1.2 Amino Acids 21A corresponding reaction with phenylisothio-
cyanate can degrade a peptide in a stepwise
fashion (Edmandegradation). The reaction is of
great importance for revealing the amino acid
sequence in a peptide chain. The phenylthiocar-
bamoyl derivative (PTC-peptide) formed in the
first step (coupling) is cleaved non-hydrolytically
in the second step (cleavage) with anhydrous
trifluoroacetic acid into anilinothiazolinone as
derivative of the N-terminal amino acid and
the remaining peptide which is shortened by
the latter. Because of its instability, the thia-
zolinone is not suited for an identification of
the N-terminal amino acid and is therefore –
after separation from the remaining peptide,
in the third step (conversion) – converted in
aqueous HCl via the phenylthiocarbamoy-
lamino acid into phenyl-thiohydantoin, while
the remaining peptide is fed into a new
cycle.
(1.41)(1.42)1.2.4.2.4 Reactions with Carbonyl Compounds.
Amino acids react with carbonyl compounds,
forming azomethines. If the carbonyl com-
pound has an electron-withdrawing group,
e. g., a second carbonyl group, transamination
and decarboxylation occur. The reaction is
known as theStreckerdegradation and plays
a role in food since food can be an abundant
source of dicarbonyl compounds generated
by theMaillard reaction (cf. 4.2.4.4.7). The
aldehydes formed from amino acids (Strecker
aldehydes) are aroma compounds (cf. 5.3.1.1).
The ninhydrin reaction is a special case of
the Strecker degradation. It is an important
reaction for the quantitative determination of