A high-throughput crystallographic investigation on several crystals of photosynthetic reaction center covalently bound to an ad-hoc synthesized artificial antenna (AE600) is presented. The investigation did not show a preferential binding site of the antenna molecule AE600 to the reaction center in the solid phase. An accurate crystallographic study allowed identifying a lysine residue sitting on periplasmic side of the protein as one of the bioconjugation sites. The residue sits on subunit M of the protein, in close proximity to the bacteriochlorophylls of the reaction center involved in the light absorption and conversion processes. Distances obtained from the crystallographic structure confirm that energy transfer between the antenna and the protein proceed with the Förster resonance mechanism.

Eumelanins, the black insoluble pigments of human skin, eyes and substantia nigra (neuromelanin), stand today as a unique source of inspiration for the design and implementation of soft biocompatible multifunctional materials for bio-optoelectronic devices. Interest in eumelanins stems from bioavailability, biocompatibility and a peculiar set of physicochemical properties, i.e. broadband absorption in the UV-visible range, intrinsic free radical character, water-dependent hybrid ionic–electronic conductor behaviour, supporting optimistic feelings about a possible rise of eumelanin-mimics as innovative bioinspired solutions for organic bioelectronics.

However, a number of conceptual and technological gaps still hinder a rapid progress of melanin-based organic electronics and bioelectronics, including in particular the limited contribution of electronic conductivity and current decay with time under biasing. Herein, we provide a concise overview of the structural and optoelectronic properties of melanins with a view to bringing to focus main issues and challenges en route to bioelectronic applications.

Diatoms are found in nearly every aqueous environment and play a vital part of the global primary production system contributing with up to 25 % and are efficient light harvesting organisms. Unique to diatoms are the hard cell wall, called the frustule surrounding the single cell. The frustule is made from bio-synthesized silicate, perforated by wavelength sized features where the morphology of the nano-structured “greenhouse” is species dependent. Diatoms would therefore make for one of the most interesting “green” resources since it has not only potential as a biomass production system but also for nano-structured inorganic material. To understand the biological significance and to integrate diatomic frustules as active material in devices a fundamental understanding of how light interacts with the frustule is needed. In this study we focus on centric diatoms, i.e. having rotational symmetry where morphological parameters vary between the different investigated species. We report how light interacts with the frustule in the wavelength range from UV-A (320-380 nm) to NIR (900 nm). High resolution spectroscopy and CCD images are used to identify photoluminescence (PL) and variations in the transmitted light caused by the nano-structured frustule. Furthermore we show, by placing the frustule on a quartz half sphere how light transmission is a function of the angle of incidence and wavelength.

The functionalization of biosilica shells (frustules) of diatoms microalgae with a tailored luminescent molecule is a convenient, scalable and biotechnological approach for obtaining new light emitting silica nanostructures with promising applications in photonics. In particular, here we report the synthesis of a red emitting organic fluorophore and its covalent linking to the surface of mesoporous biosilica extracted from Thalassiosira weissflogii diatoms cultured in our laboratories. The organic dye has a conjugated skeleton composed of thienyl, benzothiadiazolyl and phenyl units and a peripheral triethoxysilyl group which enables its stable binding onto the frustules surface. The protocol to extract the biosilica shells from living diatoms preserving their natural ornate nanostructured morphology is also discussed.

Diatoms are the most abundant resource of biosilica on Earth. These microalgae are encased in a 3-D amorphous silica “shell” called frustule whose size and morphology is strictly dependent on the diatom species. Naturally nanostructured biosilica from diatoms exhibit unique adsorption and confinement properties useful for delivery of molecules of pharmacological interest.In this work fossil biosilica was used as a carrier for Ophiobolin A (a fungal macrolide with anticancer and antiparasitic properties), with the aim to develop a model system of Ophiobolin A loading / delivery. Ophiobolin A delivery properties of fossil diatoms were investigated by spectophotometric analyses.

Bio-inspired, hybrid architectures employing quantum dots (QDs) appended with functionally active biomolecules such as enzymes have the potential to be utilized in numerous applications. Some examples include nanosensors for medical diagnostics, chemical/biological threat detection, as well as “bio-factories” in complex industrial synthetic processes. The main advantage in creating these nanofactories is increased rates in catalysis and efficiency when enzymes are associated with nanoscaffolds, as shown in numerous studies. However, the mechanism for this enhancement remains elusive. Gaining a fundamental, mechanistic understanding of enzyme-QD nanostructures is important in the development of numerous device applications. In this work, we review an array of enzymes attached to QDs and generate a hypothesis in regards to the unique architecture of the enzyme-nanoparticle (NP) construct that leads to increases in catalysis. We highlight work with phosphotiresterase (PTE) attached to two distinctly sized QDs in neutralizing a simulant nerve agent, as well as in other enzyme systems.