Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10870100 | FEBS Letters | 2015 | 9 Pages |
Abstract
Aurone synthase from Coreopsis grandiflora (cgAUS1), catalyzing conversion of butein to sulfuretin in a type-3 copper center, is a rare example of a polyphenol oxidase involved in anabolism. Site-directed mutagenesis around the CuA site of AUS1 was performed, and recombinant enzymes were analyzed by mass spectrometry. Replacement of the coordinating CuA histidines with alanine resulted in the presence of a single copper and loss of diphenolase activity. The thioether bridge-building cysteine and a phenylalanine over the CuA site, exchanged to alanine, have no influence on copper content but appear to play an important role in substrate binding.
Keywords
PPOF-AAS4-tert-ButylcatecholGF-AASPHCPMSFGSTIPTGTBCPESAASTHCLC/MSSite-directed mutagenesisisopropyl-β-d-thiogalactopyranosideAtomic absorption spectroscopyflame atomic absorption spectroscopyGraphite furnace atomic absorption spectroscopyPolyphenol oxidasePolyphenol oxidase (PPO)liquid chromatographyglutathione S-transferase
Related Topics
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Authors
Cornelia Kaintz, Rupert L. Mayer, Franz Jirsa, Heidi Halbwirth, Annette Rompel,