反応 #78828
ord-e7f1a623706c40468e11efc782f9fa6d
溶媒
反応条件
後処理
- 1その他Substrate stock solutions were prepared
- 2その他to provide substrate
- 3濃縮solutions of various concentrations (final concentration of DMSO in each substrate solution
- 4その他30-100 mg, were placed in a microcentrifuge tube
- 5workup.ADDITION1.3 ml of substrate solution was added
- 6その他the mixture was bath-sonicated
- 7workup.ADDITIONto completely disperse the particles
- 8その他provided every 45-60 minutes
- 9その他The mixture was then removed from the water bath
- 10workup.WAITcentrifuged at 14,000 rpm for 30 minutes
- 11その他sonication to the beginning of centrifugation
- 12温度increase in free p-nitrophenol
- 13濃縮concentration
- 14その他from the absorbance due to light scattering of the particle dispersion of particles in 0.1 M Tris buffer (prepared identically as above) at 410 nm
実験手順
Substrate stock solutions were prepared by dissolving ˜50 mg BAPNA or suc-AAPF-PNP in DMSO; these stock solutions were then diluted with DMSO and 0.1 M TRIS/HCl buffer (pH 7.4) to provide substrate solutions of various concentrations (final concentration of DMSO in each substrate solution was 15% v/v). A measured quantity of particles; 30-100 mg, were placed in a microcentrifuge tube, 1.3 ml of substrate solution was added, and the mixture was bath-sonicated to completely disperse the particles. The mixture was then placed in a water bath at 30° C. for 5-6 hours, with additional agitation provided every 45-60 minutes. The mixture was then removed from the water bath and centrifuged at 14,000 rpm for 30 minutes. The reaction time was measured from initial sonication to the beginning of centrifugation. Catalytic activity was determined from the increase in free p-nitrophenol concentration, measured by UV/VIS spectroscopy at 410 nm with an extinction coefficient of 8500 M−1 cm−1. The measured absorbance was compared to that of the substrate solution at 410 nm and from the absorbance due to light scattering of the particle dispersion of particles in 0.1 M Tris buffer (prepared identically as above) at 410 nm. These contributions to the absorbance were subtracted from the total absorbance at 410 nm to obtain the absorbance due to free p-nitrophenol. Each data point was calculated based on the average of 3 to 7 trials.