="iso-abbrev">Plant Physiol</journal-id><journal-id journal-id-type="hwp">plantphysiol</journal-id><journal-id journal-id-type="publisher-id">aspb</journal-id><journal-title-group><journal-title>Plant Physiology</journal-title></journal-title-group><issn pub-type="ppub">0032-0889</issn><issn pub-type="epub">1532-2548</issn><publisher><publisher-name>American Society of Plant Biologists</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">22573801</article-id><article-id pub-id-type="pmc">3387693</article-id><article-id pub-id-type="publisher-id">198457</article-id><article-id pub-id-type="doi">10.1104/pp.112.198457</article-id><article-categories><subj-group subj-group-type="heading"><subject>Development and Hormone Action</subject></subj-group></article-categories><title-group><article-title>Biosynthesis of the Halogenated Auxin, 4-Chloroindole-3-Acetic Acid<xref ref-type="author-notes" rid="fn1"><sup>1</sup></xref><xref ref-type="author-notes" rid="fn2"><sup>[W]</sup></xref><xref ref-type="author-notes" rid="fn3"><sup>[OA]</sup></xref></article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Tivendale</surname><given-names>Nathan D.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Davidson</surname><given-names>Sandra E.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Davies</surname><given-names>Noel W.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Smith</surname><given-names>Jason A.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Dalmais</surname><given-names>Marion</given-names></name></contrib><contrib contrib-type="author"><name><surname>Bendahmane</surname><given-names>Abdelhafid I.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Quittenden</surname><given-names>Laura J.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Sutton</surname><given-names>Lily</given-names></name></contrib><contrib contrib-type="author"><name><surname>Bala</surname><given-names>Raj K.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Le Signor</surname><given-names>Christine</given-names></name></contrib><contrib contrib-type="author"><name><surname>Thompson</surname><given-names>Richard</given-names></name></contrib><contrib contrib-type="author"><name><surname>Horne</surname><given-names>James</given-names></name></contrib><contrib contrib-type="author"><name><surname>Reid</surname><given-names>James B.</given-names></name></contrib><contrib contrib-type="author"><name><surname>Ross</surname><given-names>John J.</given-names></name><xref ref-type="corresp" rid="cor1">*</xref></contrib><aff>School of Plant Science (N.D.T., S.E.D., L.J.Q., L.S., R.K.B., J.B.R., J.J.R.), Central Science Laboratory (N.W.D., J.H.), and School of Chemistry (N.D.T., J.A.S.), University of Tasmania, Sandy Bay, Tasmania, Australia 7005; Unité de Recherche en Génomique Végétale, 2 Evry, France 91018 (M.D., A.I.B.); and Unité Mixte de Recherche 1347 Agroécologie, Institut National de la Recherche Agronomique, Dijon, France 21065 (C.L.S., R.T.)</aff></contrib-group><author-notes><fn id="fn1" fn-type="supported-by"><label>1</label><p>This work was supported by the Australian Research Council.</p></fn><fn id="fn2"><label>[W]</label><p>The online version of this article contains Web-only data.</p></fn><fn id="fn3"><label>[OA]</label><p>Open Access articles can be viewed online without a subscription.</p></fn><fn><p><ext-link ext-link-type="uri" xlink:href="www.plantphysiol.org/cgi/doi/10.1104/pp.112.198457">www.plantphysiol.org/cgi/doi/10.1104/pp.112.198457</ext-link></p></fn><fn><p>The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (<ext-link ext-link-type="uri" xlink:href="www.plantphysiol.org">www.plantphysiol.org</ext-link>) is: John J. Ross (<email>john.ross@utas.edu.au</email>).</p></fn><corresp id="cor1"><label>*</label>Corresponding author; e-mail <email>john.ross@utas.edu.au</email>.</corresp></author-notes><pmc-comment>Fake ppub date generated by PMC from publisher pub-date/@pub-type='epub-ppub' </pmc-comment>
<pub-date pub-type="ppub"><month>7</month><year>2012</year></pub-date><pub-date pub-type="epub"><day>9</day><month>5</month><year>2012</year></pub-date><pub-date pub-type="pmc-release"><day>9</day><month>5</month><year>2012</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on the
<volume>159</volume><issue>3</issue><fpage>1055</fpage><lpage>1063</lpage><history><date date-type="received"><day>10</day><month>4</month><year>2012</year></date><date date-type="accepted"><day>08</day><month>5</month><year>2012</year></date></history><permissions><copyright-statement>© 2012 American Society of Plant Biologists. All rights reserved.</copyright-statement><copyright-year>2012</copyright-year></permissions><abstract><p>Seeds of several agriculturally important legumes are rich sources of the only halogenated plant hormone, 4-chloroindole-3-acetic acid. However, the biosynthesis of this auxin is poorly understood. Here, we show that in pea (<italic>Pisum sativum</italic>) seeds, 4-chloroindole-3-acetic acid is synthesized via the novel intermediate 4-chloroindole-3-pyruvic acid, which is produced from 4-chlorotryptophan by two aminotransferases, TRYPTOPHAN AMINOTRANSFERASE RELATED1 and TRYPTOPHAN AMINOTRANSFERASE RELATED2. We characterize a <italic>tar2</italic> mutant, obtained by Targeting Induced Local Lesions in Genomes, the seeds of which contain dramatically reduced 4-chloroindole-3-acetic acid levels as they mature. We also show that the widespread auxin, indole-3-acetic acid, is synthesized by a parallel pathway in pea.</p></abstract></article-meta><notes><glossary><title>Glossary</title><def-list><def-item><term id="term1">4-Cl-IAA</term><def id="def1"><p>4-chloroindole-3-acetic acid</p></def></def-item><def-item><term id="term2">IAA</term><def id="def2"><p>indole-3-acetic acid</p></def></def-item><def-item><term id="term3">IPyA</term><def id="def3"><p>indole-3-pyruvic acid</p></def></def-item><def-item><term id="term4">UPLC</term><def id="def4"><p>ultra-performance liquid chromatography</p></def></def-item><def-item><term id="term5">MS</term><def id="def5"><p>mass spectrometry</p></def></def-item><def-item><term id="term6">4-Cl-IPyA</term><def id="def6"><p>4-chloroindole-3-pyruvic acid</p></def></def-item><def-item><term id="term7">4-Cl-Trp</term><def id="def7"><p>4-chloro-tryptophan</p></def></def-item><def-item><term id="term8">RT</term><def id="def8"><p>retention time</p></def></def-item><def-item><term id="term9">MRM</term><def id="def9"><p>multiple reaction monitoring</p></def></def-item><def-item><term id="term10"><italic>m</italic>/<italic>z</italic></term><def id="def10"><p>mass-to-charge ratio</p></def></def-item><def-item><term id="term11">DPA</term><def id="def11"><p>d post anthesis</p></def></def-item><def-item><term id="term12">PLP</term><def id="def12"><p>pyridoxal-5-phosphate</p></def></def-item><def-item><term id="term13">IAM</term><def id="def13"><p>indole-3-acetamide</p></def></def-item><def-item><term id="term14">NEB</term><def id="def14"><p>New England Biolabs</p></def></def-item><def-item><term id="term15">OD<sub>600</sub></term><def id="def15"><p>optical density at 600 nm</p></def></def-item><def-item><term id="term16">CE</term><def id="def16"><p>collision energy</p></def></def-item><def-item><term id="term17">TILLING</term><def id="def17"><p>Target-Induced Local Lesions In Genome</p></def></def-item><def-item><term id="term18">cDNA</term><def id="def18"><p>to be defined</p></def></def-item></def-list></glossary></notes></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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