Subject area |
Biochemistry |
More specific subject area |
Enzymology |
Type of data |
Synthetic experimentals/characterization, tables, graphs, figures |
How data was acquired |
NMR (JEOL ECS-400 400 MHz), IR (Nicolet Avatar FTIR), UV–vis (Shimadzu UV-2450 with TCC-240A cell chamber), HPLC (Agilent 1200 system with degasser, photodiode array detector, and temperature-controlled autosampler) |
Data format |
Analyzed |
Experimental factors |
All analytical standards and reagents were confirmed to be >95% purity |
Experimental features |
The synthesis and characterization of 2,2-diphenylethyl glucosinolate; HPLC standardization of glucosinolate, isothiocyanate, nitrile, and amine analytes; HPLC reaction progress curves for experiments with (1) variable substrate concentration, (2) variable enzyme concentration, (3) variable buffer pH, and (4) variable temperature; tables of initial velocities of hydrolysis/formation |
Data source location |
Sioux Falls, SD |
Data accessibility |
The data are available with this article. |