RESUMO
Rapid progress in algal biotechnology has triggered a growing interest in hydrogel-encapsulated microalgal cultivation, especially for the engineering of functional photosynthetic materials and biomass production. An overlooked characteristic of gel-encapsulated cultures is the emergence of cell aggregates, which are the result of the mechanical confinement of the cells. Such aggregates have a dramatic effect on the light management of gel-encapsulated photobioreactors and hence strongly affect the photosynthetic outcome. To evaluate such an effect, we experimentally studied the optical response of hydrogels containing algal aggregates and developed optical simulations to study the resultant light intensity profiles. The simulations are validated experimentally via transmittance measurements using an integrating sphere and aggregate volume analysis with confocal microscopy. Specifically, the heterogeneous distribution of cell aggregates in a hydrogel matrix can increase light penetration while alleviating photoinhibition more effectively than in a flat biofilm. Finally, we demonstrate that light harvesting efficiency can be further enhanced with the introduction of scattering particles within the hydrogel matrix, leading to a fourfold increase in biomass growth. Our study, therefore, highlights a strategy for the design of spatially efficient photosynthetic living materials that have important implications for the engineering of future algal cultivation systems.
Assuntos
Hidrogéis , Luz , Microalgas , Fotossíntese , Hidrogéis/química , Microalgas/crescimento & desenvolvimento , Microalgas/metabolismo , Biomassa , FotobiorreatoresRESUMO
Naturally-sourced cellulose nanocrystals (CNCs) are elongated, birefringent nanoparticles that can undergo cholesteric self-assembly in water to produce vibrant, structurally colored films. As such, they are an ideal candidate for use as sustainable and cost-effective inks in the printing of scalable photonic coatings and bespoke patterns. However, the small volume and large surface area of a sessile CNC drop typically leads to rapid evaporation, resulting in microfilms with a coffee-stain-like morphology and very weak coloration. Here, it is demonstrated that inkjet printing of CNC drops directly through an immiscible oil layer can immediately inhibit water loss, resulting in reduced internal mass flows and greater time for cholesteric self-assembly. The color of each microfilm is determined by the initial composition of the drop, which can be tuned on-demand by exploiting the overprinting and coalescence of multiple smaller drops of different inks. This enables the production of multicolored patterns with complex optical behaviors, such as angle-dependent color and polarization-selective reflection. Finally, the array can be made responsive to stimuli (e.g., UV light, polar solvent) by the inclusion of a degradable additive. This suite of functional properties promotes inkjet-printed photonic CNC arrays for smart colorimetric labeling or optical anticounterfeiting applications.
RESUMO
Marine life is populated by a huge diversity of organisms with an incredible range of colour. While structural colour mechanisms and functions are usually well studied in marine animal species, there is a huge knowledge gap regarding the marine macroalgae (red, green and brown seaweeds) that have structural coloration and the biological significance of this phenomenon in these photosynthetic organisms. Here we show that structural colour in the gametophyte life history phase of the red alga Chondrus crispus plays an important role as a photoprotective mechanism in synergy with the other pigments present. In particular, we have demonstrated that blue structural coloration attenuates the more energetic light while simultaneously favouring green and red light harvesting through the external antennae (phycobilisomes) which possess an intensity-dependent photoprotection mechanism. These insights into the relationship between structural colour and photosynthetic light management further our understanding of the mechanisms involved.