treatments-xml/data/AA/6F/87/AA6F87ECFFA54B0D61393C85FC1DFD2E.xml
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<document id="89B9ADE33E9F851225E5B8C922C543A9" ID-DOI="10.1016/j.phytochem.2021.112847" ID-ISSN="1873-3700" ID-Zenodo-Dep="8273033" IM.bibliography_approvedBy="julia" IM.illustrations_approvedBy="julia" IM.materialsCitations_approvedBy="julia" IM.metadata_approvedBy="julia" IM.tables_approvedBy="julia" IM.taxonomicNames_approvedBy="julia" IM.treatments_approvedBy="julia" checkinTime="1692303169482" checkinUser="felipe" docAuthor="Fan, Honghong, Wei, Guo, Chen, Xinlu, Guo, Hong, Crandall-Stotler, Barbara, Kollner, Tobias G. &amp; Chen, Feng" docDate="2021" docId="AA6F87ECFFA54B0D61393C85FC1DFD2E" docLanguage="en" docName="Phytochemistry.190.112847.pdf" docOrigin="Phytochemistry (112847) 190" docSource="http://dx.doi.org/10.1016/j.phytochem.2021.112847" docStyle="DocumentStyle:F36D69FC8B198FBE91029DF9C24697D3.5:Phytochemistry.2020-.journal_article" docStyleId="F36D69FC8B198FBE91029DF9C24697D3" docStyleName="Phytochemistry.2020-.journal_article" docStyleVersion="5" docTitle="Radula lindenbergiana" docType="treatment" docVersion="2" lastPageNumber="2" masterDocId="5656FF94FFA44B0C620B3D0AFFE9FF97" masterDocTitle="Sesquiterpene biosynthesis in a leafy liverwort Radula lindenbergiana Gottsche ex C. Hartm" masterLastPageNumber="8" masterPageNumber="1" pageNumber="2" updateTime="1692729354687" updateUser="julia">
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<mods:title id="5E7E180BCFA2F3013420117B80E3ACAE">Sesquiterpene biosynthesis in a leafy liverwort Radula lindenbergiana Gottsche ex C. Hartm</mods:title>
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<mods:namePart id="6DB1B7ACFBEB4DCBC0E40DC034998B84">Fan, Honghong</mods:namePart>
<mods:affiliation id="04EAD53DF76AABF943432DA4D94CE0EE">* &amp; Department of Plant Sciences, University of Tennessee, Knoxville, TN, 37996, USA &amp; School of Life Sciences, Anhui Agricultural University, Hefei, 230036, China</mods:affiliation>
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<mods:namePart id="37CA2EC458B4A3A6B4B613E2BF4DC8D5">Wei, Guo</mods:namePart>
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<mods:namePart id="A26D1BA26E8A20EF750F143C03359F5E">Chen, Xinlu</mods:namePart>
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<mods:namePart id="020CBBDBA2742C83C4E83C33D43E35BD">Guo, Hong</mods:namePart>
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<mods:namePart id="24956E0FB6D82D4BAB1AF2F9C05F81F4">Crandall-Stotler, Barbara</mods:namePart>
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<mods:namePart id="950B41384F33D1B2C5458CC94D9892BA">Kollner, Tobias G.</mods:namePart>
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<mods:namePart id="20E9CB64794665EF814C9341A449C065">Chen, Feng</mods:namePart>
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<mods:title id="B680E56AB74A17503FD942BCCA829AD6">Phytochemistry</mods:title>
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<mods:date id="6785BF93A63DC8B8DF086036BFD3FABD">2021</mods:date>
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<mods:title id="1C61CBAA0B22A482DFE1BCAFF0541460">112847</mods:title>
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<mods:number id="A9FD06DAC5C8B329C8BD7037A1865D98">2021-10-31</mods:number>
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<mods:identifier id="63C333961E8CCC88125D919BD4E6A8E0" type="ISSN">1873-3700</mods:identifier>
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<treatment id="AA6F87ECFFA54B0D61393C85FC1DFD2E" LSID="urn:lsid:plazi:treatment:AA6F87ECFFA54B0D61393C85FC1DFD2E" httpUri="http://treatment.plazi.org/id/AA6F87ECFFA54B0D61393C85FC1DFD2E" lastPageNumber="2" pageId="1" pageNumber="2">
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<paragraph id="227936FAFFA54B0D61393C85FA49FE35" blockId="1.[818,1440,399,418]" box="[818,1440,399,418]" pageId="1" pageNumber="2">
<heading id="79318196FFA54B0D61393C85FA49FE35" bold="true" box="[818,1440,399,418]" fontSize="36" level="1" pageId="1" pageNumber="2" reason="1">
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2.1. Diverse sesquiterpenes in the gametophytes of
<taxonomicName id="E5C64D79FFA54B0D66F53C85FA49FE35" ID-CoL="4R9QX" ID-ENA="697108" authority="Gottsche ex C. Hartm" box="[1278,1440,399,418]" class="Jungermanniopsida" family="Radulaceae" genus="Radula" kingdom="Plantae" order="Porellales" pageId="1" pageNumber="2" phylum="Marchantiophyta" rank="species" species="lindenbergiana">R. Lindenbergiana</taxonomicName>
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In this study, axenically cultured
<taxonomicName id="E5C64D79FFA54B0D66853CCDFAC3FE4D" authority="Gottsche ex C. Hartm" box="[1166,1322,455,474]" class="Jungermanniopsida" family="Radulaceae" genus="Radula" kingdom="Plantae" order="Porellales" pageId="1" pageNumber="2" phylum="Marchantiophyta" rank="species" species="lindenbergiana">
<emphasis id="10B2EAE8FFA54B0D66853CCDFAC3FE4D" bold="true" box="[1166,1322,455,474]" italics="true" pageId="1" pageNumber="2">R. lindenbergiana</emphasis>
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plants were used for chemical and molecular experiments. For chemical profiling, plants were taken from axenic culture and subjected to organic extraction. The extracts were analyzed using gas chromatography-mass spectrometry (GC-MS). A total of 25 terpenoids were detected (
<figureCitation id="BAFD2A7FFFA54B0D670C3F3DFAD5FDDD" box="[1287,1340,567,586]" captionStart="Fig" captionStartId="1.[818,848,1786,1803]" captionTargetBox="[824,1483,1580,1757]" captionTargetId="figure-1138@1.[823,1484,1579,1758]" captionTargetPageId="1" captionText="Fig. 1. Chemical profiling of R. lindenbergiana. 5, striatene; 6, pentalenene; 8, α-funebrene; 9, β-elemene; 10, petasitene; 11, α-cedrene; 12, isobazzanene; 13, (E)-α-bergamotene; 14, epi-β-santalene; 15, (E)-β-farnesene; 17, β-santalene; 18, β-acoradiene; 19, 4,5-di-epi-aristolochene; 20, ar-curcumene; 21, unidentified sesquiterpene; 22, eremophilene; 23, α-selinene; 24, (E,E)-α-farnesene and β-curcumene; 25, (Z)-β-bisabolene; All listed compounds are tentatively identified using mass spec libraries. All numbered compounds that are not listed represent unidentified sesquiterpenes." figureDoi="http://doi.org/10.5281/zenodo.8273035" httpUri="https://zenodo.org/record/8273035/files/figure.png" pageId="1" pageNumber="2">Fig. 1</figureCitation>
), and retention indices of these compounds were calculated (
<tableCitation id="6F440341FFA54B0D66E83F59FAC3FDF1" box="[1251,1322,595,614]" captionStart="Table 1" captionStartId="2.[100,150,150,166]" captionTargetPageId="2" captionText="Table 1 Terpene profile of vegetative plants of Radula lindenbergiana." httpUri="http://table.plazi.org/id/76B96672FFA64B0E626F3D9CFD81FF57" pageId="1" pageNumber="2" tableUuid="76B96672FFA64B0E626F3D9CFD81FF57">Table 1</tableCitation>
). All of them are sesquiterpenes, including 7 unidentified compounds. (
<emphasis id="10B2EAE8FFA54B0D67273F65FAA3FD15" bold="true" box="[1324,1354,623,642]" italics="true" pageId="1" pageNumber="2">E,E</emphasis>
)-α- farnesene/ β- curcumene and (
<emphasis id="10B2EAE8FFA54B0D61E53F81FC13FD09" bold="true" box="[1006,1018,651,670]" italics="true" pageId="1" pageNumber="2">Z</emphasis>
)-β- bisabolene were among the most abundant constituents (
<figureCitation id="BAFD2A7FFFA54B0D61BA3FACFC0FFD2E" box="[945,998,678,697]" captionStart="Fig" captionStartId="1.[818,848,1786,1803]" captionTargetBox="[824,1483,1580,1757]" captionTargetId="figure-1138@1.[823,1484,1579,1758]" captionTargetPageId="1" captionText="Fig. 1. Chemical profiling of R. lindenbergiana. 5, striatene; 6, pentalenene; 8, α-funebrene; 9, β-elemene; 10, petasitene; 11, α-cedrene; 12, isobazzanene; 13, (E)-α-bergamotene; 14, epi-β-santalene; 15, (E)-β-farnesene; 17, β-santalene; 18, β-acoradiene; 19, 4,5-di-epi-aristolochene; 20, ar-curcumene; 21, unidentified sesquiterpene; 22, eremophilene; 23, α-selinene; 24, (E,E)-α-farnesene and β-curcumene; 25, (Z)-β-bisabolene; All listed compounds are tentatively identified using mass spec libraries. All numbered compounds that are not listed represent unidentified sesquiterpenes." figureDoi="http://doi.org/10.5281/zenodo.8273035" httpUri="https://zenodo.org/record/8273035/files/figure.png" pageId="1" pageNumber="2">Fig. 1</figureCitation>
).
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