Home LiteratureArticle Details
PMID: 16367960 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Localization of a flavonoid biosynthetic polyphenol oxidase in vacuoles.

The Plant journal : for cell and molecular biology ·Vol. 45 ·No. 2 ·2006-01-00 ·Pages 133-43

Ono E, Hatayama M, Isono Y, Sato T, Watanabe R, Yonekura-Sakakibara K, Fukuchi-Mizutani M, Tanaka Y, Kusumi T, Nishino T, Nakayama T

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.

MeSH Terms
Amino Acid Sequence Blotting, Western Catechol Oxidase/chemistry,metabolism Electrophoresis, Polyacrylamide Gel Endoplasmic Reticulum/enzymology Flavonoids/biosynthesis Genetic Vectors Golgi Apparatus/enzymology Molecular Sequence Data Plastids/enzymology Protein Transport Sequence Homology, Amino Acid Vacuoles/enzymology
Chemicals
Flavonoids Catechol Oxidase
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Ono Eiichiro
Suntory Research Center, Shimamoto-cho, Mishima-gun, Osaka 618-8503, Japan.
Hatayama Masayoshi
Isono Yuri
Sato Takuya
Watanabe Ryoko
Yonekura-Sakakibara Keiko
Fukuchi-Mizutani Masako
Tanaka Yoshikazu
Kusumi Takaaki
Nishino Tokuzo
Nakayama Toru
Article Info
Journal
The Plant journal : for cell and molecular biology
Abbr.
Plant J
ISSN
0960-7412
Published
2006-01-00
Pages
133-43
Language
English
Region
England
NLM ID
9207397
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com