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Identification and characterization of xanthone biosynthetic genes contributing to the vivid red coloration of red‐flowered gentian
Summary Cultivated Japanese gentians traditionally produce vivid blue flowers because of the accumulation of delphinidin‐based polyacylated anthocyanins. However, recent breeding programs developed several red‐flowered cultivars, but the underlying mechanism for this red coloration was unknown. Thus...
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Published in: | The Plant journal : for cell and molecular biology 2021-09, Vol.107 (6), p.1711-1723 |
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creator | Sasaki, Nobuhiro Nemoto, Keiichirou Nishizaki, Yuzo Sugimoto, Naoki Tasaki, Keisuke Watanabe, Aiko Goto, Fumina Higuchi, Atsumi Morgan, Ed Hikage, Takashi Nishihara, Masahiro |
description | Summary
Cultivated Japanese gentians traditionally produce vivid blue flowers because of the accumulation of delphinidin‐based polyacylated anthocyanins. However, recent breeding programs developed several red‐flowered cultivars, but the underlying mechanism for this red coloration was unknown. Thus, we characterized the pigments responsible for the red coloration in these cultivars. A high‐performance liquid chromatography with photodiode array analysis revealed the presence of phenolic compounds, including flavones and xanthones, as well as the accumulation of colored cyanidin‐based anthocyanins. The chemical structures of two xanthone compounds contributing to the coloration of red‐flowered gentian petals were determined by mass spectrometry and nuclear magnetic resonance spectroscopy. The compounds were identified as norathyriol 6‐O‐glucoside (i.e., tripteroside designated as Xt1) and a previously unreported norathyriol‐6‐O‐(6′‐O‐malonyl)‐glucoside (designated Xt2). The copigmentation effects of these compounds on cyanidin 3‐O‐glucoside were detected in vitro. Additionally, an RNA sequencing analysis was performed to identify the cDNAs encoding the enzymes involved in the biosynthesis of these xanthones. Recombinant proteins encoded by the candidate genes were produced in a wheat germ cell‐free protein expression system and assayed. We determined that a UDP‐glucose‐dependent glucosyltransferase (StrGT9) catalyzes the transfer of a glucose moiety to norathyriol, a xanthone aglycone, to produce Xt1, which is converted to Xt2 by a malonyltransferase (StrAT2). An analysis of the progeny lines suggested that the accumulation of Xt2 contributes to the vivid red coloration of gentian flowers. Our data indicate that StrGT9 and StrAT2 help mediate xanthone biosynthesis and contribute to the coloration of red‐flowered gentians via copigmentation effects.
Significance Statement
We identified two key genes encoding UDP‐glucose‐dependent glucosyltransferase and malonyl‐CoA acyltransferase, which are involved in xanthone biosynthesis in red‐flowered gentian. In vitro assays involving different pigment combinations demonstrated that a malonylated tripteroside synthesized from norathyriol via these two enzymes increases the absorption of cyanidin 3‐O‐glucoside, and a progeny line analysis suggested that the presence of malonylated tripteroside is associated with the vivid red coloration of gentian flowers. |
doi_str_mv | 10.1111/tpj.15412 |
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Cultivated Japanese gentians traditionally produce vivid blue flowers because of the accumulation of delphinidin‐based polyacylated anthocyanins. However, recent breeding programs developed several red‐flowered cultivars, but the underlying mechanism for this red coloration was unknown. Thus, we characterized the pigments responsible for the red coloration in these cultivars. A high‐performance liquid chromatography with photodiode array analysis revealed the presence of phenolic compounds, including flavones and xanthones, as well as the accumulation of colored cyanidin‐based anthocyanins. The chemical structures of two xanthone compounds contributing to the coloration of red‐flowered gentian petals were determined by mass spectrometry and nuclear magnetic resonance spectroscopy. The compounds were identified as norathyriol 6‐O‐glucoside (i.e., tripteroside designated as Xt1) and a previously unreported norathyriol‐6‐O‐(6′‐O‐malonyl)‐glucoside (designated Xt2). The copigmentation effects of these compounds on cyanidin 3‐O‐glucoside were detected in vitro. Additionally, an RNA sequencing analysis was performed to identify the cDNAs encoding the enzymes involved in the biosynthesis of these xanthones. Recombinant proteins encoded by the candidate genes were produced in a wheat germ cell‐free protein expression system and assayed. We determined that a UDP‐glucose‐dependent glucosyltransferase (StrGT9) catalyzes the transfer of a glucose moiety to norathyriol, a xanthone aglycone, to produce Xt1, which is converted to Xt2 by a malonyltransferase (StrAT2). An analysis of the progeny lines suggested that the accumulation of Xt2 contributes to the vivid red coloration of gentian flowers. Our data indicate that StrGT9 and StrAT2 help mediate xanthone biosynthesis and contribute to the coloration of red‐flowered gentians via copigmentation effects.
Significance Statement
We identified two key genes encoding UDP‐glucose‐dependent glucosyltransferase and malonyl‐CoA acyltransferase, which are involved in xanthone biosynthesis in red‐flowered gentian. In vitro assays involving different pigment combinations demonstrated that a malonylated tripteroside synthesized from norathyriol via these two enzymes increases the absorption of cyanidin 3‐O‐glucoside, and a progeny line analysis suggested that the presence of malonylated tripteroside is associated with the vivid red coloration of gentian flowers.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.15412</identifier><identifier>PMID: 34245606</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Accumulation ; Acyltransferases - genetics ; Acyltransferases - metabolism ; Anthocyanins ; Anthocyanins - genetics ; Anthocyanins - metabolism ; Biosynthesis ; Chromatography, High Pressure Liquid ; Coloration ; copigmentation ; Cultivars ; Flavones ; Flowers ; Flowers - genetics ; Flowers - physiology ; Gene sequencing ; Genes ; gentian ; Gentiana - genetics ; Gentiana - physiology ; Gentianaceae ; Glucose ; Glucosides ; Glucosyltransferase ; Glucosyltransferases - genetics ; Glucosyltransferases - metabolism ; Liquid chromatography ; Magnetic resonance spectroscopy ; malonyltransferase ; Mass spectrometry ; Mass spectroscopy ; Molecular Structure ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Phenolic compounds ; Phenols ; Photodiodes ; Pigmentation - genetics ; Pigments ; Pigments, Biological - genetics ; Pigments, Biological - metabolism ; Plant breeding ; Plant Proteins - genetics ; Plant Proteins - metabolism ; Progeny ; Proteins ; red flower ; Sequence analysis ; Sequence Analysis, RNA ; Wheat germ ; Xanthenes - metabolism ; xanthone ; Xanthones - chemistry ; Xanthones - isolation & purification ; Xanthones - metabolism</subject><ispartof>The Plant journal : for cell and molecular biology, 2021-09, Vol.107 (6), p.1711-1723</ispartof><rights>2021 Society for Experimental Biology and John Wiley & Sons Ltd.</rights><rights>Copyright © 2021 John Wiley & Sons Ltd and the Society for Experimental Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3</citedby><cites>FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3</cites><orcidid>0000-0002-1454-8785 ; 0000-0001-7081-2176 ; 0000-0002-5353-2639</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34245606$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sasaki, Nobuhiro</creatorcontrib><creatorcontrib>Nemoto, Keiichirou</creatorcontrib><creatorcontrib>Nishizaki, Yuzo</creatorcontrib><creatorcontrib>Sugimoto, Naoki</creatorcontrib><creatorcontrib>Tasaki, Keisuke</creatorcontrib><creatorcontrib>Watanabe, Aiko</creatorcontrib><creatorcontrib>Goto, Fumina</creatorcontrib><creatorcontrib>Higuchi, Atsumi</creatorcontrib><creatorcontrib>Morgan, Ed</creatorcontrib><creatorcontrib>Hikage, Takashi</creatorcontrib><creatorcontrib>Nishihara, Masahiro</creatorcontrib><title>Identification and characterization of xanthone biosynthetic genes contributing to the vivid red coloration of red‐flowered gentian</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Summary
Cultivated Japanese gentians traditionally produce vivid blue flowers because of the accumulation of delphinidin‐based polyacylated anthocyanins. However, recent breeding programs developed several red‐flowered cultivars, but the underlying mechanism for this red coloration was unknown. Thus, we characterized the pigments responsible for the red coloration in these cultivars. A high‐performance liquid chromatography with photodiode array analysis revealed the presence of phenolic compounds, including flavones and xanthones, as well as the accumulation of colored cyanidin‐based anthocyanins. The chemical structures of two xanthone compounds contributing to the coloration of red‐flowered gentian petals were determined by mass spectrometry and nuclear magnetic resonance spectroscopy. The compounds were identified as norathyriol 6‐O‐glucoside (i.e., tripteroside designated as Xt1) and a previously unreported norathyriol‐6‐O‐(6′‐O‐malonyl)‐glucoside (designated Xt2). The copigmentation effects of these compounds on cyanidin 3‐O‐glucoside were detected in vitro. Additionally, an RNA sequencing analysis was performed to identify the cDNAs encoding the enzymes involved in the biosynthesis of these xanthones. Recombinant proteins encoded by the candidate genes were produced in a wheat germ cell‐free protein expression system and assayed. We determined that a UDP‐glucose‐dependent glucosyltransferase (StrGT9) catalyzes the transfer of a glucose moiety to norathyriol, a xanthone aglycone, to produce Xt1, which is converted to Xt2 by a malonyltransferase (StrAT2). An analysis of the progeny lines suggested that the accumulation of Xt2 contributes to the vivid red coloration of gentian flowers. Our data indicate that StrGT9 and StrAT2 help mediate xanthone biosynthesis and contribute to the coloration of red‐flowered gentians via copigmentation effects.
Significance Statement
We identified two key genes encoding UDP‐glucose‐dependent glucosyltransferase and malonyl‐CoA acyltransferase, which are involved in xanthone biosynthesis in red‐flowered gentian. In vitro assays involving different pigment combinations demonstrated that a malonylated tripteroside synthesized from norathyriol via these two enzymes increases the absorption of cyanidin 3‐O‐glucoside, and a progeny line analysis suggested that the presence of malonylated tripteroside is associated with the vivid red coloration of gentian flowers.</description><subject>Accumulation</subject><subject>Acyltransferases - genetics</subject><subject>Acyltransferases - metabolism</subject><subject>Anthocyanins</subject><subject>Anthocyanins - genetics</subject><subject>Anthocyanins - metabolism</subject><subject>Biosynthesis</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Coloration</subject><subject>copigmentation</subject><subject>Cultivars</subject><subject>Flavones</subject><subject>Flowers</subject><subject>Flowers - genetics</subject><subject>Flowers - physiology</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>gentian</subject><subject>Gentiana - genetics</subject><subject>Gentiana - physiology</subject><subject>Gentianaceae</subject><subject>Glucose</subject><subject>Glucosides</subject><subject>Glucosyltransferase</subject><subject>Glucosyltransferases - genetics</subject><subject>Glucosyltransferases - metabolism</subject><subject>Liquid chromatography</subject><subject>Magnetic resonance spectroscopy</subject><subject>malonyltransferase</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Molecular Structure</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Phenolic compounds</subject><subject>Phenols</subject><subject>Photodiodes</subject><subject>Pigmentation - genetics</subject><subject>Pigments</subject><subject>Pigments, Biological - genetics</subject><subject>Pigments, Biological - metabolism</subject><subject>Plant breeding</subject><subject>Plant Proteins - genetics</subject><subject>Plant Proteins - metabolism</subject><subject>Progeny</subject><subject>Proteins</subject><subject>red flower</subject><subject>Sequence analysis</subject><subject>Sequence Analysis, RNA</subject><subject>Wheat germ</subject><subject>Xanthenes - metabolism</subject><subject>xanthone</subject><subject>Xanthones - chemistry</subject><subject>Xanthones - isolation & purification</subject><subject>Xanthones - metabolism</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kb1OHDEURi2UCDYkBS8QWUpDigF7_DdTIgSBCCkptkg38njuLF7N2hvbAyxVmvR5Rp4ELwMUSHFj67tH51r6EDqg5Ijmc5zWyyMqOC130IwyKQpG2a93aEZqSQqV8z30IcYlIVQxyXfRHuMlF5LIGfp72YFLtrdGJ-sd1q7D5loHbRIEez-Fvsd32qVr7wC31sdNfkOyBi_AQcTGuxRsOybrFjh5nIf4xt7YDgfINj_48OrJycOff_3gb2E7XGyXa_cRve_1EOHT872P5udn89OL4urHt8vTk6vCcMHLwgjJuGHM0K4TjPYVExVphTTc1ERr3opeSaiVIKpkwKuq7KAjdUWM0j3TbB8dTtp18L9HiKlZ2WhgGLQDP8amFIKUslIVy-iXN-jSj8Hlz2VKKZ6ldZWprxNlgo8xQN-sg13psGkoabbVNLma5qmazH5-No7tCrpX8qWLDBxPwK0dYPN_UzP_-X1SPgJEtJtj</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Sasaki, Nobuhiro</creator><creator>Nemoto, Keiichirou</creator><creator>Nishizaki, Yuzo</creator><creator>Sugimoto, Naoki</creator><creator>Tasaki, Keisuke</creator><creator>Watanabe, Aiko</creator><creator>Goto, Fumina</creator><creator>Higuchi, Atsumi</creator><creator>Morgan, Ed</creator><creator>Hikage, Takashi</creator><creator>Nishihara, Masahiro</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1454-8785</orcidid><orcidid>https://orcid.org/0000-0001-7081-2176</orcidid><orcidid>https://orcid.org/0000-0002-5353-2639</orcidid></search><sort><creationdate>202109</creationdate><title>Identification and characterization of xanthone biosynthetic genes contributing to the vivid red coloration of red‐flowered gentian</title><author>Sasaki, Nobuhiro ; Nemoto, Keiichirou ; Nishizaki, Yuzo ; Sugimoto, Naoki ; Tasaki, Keisuke ; Watanabe, Aiko ; Goto, Fumina ; Higuchi, Atsumi ; Morgan, Ed ; Hikage, Takashi ; Nishihara, Masahiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Accumulation</topic><topic>Acyltransferases - genetics</topic><topic>Acyltransferases - metabolism</topic><topic>Anthocyanins</topic><topic>Anthocyanins - genetics</topic><topic>Anthocyanins - metabolism</topic><topic>Biosynthesis</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Coloration</topic><topic>copigmentation</topic><topic>Cultivars</topic><topic>Flavones</topic><topic>Flowers</topic><topic>Flowers - genetics</topic><topic>Flowers - physiology</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>gentian</topic><topic>Gentiana - genetics</topic><topic>Gentiana - physiology</topic><topic>Gentianaceae</topic><topic>Glucose</topic><topic>Glucosides</topic><topic>Glucosyltransferase</topic><topic>Glucosyltransferases - genetics</topic><topic>Glucosyltransferases - metabolism</topic><topic>Liquid chromatography</topic><topic>Magnetic resonance spectroscopy</topic><topic>malonyltransferase</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Molecular Structure</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Phenolic compounds</topic><topic>Phenols</topic><topic>Photodiodes</topic><topic>Pigmentation - genetics</topic><topic>Pigments</topic><topic>Pigments, Biological - genetics</topic><topic>Pigments, Biological - metabolism</topic><topic>Plant breeding</topic><topic>Plant Proteins - genetics</topic><topic>Plant Proteins - metabolism</topic><topic>Progeny</topic><topic>Proteins</topic><topic>red flower</topic><topic>Sequence analysis</topic><topic>Sequence Analysis, RNA</topic><topic>Wheat germ</topic><topic>Xanthenes - metabolism</topic><topic>xanthone</topic><topic>Xanthones - chemistry</topic><topic>Xanthones - isolation & purification</topic><topic>Xanthones - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasaki, Nobuhiro</creatorcontrib><creatorcontrib>Nemoto, Keiichirou</creatorcontrib><creatorcontrib>Nishizaki, Yuzo</creatorcontrib><creatorcontrib>Sugimoto, Naoki</creatorcontrib><creatorcontrib>Tasaki, Keisuke</creatorcontrib><creatorcontrib>Watanabe, Aiko</creatorcontrib><creatorcontrib>Goto, Fumina</creatorcontrib><creatorcontrib>Higuchi, Atsumi</creatorcontrib><creatorcontrib>Morgan, Ed</creatorcontrib><creatorcontrib>Hikage, Takashi</creatorcontrib><creatorcontrib>Nishihara, Masahiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasaki, Nobuhiro</au><au>Nemoto, Keiichirou</au><au>Nishizaki, Yuzo</au><au>Sugimoto, Naoki</au><au>Tasaki, Keisuke</au><au>Watanabe, Aiko</au><au>Goto, Fumina</au><au>Higuchi, Atsumi</au><au>Morgan, Ed</au><au>Hikage, Takashi</au><au>Nishihara, Masahiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and characterization of xanthone biosynthetic genes contributing to the vivid red coloration of red‐flowered gentian</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2021-09</date><risdate>2021</risdate><volume>107</volume><issue>6</issue><spage>1711</spage><epage>1723</epage><pages>1711-1723</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Summary
Cultivated Japanese gentians traditionally produce vivid blue flowers because of the accumulation of delphinidin‐based polyacylated anthocyanins. However, recent breeding programs developed several red‐flowered cultivars, but the underlying mechanism for this red coloration was unknown. Thus, we characterized the pigments responsible for the red coloration in these cultivars. A high‐performance liquid chromatography with photodiode array analysis revealed the presence of phenolic compounds, including flavones and xanthones, as well as the accumulation of colored cyanidin‐based anthocyanins. The chemical structures of two xanthone compounds contributing to the coloration of red‐flowered gentian petals were determined by mass spectrometry and nuclear magnetic resonance spectroscopy. The compounds were identified as norathyriol 6‐O‐glucoside (i.e., tripteroside designated as Xt1) and a previously unreported norathyriol‐6‐O‐(6′‐O‐malonyl)‐glucoside (designated Xt2). The copigmentation effects of these compounds on cyanidin 3‐O‐glucoside were detected in vitro. Additionally, an RNA sequencing analysis was performed to identify the cDNAs encoding the enzymes involved in the biosynthesis of these xanthones. Recombinant proteins encoded by the candidate genes were produced in a wheat germ cell‐free protein expression system and assayed. We determined that a UDP‐glucose‐dependent glucosyltransferase (StrGT9) catalyzes the transfer of a glucose moiety to norathyriol, a xanthone aglycone, to produce Xt1, which is converted to Xt2 by a malonyltransferase (StrAT2). An analysis of the progeny lines suggested that the accumulation of Xt2 contributes to the vivid red coloration of gentian flowers. Our data indicate that StrGT9 and StrAT2 help mediate xanthone biosynthesis and contribute to the coloration of red‐flowered gentians via copigmentation effects.
Significance Statement
We identified two key genes encoding UDP‐glucose‐dependent glucosyltransferase and malonyl‐CoA acyltransferase, which are involved in xanthone biosynthesis in red‐flowered gentian. In vitro assays involving different pigment combinations demonstrated that a malonylated tripteroside synthesized from norathyriol via these two enzymes increases the absorption of cyanidin 3‐O‐glucoside, and a progeny line analysis suggested that the presence of malonylated tripteroside is associated with the vivid red coloration of gentian flowers.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>34245606</pmid><doi>10.1111/tpj.15412</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-1454-8785</orcidid><orcidid>https://orcid.org/0000-0001-7081-2176</orcidid><orcidid>https://orcid.org/0000-0002-5353-2639</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Accumulation Acyltransferases - genetics Acyltransferases - metabolism Anthocyanins Anthocyanins - genetics Anthocyanins - metabolism Biosynthesis Chromatography, High Pressure Liquid Coloration copigmentation Cultivars Flavones Flowers Flowers - genetics Flowers - physiology Gene sequencing Genes gentian Gentiana - genetics Gentiana - physiology Gentianaceae Glucose Glucosides Glucosyltransferase Glucosyltransferases - genetics Glucosyltransferases - metabolism Liquid chromatography Magnetic resonance spectroscopy malonyltransferase Mass spectrometry Mass spectroscopy Molecular Structure NMR NMR spectroscopy Nuclear magnetic resonance Phenolic compounds Phenols Photodiodes Pigmentation - genetics Pigments Pigments, Biological - genetics Pigments, Biological - metabolism Plant breeding Plant Proteins - genetics Plant Proteins - metabolism Progeny Proteins red flower Sequence analysis Sequence Analysis, RNA Wheat germ Xanthenes - metabolism xanthone Xanthones - chemistry Xanthones - isolation & purification Xanthones - metabolism |
title | Identification and characterization of xanthone biosynthetic genes contributing to the vivid red coloration of red‐flowered gentian |
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