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Can I read The C-4 stereochemistry of leucocyanidin substrates for anthocyanidin synthase affects product selectivity on EtoBox?
The C-4 stereochemistry of leucocyanidin substrates for anthocyanidin synthase affects product selectivity by Jonathan J. Turnbull; Michael J. Nagle; Jürgen F. Seibel; Richard W.D. Welford; Guy H. Grant; Christopher J. Schofield is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
What is The C-4 stereochemistry of leucocyanidin substrates for anthocyanidin synthase affects product selectivity about?
Anthocyanidin synthase (ANS), an iron(II) and 2-oxoglutarate (2OG) dependent oxygenase, catalyses the penultimate step in anthocyanin biosynthesis by oxidation of the 2R,3S,4S-cis-leucoanthocyanidins. It has been believed that in vivo the products of ANS are the anthocyanidins. However, in vitro studies on ANS using optically active cis-and trans-leucocyanidin substrates identified cyanidin as only a minor product; instead both quercetin and dihydroquercetin are products with the distribution being dependent on the C-4 stereochemistry of the leucocyanidin substrates.
Who reads The C-4 stereochemistry of leucocyanidin substrates for anthocyanidin synthase affects product selectivity?
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Jonathan J. Turnbull; Michael J. Nagle; Jürgen F. Seibel; Richard W.D. Welford; Guy H. Grant; Christopher J. Schofield
- Publisher
- Elsevier Science; Elsevier ; Elsevier Ltd.; Elsevier BV (ISSN 0960-894X)
- Published
- 2003
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)