Respiration

Respiration

Respiration is the reaction that produces the ATP needed for other metabolic reactions in cells. It is an enzyme controlled reaction and is therefore sensitive to temperature and pH changes.

Glucose is broken down to release the ATP, but if there is no glucose, glycogen (in animals) or starch (in plants) stores of glucose left then other respiratory substrates are used. Lipids can be hydrolysed to glycerol and fatty acids. The glycerol is then phosphorylated into triose phosphate and enters aerobic respiration at the Krebs cycle. Proteins could also be modified and used. Amino acids must be hydrolysed and the amino group removed (deamination). The carbon compound that remains can enter the Krebs cycle.

Aerobic Respiration

Aerobic respiration is split into four stages:

  1. Glycolysis (cytoplasm)
  2. Link reaction (Mitochondrial matrix)
  3. Krebs cycle (Mitochondrial matrix)
  4. Oxidative Phosphorylation (Cristae)

Respiration, figure 1

Respiration, figure 2

Glycolysis

Glycolysis is the first stage and as it does not require oxygen and occurs in the cytoplasm it is in both anaerobic and aerobic respiration. Glycolysis (sugar splitting) involves three key stages:

  1. Substrate level phosphorylation - The glycose has two phosphate groups added to it from two ATP molecules.
  2. Phosphorylation makes the glucose-2-phosphate unstable and it splits into two 3-carbon compounds, triose phosphate (TP).
  3. The two TP molecules are both oxidised to form two pyruvate molecules by removing a hydrogen from each. The hydrogen is picked up by two NAD molecules to become NADH. This process also releases 4 ATP.

Therefore glycolysis results in the production of 2 NADH, 2 pyruvate and a net gain of 2 ATP. The NADH and pyruvate are both needed for subsequent stages in aerobic respiration and therefore are actively transported into the mitrochondrial matrix.

This reaction occurs in the mitochondrial matrix and converts pyruvate into acetyl CoA.

Pyruvate contains 3 carbons whereas acetyl CoA contains two, so a carbon is removed in this stage in the form of carbon dioxide. This is known as decarboxylation and requires decarboxylase enzymes. 2 hydrogen atoms are also removed to oxidise the carbon compound further to create acetate. This is known as dehydrogenation and is catalysed by dehydrogenase enzymes. The NAD picks up the hydrogen to become NADH. The coenzyme CoA combines with the acetate that is formed to create acetyl CoA, this is to assist in acetyl reacting in the Krebs cycle.

The reaction occurs twice per glucose molecule as there are two pyruvate molecules.

Respiration, figure 1

The overall products from the link reaction per glucose molecule are:

  • 2 x Acetyl CoA
  • 2 CO2
  • 2 reduced NAD

Krebs Cycle

The acetyl CoA reacts with a four-carbon molecule, releasing coenzyme A and producing a six-carbon molecule that enters the Krebs cycle. In a series of oxidation-reduction reactions, the Krebs cycle generates 8 reduced coenzymes, 2 ATP by substrate-level phosphorylation, and 4 carbon dioxide are lost. In total therefore, per glucose molecule 2 ATP, 6 NADH and 2 FADH are produced. The Krebs cycle is also known as the citric acid cycle.

Respiration, figure 1

Oxidation Phosphorylation

This is the final stage of aerobic respiration where most ATP is syntehsised and oxygen is used. This stage involves the transfer of electrons down the electron transfer chain and the movement of protons across the inner mitochondrial membranes. The movement of these protons is down a concentration gradient catalysed by ATP synthase,embedded in these membranes- this is another example of chemiosomotic theory.

Respiration, figure 1

Is this stage all of the accumulated reduced coenzymes release the hydrogens and these split into protons (H+) and electrons (e-). The e- are passed down a series of electron carrier proteins embedded in the inner mitochondrial membrane, losing energy as the move (electron transport chain). The small amount of energy the electrons release pumps protons from the mitochondrial matrix into the intermembrane space. This creates an electrochemical gradient across the membrane. Therefore the protons move down the electrochemical gradient back into the matrix via ATP synthase making ATP. This movement of H+ is known as Chemiosmosis. Oxygen is the final electron acceptor in the electron transport chain. The oxygen combines with the electrons and the protons to form water.

Respiration, figure 2

Anaerobic Respiration

In the absence of oxygen respiration occurs anaerobically. The pyruvate produced in glycolysis is reduced to form ethanol (in plants and microbes) or lactate (in animals) by gaining the hydrogen from reduced NAD. This oxidises NAD so that it can be reused in glycolysis and ensure more ATP is continued to be produced.

Respiration, figure 1

Efficiency

1 reduced NAD can result in a yield of 3 ATP molecules, whereas 1 reduced FAD can result in a yield of 2 ATP molecules. Therefore, the total yield of ATP from one glucose molecule should be 38 molecules of ATP. Aerobic respiration is approximately 32% efficient. This is due to some protons leaking across the mitochondrial membrane during oxidative phosphorylation, ATP being used to actively transport pyruvate and NADH into the matrix and because some energy is lost as heat.

Anaerobic respiration is even less efficient, because only 2 ATP molecules and produced from one glucose molecule.

How many carbons does glucose have?
6
Where does glycolysis take place?
Cytoplasm
Why are the glycolysis reactions described as anaerobic?
Your answer should include: require / no / oxygen
Where does the Krebs cycle take place?
Your answer should include: Mitochondrial / matrix
How many carbons does the intermediate that reacts with acetyl CoA have?
4
How many carbon dioxides are lost per turn of the Krebs cycle?
2
Why must oxidative phosphorylation occur for the Krebs cycle to continue?
Your answer should include: NADH / to / NAD
What is the final electron and hydrogen acceptor in oxidative phosphorylation?
Oxygen