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Enzymes as organic catalystsEnzymes as organic catalysts
• Enzyme is for Enzyme is for lowering of lowering of activation energy.activation energy.
Energy level of substrate particles
No. of substrate particles
EE’
E: Activation energy when enzyme is not added.
E’:Activation energy when enzyme is added.
Lock and key hypothesisLock and key hypothesis
Enzyme
Active site
substrate
Enzyme-substrate complex
Products
Induced fit model
The active site is induced by the substrate to change its shape to fit
the shape of the substrate.
Enzyme can catalyze both forward and backward reactions. It does not alter the equilibrium position of a biochemical reaction. The normal progress of a biochemical reaction is due to the immediate removal of the end product.
Specificity
The degree of specificity varies from one enzyme to another.Intracellular enzyme works on one particular substrate.Extracellular enzyme works on a range of related substrates.
Factors affecting enzymatic Factors affecting enzymatic activity activity
temperature pH value Substrate concentration
enzymeconcentration
cofactors inhibitors
Temperature affects the energy content and hence the mobility of the enzyme and substrate molecules. Higher temperature enables enzyme and substrate molecules to collide more frequently and therefore facilitates the substrate molecule to bind with the active site of the enzyme.
If the temperature is too high (above optimum), the polypeptide chains made up the enzyme will vibrate too much so that the structure will be disrupted, and the enzyme is said to be denatured.
Temperature coefficient QTemperature coefficient Q1010
Q10 = Reaction rate at (X+10)oC
Reaction rate at XoC
When the temperature is below the optimum temperature, Q10 usually is 2.
When the temperature is above the optimum temperature, Q10 usually is less than 1.
pH
Changes in pH alter the ionic charge on the enzyme surface, thus causing change in shape of its active site, thus diminishing its catalytic activity. If extremes of pH is encountered, the enzyme is denatured and loses its catalytic function.
Reversible inhibitors: The effect is temporary. The inhibiting effect can be eliminated if the reversible inhibitor is removed.
Irreversible inhibitors: This kind of inhibitor disrupts the bonds of the polypeptides which form the enzyme. Therefore the shape of the active site is altered permanently and loses its catalytic properties.
Usually the end product of a biochemical reaction acts as competitive inhibitor. This is known as end-product inhibition. Immediate removal of the end product facilitates enzyme reaction.
Non-competitive Inhibitor
Non-competitive Inhibitor
Normal substrate
Allosteric site
The shape of the enzyme changes so that the normal substrate cannot bind to it.
Example of competitive inhibitor
Sulphonamides have very similar molecular shape to amino benzoic acid, a compound essential for growth of many pathogenic bacteria. Therefore, sulphonamide acts as competitive inhibitor to check the growth of many bacteria in treatment of many diseases caused by bacteria.
Example of non-competitive inhibitor
Diisopropylflurophosphate (DFP), a nerve gas used in warfare is a non‑competitive inhibitor. DFP acts on enzyme cholinesterase which is involved in synaptic transmission. DFP causes prolonged muscle contraction and death is the end result.
Enzyme concentration and substrate concentration affects the concentration of the enzyme-substrate complex and hence the rate of enzyme-catalysed biochemical reaction.
Enzyme cofactorIt is non-protein substance which makes some
enzyme to function more efficiently.
Enzymeactivator
Coenzyme Prostheticgroup
Cofactors
Enzyme activator
• It is an inorganic ion which loosely bound to an enzyme or an substrate to increase the chance to an enzyme-substrate complex forming. Some times, the inorganic ions are free and does not bind to the enzyme or substrate,
• e.g. copper, iron, calcium, Cl- etc.
Coenzyme
• It is an organic non-protein molecule firmly associated with the enzyme and is essential for enzyme activity.
• It acts a carrier for transferring chemical groups or atoms from one enzyme to another.
• Many coenzymes are synthesized from vitamins.
• e.g. NAD
Prosthetic group
• It is an organic non-protein group which is tightly bound to the enzyme or as an integral part with the enzyme.
• It can act as carriers of atoms or electrons while transferring one compound to another in an overall metabolic pathway.
• e.g. FAD, haemoglobin etc.