Measuring the rate of the reaction

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Presentation transcript:

The effect of incubation time on the rate of an enzyme catalyzed reaction

Measuring the rate of the reaction Objectives To monitor the progress of an enzyme catalyzed reaction (Acid phosphatase). To determine the initial rate of the reaction (Vi). Important terms and points: Enzyme kinetics Measuring the rate of the reaction Initial velocity

Acid phosphatase Time Enzyme Conc pH Temp Substrate conc Inhibitor

Enzyme kinetics The central approach for studying the mechanism of an enzyme-catalyzed reaction is to study enzyme kinetics. It determines the rate of the enzymatic reaction (velocity) and its changes in response with the changes in parameters such as substrate concentration, enzyme concentration, pH, temperature.

Measuring the rate of reaction (velocity) The progress of an enzyme catalyzed reaction may be followed by measuring either the amount of substrate consumed, or Amount of product formed Velocity (V) = rate of reaction= change in [P] or [S] per unit time Unit : µmoles/minute per unit time.

Product formed (µmole) initial velocity The initial rate of reaction is used in the study of enzyme kinetics The initial rate of reaction (Vi) is measured as the slope at the origin (time= 0). Product formed (µmole) Plateau

Why we measure initial velocity? Product formed (µmole) Plateau The rate of the reaction is highest at time zero and decreases with increasing time, eventually falling to zero itself, reaching a plateau. This usually occurs either when all the substrate is used up or when equilibrium is reached. The Solution is to Measure V at very early times in reaction, before [S] decreases significantly The initial rate of reaction, vi, measured as the slope to the above curve at the origin (time= 0)

Acid phosphatase In this experiment, you will measure the velocity of the reaction catalyzed by purified acid phosphatase (ACP) from wheat germ. Acid phosphatase is a phosphatase that acts on monoesters of orthophosphoric acid. It does not act on phosphoric diesters or triesters. Acid phosphatase is an important enzyme that plants use to obtain their energy from phosphate. Acid phosphatase’s function in plants is to hydrolyze phosphate esters during energy metabolism.

Acid phosphatase from wheat germ The enzyme catalyzes the hydrolysis of p-nitrophenyl phosphate to inorganic phosphate and p-nitrophenol, under acidic conditions (pH=5.7), with optimum temperature 37◦C Mg++ ion act as an activator for the enzyme ACP Mg++ pH=5.7 37◦C

Principal of the enzyme assay in vitro 2. 1. Both p-nitrophenyl phosphate and p-nitrophenol are colorless at acidic pH values. Addition of alkaline solution, p-nitrophenol is converted to a p-nitrophenolate (yellow color) and concentration can be measured at 405 nm. Note: Since ACP works under acidic condition, adding alkaline will cause the enzymatic reaction to stop.

Method: The effect of incubation Time The reaction is stopped after 5 minutes intervals (by Addition of KOH ), hence called Fixed-time assay

Method Prepare a series of seven reaction tubes labeled 0 through 30 minutes at 5 minute intervals (Blank, 5, 10 … minutes). Follow the following addition protocol for all the tubes: Place in a water bath maintained at 37 ºC for 5 minutes.

To start the reaction  add 0.5ml of E To stop the reaction  add 0.5ml of KOH Start at (min) 2 4 6 8 10 Stop at (min) 5 12 19 26 33 40 Add KOH to blank ((FIRST)), to prevent the reaction from happening. After all the reactions have been terminated, determine the absorbance at 405 nm for each sample against blank.

To convert the time table to an easier way try the following Tube 5 10 15 20 25 30 Start at (min) 2 4 6 8 Stop at (min) 12 19 26 33 40 To convert the time table to an easier way try the following

Results [P] (µmoles) Absorbance at 405nm Time (min) 5 10 15 20 25 30 5 10 15 20 25 30 [P] = ( A x 106 ) / E X L= µmole E= extension coefficient=18.8x103 A= absorbance L= path length (1 cm)

Product formed (µmole)

Discussion Draw the graph [ do not forget the title and the units ] X axis = Time (min) Y axis = [P] (µmoles) Calculate from the graph the value initial velocity Principle Comment on the graph that you get in details

Questions How is the initial velocity of an enzymatic reaction determined? What are the factors that influence the rate of enzyme catalyzed reactions? What is the pH which the acid phosphatase activity is measured?