MOCK 1 Flashcards

(309 cards)

1
Q

Energy in living organisms needed for:

A

 Anabolic reactions:
 Protein synthesis / DNA replication / glycogenesis / polymerisation
 Cellular work:
 Active transport / movement of chromosomes / sliding filaments /
movement of vesicles
 Movement
 Maintenance of body temperature in endotherms

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2
Q

Glucose is stable due to

A

its activation energy – lowered by enzymes and raising the energy
level of glucose by phosphorylation

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3
Q
A
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4
Q

Features of ATP that make it suitable as the universal energy currency:

A

 Loss of phosphate / hydrolysis, leads to energy release
 Small packets of energy
 Small / water-soluble, so can move around cell
 Immediate energy donor
 Acts as link between energy-yielding and energy-requiring reactions
 High turnover

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5
Q

Excess energy during transfer and reactions are converted into

A

thermal energy

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6
Q
A
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7
Q

glycolysis happens in

A

cytoplasm

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8
Q

Glycolysis

A

 Glucose phosphorylated by ATP
 Raises energy level / overcomes activation energy to form fructose bisphosphate
 Lysis / splitting of glucose / hexose
 Breaks down to two TP (triose phosphate)
 6C (hexose bisphosphate) into 2 3C (triose phosphate) which is then
dehydrogenated; hydrogen transferred to NAD
 2 reduced NAD formed from each TP
 4 ATP produced; final net gain of 2 ATP
 Pyruvate produced

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9
Q

link reaction happens in

A

mitochondrial matrix:

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10
Q

link reaction

A

 Pyruvate passes by active transport from the cytoplasm through the outer and
inner membranes of a mitochondrion
 Undergoes decarboxylation, dehydrogenation (hydrogen transferred to NAD) and
combined with coenzyme A (CoA) to give acetyl coenzyme A

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11
Q

role of CoA in link reaction

A

 Combines with acetyl group in the link reaction
 Delivers acetyl group to the Krebs cycle
 Acetyl group combines with oxaloacetate

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12
Q

krebs cycle happens in

A

mitochondrial matrix

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13
Q

krebs cycle

A

 Reactions are catalysed by enzymes
 Acetyl CoA combines with a four-carbon compound (oxaloacetate) to form a six
carbon compound (citrate)
 Citrate is decarboxylated and dehydrogenated – through intermediate compounds – to yield CO2 (waste gas) and hydrogens are accepted by hydrogen carriers (NAD
and FAD) to form reduced NAD and reduced FAD
 Oxaloacetate is regenerated to combine with another acetyl CoA
 Two CO2 are produced
 One FAD and three NAD molecules are reduced
 One ATP molecule is generated (substrate-level phosphorylation)

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14
Q

oxidative phosphorylation happens in

A

inner mitochondrial membrane

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15
Q

Oxidative phosphorylation

A

 Reduced NAD / FAD are passed to the electron transport chain (ETC) on the inner
membrane of the mitochondria (cristae)
 Hydrogen released from reduced NAD / FAD and splits into electron and proton
 Electrons are passed along the electron carriers on the ETC
 Energy released from the electrons, pumps protons into the intermembrane space
 Proton gradient is set up
 Protons diffuse back through the membrane – through ATP synthase – down the
potential gradient
 Oxygen acts as the final electron acceptor; acts as proton acceptor to form water;
allows ETC to continue and ATP to be produced

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16
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A
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17
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18
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19
Q
A

NAD

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20
Q

Comparison between the structures of ATP and NAD:

A

 Both have ribose sugars
 ATP has 1 ribose, while NAD has 2
 Both have adenine base
 NAD has nicotinamide base
 ATP has three phosphates

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21
Q

Function of NAD in the cytoplasm of a cell:

A

 Acts as a hydrogen carrier
 Acts as a coenzyme / enables dehydrogenases to work
 Used in glycolysis / anaerobic respirations

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22
Q

 Anaerobic respiration:

A

Alcoholic fermentation (conversion of glucose to ethanol):
 Lactic fermentation (conversion of glucose to lactate):

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23
Q

Alcoholic fermentation (conversion of glucose to ethanol):

A

 In various microorganisms (e.g. yeast) and in some plant tissues
 The hydrogen from reduced NAD is passed to ethanol (CH3CHO); releasing the NAD
and allows glycolysis to continue
 Pyruvate is decarboxylated into ethanal, which gets reduced to ethanol (C2H5OH) by
the enzyme ethanol dehydrogenase
 Irreversible reaction
 NAD regenerated, hence glycolysis can continue

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24
Q

 Lactic fermentation (conversion of glucose to lactate):

A

 In mammalian muscles when deprived of oxygen
 Pyruvate and reduced NAD formed by glycolysis
 Pyruvate is decarboxylated by pyruvate decarboxylase into ethanal – which acts as
a hydrogen acceptor from reduced NAD
 NAD regenerated, hence glycolysis can continue
 Reversible reaction

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The structure of the mitochondrion is related to its function:
 Double membrane  Inner membrane is folded / cristae has a large surface area; has ATP synthase / stalked particles; has carrier proteins / cytochromes for the site of ETC / chemiosmosis  Mitochondrial matrix contains enzymes; is the site of link reaction and the Krebs cycle  Outer membrane has protein carriers for pyruvate and reduced NAD  Intermembrane space has low pH due to high concentration of protons from ETC, creating a proton gradient between intermembrane space and matrix, resulting to the synthesis of ATP
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 The post-exercise uptake of extra oxygen is called the oxygen debt
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 Respiratory substrates:  Most energy liberated in aerobic respiration comes from the
oxidation of hydrogen to water, hence the greater the number of hydrogens in the structure the greater the energy value
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The energy value of a substrate us determined by
burning a known mass of the substance in oxygen in a calorimeter, where the energy liberated can be determined from the rise in temperature of a known mass of water in the calorimeter
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Lipids have a higher energy value than carbohydrates due to the
higher number of C-H bonds, hence yields more reduced NAD, so produces more ATP per gram, thus more aerobic respiration / oxidative phosphorylation / chemiosmosis; fats can only be broken down aerobically
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 Respiratory quotient:  Shows the
substrate used in respiration and whether or not anaerobic respiration is occurring
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RQ=
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For the aerobic respiration of glucose:
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For the aerobic respiration of fatty acid oleic acid:
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For anaerobic respiration (e.g. alcoholic fermentation):
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Or yields a high value (> 1.0), as some of the
respiration might still be aerobic  No RQ can be calculated for muscle cells using lactate pathway, as no CO2 is produced:
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he respiration of glucose in anaerobic conditions
oxygen is not available as a final electron acceptor, hence oxidative phosphorylation on the ETC, where most ATP are produced – produces less ATP than in aerobic conditions as only glycolysis (substrate-linked phosphorylation) occurs (only produces a net gain of 2 ATP); pyruvate converted to lactate which is energy rich
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Oxygen debt is needed to
Convert lactate to pyruvate in the liver cells, re-oxygenate haemoglobin, and to meet demands of continued increased in metabolic rate
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Adaptations of rice to grow with its roots submerged in water in terms of tolerance to ethanol from respiration in anaerobic conditions and the presence of aerenchyma:
 Aerenchyma in stem and roots which help oxygen to, move / diffuse, to the roots ;  Shallow roots  Air film trapped on underwater leaves  Has fast internode growth  Modified growth regulated by gibberellin  Anaerobic respiration underwater  Tolerance to high ethanol concentration  Ethanol dehydrogenase switched on in anaerobic conditions  Carbohydrates conserved
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Respirometers
 To measure rate of oxygen consumption during respiration  CO2 produced absorbed by concentrated solution of KOH / NaOH  Oxygen consumption in unit time read through the level of the manometer fluid against the scale, decrease or increase  Changes in temperature and pressure alter the volume of air in the apparatus, hence needed to be kept constant (e.g. electronic water bath & a control tube – with equal volume of inert material to the volume of the organisms to compensate for changes in pressure)  Can be used to measure the RQ of an organism done by noting down the found oxygen consumptions; set up with the same controls, but with no CO2 absorbing chemicals
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DCPIP / methylene blue – investigating the rate of respiration using a redox dye
 Turns from blue to colourless; the rate of change from blue to colourless is a measure of the rate of respiration; can be used to investigate effects of temperature / different substrate concentrations
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Photosynthesis is the
the fixation of CO2 and its subsequent reduction to carbohydrate, using hydrogen from water, taking place in the chloroplast; where two reactions are involved: light dependent reactions and light independent reactions
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The photosynthetic pigments involved fall into two categories:
primary pigments (chlorophylls) and accessory pigments (carotenoids) of which are arranged in light harvesting clusters called photosystems (I and II), where several hundred accessory pigment molecules surround a primary pigment molecule to pass absorbed light energy towards the primary pigment – the reaction centre
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light dependent reactions happens in
thylakoids (holds ATP synthase):
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Light energy is necessary for the synthesis of
ATP in photophosphorylation and the splitting of water (photolysis – photosystem II) into hydrogen ions (combine with a carrier molecule NADP to make reduced NADP) and oxygen – waste product
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Photophosphorylation of ADP to ATP are of two types:
cyclic and non-cyclic
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Cyclic phosphorylatio
 Only involves photosystem I  Light absorbed by photosystem I passed to the primary pigment resulting to the excitation of an electron for which is emitted from the chlorophyll molecule (photoactivation) and captured by an electron acceptor to be passed onto the electron transport chain  Protons from photolysis pumped into the membrane space to synthesise ATP from ADP and an inorganic phosphate group (Pi) by the process of chemiosmosis for which goes to the light independent stage (Calvin cycle) to produce complex organic molecules
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Non-cyclic phosphorylation
 Involves both the photosystems  Light is absorbed by both photosystems resulting to excited electrons emitted from the primary pigments of both reaction centres, which are then absorbed by electron acceptors and pass along the ETC  The primary pigment of photosystem I absorbs electrons from photosystem II for which receives replacement electrons from the splitting of water (photolysis)  Protons from photolysis pumped into the membrane space to synthesise ATP from ADP and an inorganic phosphate group (Pi) by the process of chemiosmosis for which goes the light independent stage (Calvin cycle) to produce complex organic molecules
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Light independent reaction (Calvin cycle) happens in
stroma
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Light independent reaction (Calvin cycle) – stroma :
 Carbon dioxide reaches the inside of a palisade mesophyll cell from the external atmosphere through the stomata by diffusion down a concentration gradient, and passes through air spaces; dissolves in film of water on cell surface then diffuses through cell wall / surface membrane of palisade cells  Using a series of enzyme-controlled reactions:  Fixation of carbon dioxide by combination with RuBP, a 5C compound, (carboxylation) – using Rubisco enzyme – to form an unstable 6C intermediate, resulting to 2 molecules of GP, a 3C compound; using ATP and reduced NADP from the light dependent reaction reduces GP to TP for which most of it regenerates to form RuBP while others undergo rearrangement of carbons to form pentose sugars / lipids / amino acids / hexose sugars; ATP is required for the phosphorylation of ribulose phosphate into ribulose bisphosphate
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Role of accessory pigment in photosynthesis:
passes energy to primary pigment; absorb light wavelengths that primary pigment does not; forms part of the light-harvesting cluster of pigments (photosystem)
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Chlorophyll absorb mainly in the
red and blue-violet regions of the line spectrum and reflects green light; whereas carotenoids absorb mainly in the blue-violet region of the spectrum
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An absorption spectrum
is a graph that shows the, absorbance / absorption, of different wavelengths of light by chloroplast pigments
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An action spectrum
is a graph of the rate of photosynthesis at different wavelengths of light, showing the effectiveness of different wavelengths related to their absorption and energy content
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action spectrum
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nvestigation to determine the effect of light intensity or light wavelength on the rate of photosynthesis using a
redox indicator (e.g. DCPIP) and a suspension of chloroplasts (the Hill reaction):
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The main external factors that affects the rate of photosynthesis:
light intensity and wavelength, temperature, and carbon dioxide concentration
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The rate of any process which depends on a series of reactions is limited by
the slowest reaction in the series
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Chromatography – to
separate and identify chloroplast pigments and carry out an investigation to compare the chloroplast pigments in different plants (reference should be made to Rf values in identification):
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chromatography process
 Usage of a chromatogram  Place spot of pigments on pencil mark at base of the paper  Dry and repeat to concentrate spot  Dip the paper / chromatogram in the solvent (ethanol) to travel up the paper  Measure distance travelled by solvent (front) and pigment (spot)  Calculate the Rf value = distance travelled by pigment spot / distance travelled by solvent front  Look up / compare results with known Rf values to identify pigments
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Chloroplasts can move within
palisade cells to maximise the amount of light absorption of light and to avoid damage by high light intensities
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In the light independent stage of photosynthesis, carbon dioxide combines with RuBP
to form a six-carbon compound, which immediately splits to form two three-carbon molecules (GP), these plants are called C3 plants; However, maize and sorghum plants – and most other tropical grasses – do something different, as their first compound that isproduced in the light independent reaction contains four carbon atoms, therefore are called C4 plants
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Rubisco catalyses
he reaction of both carbon dioxide and RuBP; oxygen with RuBP (photorespiration), causing less photosynthesis to take place as less RuBP available to combine with carbon dioxide; occurs readily in high temperatures and light intensity
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C4 plants keep
RuBP and Rubisco away from high oxygen concentrations in the bundle sheath cells around the vascular bundles
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Carbon dioxide is absorbed by the
tightly mesophyll cells (so O2 cannot reach the bundle sheath cells), which contains PEP carboxylase enzyme (has high optimum temperature and does not accept O2) catalysing the combination of CO2 with a 3C compound, PEP, resulting to oxaloactetate, 5C, which is converted into malate and passed to the bundle sheath cells – hence maintaining a high concentration of carbon dioxide – for which CO2 is fixated with RuBP in the light independent reaction; photorespiration is avoided
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The high surface area of the
thylakoid membrane and the large size and number of grana results to the high absorption of light, hence high photophosphorylation and more chemiosmosis; the large thylakoid space helps increase the proton gradient hence more ATP and reduced NADP produced, thus high rate of light independent reaction
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Homeostasis
to maintain a constant/stable internal environment in the body
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The importance of homeostasis in a mammal:
 To maintain a constant internal environment of blood and tissue fluids within narrow limits / set point, effects:  Low temperature, consequence: slowed metabolism / enzymes less active  High temperature, consequence: enzymes denatured  Low water potential, consequence: water leaving cells / cells shrink  High water potential, consequence: water enters cells / cells burst  Low blood glucose, consequence: effect on respiration  High blood glucose, consequence: water leaving cells / cells shrink  Control of pH, consequence: enzymes become less active
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Control mechanisms use a negative feedback loop involving:
 Receptor (sensor) detects changes in both internal and external stimuli (any change in a physiological factor being regulated) away from the set-point; nerve impulse sent to a central control or hormone released, which then reaches the effectors (muscles and glands) / target organs; effector performs corrective action, hence factor returns to set-point
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Continuous monitoring of the factor by receptors produces a
steady stream of information to the control centre that makes continuous adjustments to the output, hence the factor fluctuates around a particular set point
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Negative feedback:
the mechanism to keep changes in the factor within narrow limits, by increasing or decreasing accordingly during a change in the factor
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Two coordination systems in mammals:
 Nervous system, by electrical impulses transmitted along neurones  Endocrine system, by hormones (chemical messengers) travel in the blood
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Thermoregulation
is the control of body temperature involving both coordination systems, controlled by the hypothalamus – receives constant input of sensory information about temperature of the blood (by the themorecepter cells monitoring the core temperature) and the surroundings (skin receptors)
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If there is a decrease in temperature,
ypothalamus sends impulses that activate several physiological responses which decreases the loss of heat from the body and increases heat production:
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physiological responses which decreases the loss of heat from the body and increases heat production:
 Vasoconstriction – contraction of the muscles in the walls of the arterioles in skin surface, narrowing the lumens, reducing the supply of blood, hence less heat lost from the blood  Shivering – involuntary contraction of the skeletal muscles generate heat, absorbed by the blood  Raising body hairs – contraction of the muscles attached to the hairs, increasing the depth of fur and the layer of insulation, trapping air close to the skin  Decrease in sweat production – reduces heat loss by evaporation from skin surface  Increase secretion of adrenaline – increases the rate of heat production in the liver
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A decrease in temperature gradually (e.g. winter),
the hypothalamus releases a hormone which activates the anterior pituitary gland to release thyroid stimulating hormone (TSH)
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what does TSH do
 TSH stimulates the thyroid gland to secrete thyroxine hormone into the blood, increases the metabolic rate, increases the heat production  When temperature starts to increase again, the hypothalamus responds by reducing the release of TSH by the anterior pituitary gland, hence less thyroxine released from the thyroid gland
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If there is a increase in temperature
hypothalamus increases the loss of heat from the body and reduces heat production:
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hypothalamus increases the loss of heat from the body and reduces heat production:
 Vasodilation – relaxation of the arterioles in skin, hence it widens, more blood flows to the capillaries, heat energy lost  Increasing sweat production – sweat glands increase production of sweat which evaporates on the surface of the skin, removing heat from the body  Lowering body hairs – relaxation of the muscles attached to the hairs, hence they lie flat, reducing the depth of fur and layer of insulation
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Excretion:
the removal of unwanted products (e.g. ammonia – toxic) of metabolism
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 Urea is produced in the
liver from excess amino acids, transported to the kidney in solution in the blood plasma through diffusion from liver cells, which will then be removed from the blood, dissolved in water and excreted as urine
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The formation of urea from excess amino acids by liver cells:
 Deamination / removal of amine group and ammonia (NH3) formed, which is then combined with carbon dioxide forming the urea cycle  Ammonia is a soluble and toxic compound, hence needed to be converted into urea (main nitrogenous excretory product) – less soluble and less toxic
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Structure of kidney:
 Each kidney receives blood from a renal artery; return blood via a renal vein  Narrow tube – ureter – carries urine from kidney to bladder  Urethra – single tube – carries urine to the outside of the body
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A longitudinal section through a kidney (Fig 14.6) shows its main areas
 Capsule covering the whole kidney  Cortex lying beneath the capsule  Medulla – central area of kidney  Pelvis – where ureter joins
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A kidney is made up of thousands of
tiny tubes called nephrons and many blood vessels
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nephron structure
One end of the nephron forms a cup-shaped structure called Bowman’s capsule, surrounding a tight network of capillaries called a glomerulus (both located on the cortex)  The tube then forms a twisted region called the proximal convoluted tubule  Which then runs down towards the centre of the kidney (medulla) forming the loop of Henle  It then runs back upwards into the cortex forming another twisted region called distal convoluted tubule  Before finally joining a collecting duct that leads down through the medulla and into the pelvis of the kidney  Each glomerulus is supplied with blood from a branch of renal artery called an afferent arteriole  The capillaries of the glomerulus rejoins to form an efferent arteriole, which leads off to form a network of capillaries running closely alongside the rest of the nephron, where it then flows into a branch of the renal vein
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The kidney makes urine in a two-stage process:
 Ultrafiltration – filtering of small molecules including urea into the Bownman’s capsule from the blood  Selective reabsorption – taking back useful molecules from the fluid in the nephron as it flows along
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Water potential:
tendency of water molecules to move from one region to another
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Ultrafiltration
The blood in the glomerular capillaries is separated from the lumen of the Bowman’s capsule by two cell layers (endothelium of the capillary and epithelial cells (podocytes – having finger-like projections with gaps in between them) making the inner lining of the Bowman’s capsule) and a basement membrane  The diameter of lumen of the afferent arteriole is wider than efferent arteriole, which leads to high blood pressure (hydrostatic pressure) and low pressure in the Bowman’s capsule, hence plasma/fluid passes through the fenestrations between the endothelial cells of the capillaries; however, red and white blood cells / large proteins (plasma proteins) / molecules greater than 68 000(MM), cannot pass through due to the basement membrane which acts as a selective barrier; filtrate through the basement membrane can freely pass through the podocytes due to its fenestrations and forced into the Bowman’s capsule (renal capsule)
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Reabsorption in the proximal convoluted tubule
 Process called selective reabsorption (above 180 mg, no further absorption, as carriers in the PCT are saturated)  Lining of the proximal convoluted tubule is made of a single layer of cuboidal epithelial cells
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single layer of cuboidal epithelial cells which are adapted to their function of reabsorption by having:
 Microvilli to increase the surface area of the inner surface facing the lumen to increase absorption of Na+ / glucose / amino acids  Tight junctions to hold adjacent cells together so that fluid cannot pass between the cells (all reabsorbed substances must go through the cells)  Many mitochondria to provide ATP for sodium-potassium (Na+-K+) pump proteins in the outer membranes of the cells  Many co-transporter proteins in the membrane facing the lumen  Folded basal membrane to increase surface area to increase sodium potassium pumps to move Na+ into the blood  More ER for increase in protein synthesis
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 The folded basal membranes of the cells lining the proximal convoluted tubule are those nearest the blood capillaries; s
odium–potassium pumps in these membranes move sodium ions out of the cells; the sodium ions are carried away in the blood, lowering the concentration of sodium ions inside the cell, so that they passively diffuse into it, down their concentration gradient, from the fluid in the lumen of the tubule; however, sodium ions do not diffuse freely through the membrane – only enter through special co-transporter proteins in the membrane, each of which transports something else, such as a glucose molecule or an amino acid, at the same time as the sodium ion (the passive movement of sodium ions into the cell down their concentration gradient provides the energy to move glucose molecules, against a concentration gradient – indirect or secondary active transport, since the energy (as ATP) is used in the pumping of sodium
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All of the glucose, amino acids, vitamins and many Na+ and Cl- ions, some urea and most water are
reabsorbed from the glomerular filtrate into the blood, which increases the water potential in the filtrate, hence water moves down this gradient through the cells into the blood
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 Reabsorption in the loop of Henle and collecting duct
absorption in the loop of Henle and collecting duct  Descending limb is permeable to water, ascending limb does not  In the ascending limb, active transport of Na+ and Cl- ions out of loop into the tissue fluid, which decreases the water potential in the tissue fluid and increases the water potential of the ascending limb’s water potential  Descending limb permeable to both water and Na+ and Cl- ions, hence as fluid moves down the loop, water from filtrate moves down a water potential gradient into the tissue fluid by osmosis, while Na+ and Cl- ions diffuse into the loop, down their potential gradient, thus the fluid becomes more concentrated towards the bottom of the loop; the longer the loop, the more concentrated the fluid can become  Concentrated fluid flows up the ascending limb where Na+ and Cl- ions diffuse out in the lower part of ascending limb; and active transported out on the upper part of ascending limb Counter-current multiplier mechanism used – fluid flowing in vertically opposite directions to maximise the concentration built up of solutes both inside and outside the tube at the bottom of the loop
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As fluid flows up the ascending limb of the loop of Henle,
it loses sodium and chloride ions as it goes, so becoming more dilute and having a higher water potential; cells of the ascending limb of the loop of Henle and the cells lining the collecting ducts are permeable to urea which diffuses into the tissue fluid, hence urea is also concentrated in the tissue fluid in the medulla, so water can move out of the collecting duct by osmosis, due to the tissue fluid’s high solute concentration and low water potential
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Reabsorption in the distal convoluted tubule and collecting duct
 Na+ ions are actively pumped from the fluid in the tubule into the tissue fluid, into the blood  K+ ions are actively transported into the tubule, where the rate of transfer of the two ions are variable, helps regulate the concentration of these ions in the blood
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Osmoregulation:
: the control of the water potential of body fluids
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Roles of hypothalamus, posterior pituitary, collecting ducts and ADH in osmoregulation:
 Hypothalamus detects changes in water potential of the blood, as osmoreceptors (in the hypothalamus) shrink when there is a low water potential (ADH produced in hypothalamus), and released into the blood via the posterior pituitary gland  Nerve impulses are sent from the hypothalamus to posterior pituitary gland  ADH bind to receptor proteins on the collecting duct cell surface membranes and affects the collecting duct by activating series of enzyme controlled reactions, activating vesicles containing aquaporins in their membranes to move to cell surface membrane on lumen side; fuses with the cell surface membrane, hence increases water permeability of collecting duct cells, causing more water reabsorption / more concentrated urine, as water moves through the aquaporins, out of the tubule into the tissue fluid down water potential gradient
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Homeostatic control of blood glucose concentration is carried out by
two hormones secreted by endocrine tissue – consisting of groups of cells known as islets of Langerhans (containing cells secreting glucagon; cells secreting insulin) in the pancreas
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Insulin is
a signalling molecule which binds to a receptor in the cell surface membrane and affects the cell indirectly through the mediation of intracellular messengers
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signalling molecule which binds to a receptor in the cell surface membrane and affects the cell indirectly through the mediation of intracellular messengers, following these steps
 Increase in blood glucose concentration detected by β cells in the islets of Langerhans, hence more insulin secreted into the blood  Resulting to increase in glucose absorption in the liver by phosphorylating glucose – traps glucose inside cells as phosphorylated glucose cannot pass through the transporters in the cell surface membrane; increases the permeability of glucose in muscle / fat cells by addition of GLUT 4 proteins to cell surface membranes of these cells; increases the rate of respiration of glucose; conversion of glucose to glycogen; inhibits secretion of glucagon; process called negative feedback
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 The action of glucagon on liver cells in the regulation of blood glucose concentration:
 Decrease in blood glucose concentration detected by cells and responds by secreting glucagon  Glucagon binds to receptors in cell surface membrane of liver cell  Receptor changes conformation and G-protein activated  Adenylate cyclase activated causing ATP to be converted to cyclic AMP which is a second messenger  Cyclic AMP activates kinase protein which activate enzymes through phosphorylation resulting to enzyme cascade  Glycogen phosphorylase activated catalysing the breakdown of glycogen to glucose  Glucose diffuses out of liver cell through GLUT2 transporter proteins into the blood  Gluconeogenesis – glucose made from amino acids and lipids  Increase in blood glucose concentration
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The main stages of cell signalling in the control of blood glucose concentration by adrenaline:
 Adrenaline binds to receptors in the cell surface membrane  Receptor changes conformation and G proteins activated  Adenylyl cyclase activated resulting to ATP converted to cyclic AMP which is a second messenger  Cyclic AMP activates kinase protein which activates enzymes through phosphorylation resulting to enzyme cascade  Glycogen phosphorylase activated catalysing the breakdown of glycogen to glucose  Glucose diffuses out of liver cell through GLUT2 transporter proteins into the blood  Increase in blood glucose concentration
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Diabetes mellitus are of two forms:
 Type 1 diabetes: insulin-dependent diabetes, where pancreas is incapable of secreting sufficient insulin, early onset  Type 2 diabetes: non-insulin-dependent diabetes, where pancreas does secrete insulin, but liver and muscle cells do not respond properly to it, late onset – associated with diet and obesity
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The symptoms of diabetes mellitus include the tendency to drink a lot of water and a loss of body mass because:
 High blood glucose concentration causes decrease in water potential of the blood, which is detected by osmoreceptors resulting to the feelings of thirst  Less glucose converted to glycogen, as glucose lost in urine (above the renal threshold), hence glucose is not taken up by cells, hence fats are metabolised, resulting to build up in ketones which decreases the blood pH causing come
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Dip stick can be used to measure glucose concentration by:
 Immobilised glucose oxidase enzyme stuck onto pad at the end of the stick  Dip stick lowered into urine and if it contains glucose, glucose oxidase oxidises glucose into gluconic acid (gluconolactone) and hydrogen peroxide  Peroxide reacts with chromogen (using peroxidase enzyme) on pad to form a brown compound, due to the oxygen produced resulting to the oxidation of chromogen by oxygen, which produces a range of colour  Darkness of colour / range of colours is matched against a colour chart and is proportional to concentration of glucose (the darker the colour, the more glucose present)  Does not give the current blood glucose concentration (only that it is higher than the renal threshold  Important to keep a fixed time in observing colour changes
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Biosensor can be used to measure glucose concentration by:
 The pad contains glucose oxidase enzyme reacts with glucose in the blood to produce gluconolactone and oxygen  Oxygen is detected and an electric current is generated which is detected by an electrode, amplified and gives numerical value of blood glucose concentration  The greater the current, the greater the reading from the biosensor, the greater the glucose present
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Advantages of biosensor over dip stick:
 Gives the actual reading of blood glucose concentration  Re-usable  Quantitative, hence more precise reading
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Stomata have daily rhythms of
opening and closing (opens during the day to maintain the inward diffusion of carbon dioxide and the outward diffusion of oxygen and water vapour in transpiration; the closure of stomata at night when photosynthesis does not occur to reduce rates of transpiration and conserve water) and also respond to changes in environmental conditions to allow diffusion of carbon dioxide and regulate water loss by transpiration
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stomata open in response to
 Increase in light intensity to gain CO2 for photosynthesis, allowing oxygen to diffuse out  Allows transpiration to occur for which brings water / mineral ions in for photosynthesis
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stomata close in response to
 Decrease in light intensity as CO2 is not required (no photosynthesis)  Low humidity, high temperature, high wind speed and water stress  To prevent water loss by transpiration (maintains cell turgidity)
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Guard cells open when they gain
water to become turgid and close when they lose water to become flaccid, by osmosis
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Mechanism by which guard cells open stomata:
 Proton pumps in cell surface membranes of guard cells actively pump H+ out of the cells, which causes a lower H+ concentration inside the cell, hence inside of cell is more negatively charged than the outside  K+ channels open to move K+ into the cell by facilitated diffusion down an electrochemical gradient  Water potential of cell decreases, due to increase in solute potential, hence water moves into the cell by osmosis down a water potential gradient through the aquaporins in the membrane  Volume of the guard cells increases becoming turgid opening the stoma  Unequal thickness of the cell wall of the guard cells (thicker wall adjacent to the pore
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Stomata close when
proton pumps in cell surface membranes of guard cells stop and K+ ions diffuses out of the guard cells through K+ channels to enter the neighbouring cells, creating a water potential gradient in the opposite direction, hence water leaves the guard cells so it becomes flaccid and stoma closes, reducing the CO2 uptake for photosynthesis and reduces rate of transpiration; in conditions of water stress, abscisic acid (ABA) hormone stimulates stomatal closure
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The role of abscisic acid in the closure of stomata:
 Plant secretes abscisic acid during times of water stress  Abscisic acid is a stress hormone which binds to receptors on the cell surface membranes of guard cells, and inhibits proton pump (H+ not pumped out of cell)  High H+ concentration inside cell, resulting to change in charge, stimulating Ca2+ influx into the cytoplasm which acts as second messenger, and encourages K+ efflux (K+ channels open)  Water potential of the cell increases, hence water moves out of cell by osmosis  Volume of guard cells decreases, becoming flaccid  The response is very fast
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The mammalian nervous system is made up of
central nervous system (brain and spinal cord) and peripheral nervous system (cranial and spinal nerves)
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Communication using nerve action potentials
(brief changes in the distribution of electrical change across the cell surface membrane, caused by rapid movement of Na+ and K+ ions) / impulses which travel along nerve cells (neurones) at very high speeds to their target cells
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Compare the nervous and endocrine systems as communication systems that co-ordinate responses to changes in the internal and external environment in mammals: differences
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similarities Compare the nervous and endocrine systems as communication systems that co-ordinate responses to changes in the internal and external environment in mammals
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 Motor neurone:
 Dendrites lead to cell body containing nucleus, many mitochondria and RER  Has one long axon with synaptic knobs at the end furthest from cell body  For some of its length, covered in myelin sheath made by specialised cells: Schwann cells  Has small uncovered areas of axon between Schwann cells: nodes of Ranvier
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 Sensory neurone:
 Dendrites at the ends of the long axon with synaptic knobs, with the cell body containing nucleus, many mitochondria and RER near the source of stimuli or ganglion  For some of its length, covered in myelin sheath made by specialised cells: Schwann cells
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Relay neurone found in the
central nervous system
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The functions of sensory, relay and motor neurones in a reflex arc:
 Sensory neurone – receives impulses from receptor  relay neurone – passes impulses on to motor neurone  motor neurone – sends impulses to the effector
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The transmission of action potential in a myelinated neurone and its initiation from a resting potential
 Initially at a resting potential (p.d. between -60 mV to -70mV), as inside is slightly more negative than the outside, which is produced and maintained by sodium potassium pumps in the cell surface membrane (3 Na+ removed for every 2 K+ brought in across the potential gradient by active transport)  Na+ channels open and Na+ enters the cell down their electrochemical gradient, where the p.d. becomes positive (+40 mV) due to depolarisation  Na+ channels close and K+ channels open, hence K+ moves out of cell down their concentration gradient, hence p.d., becomes negative due to repolarisation  Local circuits occur  Myelin sheath acts as an insulator hence prevents movement of ions, hence action potentials / depolarisation occurs only at nodes of Ranvier, process called saltatory conduction (action potential jumps from node to node)  Process is a one-way transmission due to the refractory period  If the p.d. generated does not reach the threshold potential (between – 60 mV and –70 mV), action potential does not occur
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The length of the refractory period determines the
maximum frequency at which impulses are transmitted along neurones, as the transferred region will still be recovering from the action potential it just had (sodium ion voltage-gated channels are ‘shut tight’ and cannot be stimulated to open, however great the stimulus)
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The difference in strength of stimulus causes the
different frequency of action potentials, where a strong stimulus produces a rapid succession of action potentials, each one following along the axon just behind its predecessor; a weak stimulus results in fewer action potentials per second; a strong stimulus stimulate more neurones than a weak stimulus  The brain can therefore interpret the frequency of action potentials arriving along the axon of a sensory neurone, and the number of neurones carrying action potentials, to get information about the strength of the stimulus being detected. The nature of the stimulus, whether it is light, heat, touch or so on, is deduced from the position of the sensory neurone bringing the information. If the neurone is from the retina of the eye, then the brain will interpret the information as meaning ‘light’
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Sensory receptor cell
a cell that responds and converts a stimulus into an electrical impulse by initiating an action potential (e.g. chemoreceptor)
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The roles of sensory receptor cells in detecting stimuli and stimulating the transmission of nerve impulses in sensory neurones (e.g. chemoreceptor cell found in human taste buds):
 Chemicals act as a stimulus  Each chemoreceptors contain a specific receptor protein which detects a particular chemical  Sodium ions diffuse into cell via Microvilli, causing the membrane to depolarise, which increases the positive charge inside the cell known as receptor potential  Sufficient stimulation (above the threshold potential (below will only cause a local depolarisation of the receptor cell)) of Na+, stimulates opening of calcium ion channels, hence calcium ions enter cell, causing movement of vesicles containing neurotransmitter which is released exocytosis  Neurotransmitter stimulates action potential in sensory neurone  Chemoreceptors are transducers as they convert energy in one form into emergy in an electrical impulse in a neurone  All or nothing law where neurones either transmit impulses from one end to another or they do not  Chemoreceptor cells found in the papilla of the tongue
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The gap between two neurones is called
synaptic cleft; the parts of the two neurones near the cleft, plus the cleft itself, make up a synapse
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An action potential occurs at the
cell surface membrane of the presynaptic neurone  Action potential causes the release of molecules of transmitter substance into the cleft  The molecules of neurotransmitter diffuse across the synaptic clef and bind temporarily on the postsynaptic neurone  The postsynaptic neurone responds to all the impulses arriving at any one time by depolarising; sends impulses if the overall depolarisation is above its threshold  Synapses that uses acetylcholine as its neurotransmitter is known as cholinergic synapses
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 How a cholinergic synapse functions:
 Action potential reaches presynaptic membrane causing depolarisation, and Ca2+ channels to open in the presynaptic membrane  An influx of Ca2+ ions (facilitated diffused down its electrochemical gradient), stimulates vesicles containing ACh to move towards the presynaptic membrane and fuse with it  ACh released into synaptic cleft by exocytosis, and diffuses across the cleft  ACh binds to receptor proteins on the postsynaptic membrane; proteins change shape causing Na+ channels to open  Na+ facilitated diffuse into postsynaptic neurone causing depolarisation of the postsynaptic membrane creating an action potential, if the potential difference is above the threshold for that neurone  Acetylcholinesterase catalyses the hydrolysis of each ACh molecule into acetate and choline to prevent permanent depolarisation of the postsynaptic neurone; choline is taken back into the presynaptic neurone to be combined with acetyl CoA to form ACh once more and transported into the presynaptic vesicles
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 Role of calcium ions in synaptic transmission:
 Enter the presynaptic neurone, and causes vesicles containing acetylcholine (ACh) to fuse with the presynaptic membrane, hence releasing ACh into the synaptic cleft (exocytosis)
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Some insecticides have a similar structure to acetylcholine, hence affects the functioning of acethycholinesterase by:
 Acting as a competitive inhibitor – complementary to the active site – hence binds with the active site, this ACh is not broken down
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 A: Na+ cannot enter post-synaptic neurone hence no depolarisation / action potential in the post-synaptic neurone  B: Ca2+ cannot enter pre-synaptic neurone hence vesicles cannot move towards the pre synaptic membrane  C: ACh cannot be released into synaptic cleft  D: ACh is not broken down hence continuous depolarisation / action potential, of post synaptic neurone
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Ways in which the toxin (acts at cholinergic synapses) in cobra venom may cause muscle paralysis:
 Binds to receptors on postsynaptic membrane, hence stops ACh from binding, inhibiting depolarisation, hence no action potentials / Na+ ion channels stay shut  Stimulates ACh receptors causing continuous depolarisation / opens Na+ ion channels  Stops the release of ACh from presynaptic neurone  Inhibits acetyl cholinesterase
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The roles of synapses in the nervous system
 Ensures one-way transmission as vesicles are only found in the presynaptic neurone, hence ACh will only be released from presynaptic neurone  Involved in memory and learning, where an increase in the number of synapses allows more interconnection of nerve pathways for memory, allowing a wider range of response  Allows interconnection of nerve pathways
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 The roles of synapses in the nervous system
 Ensures one-way transmission as vesicles are only found in the presynaptic neurone, hence ACh will only be released from presynaptic neurone  Involved in memory and learning, where an increase in the number of synapses allows more interconnection of nerve pathways for memory, allowing a wider range of response  Allows interconnection of nerve pathways
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Striated muscle tissue makes up the
many muscles in the body that are attached to the skeleton; only contracts when it is stimulated to do so by impulses that arrive via motor neurones; muscle tissue like this is described as being neurogenic, whereas the cardiac muscle in the heart is myogenic – it contracts and relaxes automatically, with no need for impulses arriving from neurones
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Multinucleate muscle fibres are called
synctium instead of cell; sacrolemma instead of cell surface membrane; sarcoplasm instead of cytoplasm; sarcoplasmic reticulum (SR) instead of endoplasmic reticulum; the deep infolding of the cell surface membrane into the interior of the muscle fibre is called transverse system tubules or T-tubules, which runs close to the sarcoplasmic reticulum
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Membranes of the sarcoplasmic reticulum have
huge numbers of protein pumps that transport calcium ions into the cisternae of the SR
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The sarcoplasm contains a large number of
mitochondria, packed tightly between the myofibrils to carry out aerobic respiration, generating the ATP that is required for muscle contraction
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Each myofibrils are made up of
filaments (made from protein), where parallel groups of thick filaments (made up of myosin) lie between groups of thin ones (made up of actin), creating the stripes or striations
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The darkest parts of the A band are produced by the
overlap of thick and thin filaments, while the lighter area within the A band, known as the H band, represents the parts where only the thick filaments are present
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The Z line provides an attachment for
the actin filaments, while the M line does the same for the myosin filaments; the part of a myofibril between two Z lines is called a sarcomere
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The sliding filament model of muscular contraction (shortening of I-band):
 When sarcoplasmic reticulum (SR) depolarised  Calcium ion channels open  Tropomyosin covers / uncovers the myosin binding sites on actin; when calcium ions diffuse down a potential gradient through open channels from the SR to bind to troponin hence changes shape (so tropomyosin and troponin move away), allowing myosin to bind to actin, forming cross-bridges  ATP hydrolysis (ATP → ADP + Pi) causes myosin head (acts as ATPase) to tilt  ADP and Pi detach and myosin head swings back / returns to previous position  Actin is moved and power stroke occurs  New ATP binds  Myosin head detaches from actin and the cross-bridges break
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No ATP in striated muscle results to:
 No pumping of calcium ions into SR  No detachment of myosin heads:  Hence no hydrolysis of ATP  Hence no cross bridge formation  Hence no power stroke / pulling of actin  Hence no recovery stroke / myosin head does not return to original position
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Stimulating contraction in striated muscle:
 Action potential arrives resulting to the opening of Ca2+ channels in the presynaptic membrane, hence Ca2+ enters into the presynaptic neurone  Releasing vesicles containing acetylcholine to move towards and fuse to the presynaptic membrane  Acetylcholine released by exocytosis and diffuses across the cleft; binds to receptors on the sacrolemma  Na+ channels open, hence Na+ ions enter to depolarise the sacrolemma and generate action potential  Impulses then pass along the T-tubules towards the centre of the muscle fibre  Causing Ca2+ ions to bind with the troponin molecules  When there is no longer stimulation from the motor neurone, no impulses conducted along the T-tubules, hence the Ca2+ channels close and calcium pumps move Ca2+ back into stores in the SR; as Ca2+ leaves the binding sites on troponin, tropomyosin moves back to cover the myosin-binding sites, hence no more cross bridges
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Muscles also have another source of ATO produced from
creatine phosphate, keeping their stores in their sarcoplasm as their immediate source of energy
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Venus fly trap:
 Each trap consists of a pair of modified leaves joined by a midrib of hinge cells  The modified leaves have touch-sensitive hairs; if two hairs are touched within 20 seconds, or the same hair is touched twice in rapid succession, the trap closes  The surface of the lobes has many glands that secrete enzymes for the digestion of trapped insects  The touch of insects on the sensory hairs activates calcium ion channels in cells at the base of the hair to open, causing an influx in Ca2+ to generate action potential  Auxin increase triggered in hinge cells  H+ ions pumped into the cell walls and calcium pectate ‘glue’ in cell wall dissolved  Ca2+ ions enter hinge cell  Water follows by osmosis down its water potential gradient  Hinge cells expand  Trap lobes, flip from convex to concave (change in elastic tension)
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Two types of plant growth regulators (hormones):
Auxins: influence many aspects of growth including elongation growth which determines the overall length of roots and shoots; synthesised in the growing tips (meristems) of shoots and roots, where cells are dividing; actively transported from cell to cell  Gibberellins: involved in seed germination and controlling stem elongation
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Role of auxin in cell elongation in plants:
 Acid-growth hypothesis  Auxin stimulates proton pumps in the cell surface membrane  H+ pumped into the cell wall by active transport, hence the pH of cell wall decreases, so pH-dependent enzymes activated (expansins) and loosen the bonds between cellulose microfibrils  Cell wall ‘loosens’ / becomes more elastic / able to stretch, hence more water enters the cell and turgor pressure increases, resulting to the expansion of the cell wall
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The role of gibberellin in the germination of wheat or barley:
 Seed is initially dormant  When the seed absorbs water, embryo produces gibberellin  Gibberellin diffuses onto the aleurone layer and stimulate the cells to synthesise amylase, by the affecting the gene transcription of mRNA for amylase (breakdown of DELLA proteins which inhibit germination)  Amylase hydrolyses starch in the endosperm to soluble maltose molecules, which are converted to glucose and transported to the embryo for respiration (ATP for growth)  Amylase hydrolyses starch in the endosperm to soluble maltose molecules, which are converted to glucose and transported to the embryo for respiration (ATP for growth)
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 The height of some plants is partly controlled by their genes, e.g
tallness in pea plants is affected by a gene with two alleles; if the dominant allele, Le, is present, the plants can grow tall, but plants homozygous for the recessive allele, le, always remain short  The dominant allele of this gene regulates the synthesis of the last enzyme in a pathway that produces an active form of gibberellin, GA1  Active gibberellin stimulates cell division and cell elongation in the stem, so causing the plant to grow tall  A substitution mutation in this gene gives rise to a change from alanine to threonine in the primary structure of the enzyme near its active site, producing a non-functional enzyme; this mutation has given rise to the recessive allele, le; hence homozygous plants, lele, are genetically dwarf as they do not have the active form of gibberellin
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Homologous chromosomes
are a pair of chromosomes in a diploid cell that have the same structure as each other, with the same genes (but not necessarily the same alleles of those genes) at the same loci, and that pair together to form a bivalent during the first division of meiosis
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There are 22
matching chromosomes in humans (homologous chromosomes) – autosomes – and a non-matching pair labelled X and Y (sex chromosomes); two sets of 23 chromosomes – one set of 23 from the father and one set of 23 from the mothe
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A gene
is a length of DNA that codes for a particular protein or polypeptide
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An allele
is a particular variety of a gene
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A locus
is the position at which a particular gene is found on a particular chromosome; the same gene is always found at the same locus
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Diploid cell
one that possesses two complete sets of chromosomes; the abbreviation for diploid is 2n
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Haploid cell:
: one that possesses one complete set of chromosomes; the abbreviation for haploid is n
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Without halving the number of chromosomes into
haploid gametes (meiosis – reduction division), it would double every generation
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The formation of male gametes:
: spermatogenesis (testes)
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The formation of female gametes:
: oogenesis (ovaries)
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Sperm production takes place inside
tubules in the testes. Here, diploid cells divide by mitosis to produce numerous diploid spermatogonia, which grow to form diploid primary spermatocytes. The first division of meiosis then takes place, forming two haploid secondary spermatocytes. The second division of meiosis then produces haploid spermatids, which mature into spermatozoa.
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Ovum production takes place inside the
ovaries, where diploid cells divide by mitosis to produce many oogania which begins to divide by meiosis but stops at prophase I, primary oocytes are formed. During puberty, some of the primary oocytes proceed from prophase I to the end of the first meiotic division forming two haploid cells (secondary oocyte – gets most of the cytoplasm – and polar body – has no role in reproduction)
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The male gametes are nuclei inside
pollen grains, which are made in the anthers of a flower
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The female gametes are nuclei inside
the embryo sacs, which are made in the ovules inside the ovaries of a flower
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Inside the anthers,
pollen mother cells divide by meiosis to form four haploid cells, which nuclei divide by mitosis to form two haploid nuclei in each cell; matures into pollen grains; one of the nuclei is the male gamete nucleus which can fuse with a female nucleus to produce a diploid zygote which grows into an embryo plant
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Inside each ovule,
a large, diploid spore mother cell develops, which divides by meiosis to produce four haploid cells; all but one of these degenerates, which then develops into an embryo sac, which grows larger and its haploid nucleus divides by mitosis three times, forming eight haploid nucleus (one of these will become the female gamete
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Note that in plants, unlike animals,
e gametes are not formed directly by meiosis. Instead, meiosis is used in the production of pollen grains and the embryo sac and the gametes are then formed inside these structures by mitotic divisions
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During prophase I of meiosis,
as the two homologous chromosomes lie side by side, their chromatids form links called chiasmata (singular: chiasma) with each other. When they move apart, a piece of chromatid from one chromosome may swap places with a piece from the other – crossing over – resulting in each chromosome having different combinations of alleles as it did before
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Independent assortment.
At metaphase of meiosis I, the pairs of homologous chromosomes line up on the equator independently of each other. For two pairs of chromosomes, there are two possible orientations; at the end of meiosis II, each orientation gives two types of gamete. There are therefore four types of gamete altogethe
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A genotype is
the alleles possessed by an organism
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Homozygous means
having two identical alleles of a gene (e.g. HbAHbA)
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Heterozygous means
having two different alleles of a gene (e.g. HbAHbS)
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Genotype affects phenotype:
 HbSHbS: coding for the production of the sickle cell -globin polypeptide, sickle cell anaemia  HbAHbA: coding for the normal -globin polypeptide  HbAHbS: Half of the person’s Hb will be normal, and half will be sickle cell Hb - sickle cell trait – can be referred to as ‘carriers’ – they have enough normal haemoglobin to carry enough oxygen, and so will have no problems at all and immune to malaria
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An organism’s phenotype is its
characteristics, often resulting from an interaction between its genotype and its environment
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During every fertilisation,
either an HbA sperm or an HbS sperm may fertilize either an HbA egg or an HbS egg. The possible results can be shown like this:
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Codominant alleles both have
an effect on the phenotype of a heterozygous organism
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A dominant allele is
one whose effect on the phenotype of a heterozygote is identical to its effect in a homozygote
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A recessive allele is
one that is only expressed when no dominant allele is present  Dominant and recessive example (tomato plants):
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The F1 generation
is the offspring resulting from a cross between an organism with a homozygous dominant genotype, and one with a homozygous recessive genotyp
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The F2 generation
is the offspring resulting from a cross between two F1 (heterozygous( organisms
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A test cross is a
genetic cross in which an organism showing a characteristic caused by a dominant allele is crossed with an organism that is homozygous recessive; the phenotypes of the offspring can be a guide to whether the first organism is homozygous or heterozygous:  E.g. a purple stem tomato plant might have the genotype AA or Aa; to find out its genotype, it could be crossed with a green-stemmed tomato plant aa
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XX:
female
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XY
malewhere Y chromosome is much shorter than the X
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Sex linkage.
E.g. haemophilia (sex-linked gene), in which the blood fails to clot properly due to the recessive allele h, resulting to the lack of factor VIII; where dominant allele, H, produces normal factor VIII
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The gene for haemophilia is on the
X chromosome, and not on the autosome, hence affects the way that is inherited, e.g. a man does not have haemophilia while the woman is a carrier (0.25 probability: normal girl, boy, carrier girl and boy with haemophilia):
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Dihybrid crosses
(inheritance of two genes at once
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dihybrid cross between a heterozygous organism and a homozygous recessive organism where the alleles show complete dominance
1 : 1 : 1 : 1 ratio
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dihybrid cross between two heterozygous organisms where the two alleles show complete dominance and where the genes are on different chromosomes
9 : 3 : 3 : 1 ratio
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Linkage
is the presence of two genes on the same chromosome, so that they tend to be inherited together and do not assort independently (e.g. the fruit fly, Drosophila. The gene for body colour and the gene for antennal shape are close together on the same chromosome and so are linked)
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Recombinant (offspring caused by crossing over):
Cross over value is the percentage of offspring that belong to the recombinant class
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Chi-squared (χ2) test
allows comparison between observed results and expected results, and decide whether there is a significant difference between them (e.g. two heterozygous tomato plants – 144 offspring):
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Gene mutation:
a change in the structure of a DNA molecule, producing a different allele of a gene
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Mutagen
a substance that increases the chances of mutation occurring
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Three different ways in which the sequence of bases in a gene may be altered (gene mutations):
 Base substitution, where one base takes the place of another, e.g. CCT GAG GAG into CCT GTG GAG  Base addition, where one or more extra bases are added to the sequence, e.g. CCT GAG GAG into CCA TGA GGA G  Base deletion, where one or more bases are lost from the sequence, e.g. CCT GAG GAG into CCG AGG AG
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Base deletion and addition have significant effect on
the structure, therefore function of the polypeptide that the allele codes for, and causes frame shifts
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Base substitution may not have
any apparent effect, called silent mutation
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Sickle cell anaemia:
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Huntington’s disease:
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Albinism:
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Genetic variation is caused by:
 Independent assortment of chromosomes, and therefore alleles, during meiosis  Crossing over between chromatids of homologous chromosomes during meiosis  Random mating between organisms within a species  Random fertilisation of gametes  Mutation (excluding somatic cells – apart of cells in the reproductive organs
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Genetic variation provides the
raw material on which natural selection can act, where some individual have features that give them an advantage over other members in a population
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Phenotypic variation is also caused by
the environment, e.g. some organisms might be larger than others due to better access of quality food while they were growing, however these variations will not be passed onto the offsprin
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Qualitative differences fall into
learly distinguishable categories, with no intermediates – e.g. four possible ABO blood groups: A, B, AB or O. This is discontinuous variatio
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Quantitative differences where there is a
range of heights between two extremes (Figure 17.2). This is continuous variation
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Both qualitative and quantitative differences in phenotype may be inherited; may involve several different genes; differences between them are:
 In discontinuous (qualitative) variation:  Different alleles at a single gene locus have large effects on the phenotype  Different genes have quite different effects on the phenotype  In continuous (quantitative) variation (e.g. organism’s height):  Different alleles at a single gene locus have small effects on the phenotype  Different genes have the same, often additive, effect on the phenotype  A large number of genes may have a combined effect on a particular phenotypic trait; these genes are known as polygenes
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Environmental effects may allow the full genetic potential height to be reached or may stunt it in some way:
 One individual might have less food, or less nutritious food, than another with the same genetic contribution  A plant may be in a lower light intensity or in soil with fewer nutrients than another with the same genetic potential height.  Himalayan colouring of rabbits and of Siamese and Burmese cats, colouring is caused by an allele which allows the formation of the dark pigment only at low temperature, hence the extremities are the coldest parts of the animals
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The t-test is used to
assess whether or not the means of two sets of data with roughly normal distributions, are significantly different from one another (p. 500)
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Various environmental factors come into play to keep down a population’s number
 Biotic – caused by other living organisms such as through predation, competition for food, or infection by pathogens  Abiotic – caused by non-living components of the environment such as water supply or nutrient levels in the soil
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Once the population increases,
the pressure of the environmental factors will be sufficiently great, then the population size will decrease, only when they have fallen considerably will the numbers be able to grow again; over a period of time, the population will oscillate about a mean level
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Natural selection occurs as
populations have the capacity to produce many offspring that compete for resources; in the ‘struggle for existence’ only the individuals that are best adapted survive to breed and pass on their alleles to the next generation (selection pressure)
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Fitness
is the capacity of an organism to survive and transmit its genotype to its offspring
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Selection pressure
an environmental factor that gives greater chances of survival and reproduction on some individuals than on others in a population (e.g. predation and camouflage)
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Environmental factors can act as:
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Changes in allele frequency creates the
basis of evolution
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Antibiotic resistance:
 There may be one or more individual bacteria with an allele giving resistance to penicillin – such as Staphylococcus – by producing penicillinase, which inactivates penicillin. These bacteria can survive and reproduce, while others will die (selection pressure)
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Industrial melanism
 Black forms of moth with allele, C, increases in areas near industrial cities; whereas speckled forms of moth with allele, c, stays constant in non-industrial areas (predation selection pressure)  These mutations are not caused by pollution (changes in environmental factors only affect the likelihood of an allele surviving in a population; not affecting the likelihood of such an allele arising by mutation
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Sickle cell anaemia:
 Places where sickle cell allele is most common are parts of the world where malaria (caused by protoctist parasite, Plasmodium, where it enters the RBC and multiply) is found (selection pressure occurs hence selective advantage occurs)  There are two strong selection pressures acting on these two allele:  Selection against people who are homozygous for the sickle cell allele, HbSHbS, is very strong, because they become seriously anaemic  Selection against people, who are homozygous HbAHbA is also very strong, as they are more likely to die from malaria  Heterozygous people with malaria only have about one-third the number of Plasmodium in their blood as do HbAHbA homozygotes
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Genetic drift
s a change in allele frequency that occurs by chance, as only some of the organisms of each generation reproduce (e.g. when a small number of individuals are separated (isolated) from the rest of a large population, resulting to different allele frequencies; further genetic drift will alter the allele frequencies even more and evolution will cause significant difference with the parent population) – founder effect
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Hardy-Weinberg principle
allow the proportions of each of the genotypes in a large, randomly mating population to be calculated (the frequency of a genotype is its proportion to the total population; p represents the frequency of the dominant allele & q represents the frequency of the recessive allele):  E.g. two alleles of a single gene, A/a, thus three genotypes will be in the population
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Hardy-Weinberg calculations do not apply when the population is small or when there is:
 Significant selective pressure against one of the genotypes  Migration of individuals carrying one of hte two alleles into, or out of, the population  Non-random mating
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Selective breeding of dairy cattle:
 Artificial selection: When humans purposely apply selection pressures to populations  Desired features include docility (making the animal easier to control), fast growth rates and high milk yields have been achieved by selective breeding  Individuals showing one or more of these desired features are chosen for breeding  Some of the alleles granting these features are passed on to the individuals’ offspring  Over many generations, alleles granting the desired characteristics increase in frequency, while those conferring characteristics not desired by the breeder decrease in frequency  Background genes (the alleles of genes that adapt to its particular environment) results in offspring obtaining the same adaptations, however will not be well adapted to a new environment (even though it will show selected traits)
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Crop improvement:
 Gene technology is used to alter or add genes into a species in order to change it characteristics  Selective breeding:  Produced many different varieties of wheat and rice – most is grown to produce grains rich in gluten  Resistance towards various diseases (wheat and rice)  Shorter stems, for easy harvest hence higher yields (less energy used to grow tall, more to growing of seeds) – wheat and rice  Most of the dwarf varieties of wheat carry mutant alleles of two reduced height (Rht) genes, which code for DELLA proteins to reduce the effect of gibberellins ongrowth. The mutant alleles cause dwarfism by producing more of, or more active forms of, these transcription inhibitors  A mutant allele of a different gene, called ‘Tom Thumb’, has its dwarfing effect because the plant cells do not have receptors for gibberellins and so cannot respond to the hormone  Interbreeding and hybridisation of maize for uniformity and heterozygosity:  If maize plants are inbred (crossed with other plants with genotypes like their own), the plants in each generation become progressively smaller and weaker – inbreeding depression – due to the less vigorous homozygous plants compared to heterozygous  Homozygous plants obtained from companies, then crossing them, producing F1 plants that all have the same genotype which have characteristics such as high yields, resistance to more pests and diseases, and good growth in nutrient-poor soils or where water is in short supply
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Speciation
: The production of new species
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A species
is a group of organisms with similar morphological, physiological, biochemical and behavioural features, which can breed together naturally to produce fertile offspring, and are reproductively isolated from other species
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Reproductive isolation:
The inability of two groups of organisms of the same species to breed with one another, e.g. because of geographical separation or because of behavioural differences
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Reproductive isolation can take very different forms:
pre zygotic and postzygotic
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Prezygotic (before a zygote is formed) isolating mechanisms include:
 Individuals not recognising one another as potential mates or not responding to mating behaviour  Animals being physically unable to mate  Incompatibility of pollen and stigma in plants  Inability of a male gamete to fuse with a female gamete
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Postzygotic isolating mechanisms include:
 Failure of cell division in the zygote  Non-viable offspring (offspring that soon die)  Viable, but sterile offspring
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 Allopatric speciation (geographical isolation/separation):
 Requires a barrier to arise between two populations of the same species, preventing them from mixing (e.g. a stretch of water, deforestation)  The selection pressures on these two places might be very different, resulting in different alleles being selected for  Over time, the two population can no longer interbreed, hence a new species had evolved
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Sympatric speciation (ecological and behavioural separation):
 Two groups of individuals living in the same area may become unable to breed together (e.g. one group develops courtship behaviours that no longer match with the other groups, because they love in different habitats in the same area (ecological separation))
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Molecular evidence that reveals similarities between closely related organisms with reference to mitochondrial DNA and protein sequence data:
 Mitochondria contain a single DNA molecule that is passed on down the female line; analysis of mitochondrial DNA (mtDNA) can be used to determine how closely related two different species are; the more similar the sequence of bases in the DNA, the more closely related they are considered to be  Amino acid sequences in proteins can be used (the protein cytochrome c, involved in the electron transport chain, is found in a very wide range of different organisms, suggesting that they all evolved from a common ancestor, where differences in the amino acid sequences in cytochrome c suggest how closely related particular species are
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Extinctions tend to be caused by:
 Climate change, for example, global warming can result in some species inability to find adapted habitats  Competition, for example, a newly evolved species or an alien species, may out compete a resident species  Habitat loss, for example, large deforestations  Direct killing by humans
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Structural genes:
 Genes that code for proteins required by a cell
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Regulatory genes:
 Genes that code for proteins that regulate the expression of other genes
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Difference between repressible and inducible enzymes
 The synthesis of a repressible enzyme can be prevented by binding a repressor protein to a specific site, called an operator, on bacterium’s DNA  The synthesis of an inducible enzyme occurs only when its substrate is present (transcription of a gene occurs as a result of the inducer (enzyme’s substrate) interacting with the protein produced by the regulatory gene)
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 The lac operon consists of a cluster of three structural genes and a length of DNA including operator and promoter regions, the three structural genes are
 lacZ, coding for -galactosidase  lacY, coding for permease (allows lactose to enter the cell)  lacA, coding for transacetylase
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When there is no lactose in the medium in which the bacterium is growing:
 The regulatory gene codes for a protein called a repressor  The repressor binds to the operator region, close to gene lacZ  In the presence of bound repressor at the operator, RNA polymerase cannot bind to DNA at the promoter region  No transcription of the three structural genes take place
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The repressor protein is
allosteric (two binding sites), hence when lactose binds to its site, the shape of the protein changes so that the DNA-binding site is closed
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When lactose is present in the medium in which the bacterium is growing:
 Lactose is taken up by the bacterium  Lactose binds to the repressor protein, distorting its shape and preventing it from binding to DNA at the operator site  Transcription is no longer inhibited and messenger RNA is produced from the three structural genes  -galactosidase is an inducible enzyme
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Transcription of a gene is controlled by transcription factors
proteins that bind to a specific DNA sequence and control the flow of information from DNA to RNA by controlling the formation of mRNA, role is to make sure that genes are expressed in the correct cell at the correct time and to the correct extend
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effects of mrna
 Necessary for transcription to occur, form part of the protein complex that binds to the promoter region of the gene concerned  Activate appropriate genes in sequence  Responsible for the determination of sex in mammals  Allow responses to environmental stimuli, e.g. switching on the correct genes to respond to high environmental temperatures  Hormones have their effect through transcription factors
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Gibberellin controls seed germination in plants by
increasing the transcription of mRNA coding for amylase, done by breaking down of DELLA proteins (inhibits the binding of a transcription factor, such as PIF to a gene promoter), causing PIF to bind to its target promoter resulting to an increase in amylase production
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