Localization of a flavonoid biosynthetic polyphenol oxidase in vacuoles
Aureusidin synthase, a polyphenol oxidase (PPO), specifically catalyzes the oxidative formation of aurones from chalcones, which are plant flavonoids, and is responsible for the yellow coloration of snapdragon (Antirrhinum majus) flowers. All known PPOs have been found to be localized in plastids, w...
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creator | Ono, Eiichiro Hatayama, Masayoshi Isono, Yuri Sato, Takuya Watanabe, Ryoko Yonekura-Sakakibara, Keiko Fukuchi-Mizutani, Masako Tanaka, Yoshikazu Kusumi, Takaaki Nishino, Tokuzo Nakayama, Toru |
description | Aureusidin synthase, a polyphenol oxidase (PPO), specifically catalyzes the oxidative formation of aurones from chalcones, which are plant flavonoids, and is responsible for the yellow coloration of snapdragon (Antirrhinum majus) flowers. All known PPOs have been found to be localized in plastids, whereas flavonoid biosynthesis is thought to take place in the cytoplasm [or on the cytoplasmic surface of the endoplasmic reticulum (ER)]. However, the primary structural characteristics of aureusidin synthase and some of its molecular properties argue against localization of the enzyme in plastids and the cytoplasm. In this study, the subcellular localization of the enzyme in petal cells of the yellow snapdragon was investigated. Sucrose-density gradient and differential centrifugation analyses suggested that the enzyme (the 39-kDa mature form) is not located in plastids or on the ER. Transient assays using a green fluorescent protein (GFP) chimera fused with the putative propeptide of the PPO precursor suggested that the enzyme was localized within the vacuole lumen. We also found that the necessary information for vacuolar targeting of the PPO was encoded within the 53-residue N-terminal sequence (NTPP), but not in the C-terminal sequence of the precursor. NTPP-mediated ER-to-Golgi trafficking to vacuoles was confirmed by means of the co-expression of an NTPP-GFP chimera with a dominant negative mutant of the Arabidopsis GTPase Sar1 or with a monomeric red fluorescent protein (mRFP)-fused Golgi marker (an H⁺-translocating inorganic pyrophosphatase of Arabidopsis). We identified a sequence-specific vacuolar sorting determinant in the NTPP of the precursor. We have demonstrated the biosynthesis of a flavonoid skeleton in vacuoles. The findings of this metabolic compartmentation may provide a strategy for overcoming the biochemical instability of the precursor chalcones in the cytoplasm, thus leading to the efficient accumulation of aurones in the flower. |
doi_str_mv | 10.1111/j.1365-313x.2005.02625.x |
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All known PPOs have been found to be localized in plastids, whereas flavonoid biosynthesis is thought to take place in the cytoplasm [or on the cytoplasmic surface of the endoplasmic reticulum (ER)]. However, the primary structural characteristics of aureusidin synthase and some of its molecular properties argue against localization of the enzyme in plastids and the cytoplasm. In this study, the subcellular localization of the enzyme in petal cells of the yellow snapdragon was investigated. Sucrose-density gradient and differential centrifugation analyses suggested that the enzyme (the 39-kDa mature form) is not located in plastids or on the ER. Transient assays using a green fluorescent protein (GFP) chimera fused with the putative propeptide of the PPO precursor suggested that the enzyme was localized within the vacuole lumen. We also found that the necessary information for vacuolar targeting of the PPO was encoded within the 53-residue N-terminal sequence (NTPP), but not in the C-terminal sequence of the precursor. NTPP-mediated ER-to-Golgi trafficking to vacuoles was confirmed by means of the co-expression of an NTPP-GFP chimera with a dominant negative mutant of the Arabidopsis GTPase Sar1 or with a monomeric red fluorescent protein (mRFP)-fused Golgi marker (an H⁺-translocating inorganic pyrophosphatase of Arabidopsis). We identified a sequence-specific vacuolar sorting determinant in the NTPP of the precursor. We have demonstrated the biosynthesis of a flavonoid skeleton in vacuoles. The findings of this metabolic compartmentation may provide a strategy for overcoming the biochemical instability of the precursor chalcones in the cytoplasm, thus leading to the efficient accumulation of aurones in the flower.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/j.1365-313x.2005.02625.x</identifier><identifier>PMID: 16367960</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Science Ltd</publisher><subject>Amino Acid Sequence ; Analytical, structural and metabolic biochemistry ; aurone ; Biological and medical sciences ; biosynthesis of flavonoids ; Blotting, Western ; Catechol Oxidase - chemistry ; Catechol Oxidase - metabolism ; Electrophoresis, Polyacrylamide Gel ; Endoplasmic Reticulum - enzymology ; Enzymes and enzyme inhibitors ; Flavonoids - biosynthesis ; flower coloration ; Fundamental and applied biological sciences. Psychology ; Genetic Vectors ; Golgi Apparatus - enzymology ; Molecular Sequence Data ; Oxidoreductases ; Plastids - enzymology ; polyphenol oxidase ; Protein Transport ; Sequence Homology, Amino Acid ; subcellular localization ; vacuole ; Vacuoles - enzymology</subject><ispartof>The Plant journal : for cell and molecular biology, 2006-01, Vol.45 (2), p.133-143</ispartof><rights>2006 INIST-CNRS</rights><rights>2005 The Authors Journal compilation 2005 Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5645-b534debde5496be57af5229afb86f6b2de766fc00e55a687c9047c68bea76c783</citedby><cites>FETCH-LOGICAL-c5645-b534debde5496be57af5229afb86f6b2de766fc00e55a687c9047c68bea76c783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-313X.2005.02625.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-313X.2005.02625.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17470760$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16367960$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ono, Eiichiro</creatorcontrib><creatorcontrib>Hatayama, Masayoshi</creatorcontrib><creatorcontrib>Isono, Yuri</creatorcontrib><creatorcontrib>Sato, Takuya</creatorcontrib><creatorcontrib>Watanabe, Ryoko</creatorcontrib><creatorcontrib>Yonekura-Sakakibara, Keiko</creatorcontrib><creatorcontrib>Fukuchi-Mizutani, Masako</creatorcontrib><creatorcontrib>Tanaka, Yoshikazu</creatorcontrib><creatorcontrib>Kusumi, Takaaki</creatorcontrib><creatorcontrib>Nishino, Tokuzo</creatorcontrib><creatorcontrib>Nakayama, Toru</creatorcontrib><title>Localization of a flavonoid biosynthetic polyphenol oxidase in vacuoles</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Aureusidin synthase, a polyphenol oxidase (PPO), specifically catalyzes the oxidative formation of aurones from chalcones, which are plant flavonoids, and is responsible for the yellow coloration of snapdragon (Antirrhinum majus) flowers. All known PPOs have been found to be localized in plastids, whereas flavonoid biosynthesis is thought to take place in the cytoplasm [or on the cytoplasmic surface of the endoplasmic reticulum (ER)]. However, the primary structural characteristics of aureusidin synthase and some of its molecular properties argue against localization of the enzyme in plastids and the cytoplasm. In this study, the subcellular localization of the enzyme in petal cells of the yellow snapdragon was investigated. Sucrose-density gradient and differential centrifugation analyses suggested that the enzyme (the 39-kDa mature form) is not located in plastids or on the ER. Transient assays using a green fluorescent protein (GFP) chimera fused with the putative propeptide of the PPO precursor suggested that the enzyme was localized within the vacuole lumen. We also found that the necessary information for vacuolar targeting of the PPO was encoded within the 53-residue N-terminal sequence (NTPP), but not in the C-terminal sequence of the precursor. NTPP-mediated ER-to-Golgi trafficking to vacuoles was confirmed by means of the co-expression of an NTPP-GFP chimera with a dominant negative mutant of the Arabidopsis GTPase Sar1 or with a monomeric red fluorescent protein (mRFP)-fused Golgi marker (an H⁺-translocating inorganic pyrophosphatase of Arabidopsis). We identified a sequence-specific vacuolar sorting determinant in the NTPP of the precursor. We have demonstrated the biosynthesis of a flavonoid skeleton in vacuoles. The findings of this metabolic compartmentation may provide a strategy for overcoming the biochemical instability of the precursor chalcones in the cytoplasm, thus leading to the efficient accumulation of aurones in the flower.</description><subject>Amino Acid Sequence</subject><subject>Analytical, structural and metabolic biochemistry</subject><subject>aurone</subject><subject>Biological and medical sciences</subject><subject>biosynthesis of flavonoids</subject><subject>Blotting, Western</subject><subject>Catechol Oxidase - chemistry</subject><subject>Catechol Oxidase - metabolism</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Endoplasmic Reticulum - enzymology</subject><subject>Enzymes and enzyme inhibitors</subject><subject>Flavonoids - biosynthesis</subject><subject>flower coloration</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Vectors</subject><subject>Golgi Apparatus - enzymology</subject><subject>Molecular Sequence Data</subject><subject>Oxidoreductases</subject><subject>Plastids - enzymology</subject><subject>polyphenol oxidase</subject><subject>Protein Transport</subject><subject>Sequence Homology, Amino Acid</subject><subject>subcellular localization</subject><subject>vacuole</subject><subject>Vacuoles - enzymology</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEFvFCEUx4nR2LX6FZSY6G3GBwwwHDyYplbNJjWxTbwRhgHLhh3WYafd9dPLdNc06UkukLzf_73HDyFMoCblfFjVhAleMcJ2NQXgNVBBeb17ghb_Cj-fogUoAZVsCD1BL3JeARDJRPMcnRDBhCzFBbpYJmti-GO2IQ04eWywj-Y2DSn0uAsp74ftjdsGizcp7jc3bkgRp13oTXY4DPjW2ClFl1-iZ97E7F4d71N0_fn86uxLtby8-Hr2aVlZLhpedZw1vet6xxslOsel8ZxSZXzXCi862jsphLcAjnMjWmkVNNKKtnNGCitbdoreH_puxvR7cnmr1yFbF6MZXJqyFpK3SilawLePwFWaxqHspilhTauIggK1B8iOKefReb0Zw9qMe01Az6b1Ss9C9SxUz6b1vWm9K9HXx_5Tt3b9Q_CotgDvjoDJRbEfzWBDfuBkI0Hecx8P3F2Ibv_fC-ir79_mV8m_OeS9Sdr8GsuM6x8UCAMCbfkjsL_r76M7</recordid><startdate>200601</startdate><enddate>200601</enddate><creator>Ono, Eiichiro</creator><creator>Hatayama, Masayoshi</creator><creator>Isono, Yuri</creator><creator>Sato, Takuya</creator><creator>Watanabe, Ryoko</creator><creator>Yonekura-Sakakibara, Keiko</creator><creator>Fukuchi-Mizutani, Masako</creator><creator>Tanaka, Yoshikazu</creator><creator>Kusumi, Takaaki</creator><creator>Nishino, Tokuzo</creator><creator>Nakayama, Toru</creator><general>Oxford, UK : Blackwell Science Ltd</general><general>Blackwell Science Ltd</general><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><scope>FBQ</scope><scope>IQODW</scope><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></search><sort><creationdate>200601</creationdate><title>Localization of a flavonoid biosynthetic polyphenol oxidase in vacuoles</title><author>Ono, Eiichiro ; Hatayama, Masayoshi ; Isono, Yuri ; Sato, Takuya ; Watanabe, Ryoko ; Yonekura-Sakakibara, Keiko ; Fukuchi-Mizutani, Masako ; Tanaka, Yoshikazu ; Kusumi, Takaaki ; Nishino, Tokuzo ; Nakayama, Toru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5645-b534debde5496be57af5229afb86f6b2de766fc00e55a687c9047c68bea76c783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Amino Acid Sequence</topic><topic>Analytical, structural and metabolic biochemistry</topic><topic>aurone</topic><topic>Biological and medical sciences</topic><topic>biosynthesis of flavonoids</topic><topic>Blotting, Western</topic><topic>Catechol Oxidase - chemistry</topic><topic>Catechol Oxidase - metabolism</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Endoplasmic Reticulum - enzymology</topic><topic>Enzymes and enzyme inhibitors</topic><topic>Flavonoids - biosynthesis</topic><topic>flower coloration</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Vectors</topic><topic>Golgi Apparatus - enzymology</topic><topic>Molecular Sequence Data</topic><topic>Oxidoreductases</topic><topic>Plastids - enzymology</topic><topic>polyphenol oxidase</topic><topic>Protein Transport</topic><topic>Sequence Homology, Amino Acid</topic><topic>subcellular localization</topic><topic>vacuole</topic><topic>Vacuoles - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ono, Eiichiro</creatorcontrib><creatorcontrib>Hatayama, Masayoshi</creatorcontrib><creatorcontrib>Isono, Yuri</creatorcontrib><creatorcontrib>Sato, Takuya</creatorcontrib><creatorcontrib>Watanabe, Ryoko</creatorcontrib><creatorcontrib>Yonekura-Sakakibara, Keiko</creatorcontrib><creatorcontrib>Fukuchi-Mizutani, Masako</creatorcontrib><creatorcontrib>Tanaka, Yoshikazu</creatorcontrib><creatorcontrib>Kusumi, Takaaki</creatorcontrib><creatorcontrib>Nishino, Tokuzo</creatorcontrib><creatorcontrib>Nakayama, Toru</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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>Ono, Eiichiro</au><au>Hatayama, Masayoshi</au><au>Isono, Yuri</au><au>Sato, Takuya</au><au>Watanabe, Ryoko</au><au>Yonekura-Sakakibara, Keiko</au><au>Fukuchi-Mizutani, Masako</au><au>Tanaka, Yoshikazu</au><au>Kusumi, Takaaki</au><au>Nishino, Tokuzo</au><au>Nakayama, Toru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Localization of a flavonoid biosynthetic polyphenol oxidase in vacuoles</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2006-01</date><risdate>2006</risdate><volume>45</volume><issue>2</issue><spage>133</spage><epage>143</epage><pages>133-143</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Aureusidin synthase, a polyphenol oxidase (PPO), specifically catalyzes the oxidative formation of aurones from chalcones, which are plant flavonoids, and is responsible for the yellow coloration of snapdragon (Antirrhinum majus) flowers. All known PPOs have been found to be localized in plastids, whereas flavonoid biosynthesis is thought to take place in the cytoplasm [or on the cytoplasmic surface of the endoplasmic reticulum (ER)]. However, the primary structural characteristics of aureusidin synthase and some of its molecular properties argue against localization of the enzyme in plastids and the cytoplasm. In this study, the subcellular localization of the enzyme in petal cells of the yellow snapdragon was investigated. Sucrose-density gradient and differential centrifugation analyses suggested that the enzyme (the 39-kDa mature form) is not located in plastids or on the ER. Transient assays using a green fluorescent protein (GFP) chimera fused with the putative propeptide of the PPO precursor suggested that the enzyme was localized within the vacuole lumen. We also found that the necessary information for vacuolar targeting of the PPO was encoded within the 53-residue N-terminal sequence (NTPP), but not in the C-terminal sequence of the precursor. NTPP-mediated ER-to-Golgi trafficking to vacuoles was confirmed by means of the co-expression of an NTPP-GFP chimera with a dominant negative mutant of the Arabidopsis GTPase Sar1 or with a monomeric red fluorescent protein (mRFP)-fused Golgi marker (an H⁺-translocating inorganic pyrophosphatase of Arabidopsis). We identified a sequence-specific vacuolar sorting determinant in the NTPP of the precursor. We have demonstrated the biosynthesis of a flavonoid skeleton in vacuoles. The findings of this metabolic compartmentation may provide a strategy for overcoming the biochemical instability of the precursor chalcones in the cytoplasm, thus leading to the efficient accumulation of aurones in the flower.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Science Ltd</pub><pmid>16367960</pmid><doi>10.1111/j.1365-313x.2005.02625.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Analytical, structural and metabolic biochemistry aurone Biological and medical sciences biosynthesis of flavonoids Blotting, Western Catechol Oxidase - chemistry Catechol Oxidase - metabolism Electrophoresis, Polyacrylamide Gel Endoplasmic Reticulum - enzymology Enzymes and enzyme inhibitors Flavonoids - biosynthesis flower coloration Fundamental and applied biological sciences. Psychology Genetic Vectors Golgi Apparatus - enzymology Molecular Sequence Data Oxidoreductases Plastids - enzymology polyphenol oxidase Protein Transport Sequence Homology, Amino Acid subcellular localization vacuole Vacuoles - enzymology |
title | Localization of a flavonoid biosynthetic polyphenol oxidase in vacuoles |
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