The enzymatic hydrolysis of a model poly(D, L-lactide) by cutinase was
studied by using a barostat surface balance. A theoretical approach b
ased on the adaptation of the Michaelis-Menten scheme at the interface
and a process of random fragmentation of the macromolecules was devel
oped. The role of the interfacial organisation of the reaction product
s was discussed. Hydrolysis rate constant values and the specific acti
vity were estimated and compared with those obtained for the hydrolysi
s of lipid monolayers. The process of fragmentation of the interfacial
polymer structures was visualised by using AFM imaging.