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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Veröffentlicht in:The Plant journal : for cell and molecular biology 2006-01, Vol.45 (2), p.133-143
Hauptverfasser: Ono, Eiichiro, Hatayama, Masayoshi, Isono, Yuri, Sato, Takuya, Watanabe, Ryoko, Yonekura-Sakakibara, Keiko, Fukuchi-Mizutani, Masako, Tanaka, Yoshikazu, Kusumi, Takaaki, Nishino, Tokuzo, Nakayama, Toru
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container_title The Plant journal : for cell and molecular biology
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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.
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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. 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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 &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>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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