On the oxidation of cystathionamine and selenocystathionamine by plant amineoxidase.
作者信息
Cini C, Blarzino C, Coccia R, Foppoli C, de Marco C
机构信息
Dipartimento di Scienze Biochimiche A. Rossi Fanelli, Università La Sapienza, Roma, Italy.
出版信息
Biochem Mol Biol Int. 1994 Mar;32(3):575-84.
PMID:8032325
Abstract
Cystathionamine and selenocystathionamine, diamines analogous to 1,6-diaminohexane but having the third methylene group of the carbon chain substituted by a S or a Se atom, are asymmetrical thio- (seleno-) ethers. They can give rise by oxidative monodeamination to two different aminoaldehydes. It has been shown that lentil seedlings amineoxidase catalyzes the oxidative deamination of either the one or the other aminogroup of cystathionamine or of selenocystathionamine, giving rise to both possible aminoaldehydes.
摘要
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