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Announcements Post Lab 3 and Pre Lab 4 are due by the time your lab meets next. LNA Enzymes is assigned today, and due next week within the first 5 minutes of your lab period.
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Exercise 2B: 1.Experimental Plates: Examine your plates and observe the type of bacteria or fungal growth that appears on each. 2.Streak Plates: Examine the colonies; TA will be around to assign your “Skills” score 3.Complete your LNA: Exercise 2 and turn it in as directed by your TA.
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Exercise 3A: Spectrophotometry Goals: Understand the process by which spectrophotometry can be used to quantify experimental results. Develop skills taking measurements using a spectrophotometer.
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Spectrophotometry Measurement of light absorption or transmission through a solution
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Types of photometers: Colorimeters and spectrophotometers measure the amount of light absorbed by solutions. Turbidimeters and nephelometers measure the light scattered by suspensions. Fluorimeters measure the fluorescence produced by absorbed light.
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Light through a solution: Example ONP (o-nitrophenol) Absorbs blue light and allows yellow light to pass through. Solution therefore appears yellow.
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Absorption Spectrum A plot of the relative amount of light absorbed by a compound as a function of the wavelength Absorption spectrum of ONP
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Components of a Typical SpectrophotometerComponents of a Typical Spectrophotometer
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3A Techniques: Using colored water, take measurements using a spectrophotometer. Keep cuvettes free from fingerprints. Align cuvette correctly each time you take a measurement.
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3B: Enzymes Goals: Describe the principles of enzymatic reactions Use the principes of spectrophotometry to determine the concentration of the product of an enzyme- catalyzed reaction. Determine the effect of ß-galactosidase concentration on the rate of cleavage of ONPG.
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Introduction: Enzymes increase the rate of reactions, but do not allow reactions to occur that could not occur otherwise.
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There are two ways to increase the rate of a chemical reaction 1.Increase the average kinetic energy by raising the temperature, or 2.Lower the activation energy by adding a catalyst
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Catalyzed Reaction Reach a Maximum Rate
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Enzyme Regulation
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-galactosidase O-nitrophenyl- -D-galactopyranoside (ONPG)
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Hypothesis Generation Identify one characteristic you expect to change as you add ONPG, buffer, and enzyme A yellow solution is produced as o- nitrophenolate is produced
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Rephrase your speculation to the if, then format If ONPG is catalyzed by -galactosidase, and I add the enzyme in various amounts, the products of o- nitrophenolate (yellow color) will differ as well
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Independent Variable Amount of -galactosidase
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Dependent Variable OD 420 reading of o-nitrophenolate produced
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Controls ONPG + Buffer, but no enzyme added and Buffer + enzyme, but no ONPG added
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The Experiment: Take measurements of various amounts of ONPG catalyzed by -galactosidase
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