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The Effect Of Enzyme Enzymes On The Concentration Of An Enzyme

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Introduction
Organisms cannot rely entirely on spontaneous reactions to produce all the materials necessary for life. These reactions occur much too slowly. To produce these materials quicker, cells rely on enzymes, biological catalysts, to speed up these reactions without being consumed. (General Biology I, Martineau, Dean, Gilliland, & Soderstrom, Lab Manual, 2017, 43). To produce these materials quicker, the activation reaction much be lowered, a very important part of this lab. Each enzyme acts on a specific molecule, or set of molecules, called a substrate (43). The enzyme binds to this substrate, forming an enzyme-substrate complex. An enzyme is a protein whose structure is determined by the sequence of amino acids groups that …show more content…

Methods
Experiment 1: Constructing a Standard Curve
The students first prepared to construct a standard curve. To do this, each group measured the absorbance of starch solutions of unknown concentrations treated with IKI (General Biology I, Martineau, Dean, Gilliland, & Soderstrom, Lab Manual, 2017, 45). The absorbance values were determined for a range of samples, and plotted on a graph. A line of best fit was then used as a reference to determine the amount of starch present in unknown samples.
Using the yellow tube, which included everything but starch, as the blank, each group zeroed their spectrophotometer. This was done so that any absorbance observed depends only on the amount of starch present, not on any other reagents (buffer, IKI). To zero the spectrophotometer, the wavelength was first set at 580nm, using knob 3 (45). Next, the groups made sure that the light next to “transmittance” was lit, and the chamber to be tightly closed. Having the chamber empty & closed tightly provides reference for the darkest condition possible. Using knob 1, the transmittance was turned until it read 0.0 (45). Before the groups used their blank test tube to zero the spectrophotometer, each needed to wipe the tube with kimwipes to ensure a clean reading. Turning knob 2, each group was then instructed to zero the absorbance, 0.000. Upon removing the blank, each trial was inserted into the chamber (46). The

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