Schiff's bases of ortho-, meta- and para-hydroxybenzaldehydes with poly(l-α,γ-diaminobutyric acid) and poly(l-lysine) were investigated in solution of methanol and methanol-water mixtures by circular dichtroism, absorption spectroscopy and equilibrium dialysis techniques. The results so far obtained allow us to propose a molecular model, which fully justifies the stereospecific binding of ortho-hydroxybenzaldehyde with the polypeptide chain; moreover it is able to explain the dramatic change of the chemical equilibrium in the hydrolysis reaction.
Circular dichroism and structure of Schiff's bases of hydroxybenzaldehydes anchored to poly(L-lysine) and poly(L-α,γ-diaminobutyric acid) / Dentini, Mariella; DE SANTIS, Pasquale; Savino, Maria; M. P., Sforza; A. S., Verdini. - In: DIE MAKROMOLEKULARE CHEMIE. - ISSN 0025-116X. - STAMPA. - 179:(1978), pp. 1041-1049. [10.1002/macp.1978.021790418]
Circular dichroism and structure of Schiff's bases of hydroxybenzaldehydes anchored to poly(L-lysine) and poly(L-α,γ-diaminobutyric acid).
DENTINI, Mariella;DE SANTIS, Pasquale;SAVINO, Maria;
1978
Abstract
Schiff's bases of ortho-, meta- and para-hydroxybenzaldehydes with poly(l-α,γ-diaminobutyric acid) and poly(l-lysine) were investigated in solution of methanol and methanol-water mixtures by circular dichtroism, absorption spectroscopy and equilibrium dialysis techniques. The results so far obtained allow us to propose a molecular model, which fully justifies the stereospecific binding of ortho-hydroxybenzaldehyde with the polypeptide chain; moreover it is able to explain the dramatic change of the chemical equilibrium in the hydrolysis reaction.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.