Reaktionsgleichung
[N+](C1C=CC(/C(=C\C2C=CC(O)=C(OC)C=2)/C([O-])=O)=CC=1)([O-])=O.[N+](C1C=CC(CC([O-])=O)=CC=1)([O-])=O.C(O)C(N)(CO)CO.Cl.[N+:46]([C:49]1[CH:54]=[CH:53][C:52]([O-:55])=[CH:51][CH:50]=1)([O-:48])=[O:47]>CS(C)=O.C([O-])(=O)C.[Na+]>[CH:50]1[C:49]([N+:46]([O-:48])=[O:47])=[CH:54][CH:53]=[C:52]([OH:55])[CH:51]=1Komponenten
Versuchsvorschrift
A p-nitrophenylferulate 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-nitrophenylferulate 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 a SPECTRAMAX™ 340 PC plate reader (Molecular Devices, Sunnyvale, Calif., USA). One unit of feruloyl 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
- waitAt 10 minutes
- additionmixed
- customat pH 5, 25° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-5b67f0f84b55475da90280ec74c02115
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08609933B2
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