TL;DR: Results indicate that endocytic vesicles become acidic prior to fusion with lysosomes, as measured by the pH changes in the microenvironment of internalized ligands following receptor-mediated endocytosis.
TL;DR: The NPN uptake assay with the automated spectrofluorometer serves as a convenient method in analysing and quantifying the effects of external agents, including potential food preservatives, on Gram‐negative bacteria.
Abstract: Uptake of the fluorescent probe 1-N-phenylnaphthylamine (NPN), as adapted to an automated spectrofluorometer enabling multiwell reading of microtitre plates, was applied to determine permeability changes in Gram-negative bacteria. An intact outer membrane is a permeability barrier, and excludes hydrophobic substances such as NPN but, once damaged, it can allow the entry of NPN to the phospholipid layer, resulting in prominent fluorescence. With Escherichia coli O157, Pseudomonas aeruginosa, and Salmonella typhimurium as test organisms and ethylenediaminetetraacetic acid and sodium hexametaphosphate as the model permeabilizers, quantitative and highly reproducible NPN uptake levels were obtained that differed characteristically between the test bacteria. Furthermore, citric acid was shown to be a potent permeabilizer at millimolar concentrations, its effect being partly (Ps. aeruginosa, Salm. typhimurium) or almost totally (E. coli O157) abolished by MgCl2, suggesting that part of the action occurs by chelation. Sodium citrate induced weak NPN uptake, which was totally abolished by MgCl2. In conclusion, the NPN uptake assay with the automated spectrofluorometer serves as a convenient method in analysing and quantifying the effects of external agents, including potential food preservatives, on Gram-negative bacteria.
TL;DR: Norepinephrine has been identified chemically as a normal constituent of brain and a simple, rapid fluorometric method for the estimation of catechol amines in brain and other tissues is described.
Abstract: Norepinephrine has been identified chemically as a normal constituent of brain. A simple, rapid fluorometric method for the estimation of catechol amines in brain and other tissues is described. The procedure involves extraction of catechol amines from tissue homogenates into butanol. After returning the amines to an aqueous phase, they are oxidized to form fluorescent derivatives which are measured in a spectrofluorometer.
TL;DR: In this paper, a high-sensitivity spectrofluorometer without preconcentration of the samples was used to record the corrected fluorescence spectra of open marine water and the results showed that with an adequate excitation wavelength (313 nm) fluorescence signature can be used to differentiate water masses.
TL;DR: The impulse of the shock wave was a dominant factor for causing fluorophore uptake into living cells, and that shock waves might have changed the permeability of the nuclear membrane and transferred molecules directly into the nucleus.