Specificity analysis and mechanism of aurone synthesis catalyzed by aureusidin synthase, a polyphenol oxidase homolog responsible for flower coloration

Toru Nakayama, Takuya Sato, Yuko Fukui, Keiko Yonekura-Sakakibara, Hideyuki Hayashi, Yoshikazu Tanaka, Takaaki Kusumi, Tokuzo Nishino

Research output: Contribution to journalArticlepeer-review

94 Citations (Scopus)

Abstract

Aureusidin synthase, which plays a key role in the yellow coloration of snapdragon flowers, is a homolog of plant polyphenol oxidase (PPO). The enzyme specifically acted on chalcones with a 4-monohydroxy or 3,4-dihydroxy B-ring to produce aurones, for whose production the oxidative cyclization of chalcones must be preceded by 3-oxygenation. However, it exhibited virtually no PPO activity toward non-chalcone phenolics. The enzyme was competitively inhibited by phenylthiourea, a specific PPO inhibitor. These results led us to propose a mechanism of aurone synthesis by aureusidin synthase on the basis of known PPO-catalyzed reactions and conclude that the enzyme is a chalcone-specific PPO specialized for aurone biosynthesis.

Original languageEnglish
Pages (from-to)107-111
Number of pages5
JournalFEBS Letters
Volume499
Issue number1-2
DOIs
Publication statusPublished - 2001 Jun 15

Keywords

  • 2′,3,4,4′,6′- Pentahydroxychalcone
  • 2′,4,4′,6′-Tetrahydroxychalcone
  • Aureusidin synthase
  • Aurone
  • Bracteatin
  • Polyphenol oxidase
  • Tyrosinase

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Cell Biology

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