We used fluorogenic substrates, namely, alkyldiacyl glycerols labeled with
a fluorophore and a fluorescence quencher, to measure lipase activities. Fo
r this optical lipase assay it is necessary that the water-insoluble fluoro
genic substrates are dispersed in an aqueous medium in the presence of appr
opriate detergents in order to obtain well-defined and reproducible systems
with high optical transparency. The activity of lipases critically depends
on the supramolecular organization of the substrate. Therefore, we tested
different solutions containing nonionic surfactants and organic phases for
their potential use as host systems for fluorogenic lipids. We then determi
ned the pseudoternary phase diagram for the system buffer-alkyl polyglucosi
de-hexanol, which showed the highest apparent enzyme activities, in the buf
fer corner. We performed structural investigations on micellar sugar surfac
tant solutions within the L-1 phase with and without hexanol using small-an
gle neutron scattering (SANS), small-angle X-ray scattering (SAXS), and dyn
amic light scattering (DLS) in order to investigate a possible correlation
between Lipase activity and the structure of the aggregates present in the
host system.