Phaeodactylum tricornutum is a promising host for light-driven synthesis of heterologous proteins. However, the marine cold-water environment and alkaline-acidic pH shifts in the culture, necessitated by the diatom's growth requirements. In this study, we analyzed the influence of growth condition on maturation and dynamics of the yellow fluorescent protein (YFP) in episomal-transformant P. tricornutum. A mathematical model was developed to detect the parameters that affect biomass and YFP production. Optimized conditions increased YFP mean fluorescence intensity (MFI) per cell by 4.2-fold (3.6 ± 0.6 to 15.4 ± 1.1) and total protein levels in the culture by 1.8-fold (123 ± 4 to 219 ± 9 µg L), without affecting biomass. YFP stability studies in P. tricornutum showed that the ubiquitin-proteasome system contributes the degradation of the recombinant protein, whereas newly synthesized YFP remains stable for up to 12 h. This optimization provides insights into the fluorescent protein-based heterologous production in diatoms.
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http://dx.doi.org/10.1016/j.biortech.2025.132336 | DOI Listing |
Nanomaterials (Basel)
February 2025
Institute of Nanochemistry and Nanobiology, School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China.
Methyl orange (MO) is an organic synthetic dye widely used in laboratory and industrial applications. In laboratory settings, it serves as an acid-base indicator due to its distinct color change in both acidic and alkaline environments. Industrially, it is primarily utilized in the textile industry for its ultraviolet (UV) absorption properties.
View Article and Find Full Text PDFCurrently, static fluorescent anti-counterfeiting technology struggles to cope with the increasingly sophisticated counterfeiting techniques, making the dynamic multimode regulation scheme an urgent necessity. Herein, Sm3+ mono-/co-doped LiTaO3 (LTO) phosphors are prepared by high temperature solid state method. Under 254 nm excitation, the emission chromaticity of LTO: Tb3+, Sm3+ is modulated from green to yellow by increasing Sm3+ content due to Tb3+ → Sm3+ energy transfer.
View Article and Find Full Text PDFChem Sci
March 2025
Centre of Physiology and Pharmacology, Institute of Pharmacology, Medical University of Vienna Währinger Straβe 13A 1090 Vienna Austria
Fluorescent labeling techniques have enabled the visualization of various biomolecules, cellular structures, and their associated physiological processes. At the same time, there remains a demand for developing novel fluorescent compounds possessing unique chemical properties for biological imaging. A recently developed class of fluorophores, termed , displays optimal brightness and large Stokes shifts that are ideal for fluorescence microscopy.
View Article and Find Full Text PDFArch Microbiol
March 2025
Department of Microbiology, School of Biology, University College of Sciences, University of Tehran, Tehran, Iran.
Detection of Helicobacter pylori, Staphylococcus, Nocardia and Cyanobacteria inside the yeast Candida tropicalis raised the question whether treating yeast with antibiotics mix (ABM) eliminates intracellular bacteria. Live/Dead staining showed occurrence of viable bacteria inside the vacuole of C. tropicalis.
View Article and Find Full Text PDFUnlabelled: Light scattering in biological tissue presents a significant challenge for deep imaging. Our previous work demonstrated the ability to achieve optical transparency in live mice using intensely absorbing dye molecules, which created transparency in the red spectrum while blocking shorter-wavelength photons. In this paper, we extend this capability to achieve optical transparency across the entire visible spectrum by employing molecules with strong absorption in the ultraviolet spectrum and sharp absorption edges that rapidly decline upon entering the visible spectrum.
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