Cell immobilization is a promising approach to create efficient photosynthetic cell factories for sustainable chemicals production. Here, we demonstrate a novel photosynthetic solid-state cell factory design for sustainable biocatalytic ethylene...

Versatile templates were fabricated using plant-derived nanomaterials, TEMPO-oxidized cellulose nanofibrils (TEMPO CNF) for the efficient and sustainable production of biofuels from cyanobacteria and green algae. We used three different approaches to immobilize the model filamentous cyanobacteria or green algae to the TEMPO CNF matrix. These approaches involved the fabrication of: (A) a pure TEMPO CNF hydrogel; (B) a Ca 2+ -stabilized TEMPO CNF hydrogel; and (C) a solid TEMPO CNF film, which was crosslinked with polyvinyl alcohol (PVA). The different immobilization approaches resulted in matrices with enhanced water stability performance. In all cases, the photosynthetic activity and H 2 photoproduction capacity of cyanobacteria and algae entrapped in TEMPO CNF were comparable to a conventional alginate-based matrix. Green algae entrapped in Ca 2+ -stabilized TEMPO CNF hydrogels showed even greater rates of H 2 production than control alginate-entrapped algae under the more challenging submerged cultivation condition. Importantly, cyanobacterial filaments entrapped within dried TEMPO CNF films showed full recovery once rewetted, and they continued efficient H 2 production. The immobilization mechanism was passive entrapment, which was directly evidenced using surface sensitive quartz crystal microbalance with dissipation monitoring (QCM-D). The results obtained demonstrate a high compatibility between CNF and photosynthetic microbes. This opens new possibilities for developing a novel technology platform based on CNF templates with tailored pore-size and controllable surface charges that target sustainable chemical production by oxygenic photosynthetic microorganisms.

Crosslinked cellulose nanofiber-polyvinyl alcohol antifouling membrane.

Osmotic dehydration (OD) was introduced as a method to reproducibly tune the water content and porosity of cellulose nanofiber (CNF) hydrogels. The hierarchical porosity was followed by electron microscopy (pores with a >100 μm diameter) and thermoporosimetry (mesopores), together with mechanical testing, in hydrogels with solid contents ranging from 0.7 to 12 wt %. Furthermore, a reciprocal correlation between proton conductivity and the ratio of water bound to the nanocellulose network was established, suggesting the potential of these systems toward tunable energy materials.

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