Enzyme-membrane reactors (EMR) with enzyme covalently immobilized on the pore walls are interesting alternatives for continuous processes, esp. for polymns. However, the effective mass transfer in the pores is crit., and the synthesis of the high-mol. wt. inulin from sucrose using fructosyltransferase (FTF) immobilized in the pores of track-etched membranes had been very much limited by a fast enzyme deactivation via aggregation with the product along with extensive pore blocking of the membranes. In this work, EMR had been prepd. by covalent immobilization of FTF onto amino-functionalized track-etched poly(ethylene terephthalate) (PET) membranes with nominal pore diams. of 400, 1000 or 3000 nm, and in all cases the loss of enzyme activity was fast, and the extent of pore blocking was increasing with decreasing pore diam. Expts. at varied cross-flow velocity with the FTF covalently immobilized on the surface of an epoxy-reactive non-porous film suggested that the rate of FTF deactivation could be much reduced by increasing mass transfer efficiency. Consequently, FTF-EMR with pore diams. of 1000 nm had been operated using regular backpulsing during flow-through or with dispersed inert nanoparticles (diam. 110 nm) in the feed soln. flowing through the pores. For both variants, a significant performance improvement had been obtained. Finally, a novel nanoparticle composite membrane had been prepd. via the covalent immobilization of epoxy-reactive nanoparticles (diam. 200-230 nm) on the pore walls of the track-etched membranes. Spacing between the particles had been achieved by using a mixt. of reactive and inert nanoparticles and suited reaction and washing conditions. The FTF-EMR based on the novel nanoparticle composite membranes had a much higher productivity (prolongation of EMR operation time and more formation of inulin) as compared with all the other membranes or variants investigated in this study. Also a much lower pore-blocking tendency had been obsd. This improved performance had been explained by the two functions of the nanoparticles in the membrane - turbulence promoter and support providing increased surface area for covalent enzyme immobilization.