Tromethamine hydrochloride → 4-Nitrophenol

HRID 244290

Reaktionsgleichung

Reaktionsgleichung von HRID 244290
[N+](C1C=CC(CC([O-])=O)=CC=1)([O-])=O.C(O)C(N)(CO)CO.Cl.[N+:23]([C:26]1[CH:31]=[CH:30][C:29]([O-:32])=[CH:28][CH:27]=1)([O-:25])=[O:24]>CS(C)=O.C([O-])(=O)C.[Na+]>[CH:27]1[C:26]([N+:23]([O-:25])=[O:24])=[CH:31][CH:30]=[C:29]([OH:32])[CH:28]=1

Komponenten

6

Versuchsvorschrift

A p-nitrophenylacetate stock solution is made by dissolving p-nitrophenylacetate in dimethylsulfoxide (DMSO) to constitute a 0.1 M solution. Before assay, a sample of the stock solution is diluted 100-fold in 50 mM sodium acetate pH 5.0 to make a 1 mM solution. A 100 μl volume of 1 mM p-nitrophenylacetate is mixed with each dilution of the enzyme and then incubated at 25° C. for 10 minutes. Substrate alone, enzyme alone, and buffer alone are run as controls. p-Nitrophenol standard solutions of 0.25, 0.2, 0.1, 0.05, and 0.02 mM are prepared by diluting a 10 mM stock solution in 50 mM sodium acetate pH 5.0. At 10 minutes, 50 μl of 1.0 M Tris-HCl pH 8.0 buffer is added to each well (including samples, substrate control, enzyme control, reagent control, and standards), mixed, and the absorbance at 405 nm immediately measured on e.g. a SPECTRAMAX™ 340 PC plate reader (Molecular Devices, Sunnyvale, Calif., USA). One unit of acetyl xylan esterase activity is defined as the amount of enzyme capable of releasing 1 μmole of p-nitrophenolate anion per minute at pH 5, 25° C.

Aufarbeitung

  1. waitAt 10 minutes
  2. additionmixed
  3. customat pH 5, 25° C.

Quellen und Nachweise

ORD-Eintrag
ord-dff474463ee34250ac43ac2b320cc545
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08658409B2

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