Why was absorbance measured at 420 nm in the enzyme kinetics experiment? To monitor the
pls explain
Why was absorbance measured at 420 nm in the enzyme kinetics experiment? To
monitor the
a. decrease in catechol concentration
b. increase in quinone concentration
c. decrease in polyphenol oxidase concentration
d. polyphenol oxidase-catechol complex concentration
Lineweaver-Burk plot is the most used linearization method of the MichaelisMenten equation, but the main drawback is a/an:
a. overemphasis to low substrate concentration and less emphasis to high
substrate concentration.
b. overemphasis to high substrate concentration and less emphasis to low
substrate concentration.
c. exaggeration to both ends of the reciprocal of the substrate concentration.
d. lack of independent variables to x- and y- coordinates
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