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Biology subjects

Srubar, W. V.

Publications and source records attributed to Srubar, W. V..

2 recordsLinked to original sources

Chemical Stimulation Sustains Bioluminescence of Living Light Materials

Bioluminescence offers a powerful tool for real-time, label-free sensing for living materials. However, conventional approaches often rely on mechanical stimulation, which is difficult to standardize, spatially localize, and sustain over time. Here, we introduce a chemical strategy to stimulate and sustain bioluminescence in the marine dinoflagellate Pyrocystis lunula, enabling the fabrication of robust, adaptive, light-emitting living materials. By embedding P. lunula into 3D-printed, ionically crosslinked alginate hydrogel scaffolds, we engineered architecturally stable living materials with long-term cellular retention, viability, and light-emitting capacity. Exposure to acidic and basic environments enabled chemically resolved sensing and response via distinct bioluminescent signatures: acid triggers intense, localized, and persistent emission up to 25 minutes, while base induces a diffuse, biphasic emission indicative of cellular stress. Notably, coupling chemical with mechanical stimulation yields a synergistic enhancement of bioluminescence, achieving significantly greater amplitude and duration of light emission without compromising cell reactivity. Longitudinal studies over four weeks demonstrated that our living-light materials retain responsiveness and structural integrity across repeated stimulation cycles, overcoming the limitations of single-use mechanical activation. Together, these findings establish a robust new platform for programmable, light-emitting living materials with applications in biosensing, soft robotics, and environmental monitoring.

bioengineering↗

Engineered bacteria that self-assemble ''bioglass'' polysilicate coatings display enhanced light focusing

Photonic devices are cutting-edge optical materials that produce narrow, intense beams of light, but their synthesis typically requires toxic, complex methodology. Here we employ a synthetic biology approach to produce environmentally-friendly, living microlenses with tunable structural properties. We engineered Escherichia coli bacteria to display the silica biomineralization enzyme silicatein from aquatic sea sponges. Our silicatein-expressing bacteria can self-assemble a shell of polysilicate "bioglass" around themselves. Remarkably, the polysilicate-encapsulated bacteria can focus light into intense nanojets that are nearly an order of magnitude brighter than unmodified bacteria. Polysilicate-encapsulated bacteria are metabolically active for up to four months, potentially allowing them to sense and respond to stimuli over time. Our data demonstrate that engineered bacterial particles have the potential to revolutionize the development of multiple optical and photonic technologies. Significance StatementIn this work, we apply the principles of synthetic biology to create living optical devices. Utilizing the ability of sea sponges to polymerize bioglass from silica precursors in the ocean water using only a single enzyme, silicatein, we have fused this same enzyme to the surface of Escherichia coli bacterial cells. The modified bacteria can polymerize a layer of bioglass at their surface. This bioglass shell allows the bacteria to act as engineered optical devices that are able to scatter high intensity, focused light while also surviving for several months, opening the door to a wide range of sense-and-respond applications. ClassificationBiological Sciences, Applied Biological Sciences

synthetic biology↗