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In this report, we describe the synthesis of a molecularly imprinted polymer (MIP) nanotube membrane, using a porous anodic alumina oxide (AAO) membrane by surface-initiated atom transfer radical polymerization (ATRP). The use of a MIP nanotube membrane in chemical separations gives the advantage of high affinity and selectivity. Furthermore, because the molecular imprinting technique can be applied to different kinds of target molecules, ranging from small organic molecules to peptides and proteins, such MIP nanotube membranes will considerably broaden the application of nanotube membranes in chemical separations and sensors. This report also shows that the ATRP route is an efficient procedure for the preparation of molecularly imprinted polymers. Furthermore, the ATRP route works well in its formation of MIP nanotubes within a porous AAO membrane. The controllable nature of ATRP allows the growth of a MIP nanotube with uniform pores and adjustable thickness. Thus, using the same route, it is possible to tailor the synthesis of MIP nanotube membranes with either thicker MIP nanotubes for capacity improvement or thinner nanotubes for efficiency improvement.

In this paper, we present a general protocol for the making of surface-imprinted core-shell nanoparticles via surface reversible addition-fragmentation chain-transfer (RAFT) polymerization using RAFT agent functionalized model silica nanoparticles as the chain-transfer agent. In this protocol, trichloro(4-chloromethylphenyl)silane was immobilized on the surface of SiO2 nanoparticles, forming chloromethylphenyl functionalized silica (silica-Cl). RAFT agent functionalized silica was subsequently produced by substitute reaction of silica-Cl with PhC(S)SMgBr. The grafting copolymerization of 4-vinylpyridine and ethylene glycol dimethacrylate using surface RAFT polymerization and in the presence of 2,4-dichlorophenoxyacetic acid as the template led to the formation of surface-imprinted core-shell nanoparticles. The resulting surface-imprinted core-shell nanoparticles bind the original template 2,4-D with an appreciable selectivity over structurally related compounds. The potential use of the surface-imprinted core-shell nanoparticles as the recognition element in the competitive fluorescent binding assay for 2,4-D was also demonstrated.

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A case study to investigate the relationship between antibacterial activity and quorum sensing mechanisms was carried out on a sponge-associated bacterium with remarkable biological activities: Pseudoalteromonas sp. NJ6-3-1. The dependence of active substance production on cell density was studied under various growth conditions. Bacteria NJ6-3-1 was found to start producing antibacterial compounds only when cell density reached the threshold value of OD 630 =0.4. To simulate the competitive real marine environment, NJ6-3-1 at low cell density (OD 630 value below the required threshold value) was cocultured with the terrestrial bacterium Staphylococcus aureus. Antibacterial activity assays indicated the existence of some signal molecules in the metabolites of S. aureus that could induce NJ6-3-1 to produce antibacterial substances even at low cell density. Three diketopiperazines (DKPs) as metabolites and potential autoinducers of NJ6-3-1 were synthesized and co-cultured with low density NJ6-3-1. The antibacterial activity assay showed that one of these DKPs-cyclo-(L-Phe-L-Val)-was the autoinducer and could indeed induce NJ6-3-1 to produce antibacterial substances under low cell density. Our results thus provide preliminary support to the hypothesis that the antibacterial activity of NJ6-3-1 is controlled by the quorum sensing system in both an intra-species and an inter-species manner.