Biological catalysts Enzymes.

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Presentation transcript:

Biological catalysts Enzymes

Catalysts A catalyst is a substance that speeds up the rate of a chemical reaction but is not itself changed by the reaction.

hydrogen peroxide water + oxygen 2H2O2 2H2O + O2 Potassium Iodide Hydrogen peroxide breaks down to water and oxygen hydrogen peroxide Potassium Iodide water + oxygen 2H2O2 2H2O + O2

Potassium Iodide (KI) Is not a biological chemical, it is not an enzyme. But there is an enzyme, called Catalase, which speeds up the decomposition of Hydrogen peroxide to water and Oxygen

Enzymes act as biological catalysts They occur inside cells or are secreted by the cells. Catalase is the enzyme that catalyses the break down of hydrogen peroxide. Catalase

Catalase is found in liver Add a little liver to some Hydrogen peroxide and observe what happens. Have a paper towel handy Friday’s Practical!

Enzymes are proteins Proteins are long molecules (made up of Amino acids) that are folded into a specific shape. catalase amylase pepsin trypsin

The part of an enzyme where the reaction occurs is known as the active site

The molecule the enzyme acts on is known as the substrate molecule Substrate molecules Active site: The site on the enzyme where the reaction occurs Enzyme

The molecule the enzyme produces is known as the product molecule Product molecules Active site: The site on the enzyme where the reaction occurs Enzyme

The enzyme can be re-used

Each enzyme is specific to one substrate molecule or type of molecule The lock and key hypothesis states that the active site specifically matches the shape of the substrate molecule enzyme active site

The rate of an enzyme controlled reaction is affected by temperature At low temperatures enzyme controlled reactions go slowly because the molecules have low kinetic energy.

When temperature increases the reaction also increases as the molecules have more kinetic energy The temperature at which the rate of reaction is fastest is known as the optimum temperature

After the optimum temperature the heat causes the enzyme to denature The enzyme changes shape (denatured) and the active site no longer matches the shape of the substrate molecule. Enzyme is not ‘killed’ off! Running a high temperature is not good

Rate of reaction of an enzyme reaction changes at different temperatures Optimum temperature Enzyme is denaturing Molecules gain kinetic energy Rate Of Reaction 0 10 20 30 40 50 60 70 Temperature/oC

The activity and shape of enzymes is also affected by pH Enzymes prefer to work at an optimum pH. Outside of its pH range the enzyme is denatured. Enzymes in the stomach have an optimum pH of 2 Optimum pH pepsin amylase Rate Of Reaction 1 2 3 4 5 6 7 8 9 10 11 12 pH

Prepare a Fair test investigation for…

Design a Fair Test: What affect does pH have on Liver Enzyme reaction rates? TASK: You need to design an experiment to find out how the pH of a solution affects the enzyme, Catalase (found in Liver cells), which speeds up the decomposition of Hydrogen peroxide to water and Oxygen Aim: / Hypothesis: Independent variable & Dependent variable: Other variables: (Name at least three variables that you need to keep the same.) Equipment: Liver (small amount, i.e. 0.5 cm3), Hydrogen peroxide, Detergent in dropper bottle, 3 boiling tubes, stop watch, acid, alkali, distilled water   Method: (Include diagrams) Results: / Discussion: / Conclusion:

Enzymes are used in biological washing powders Proteases break down the coloured, insoluble proteins that cause stains to smaller, colourless soluble polypeptides. Can wash at lower temperatures

Enzymes are used in the food industry Pectinase break down substances in apple cell walls and enable greater juice extraction. Lactase breaks down lactose in milk into glucose and galactose. This makes milk drinkable for lactose intolerant people.

Enzymes are used in seed germination starch amylase secreted embryo plant absorbed maltose

Summary Keywords: catalyst catalyse protein catalase amylase lactase pectinase trypsin pepsin substrate active site product temperature optimum denature pH protease enzyme