Respiration Flashcards

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1
Q

Why do living organisms need to respire

A

-respiration is process that occurs in living cells and released energy stored in organic molecules
-the energy is immediately used to synthesise molecules of ATP from ADP and inorganic phosphate (Pi)
-ATP in cells can be hydrolysed to release energy needed to drive biological processes
-microorganisms (both prokaryotes and eukaryotes), plants, animals, fungi and protoctists all respire to obtain energy

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2
Q

Why do living organisms need energy

A

-energy is the capacity to do work
-the energy that is stored in complex organism molecules - e.g. fats, proteins, carbohydrates - is potential energy
-it is also chemical energy converted from light energy during process of photosynthesis
-when this energy is released from organic molecules via respiration, it can be used to make ATP to drive biological processes:
-active transport
-endocytosis/exocytosis
-activation chemicals
-cell division
-DNA replication etc

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3
Q

Describe the different metabolic reactions

A

-anabolic reactions are metabolic reactions where large molecules are synthesised from smaller molecules
-catabolic reactions are metabolic reactions involving hydrolysis of large molecules to smaller ones

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4
Q

Importance of kinetic energy

A

-within living cells atoms, ions and molecules have kinetic energy and this allows them to move
-for example when molecules diffuse down concentration gradient, moving from one place to another, they use kinetic energy to do so

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5
Q

Describe the structure of ATP

A

-ATP is standard intermediary between energy-releasing and energy-consuming metabolic reactions in both eukaryotic and prokaryotic cells
-structure of ATP is phosphorylated nucleotide
-each molecule of ATP consists of adenosine, which is the nitrogenous base adenine plus five-carbon sugar ribose and three phosphate (phosphoryl) groups

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6
Q

Describe ATP in solution

A

-ATP is relatively stable (it does not break down ADP and Pi) when in solution but is readily hydrolysed by enzyme catalysis
-However, whilst in solution, it can easily be moved from place to place within a cell

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7
Q

How efficient is the release of ATP

A

-energy-releasing hydrolysis of ATP is coupled with an energy-consuming metabolic reaction
-when ATP is hydrolysed to ADP and Pi a small quantity of energy is released for use in cells
-cells can therefore obtain energy they need for process in small manageable amounts that will not cause damage or be wasteful
-ATP is referred to as universal energy currency as it occurs in all living cells and is source of energy that can be used by cells in small amounts

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8
Q

Describe the release of ATP as heat

A

-some energy is released from hydrolysis of ATP as heat
-the release of heat, both in respiration and during ATP hydrolysis, may appear to be inefficient and wasteful
-heat however helps keep living organisms ‘warm’ and enables their enzyme catalysed reactions to proceed at or near optimum rate

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9
Q

What is glycolysis

A

-glycolysis is a biochemical pathway that occurs in cytoplasm of all living organisms that respire, including many prokaryotes
-the pathway involves a sequence of 10 reactions, each catalysed by a different enzyme, some with help of coenzyme NAD

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10
Q

What are the three main stages of glycolysis

A

1) phosphorylation of glucose to hexose biphosphate
2)splitting each hexose biphosphate molecules into two triose phosphate molecules
3)
oxidation of triose phosphate to pyruvate

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11
Q

What is NAD

A

-enzymes that catalyse oxidation and reduction reactions need help of coenzymes that accept hydrogen atoms removed during oxidation
-NAD is non protein molecule that helps dehydrogenase enzymes to carry out oxidation reactions
-NAD oxidises substrate molecules during glycolysis, the link reaction and Krebs cycle

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12
Q

How is NAD made

A

-NAD is synthesised in living cells from nicotinamide (B3 vitamin) , the five-carbon sugar ribose, the nucleotide base adenine and two phosphoryl groups
-the nicotinamide ring can accept two hydrogen atoms, becoming reduced NAD

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13
Q

Role of reduced NAD

A

-reduced NAD carries the protons and electrons to cristae of mitochondria and delivers them to be used in oxidative phosphorylation for generation of ATP from ADP and Pi
-when reduced NAD gives up the protons and electrons that it accepted during one of first three stages of respiration, it becomes oxidised and can be reused to oxidise more substrate, in process, becoming reduced again

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14
Q

Describe the process of phosphorylation

A

-glucose is a hexose sugar which means it contains 6 carbon atoms
-it molecules are stable and need to be activated before they can be split into two three carbon compounds
1) one molecule of ATP is hydrolysed and released phosphoryl group is added to glucose to make hexose monophosphate
2) another molecule of ATP is hydrolysed and the phosphoryl group added to the hexose phosphate to form a molecules of hexose biphosphate. This sugar has one phosphate group at carbon atom number one and another at carbon atom six
-the energy from hydrolysed ATP molecules activates hexose sugar and prevents it from being transported out of cell

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15
Q

Describe the splitting of the hexose biphosphate

A

-each molecule of hexose biphosphate is split into two three-carbon molecules, triose phosphate, each with a phosphate group attached

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16
Q

Describe the oxidation of triose phosphate to pyruvate

A

-although this process is anaerobic, it involves oxidation, because it involves removal of hydrogen atoms from substrate molecules
1) dehydrogenase enzymes, added by coenzyme NAD, remove hydrogens from triose phosphate
2) two molecules of NAD accept hydrogen atoms and become reduced
3)at this stage of glycolysis, two molecules of NAD are reduced for every molecule of glucose undergoing this process. Also at this stage, four molecules of ATP are made for every two triose phosphate molecules undergoing oxidation

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17
Q

What are the products of glycolysis

A

-from each molecule of glucose, at end of glycolysis there are
-two molecules of ATP: four have been made but two used to ‘kickstart’ process so net gain is two molecules of ATP
-two molecules of reduced NAD
-two molecules of pyruvate

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18
Q

What are the four main stages of respiration

A

1)glycolysis
2)link reaction
3)Krebs cycle
4) oxidative phosphorylation
-the last three stages only take place under aerobic conditions
-under aerobic conditions pyruvate molecules from glycolysis are actively transported into mitochondria for link reaction
-in absence of oxygen pyruvate converted in the cytoplasm to lactate or ethanol
-in process, reduced NAD molecules are reoxidised so glycolysis can continue to run, generating two molecules of ATP for every glucose molecule metabolised

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19
Q

Discovery of mitochondria

A

-mitochondria are organelles that are present in all types of eukaryotic cells
-mitochondria first identified in animal cells in 1840
-identified in plant cells in 1900
-ultrastructure discovered in 1950s after using electron microscope

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20
Q

Describe structure of mitochondria

A

-all mitochondria have inner and outer phospholipid membrane making up the envelope
-outer membrane smooth and inner membrane folded into cristae giving it large surface area
-embedded in inner membrane are proteins that transport electrons and protein channels associated with ATP synthase enzymes that allow protons to diffuse through them
-between inner and outer mitochondrial membranes of envelope is inter membrane space
-mitochondrial matrix enclosed by inner membrane is semirigid and gel like
-it contains mitochondrial ribosomes, looped mitochondrial DNA and enzymes for link reaction and Krebs cycle

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21
Q

MITCOHONDRIA FUNCTION: the matrix

A

-matrix is where link reaction and Krebs cycle take place
-enzymes that catalyse stages of these reactions
-molecules of coenzymes NAD and FAD (flavine adenine dinucleotide)
-oxaloacetate - four carbon compound that accepts acetyl group from link reaction
-mitochondrial DNA- some of which codes for mitochondrial enzymes and other proteins
-mitochondrial ribosomes, structurally similar to prokaryotic ribosomes, where these proteins assembled

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22
Q

MITOCHONDRIA FUNCTION: outer membrane

A

-the phospholipid composition of outer membrane similar to that of membranes around other organelles in eukaryotic cells
-it contains proteins, some of which form channels or carriers that allow passage of molecules such as pyruvate into mitochondrion

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23
Q

MITOCHONDRIA FUNCTION: inner membrane

A

-lipid composition of inner membrane differs from outer membrane
-lipid bilayer less permeable to small ions such as hydrogen ions
-the folds, cristae, in inner membrane give large surface area for electron carriers and ATP synthase enzymes embedded in them
-electron carriers are protein complexes arranged in electron transport chains
-electron transport chains are involved in final stage of aerobic respiration; oxidative phosphorylation

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24
Q

MITOCHONDRIA FUNCTION: intermembrane space

A

-intermembrane space between outer and inner layers of mitochondrial envelope is also involved in oxidative phosphorylation
-inner membrane is in close contact with mitochondrial matrix so molecules of reduced NAD and FAD can easily deliver hydrogen to electron transport chain

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25
Q

MITOCHONDRIA FUNCTION: electron transport chain - cofactor

A

-each electron carrier proteins contains a cofactor - a non protein haem group that contains an iron ion
-the iron ion can accept and donate electrons because it can become reduced (Fe2+) by gaining electron and oxidised (Fe3+) when donating electron to next electron carrier
-electron carrier proteins are oxido-reductase enzymes

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26
Q

MITOCHONDRIA FUNCTION: electron transport chain - coenzyme

A

-electron carriers also have coenzyme that, using energy released from electrons, pumps protons from matrix to intermembrane space
-protons accumulate in intermembrane space and proton gradient forms across membrane
-proton gradient can produce flow of protons through channels in ATP synthase enzymes to make ATP

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27
Q

MITOCHONDRIA FUNCTION: ATP synthase

A

-ATP synthase enzymes are large and protude from inner membrane into matrix
-protons can pass through them

28
Q

Define decarboxylation

A

removal of a carboxyl group from a substrate molecule

29
Q

Define dehydrogenation

A

removal of hydrogen atoms from substrate molecule

30
Q

Define substrate level phosphorylation

A

production of ATP from ADP and Pi during glycolysis and Krebs cycle

31
Q

Outline the importance of pyruvate in the link reaction and the Krebs cycle

A

-pyruvate produced during glycolysis is transported across the outer and inner mitochondrial membranes via a specific -H+ symport, a transport protein that transports two ions or molecules in same direction and into matrix
1) pyruvate is then converted to a two carbon acetyl group during the link reaction
2) the acetyl group is oxidised during the Krebs cycle

32
Q

What is the link reaction

A

-the link reaction occurs in the mitochondrial matrix
-pyruvate is decarboxylated and dehydrogenated, catalysed by a large multi enzyme complex, pyruvate dehydrogenase, which catalyses the sequence of reactions that occur during the link reaction
-no ATP is produced

33
Q

Steps of the link reaction

A

1) carboxyl group removed and is origin of some of carbon dioxide produced during respiration
2) this decarboxylation of pyruvate together with dehydrogenation produces an acetyl group
3) the acetyl group combines with coenzyme A (CoA) to become acetyl CoA
4) the coenzyme NAD becomes reduced

34
Q

Equation for link reaction

A

-the equation summarises the link reaction for two molecules of pyruvate derived from one molecule of glucose
2 pyruvate +2NAD+2CoA – 2CO2+ 2 reduced NAD + 2 acetyl CoA
-coenzyme A accepts the acetyl group and in form of acetyl CoA carries acetyl group onto Krebs cycle

35
Q

What is the Krebs cycle

A

-the Krebs cycle also takes place in the mitochondrial matrix
-the Krebs cycle is a series of enzyme catalysed reactions that oxidise the acetate from the link reaction to two molecules of carbon dioxide, while conserving energy by reducing the coenzymes NAD and FAD
-these reduced enzymes then carry the hydrogen atoms to the electron transport chain on the cristae, where they will be involved in the production of many more ATP molecules
-for every molecule of glucose, there are two turns of the Krebs cycle

36
Q

Steps for the Krebs cycle

A

1) acetyl group released from acetyl CoA combines with a four carbon compound, oxaloacetate to form six carbon compound, citrate
2) citrate is decarboxylated and dehydrogenated producing a five carbon compound, one molecule of carbon dioxide and one molecule of reduced NAD
3) the five carbon compound is further decarboxylated and dehydrogenated producing a four carbon compound, one molecule of carbon dioxide and one molecule of reduced NAD
4) this four carbon compound combines temporarily with and is then released from coenzyme A. At this stage, substrate level phosphorylation takes place, producing one molecule of ATP
5) the four carbon compound is dehydrogenated producing a different four carbon compound and molecule of reduced FAD
6) rearrangement of the atoms in the four carbon molecule, catalysed by an isomerase enzyme, followed by further dehydrogenation, regenerate a molecule of oxaloacetate so the cycle can continue

37
Q

Describe the products of the link reaction and the Krebs cycle

A

LINK REACTION
-2 reduced NAD
-0 reduced FAD
-2 carbon dioxide
-0 ATP
KREBS CYCLE
-6 reduced NAD
-2 reduced FAD
-4 carbon dioxide
-2 ATP
-by the end of the Krebs cycle, production of carbon dioxide from glucose is completed

38
Q

Are the reactions anaerobic

A

-although oxygen is not directly used in the link reaction and Krebs cycle, these stages will not occur in the absence of oxygen
-they are considered aerobic

39
Q

What other substrates can be respired aerobically

A
  • fatty acids are broken down to many molecules of acetate that enter the Krebs cycle via acetyl CoA
    -glycerol may be converted to pyruvate and enter Krebs cycle via the link reaction
    -amino acids may be deaminated (amino group NH2 removed) and rest of molecule enter Krebs cycle directly or changed to pyruvate or acetyl CoA
40
Q

Define chemiosmosis

A

flow of protons down their concentration gradient across a membrane through a channel associated with ATP synthase

41
Q

Define oxidative phosphorylation

A

-formation of ATP using energy released in the electron transport chain and in the presence of oxygen
-it is the last stage in aerobic respiration

42
Q

What is the final stage of aerobic respiration

A

-final stage of aerobic respiration is oxidative phosphorylation - production of ATP in the presence of oxygen
-oxidative phosphorylation takes place in mitochondria
-it involves electron carrier proteins arranged in chains called the electron transport chains embedded in the inner mitochondrial membranes (cristae) and a process called chemiosmosis
-the folded cristae gives a large surface area for the electron carrier proteins and the ATP synthase enzymes

43
Q

Staes of oxidative phosphorlyation

A

1) reduced NAD and reduced FAD are reoxidised when they deliver their hydrogen atoms to the electron transport chain
2) the hydrogen atoms released from the reduced coenzymes split into protons and electrons
3) protons go into solution in the mitochondrial matrix

44
Q

Describe the electron transport chain

A

-electrons from the hydrogen atoms pass along the chain of electron carriers
-each electron carrier protein has an iron ion at its core
-the iron ion can gain an electron becoming reduced Fe2+
-the reduced iron ion can then donate the electron to the iron ion in the next electron carrier in the chain becoming reoxidised to Fe3+
-as electrons pass along the chain some of their energy is used to pump protons across the inner mitochondrial membrane into the intermembrane spaces

45
Q

How does a proton gradient form

A

-as protons accumulate in the intermembrane spaces, a proton gradient forms across the membrane
-proton gradients generate a chemiosmotic potential that is also known as a proton motive force (pmf)
-they are a source of potential energy
-ATP is made using the energy of proton motive force

46
Q

How do protons pass through (chemiosmosis)

A

-protons cannot easily diffuse through the lipid bilayer of the mitochondrial membranes as the outer membrane has a low degree of permeability to protons and the inner membrane is impermeable to protons
-protons can however diffuse through the protein channels associated with ATP synthase enzymes that are in the inner membrane
-as protons diffuse down their concentration gradient through these channels, the flow of protons causes a conformational (shape) change in the ATP synthase enzymes that allows ADP and Pi to combine forming ATP
-this flow of protons is known as chemiosmosis
-it is coupled to the formation of ATP

47
Q

How does ATP form this way

A

-the formation of ATP in this way in the presence of oxygen is oxidative phosphorylation
-oxygen is the final electron acceptor
-it combines with electrons coming off the electron transport chain and with protons diffusing down the ATP synthase channel, forming water
4H+ +4e- +O2 – 2H2O

48
Q

Number of molecules made from one molecule of glucose in oxidative phosphorylation

A

GLYCOLYSIS
-reduced NAD=2
-reduced FAD=0
LINK REACTION
-reduced NAD=2
-reduced FAD=0
KREBS CYCLE
-reduced NAD=6
-reduced FAD=2

49
Q

How many molecules of ATP can theoretically be made

A

-the reduced coenzymes provide both protons and electrons to the electron transport chain
-the protons and electrons from the 10 molecules of reduced NAD can theoretically produce 25 molecules of ATP
-the protons and electrons from the two molecules of reduced FAD can theoretically produce three molecules of ATP
-oxidative phosphorylation may therefore produce 28 molecules of ATP per molecule of glucose

50
Q

What is the total ATP per molecule of glucose during aerobic respiration

A

-glycolysis=2
-the link reaction=0
-the krebs cycle=2
-oxidative phosphorylation=28
-total=32
-the theoretical yield is rarely achieved and the actual yield may be closer to 30 molecules of ATP per molecule of glucose or even less

51
Q

Why is theoretical yield not always met

A

-some ATP used to actively transport pyruvate into mitochondria
-some ATP used in shuttle system that transports reduced NAD made during glycolysis into mitochondria
-some protons may leak out through outer mitochondrial membrane

52
Q

What happens when oxygen is absent

A

1) oxygen cannot act as final electron acceptor at end of oxidative phosphorylation
-protons diffusing through channels associated with ATP synthase are not able to combine with electrons and oxygen to form water
2) concentration of protons increases in matrix and reduces proton gradient across inner mitochondrial membrane
3) oxidative phosphorylation ceases
4) reduced NAD and reduced FAD are not able to unload their hydrogen atoms and cannot be reoxidised
5) the Krebs cycle stops as does link reaction

53
Q

How can the organism survive in anaerobic conditions

A

-for the organism to survive these adverse conditions, glycolysis can take place but the reduced NAD generated during the oxidation of triose phosphate to pyruvate has to be reoxidised so glycolysis can continue
-these reduced coenzyme molecules cannot be reoxidised at the electron transport chain so another metabolic pathway must operate to reoxidise them

54
Q

How is reduced NAD must be reoxidised

A

-eukaryotic cells have two metabolic pathways to reoxidise the reduced NAD
-fungi and plants use ethanol fermentation pathway
-mammals use lactate fermentation pathway
-both take place in the cytoplasm of cells

55
Q

Describe the ethanol fermentation pathway

A

-pyruvate (CH3COCOOH) –ethanal (CH3CHO) –ethanol (CH3CH2OH)
-fate of pyruvate under anaerobic conditions in yeast cells is also known as alcoholic fermentation
1) each molecule of pyruvate produced during glycolysis is decarboxylated and converted to ethanal
-this stage in the pathway is catalysed by pyruvate decarboxylase which has a coenzyme, thiamine diphosphate bound to it
2)the ethanol accepts hydrogen atoms from reduced NAD becoming reduced to ethanol
-the enzyme ethanol dehydrogenase catalyses the reaction
3) in the process, the reduced NAD is reoxidised and made available to accept more hydrogen atoms from triose phosphate thus allowing continue of glycolysis

56
Q

Describe the lactate fermentation pathway

A

-lactate fermentation occurs in mammalian muscle tissue during vigorous activity such as when running fast to escape a predator, when the demand for ATP for muscle contraction is high and there is an oxygen deficit
1)pyruvate produced during glycolysis accepts hydrogen atoms from the reduced NAD, also made during glycolysis
-the enzyme lactate dehydrogenase catalyses the reaction, there are two outcomes
-pyruvate reduced to lactate
-reduced NAD becomes reoxidised
2)reoxidised NAD can accept more hydrogen atoms from triose phosphate during glycolysis and glycolysis can continue to produce enough ATP to sustain muscle contraction for short period

57
Q

Describe the fate of lactate

A

-the lactate produced in the muscle tissue is carried away from the muscles to the liver in the blood
-when more oxygen available, lactate may either be
-converted to pyruvate which may enter the Krebs cycle via the link reaction
-recycled to glucose and glycogen
-if lactate were not removed from the muscle tissue, pH would be lowered and this would inhibit action of many enzymes involved in glycolysis and muscle contraction

58
Q

Describe the yield of ATP from anaerobic respiration

A

-neither ethanol fermentation nor lactate fermentation produces any ATP
-however because this allows glycolysis to continue the net gain of two molecules of ATP per molecule of glucose is still obtained
-because glucose only partly broken down many more molecules can undergo glycolysis per minute and there overall yield of ATP quite large
-however, for each molecule of molecule glucose, the yield of ATP via anaerobic respiration is about 1/15 of that produced during aerobic respiration

59
Q

What is a respiratory substrate

A

-a respiratory substrate is an organic substrate that can be oxidised by respiration, releasing energy to make molecules of ATP
-besides carbohydrates, lipids, and proteins can also provide respiratory substrates
-they can be oxidised to produce molecules of ATP, carbon dioxide and water (in the presence of oxygen)
-they each have different relative energy values

60
Q

Energy value of carbohydrates

A

-the monosaccharide glucose is the chief respiratory substrate
-some mammalian cells, for example braincells and red blood cells use only glucose for respiration
-animals and some bacteria store carbohydrates as glycogen which can be hydrolysed to glucose for respiration:
-disaccharides can be digested to monosaccharides for respiration
-monosaccharides such as fructose and galactose can be changed by isomerase enzymes to glucose for respiration

61
Q

Energy value of lipids

A

-lipids are important respiratory substrates for a number of types of tissue including muscle
-triglycerides are hydrolysed by lipase to glycerol and fatty acids
-glycerol can be converted to triose phosphate and respired
-fatty acids are long chain hydrocarbons with a carboxylic acid
-hence in each molecule there are many carbon atoms, many hydrogen atoms and very few oxygen atoms
-these molecules are source of many protons for oxidative phosphorylation and so fats produce much more ATP than equivalent mass of carbohydrate

62
Q

Describe steps of lipid oxidation

A

1) with aid of some energy from hydrolysis of one molecule ATP to AMP each fatty acid is combined with coenzyme A
2) fatty acids-CoA complex is transported into mitochondrial matrix where it is broken down into two carbon acetyl groups each attached to CoA
3) this beta-oxidation pathway generates reduced NAD and reduced FAD
4) acetyl groups are released from CoA and enter Krebs cycle by combining with the four carbon oxaloacetate
-for every acetyl group oxidised in the Krebs cycle, three molecules of reduced NAD, one molecule of reduced FAD and molecule of ATP by substrate level phosphorylation are made

63
Q

Energy value of proteins

A

-excess amino acids released after the digestion of proteins, are deaminated in the liver
-deamination of amino acid involves removal of amino group its subsequent conversion to urea that is removed via kidney
-the rest of amino acid molecule, a keto acid, enters the respiration pathway as pyruvate, acetyl CoA or Krebs cycle acid such as oxaloacetic acid
-during fasting, starvation or prolonged exercise when insufficient glucose or lipid are available for respiration, proteins from muscle can be hydrolysed to amino acids which are then respired
-these amino acids may be converted to pyruvate or acetate and enter the krebs cycle

64
Q

Describe the energy values of different respiratory substrates

A

-most of the ATP produced during aerobic respiration is made during oxidative phosphorylation
-greater the availability of protons for chemiosmosis, the more ATP can be produced
-therefore more hydrogen atoms there are in a molecule of respiratory substrate, the more ATP can be generated per molecule of substrate
-carbohydrate=15.8kJ g-1
-lipid=39.4kJ g-1
-protein=17kJ g-1
-as the protons ultimately combine with oxygen atoms to form water, the greater the proportion of hydrogen atoms in a molecule, the more oxygen will be needed for its respiration

65
Q

What is the respiratory quotient

A

RQ=CO2 produced/ O2 consumed
-of the RQ value is greater than 1 this indicates that some anaerobic respiration is taking place because it shows that more carbon dioxide is being produced than oxygen being consumed
-e.g. glucose= 1
-fatty acids=0.7
-amino acids =0.8