Agricultural and Biological Chemistry
Online ISSN : 1881-1280
Print ISSN : 0002-1369
ISSN-L : 0002-1369
Synthesis of Selenocystine and Selenohomocystine with O-Acetylhomoserine Sulfhydrylase
Patrick CHOCATNobuyoshi ESAKIHidehiko TANAKAKenji SODAT
Author information
JOURNAL FREE ACCESS

1985 Volume 49 Issue 4 Pages 1143-1150

Details
Abstract

We describe here the synthesis of selenium araino acids with O-acetylhomoserine Sulfhydrylase, partially purified from baker's yeast. The enzyme was found to catalyze the synthesis of L-selenocystine and L-selenohomocystine from Na2Se2 with the corresponding acetyl-derivatives of serine and homoserine, respectively. L-Serine-O-sulfate also serves as a substrate of the β-replacement reaction. Na2Se2 is less efficient as a substituent donor than the physiological substrate, NaHS, and inhibits the enzyme at high concentrations. Therefore, limited amounts of Na2Se2 were added to the reaction mixture to increase the yield (50 to 60%). This provides a facile method to produce optically active Selenocystine and Selenohomocystine.

Content from these authors

This article cannot obtain the latest cited-by information.

© Japan Society for Bioscience, Biotechnology, and Agrochemistry
Previous article Next article
feedback
Top