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- W985883509 abstract "Publisher Summary This chapter discusses the fluorescence measurements of incorporation and hydrolysis of tocopherol and tocopheryl esters in biomembranes. The hydrolysis of nonfluorescent esterified chromanols can be studied by the appearance and increase of the intensity of fluorescence emitted by chromanols produced in the course of deesterification reactions. Excitation at 303 rather than 292 nm should be used to minimize the interference of protein fluorescence. The sensitivity of the assay is determined by the minimum amounts of chromanols producing a distinct fluorescence increment in the presence of a given concentration of membrane protein. Preliminary calibration by addition of standard amounts of chromanols to membrane suspensions allows obtaining the rates of hydrolysis of esterified chromanols. The chapter summarizes the data on the hydrolysis rates of α-T acetate, α-stearate, linoleate, phosphate, and 2,2,5,7,8-pentamethylchromane acetate (C 1 acetate) in suspensions of rat liver mitochondria and microsomes at three different temperatures. The de-esterification rates depend on the chemical nature of the ester and the incubation temperature, and they differ significantly in microsomes, mitochondria, and, particularly, in blood serum." @default.
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- W985883509 date "1990-01-01" @default.
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- W985883509 title "[37] Fluorescence measurements of incorporation and hydrolysis of tocopherol and tocopheryl esters in biomembranes" @default.
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- W985883509 doi "https://doi.org/10.1016/0076-6879(90)86129-j" @default.
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