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Earthen building materials are experiencing a renaissance in light of the climate crisis. To engineer high-performance sustainable and durable earthen materials for the 21st century, the importance of chemistry—and biology—cannot be underestimated. 

Biomineralization refers to the biological processes through which living organisms produce minerals. In recent years, biomineralizing microorganisms have been used to stabilize soil or to impart a self-healing or self-sealing mechanism to damaged cement and concrete materials. However, applications of biominerals in cement and concrete research can extend far beyond these applications. This article focuses on the biomineralization of calcium carbonate (CaCO3) and silicon dioxide (SiO2) and their past, present, and future potential applications in cement and concrete research. First, we review the mechanisms of CaCO3 and SiO2 biomineralization and the micro- and macroorganisms involved in their production. Second, we showcase the wide array of biomineral architectures, with an explicit focus on CaCO3 polymorphs and SiO2 morphologies found in nature. Third, we briefly summarize previous applications of CaCO3 and SiO2 biomineralization in cement and concrete research. Finally, we discuss emerging applications of biominerals in cement and concrete research, including mineral admixtures or raw meal for portland cement production, as well as other applications that extend beyond self-healing. 

Driven by the need for sustainable construction solutions, there is renewed interest in earth-based materials. Biopolymer stabilizers can enhance the rheological and structural properties of these materials to facilitate their use in 3D printing. This research examined the influence of sodium alginate on the stability, particle interaction, rheology, and 3D printability of kaolinite, a commonly found clay in soils deemed suitable for construction. Findings revealed that sodium alginate could boost electrostatic interactions to enhance the stability of kaolinite suspensions. This rise in repulsive potential energy could reduce storage modulus and yield stress by orders of magnitude. However, as the alginate content increased beyond its critical overlapping concentration (0.12 %–0.6 %), a reverse trend was observed, which was attributed to the formation of a three-dimensional polymer network. Furthermore, alginate addition shifted the “printability window” of kaolinite mixtures to higher solid contents, which has positive implications on the strength and shrinkage of the printable mixtures. 

Cutting-edge photonic devices frequently rely on microparticle components to focus and manipulate light. Conventional methods used to produce these microparticle components frequently offer limited control of their structural properties or require low-throughput nanofabrication of more complex structures. Here, we employ a synthetic biology approach to produce environmentally friendly, living microlenses with tunable structural properties. We engineeredEscherichia colibacteria 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 4 mo, potentially allowing them to sense and respond to stimuli over time. Our data demonstrate that synthetic biology offers a pathway for producing inexpensive and durable photonic components that exhibit unique optical properties.