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J Pept Sci ; 20(8): 625-9, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24817133

ABSTRACT

Oligopeptides are of high importance for various industrial applications, e.g. cosmetical or medical. Homooligomerizations and co-oligomerizations with anionic amino acid esters are well described but a successful synthesis of cationic heterooligopeptides has been missing so far. The present study reports the ficain-catalyzed heterooligomerizations of LysOEt with MetOEt, leading to cationic heterooligopeptides with a yield up to 49.5% (w/w). MALDI-ToF/ToF-MS analyses proved successful syntheses of cationic heterooligopeptides with a DP between 7 and 10 amino acid residues, with the enzyme exhibiting a clear preference for methionine.


Subject(s)
Ficain/metabolism , Lysine/analogs & derivatives , Lysine/metabolism , Methionine/analogs & derivatives , Oligopeptides/biosynthesis , Cations , Esters , Methionine/metabolism , Oligopeptides/chemistry , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
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