ADA Kinetic Assay Runs
- During the previous lab entry, the molar absorptivities of adenosine and inosine were calculated. Adenosine was found to have a higher molar absorptivity at 235.
- It was concluded from the previous period that the absorption of adenosine should decrease over time. A kinetic assay scan of the reaction containing 2.7 mL of 0.05 M sodium phosphate buffer, 300 μL of 3.07 mM adenosine, and 15 μL of 42 μM ADA was taken. The final concentration for each reagent are 0.0450 M, 0.307 mM, and 0.21 μM, respectively.
- The program was set to Kinetics with the wavelength at 235 for a collection span of 600s.
- In the scan, it can be observed that the absorption of adenosine is not decreasing over time. Instead, the absorption is increasing. Also, the signal for the absorption of adenosine is over 1.
- It was decided that the next measurements, the concentration of adenosine should be decreased by decreasing the volume in th cuvette. This is to ensure that the absorbance is below 1.
- As seen above, decreasing the concentration of adenosine maintained an absorbance below 1. However, the absorbance is still increasing. The addition of 50 μL ADA intensified the increase of absorbance in comparison to the addition of 15 μL ADA.
|Volume of ADA (μL)
||Concentration of ADA (μM)
||Volume of phosphate buffer (mL)
||Concentration of phosphate buffer (M)
||Volume of adenosine (μL)
||Concentration of adenosine (mM)
UV-vis of Adenosine and Inosine
- Due to the inconsistent behavior observed from the data above, it was decided to remeasure the absorbance of adenosine and inosine in the UV-visible spectra. The program was returned to the Spectrum setting. The measurement was adjusted to 400-200 nm.