Plant cuticle is a complex mixture of hydrophobic components that controls the uptake of pesticides by plants. Although the transport of lipophilic molecules across the cuticle has been intensively studied, development of tools to measure the cuticle polarity has received little attention. We developed a rapid and simple analytical method to evaluate the polarity of cuticles in situ. This method uses Prodan, 6-propionyl-2-(dimethylaminonaphthalene), a medium-sensitive fluorescent probe. Tests on model surfaces with varied polarity (i.e., wax paraffin, polyethylene, C18) were carried out to test the feasibility of the measurement and to optimize the application of Prodan. Moreover, on the basis of the Kamlet-Taft solvatochromic comparison method, a relationship between the emission characteristics of Prodan and the number of carbon atoms in primary alcohols mimicking the solid medium was established. After optimization, the method was validated on three natural plant cuticles (leaf of Zamiifolia, skin of green pepper, and skin of white grape).
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http://dx.doi.org/10.1021/acs.jafc.5b02779 | DOI Listing |
Chem Biomed Imaging
January 2025
Precision Healthcare University Research Institute, Queen Mary University of London, Whitechapel, London E1 4NS, United Kingdom.
Bacterial resistance, primarily stemming from misdiagnosis, misuse, and overuse of antibacterial medications in humans and animals, is a pressing issue. To address this, we focused on developing a fluorescent probe for the detection of bacteria, with a unique feature-an exceptionally long fluorescence lifetime, to overcome autofluorescence limitations in biological samples. The polymyxin-based probe (ADOTA-PMX) selectively targets Gram-negative bacteria and used the red-emitting fluorophore azadioxatriangulenium (with a reported fluorescence lifetime of 19.
View Article and Find Full Text PDFAnal Methods
January 2025
Department of Chemistry, University of South Florida, Tampa, Florida 33620, USA.
Sodium dodecyl sulfate (SDS) is widely used in numerous household products and pharmaceuticals due to its excellent water solubility, emulsification, foaming, and dispersing properties. However, the extensive use of SDS has made it a significant environmental pollutant, posing a great threat to aquatic ecosystems. Therefore, developing a rapid, efficient, and sensitive probe for detecting SDS in aqueous environments is crucial.
View Article and Find Full Text PDFPlant Mol Biol
January 2025
Graduate School of Science and Technology, Kumamoto University, 2-39-1 Kurokami, Chuo-Ku, Kumamoto, 860-8555, Japan.
The applicability of a deep learning model for the virtual staining of plant cell structures using bright-field microscopy was investigated. The training dataset consisted of microscopy images of tobacco BY-2 cells with the plasma membrane stained with the fluorescent dye PlasMem Bright Green and the cell nucleus labeled with Histone-red fluorescent protein. The trained models successfully detected the expansion of cell nuclei upon aphidicolin treatment and a decrease in the cell aspect ratio upon propyzamide treatment, demonstrating its utility in cell morphometry.
View Article and Find Full Text PDFFood Chem
January 2025
Institute for Agro-food Standards and Testing Technology, Shanghai Academy of Agricultural Sciences, 1000 Jingqi Road, Shanghai 201403, China. Electronic address:
Deoxynivalenol (DON) is one of the most harmful mycotoxins that poses great health threats to human and animals. Herein, a simple and sensitive magnetic beads-based fluorescent biosensor was successfully prepared for detection of DON in cereals. A stable double-stranded DNA (dsDNA, biotin-sDNA+FAM-cDNA/AP) was formed on the surface of streptavidin-coated magnetic beads (SMBs).
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
January 2025
Key Laboratory for Microstructural Material Physics of Hebei Province, School of Science, Yanshan University, Qinhuangdao 066004 PR China. Electronic address:
2-{[3-(1H-benzoimidazol-2-yl)-2-hydroxy-5-methylbenzylidene] amino}-benzoic acid (HBIo) based on proton transfer can serve as the fluorescent probe for detecting heavy metal ions. The excited-state intramolecular proton transfer (ESIPT) reaction mechanism of the HBIo chromophore with an intramolecular asymmetric double hydrogen bond in different solvents are investigated. The reaction barrier of the ESIPT along hydrogen bond O1-H2···N3 is higher than that of ESIPT along O4-H5···N6, which indicates that the double ESIPT is a stepwise process.
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