Professional Documents
Culture Documents
2020 Practical (1D) Investigating Properties of Cell Membrane
2020 Practical (1D) Investigating Properties of Cell Membrane
(SL / HL)
(I) Introduction
All cells are bounded by a plasma membrane, but many internal cell structures are also bounded by
membrane. These include the tonoplast, the membrane surrounding a plant cell vacuole, the double
membrane (envelope) surrounding the nucleus, mitochondria and chloroplasts, and the membranes
of other organelles such as vacuoles, vesicles, endoplasmic reticulum, and Golgi apparatus. All
these membranes have basically the same structure.
One of the roles of membranes is to control what passes across them. Membranes are partially
permeable, i.e. they do not normally allow large molecules to pass across them. Many plant cells
contain pigment molecules in the cytoplasm. In beetroot cells these molecules are large and reflect
red light, so that a solution of them turns a shade of pink. Many pigment molecules are also affected
by pH and change colour at different pH values. Litmus, for example, is a plant pigment and is blue
in alkali and red in acid. Ethanol is an organic solvent. Proteins are stable at a particular pH and
become denatured outside this. The normal pH of cells 7.2.
(II) Materials
• beet root (diced) • stopwatch
• test tubes & racks • colorimeter (absorbance at 565 nm)
• water bath (50oC & 80oC) • acetone
• ice cubes • ethanol
(III) Procedure
It is important to read through the procedure and think about what information you will need to
collect, and draw a results table before you begin the experiment.
1
3. Prepare 4 test tubes each containing 10 cm3 of water and label each with one of the
temperatures (80°C, 60°C, 40°C, room temperature, 20°C, ice 0°C) or the stable
temperatures provided by the water baths.
4. Label 4 small beakers containing 50 cm3 of water and place them in the water baths set at
approx. 80°C and 50°C, leave one at room temperature and place one on ice - allow water
to get to temperature (5 min but check with thermometer).
5. Carefully place 5 discs in the small beaker of water in the 80°C water bath and leave for
exactly 1 min. Use a timer.
6. Carefully remove the 5 discs and place in one of the labelled test tubes. Leave for 20 min
then shake gently.
7. Repeat this procedure at the other 3
temperatures.
8. Estimate the intensity of the pigment in solution
by measuring light absorbance using the
colorimeter (at 565 nm).