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Cellular Respiration
Learning Intention:
To learn about cellular respiration
Success Criteria:
By the end of the lesson I should be able to
• Describe the role of dehydrogenase in glycolysis and citric acid pathway.
• Explain the role of ATP in energy transfer and phosphorylation.
• Describe glycolysis.
• Describe the events that occur during the citric acid cycle.
• Describe the events that occur during the electron transport chain.
• State the location of the citric acid cycle and electron transfer chain.
• State the function of phosphofructokinase in respiration.
• State the role of coenzymes FAD and NAD in respiration.
ATP
• Adenosine Triphosphate
• Molecule able to provide energy immediately.
adenosine Pi Pi Pi
ATP
• Adenosine Triphosphate• This bond broken to release energy
• Adenosine Diphosphate and an inorganic phosphate are produced
adenosine Pi Pi Pi
PHOSPHORYLATION
Breakdown releasing energy
ATP ADP + Pi
Build up requiring energy
There is a constant supply of ATP in our cells because it is synthesised as fast as it is used
Importance of ATP formation• We all need energy to function and
we get this energy from the foods we eat.
• The most efficient way for cells to harvest energy stored in food is through cellular respiration
• a catabolic pathway for the production of adenosine triphosphate (ATP).
• ATP, a high energy molecule, is expended by working cells.
• Cellular respiration occurs in both eukaryotic and prokaryotic cells.
RESPIRATION
• Process by which energy is released from foods by oxidation.
• It involves the regeneration of ATP which is a high energy compound.
• Consists of 3 stages– GLYCOLYSIS– KREBS CYCLE– ELECTRON TRANSFER SYSTEM
GLYCOLYSIS• Takes place in the cytoplasm of the cell.• Is a series of enzyme controlled steps• Does not require oxygen.• Glucose (6C) is broken down into two
molecules of Pyruvic Acid (3C).• Net gain of 2 ATP.• Hydrogen released binds to a co-enzyme,
NAD/FAD by reduction.
Energy investment and payoff during glycolysis
• The first half of the chain makes up the energy investment phase
• Where 2 ATP are used per glucose molecule
• The second half of the chain makes up the energy payoff phase where 4 ATP are produced per glucose molecule
Phosphorylation occurs twice. The 2nd time by phosphofructokinase
Phosphorylation during energy investment stage
• The first phosphorylation of intermediates leads to a product that can continue to a number of other pathways
• Eg fermentation in the absence of oxygen
• The second phosphorylation catalysed by phosphofructokinase is irreversible and leads only to the glycolytic pathway
Energy payoff stage
• Hydrogen ions are released by the action of a dehydrogenase enzyme
• The co enzymes NAD and FAD pick up the H+ ions to form NADH or FADH in glycolysis and the citric acid pathways
• NADH and FADH release high energy electrons to the electron transport chain on the mitochondrial membrane
• Resulting in the synthesis of ATP
GLYCOLYSIS
GLUCOSE
PYRUVIC ACID
2 ATP
2 ADP+Pi
4 ATP
4 ADP+Pi
2 NAD
2 NADH2
MITOCHONDRIA
• Krebs Cycle takes place in the matrix.
• Electron Transfer System takes place on the cristae.
KREBS CYCLE
• Takes place in the matrix of the mitochondria.
• Requires oxygen.
• Pyruvic acid converted to Acetyl which combines with Coenzyme A (2C).
• Acetyl CoA enters Krebs and combines with oxaloactate a 4C compound to form 6C citrate.
KREBS CYCLE
• Citrate is converted back to oxaloacetate by a series of enzyme controlled reactions.
• During the cycle, carbon is released in the form of carbon dioxide, hydrogen is released and binds to NAD/FAD and ATP is formed.
KREB’S CYCLE
CO2
2NAD
2NADH2
PYRUVIC ACID (3C)
ACETYL COA (2C)
CITRIC ACID (6C)
5C COMPOUND
4C COMPOUND
4C oxaloacetate
4C COMPOUND
2NAD
2NADH2
CO2
CO2
2NAD
2FAD
2NAD2NADH2
2FADH2
2NADH2
ADP+Pi
ATP
ELECTRON TRANSFER SYSTEM• Also known as cytochrome system or hydrogen transfer
system.
• Takes place on the cristae of the mitochondria.
• The reduced NAD/FAD transfer the high energy electrons to a chain of carriers called the cytochrome system
• Energy from the electrons is used to pump H+ across the inner membrane of the mitochondria
• The return flow of H+ ions rotates part of the membrane protein ATP synthase and ATP is generated
• The final electron acceptor is oxygen which combines with hydrogen ions and low energy electron to form water
ELECTRON TRANSFER SYSTEM
• The transfer of one H molecule releases 3 ATP molecules.
• This is called oxidative phosphorylation.
ELECTRON TRANSFER SYSTEM
NADH2
NAD OXYGEN
WATER
ADP +Pi ADP +Pi ADP +Pi
ATP ATP ATP
SERIES OF HYDROGEN CARRIERS
ATP PRODUCTION
• Each NADH2 molecule produces 3 ATP
• 12 NADH2 = 36ATP from Kreb’s cycle
• 2 ATP from glycolysis
• 38 ATP in total
Substrates for respiration• Starch and glycogen are broken
down to glucose• Maltose and sucrose can be
converted to glucose or glycolysis intermediates
• Proteins can be broken down to amino acids and converted to intermediates of glycolysis and the citric acid cycle
• Fats can be broken down into fatty acids and glycerol. Glycerol is converted to a glycolytic intermediate and fatty acids converted for use in the citric acid cycle
Regulation of Cellular Respiration
• The cell conserves its resources by only producing ATP when required
• Feedback inhibition regulates and synchronises the rates of the glycolytic and citric acid cycle pathways
• If more ATP than the cell needs is produced the ATP inhibits phosphofructokinase slowing glycolysis
• High concentrations of citrate also inhibit phosphofructokinase
• When citrate concentration drops the enzyme is no longer inhibited
Energy systems in muscle cells
• During strenuous muscle activity the cell breaks down its reserves of ATP and releases energy
• Muscle cells can only store enough ATP for a few muscle contractions
• Muscle cells have an additional source of energy
Energy systems in muscle cells• Creatine phosphate
acts as a high energy reserve available to muscle cells during strenuous execrise
• During strenuous exercise creatine phosphate breaks down releasing energy and phosphate which are used to convert ADP to ATP by phosphorylation
• This system can only support strenuous muscle activity for around 10 seconds before the supply of creatine phosphate runs out
• When ATP demand is low, ATP from cellular respiration restores the levels of creatine phosphate
Lactic acid metabolism
• If strenuous exercise continues the cells respire anaerobically as they do not get enough oxygen
• Neither the citric acid cycle nor electron transport system can generate the ATP required
• Only glycolysis is able to provide more ATP
• This results in pyruvate being converted to lactic acid
• It involves the transfer of hydrogen from NADH produced during glycolysis to pyruvic acid to produce lactic acid
• NAD is regenerated to maintain ATP production during glycolysis
• Only 2 molecules of ATP are produced from each molecule of glucose
• As lactic acid builds in the muscles it causes fatigue
• An oxygen debt builds up
• When the oxygen debt is repaid, the lactic acid is converted back to pyruvic acid which then enters the aerobic pathway.
ANAEROBIC RESPIRATION
Glucose
(6C)
Pyruvic Acid
(2 X 3C)
Lactic Acid
(2 X 3C)
Oxygen debt builds up
Oxygen debt repaid
AEROBIC V ANAEROBICAerobic
RespirationAnaerobic
Respiration
Number of ATP molecules per
glucose molecule
38 2
Products of reaction (other
than ATP)
Carbon dioxide and
water
Lactic acid
Location in cell mitochondrion cytoplasm
Types of skeletal muscle• Skeletal muscles bring about movement of the
body• Two types of skeletal muscle fibres
• Type 1 slow twitch muscle fibres – These contract slowly, but sustain contractions for
longer– Good for endurance activities– Rely on aerobic respiration to generate ATP– Have many mitochondria– Have a large blood supply – Have a high concentration of myoglobin which is good
at storing oxygen ( myoglobin also extracts oxygen from the blood)
– Major storage fuel is fats
• Type 2– Muscle fibres contract quickly– Over short periods of time– Good for bursts of activity– Generates ATP through glycolysis– Have only a few mitochondria– Lower blood supply– Major storage fuels are glycogen and creatine
phosphate
• Most human muscle tissue contains both slow and fast twitch fibres
• Athletes show distinct patterns of muscle fibres that reflect their sporting activities
• Fast twitch fibres are responsible for strength. Sports requiring sudden bursts of maximum activity, such as in sprinting, throwing, jumping and lifting rely on fast twitch fibres.
•Slow twitch fibres are responsible for stamina and suppleness. The action of slow twitch fibres is dependent on aerobic respiration. So, the supply of oxygen is important. The presence of large quantity of myoglobin is necessary. Therefore, slow twitch fibres give the characteristic red colour.
Summary• Substrates for respiration. Starch and glycogen, other sugar molecules,
amino acids and fats. • Regulation of the pathways of cellular respiration by feedback inhibition —
regulation of ATP production, by inhibition of phosphofructokinase by ATP and citrate,
• synchronisation of rates of glycolysis and citric acid cycle. • Energy systems in muscle cells. • Creatine phosphate breaks down to release energy and phosphate that is
used to convert ADP to ATP at a fast rate. This system can only support strenuous muscle activity for around 10 seconds, when the creatine phosphate supply runs out. It is restored when energy demands are low.
• Lactic acid metabolism. Oxygen deficiency, conversion of pyruvate to lactic acid, muscle fatigue, oxygen debt.
• Types of skeletal muscle fibres • Slow twitch (Type 1) muscle fibres contract more slowly, but can sustain
contractions for longer and so are good for endurance activities. Fast twitch (Type 2) muscle fibres contract more quickly, over short periods, so are good for bursts of activity.