Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:The Plant journal : for cell and molecular biology 2021-09, Vol.107 (6), p.1711-1723
Main Authors: Sasaki, Nobuhiro, Nemoto, Keiichirou, Nishizaki, Yuzo, Sugimoto, Naoki, Tasaki, Keisuke, Watanabe, Aiko, Goto, Fumina, Higuchi, Atsumi, Morgan, Ed, Hikage, Takashi, Nishihara, Masahiro
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3
cites cdi_FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3
container_end_page 1723
container_issue 6
container_start_page 1711
container_title The Plant journal : for cell and molecular biology
container_volume 107
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2550268783</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2577498098</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3</originalsourceid><addsrcrecordid>eNp1kb1OHDEURi2UCDYkBS8QWUpDigF7_DdTIgSBCCkptkg38njuLF7N2hvbAyxVmvR5Rp4ELwMUSHFj67tH51r6EDqg5Ijmc5zWyyMqOC130IwyKQpG2a93aEZqSQqV8z30IcYlIVQxyXfRHuMlF5LIGfp72YFLtrdGJ-sd1q7D5loHbRIEez-Fvsd32qVr7wC31sdNfkOyBi_AQcTGuxRsOybrFjh5nIf4xt7YDgfINj_48OrJycOff_3gb2E7XGyXa_cRve_1EOHT872P5udn89OL4urHt8vTk6vCcMHLwgjJuGHM0K4TjPYVExVphTTc1ERr3opeSaiVIKpkwKuq7KAjdUWM0j3TbB8dTtp18L9HiKlZ2WhgGLQDP8amFIKUslIVy-iXN-jSj8Hlz2VKKZ6ldZWprxNlgo8xQN-sg13psGkoabbVNLma5qmazH5-No7tCrpX8qWLDBxPwK0dYPN_UzP_-X1SPgJEtJtj</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2577498098</pqid></control><display><type>article</type><title>Identification and characterization of xanthone biosynthetic genes contributing to the vivid red coloration of red‐flowered gentian</title><source>Wiley-Blackwell Read &amp; Publish Collection</source><source>EZB Electronic Journals Library</source><creator>Sasaki, Nobuhiro ; Nemoto, Keiichirou ; Nishizaki, Yuzo ; Sugimoto, Naoki ; Tasaki, Keisuke ; Watanabe, Aiko ; Goto, Fumina ; Higuchi, Atsumi ; Morgan, Ed ; Hikage, Takashi ; Nishihara, Masahiro</creator><creatorcontrib>Sasaki, Nobuhiro ; Nemoto, Keiichirou ; Nishizaki, Yuzo ; Sugimoto, Naoki ; Tasaki, Keisuke ; Watanabe, Aiko ; Goto, Fumina ; Higuchi, Atsumi ; Morgan, Ed ; Hikage, Takashi ; Nishihara, Masahiro</creatorcontrib><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><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 &amp; 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 &amp; Sons Ltd.</rights><rights>Copyright © 2021 John Wiley &amp; 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 &amp; 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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 0960-7412
ispartof The Plant journal : for cell and molecular biology, 2021-09, Vol.107 (6), p.1711-1723
issn 0960-7412
1365-313X
language eng
recordid cdi_proquest_miscellaneous_2550268783
source Wiley-Blackwell Read & Publish Collection; EZB Electronic Journals Library
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T17%3A02%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20and%20characterization%20of%20xanthone%20biosynthetic%20genes%20contributing%20to%20the%20vivid%20red%20coloration%20of%20red%E2%80%90flowered%20gentian&rft.jtitle=The%20Plant%20journal%20:%20for%20cell%20and%20molecular%20biology&rft.au=Sasaki,%20Nobuhiro&rft.date=2021-09&rft.volume=107&rft.issue=6&rft.spage=1711&rft.epage=1723&rft.pages=1711-1723&rft.issn=0960-7412&rft.eissn=1365-313X&rft_id=info:doi/10.1111/tpj.15412&rft_dat=%3Cproquest_cross%3E2577498098%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4542-c5634c33c1dd531f83580b56c4c90aa4b5f76e9750723e4882ded0980c7af3a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2577498098&rft_id=info:pmid/34245606&rfr_iscdi=true