Outline how colorimetry could be used to investigate membrane permeability.
1. Use plant tissue with soluble pigment in vacuole. Tonoplast & cell-surface membrane disrupted = ↑ permeability = pigment diffuses into solution.
2. Select colorimeter filter with complementary colour. 3. Use distilled water to set colorimeter to 0. Measure absorbance/ % transmission value of solution.
4. high absorbance/ low transmission = more pigment in solution.
Water diffuses across semi-permeable membranes from an area of higher water potential to an area of lower water potential until a dynamic equilibrium is established.
Passive process requires no energy from ATP hydrolysis.
Net movement of small, lipid-soluble molecules directly through the bilayer from an area of high concentration to an area of lower concentration (i.e. down a concentration gradient).
Specific channel or carrier proteins with complementary binding sites transport large and/ or polar molecules/ ions (not soluble in hydrophobic phospholipid tail) down concentration gradient
Channel: hydrophilic channels bind to specific ions = one side of the protein closes & the other opens
Carrier: binds to complementary molecule = conformational change releases molecule on other side of membrane; in facilitated diffusion, passive process; in active transport, requires energy from ATP hydrolysis
Active process: ATP hydrolysis releases phosphate group that binds to carrier protein, causing it to change shape.
Specific carrier protein transports molecules/ ions from area of low concentration to area of higher concentration (i.e. against concentration gradient).
Movement of a substance against its concentration gradient is coupled with the movement of another substance down its concentration/ electrochemical gradient.
Substances bind to complementary intrinsic protein: symport: transports substances in same direction antiport: transports substances in opposite direction e.g. sodium-potassium pump.
How does co- transport of a glucose molecule occur?
1. Sodium ions are actively transported out of epithelial cells, by the sodium-potassium pump, into the blood. This takes place in one type of protein-carrier molecule found in the cell-surface membrane of the epithelial cells.
2. This maintains a much higher concentration of sodium ions in the
lumen of the intestine than inside the epithelial cells.
3. Sodium ions diffuse into the epithelial cells down this concentration gradient through a different type of protein carrier (co-transport protein) in the cell-surface membrane. As the sodium ions diffuse in through this second carrier protein, they carry either amino acid molecules or glucose molecules into the cell with them.
4. The glucose/amino acids pass into the blood plasma by facilitated diffusion using another type of carrier.
Outline how colorimetry could be used to investigate membrane permeability.
1. Use plant tissue with soluble pigment in vacuole. Tonoplast & cell-surface membrane disrupted = ↑ permeability = pigment diffuses into solution.
2. Select colorimeter filter with complementary colour. 3. Use distilled water to set colorimeter to 0. Measure absorbance/ % transmission value of solution.
4. high absorbance/ low transmission = more pigment in solution.
Water diffuses across semi-permeable membranes from an area of higher water potential to an area of lower water potential until a dynamic equilibrium is established.
Passive process requires no energy from ATP hydrolysis.
Net movement of small, lipid-soluble molecules directly through the bilayer from an area of high concentration to an area of lower concentration (i.e. down a concentration gradient).
Specific channel or carrier proteins with complementary binding sites transport large and/ or polar molecules/ ions (not soluble in hydrophobic phospholipid tail) down concentration gradient
Channel: hydrophilic channels bind to specific ions = one side of the protein closes & the other opens
Carrier: binds to complementary molecule = conformational change releases molecule on other side of membrane; in facilitated diffusion, passive process; in active transport, requires energy from ATP hydrolysis
Active process: ATP hydrolysis releases phosphate group that binds to carrier protein, causing it to change shape.
Specific carrier protein transports molecules/ ions from area of low concentration to area of higher concentration (i.e. against concentration gradient).
Movement of a substance against its concentration gradient is coupled with the movement of another substance down its concentration/ electrochemical gradient.
Substances bind to complementary intrinsic protein: symport: transports substances in same direction antiport: transports substances in opposite direction e.g. sodium-potassium pump.