L-Mimosine, an amino acid with maltol-type binding properties toward copper(II), oxovanadium(IV) and other metal ions

Citation
E. Chruscinska et al., L-Mimosine, an amino acid with maltol-type binding properties toward copper(II), oxovanadium(IV) and other metal ions, J INORG BIO, 75(3), 1999, pp. 225-232
Citations number
27
Categorie Soggetti
Biochemistry & Biophysics","Inorganic & Nuclear Chemistry
Journal title
JOURNAL OF INORGANIC BIOCHEMISTRY
ISSN journal
01620134 → ACNP
Volume
75
Issue
3
Year of publication
1999
Pages
225 - 232
Database
ISI
SICI code
0162-0134(19990630)75:3<225:LAAAWM>2.0.ZU;2-G
Abstract
The complex formation between L-mimosine, alpha-amino-beta-(3-hydroxy-4-oxo -1,4-dihydropyridin-1-yl)-propanoic acid, a rare a-amino acid provided with a 3-hydroxypyridin-4(1H) one moiety, and some metal ions - Cu(II), VO(IV), Ni(II) and Zn(II) - was studied by spectroscopic (EPR and electron absorpt ion) and potentiometric techniques in aqueous solution. It was found that L -mimosine prefers the maltol-like donor set of the 3-hydroxypyridin-4 (IH)o ne fragment for binding copper(II) and oxovanadium(IV). However, the presen ce of two alternative donor centres in the ligand, (COO-, NH,) and (CO, O-) , both suitable for chelating behaviour, makes possible the formation of ve ry stable polynuclear species in which the L-mimosine ligand coordinates at both the (CO, O-) maltol-like and the (COO-, NH2) alpha-aminocarboxylate s ites. Nickel(II) interacts with the ligand, but prefers a mixed bonding mod e in the bis chelated species. Zn(II) only forms complexes with the 3-hydro xypyridin-4(1H) one fragment. (C) 1999 Elsevier Science Inc. All rights res erved.