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Diffusion
= net movement of molecules/ ions from region of higher to lower conc until evenly distributed
no net movement
equilibrim
passive: energy comes from natural, inbuilt motion of particles
not external sources e.g. ATP
particles constantly in motion due to possessing KE
random motion of particles: constantly bouncing off one another and other objects e.g. container vessel
most substances don’t easily pass across membrane
e.g. charged ions and polar molecules don’t diffuse easily due to hydrophobic nature of fatty acid phospholipid tails
can pass: small, non-polar molecules e.g. O2 and CO2
Factors affecting rate
concentration gradient
steeper = increased diffusion
= difference in concentration
e.g. blood capillary/ vessels: O2/CO2 conc
Temperature
>KE = > movement = faster diffusion
SA
increased through folding e.g. microvilli in intestine/ cristae in mitochondria
increased size = decreased SA:Vol = decreased rate
diffusion distance
> distance = < diffusion
e.g. blood capillaries 1 cell thick, alveoli walls very thin
properties of molecules/ ions
large = slower, > energy required
non-polar = quicker, as soluble in non-polar phospholipid bilayer
facilitated diffusion
= with aid of proteins
for charged ions e.g. Na+ and Cl- and large polar molecules e.g. glucose and amino acids
through transmembrane channels and carrier proteins
passive, down conc grad
Channel proteins
integral proteins forming water-filled hydrophobic channels, allowing water-soluble ions to pass
selective dur to diameter and charged groups
some always open, some gated and open only in presence of specific ion
or specific voltage
Carrier proteins
span membrane
when molecule e.g. glucose present, binds to protein
causing it to change shape so molecule released to other side of membrane
no external energy needed
direction of movement of molecules diffusing across membrane depends on relative conc on each side of membrane
but net movement always down conc grad
osmosis
= net movement of water from region of high water potential (dilute_ to region of lower water potential (concentrated) through a selectively permeable membrane
involved solutions: solution dissolved in solvent
water moves down water potential gradient until dynamic equilibrium established and no more net movement of water
solute and water molecules in random motion due to KE
selectively permeable plasma membrane only allows water molecules across it, not solute
water pot of pure water
at standard temp and P = 0kPa
0 = highest possible WP
> solute = > -ve WP (i.e. <0kPa)
Osmosis: animal cells
water in = lysis
hypotonic solution i.e. higher WP than RBC
dilute/ lower solute conc
because has no cell wall
Isotonic: dynamic equilibrium
equal WP
water out = crenation
hypertonic solution
> concentrated than blood cell
lower WP in solution than RBC
Osmosis: plant cells
water in = turgid + large vacuole
has limited expansion, so pressure builds up resisting further entry of water
protoplast (all but central vacuole adn cell wall) kept pushed against cell wall
allows plant to stand up = support + strength
water out = flaccid + plasmolysis + small vacuole
protoplast pulled away from cell wall
vol of cell decreases
plant wilts
RP3: water potential of plant tissue
Determining water potential of potato tuber cells
label 6 boiling tubes with conc of sucrose
use 1.0 moldm-3 sucrose solution to make up 20cm3 of sucrose solution of each of following concs: 0.0, 0.2, 0.4, 0.6, 0.8, 1.0
Put boiling tubes with sucrose solution in water bath at 30C
use thermometer to check temps in all tubes reach 30C
using potato chip cutter, cut 6 chips from potato tuber
remove peel and use ruler, scalpel and tile to cut all chips to same length
blot potato chips dry (don’t squeeze)
weight initial masses of each chip
transfer potato chips to boiling tubes in water bath
remove chips after 20 mins
blot chips dry and reweigh for final masses
calc change in mass and calc % change in mass
plot graph to determine conc of sucrose which has same water potential as potato tuber cells
Active transport
= movement of molecules and ions through cell membrane from region of lower conc to higher conc using ATP (from respiration) and carrier proteins
How energy released from ATP
majority of energy stored in ATP between 2nd and 3rd phosphate bond
high energy bonds = unstable with low activation energy, so are easily broken
phosphorylation = adding phosphate group to ADP to form ATP
condensation reaction
catalysed by ATP synthase
(energy added)
removal of phosphate group to form ADP and release energy
hydrolysis reaction
catalysed by ATP hydrolase
(energy released)
ATP+H2O → ADP +Pi + E
Pi = inorganic phosphate
E = energy
reversible reaction
Process of active transport
molecule/ ion binds to receptor sites on carrier protein
ATP binds to protein causing it to split into ADP and Pi
energy released used to change shape of protein and open to opposite side
molecule/ ion released to other side of membrane
phosphate molecule released, causes protein to revert to original shape
allowing process to
ADP and Pi will recombine during respiration to form ATP
Active transport vs facilitated diffusion
both use carrier proteins
f.d. down conc grad
a.t. against conc grad
carrier proteins have very specific tertiary structures with specific binding sites so will only transport specific substances to membrane
co-transport
= coupled movement of substances across cell membrane via carrier protein
2 types of molecules moved across membrane at same time (movement of one dependent on other)
involves combination of facilitated diffusion and active transport