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Palabras clave – provistas por la editorial

chitosan; Csep1p; bond selection during protein crystallization; bioremediation; education; reductants; heavy metals; biomimetic crystallization; MTT assay; protein crystallization; drug discovery; optimization; polymyxin resistance; lysozyme; ependymin-related protein (EPDR); equilibration between crystal bond and destructive energies; barium carbonate; dyes; microseed matrix screening; nanoapatites; colistin resistance; Haloalkane dehalogenase; diffusion; polyacrylic acid; random microseeding; protein ‘affinity’ to water; insulin; protein crystal nucleation; agarose; lithium ions; ependymin (EPN); {00.1} calcite; seeding; Campylobacter consisus; metallothioneins; Crohn’s disease; balance between crystal bond energy and destructive surface energies; color change; microbially induced calcite precipitation (MICP); crystallization of macromolecules; crystallization; calcein; MCR-1; Cry protein crystals; L-tryptophan; circular dichroism; crystal violet; nanocomposites; halide-binding site; calcium carbonate; PCDA; ultrasonic irradiation; adsorption; biochemical aspects of the protein crystal nucleation; GTL-16 cells; proteinase k; neutron protein crystallography; classical and two-step crystal nucleation mechanisms; thermodynamic and energetic approach; heavy metal contamination; N-acetyl-D-glucosamine; crystallization in solution flow; solubility; biomorphs; droplet array; biomimetic materials; ferritin; biomineralization; wastewater treatment; H3O+; silica; graphene; supersaturation dependence of the crystal nucleus size; pyrrole; micro-crystals; nucleation; crystallography; mammalian ependymin-related protein (MERP); high-throughput; vaterite transformation; gradients; materials science; bioprecipitation; biomedicine; human carbonic anhydrase IX; protein crystal nucleation in pores; growth; crystal growth