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Metabolism · Cellular metabolism

Cellular respiration

Before you start, make sure you know: Structures of nutrition (Biology (high school))

Imagine a soccer player finishing a match on a hot afternoon in Houston. Her cells can get energy from glucose in two ways: by burning it all at once, as in a laboratory, or by breaking it down little by little, in dozens of linked steps, capturing the energy as ATP at each one. The second option is cellular respiration, and it is the one used by almost all living things.

Glycolysis: the first step, in the cytosol

If you grow yeast or muscle cells in a container with no oxygen at all and with glucose, you find that the sugar is used up quickly and the cells survive by producing ATP: how does the cell manage to extract energy from a carbohydrate without using oxygen?

Overview of aerobic respiration in three boxes: 1 glycolysis in the cytosol, 2 Krebs cycle in the matrix, 3 electron transport chain in the inner membrane. 1 Glycolysis cytosol 2 Krebs cycle matrix 3 Electron chain inner membrane pyruvate NADH FADH₂ pyruvate is oxidized to acetyl-CoA between 1 and 2 Diagram of the two phases of glycolysis, with the initial expenditure of two ATP and the final production of four ATP, two NADH and two pyruvate molecules from one glucose. glucose (6C) glycolysis phase 1: invests 2 ATP phase 2: produces 4 ATP and 2 NADH pyruvate pyruvate
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Write the overall equation for the aerobic respiration of glucose and state which substance is oxidized and which is reduced in the process.

Write the overall equation for the aerobic respiration of glucose and state which substance is oxidized and which is reduced in the process.

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Where in the cell does glycolysis occur, and what net products are obtained from one molecule of glucose in this stage?

Where in the cell does glycolysis occur, and what net products are obtained from one molecule of glucose in this stage?

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Name the four stages of aerobic respiration and state where in the eukaryotic cell each one takes place.

Name the four stages of aerobic respiration and state where in the eukaryotic cell each one takes place.

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For each glucose molecule, glycolysis has a net balance of $2\ \text{ATP}$ and $2$ NADH. Explain why it is called a "net" balance, detailing how many ATP are consumed in…

For each glucose molecule, glycolysis has a net balance of $2\ \text{ATP}$ and $2$ NADH. Explain why it is called a "net" balance, detailing how many ATP are consumed in the first phase and how many are produced in the second.

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The fate of pyruvate: respire or ferment

Diagram of the fate of pyruvate: with oxygen it enters the mitochondrion (aerobic respiration); without oxygen it is fermented in the cytosol and lactate or ethanol is obtained. pyruvate with O₂ mitochondrion aerobic respiration without O₂ fermentation in the cytosol lactate or ethanol
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What is pyruvate and what are its two main fates after glycolysis depending on whether oxygen is available or not? State what type of metabolic pathway it follows in…

What is pyruvate and what are its two main fates after glycolysis depending on whether oxygen is available or not? State what type of metabolic pathway it follows in each case.

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Define fermentation and name the two main types with their final products, indicating an organism or tissue that carries out each one.

Define fermentation and name the two main types with their final products, indicating an organism or tissue that carries out each one.

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In lactic acid fermentation, pyruvate is converted into lactate. Explain why this process allows $\text{NAD}^+$ to be regenerated and in what situations human muscles…

In lactic acid fermentation, pyruvate is converted into lactate. Explain why this process allows $\text{NAD}^+$ to be regenerated and in what situations human muscles use it.

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Yeasts and our muscle cells can respire or ferment depending on the available oxygen. Explain how the cell "decides" between one pathway and the other (the Pasteur…

Yeasts and our muscle cells can respire or ferment depending on the available oxygen. Explain how the cell "decides" between one pathway and the other (the Pasteur effect) and what advantage it gets when, with oxygen present, it reduces glucose consumption while maintaining the same ATP supply.

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In an industrial bioreactor containing yeast (Saccharomyces cerevisiae*) fed with glucose, substrate consumption and formed metabolites are monitored. In an initial…

In an industrial bioreactor containing yeast (Saccharomyces cerevisiae) fed with glucose, substrate consumption and formed metabolites are monitored. In an initial anaerobic phase, the yeast consumes glucose at a high rate, producing ethanol and $\text{CO}_2$. When oxygen is continuously injected (second phase), the rate of glucose consumption is observed to decrease to one-fourth (Pasteur effect) and ethanol production stops completely. a) Interpret and justify at a bioenergetic level why yeast consumes much more glucose per unit time in anaerobiosis than in aerobiosis to maintain the same rate of cell division. b) If, instead of yeast, a culture of skeletal muscle cells were subjected to these same two conditions, predict which organic metabolite would accumulate in the first phase and reason whether $\text{CO}_2$ would be released. c) Justify the common metabolic need that compels both yeast and muscle cells to reduce pyruvate during fermentation.

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The Krebs cycle: in the mitochondrial matrix

When mitochondria are supplied with glucose labeled with radioactive carbon, the $\text{CO}_2$ they give off contains that label, but the amount of oxaloacetate in the matrix stays constant after millions of molecules have been broken down: how can the fuel be completely oxidised within a pathway whose components never run out?

Krebs cycle in the mitochondrial matrix: acetyl-CoA enters, two CO₂ leave, NADH, FADH₂ and ATP are produced, and oxaloacetate is regenerated to start another turn. acetyl-CoA enters CO₂ leaves (×2) NADH, FADH₂, ATP oxaloacetate regenerated Krebs cycle mitochondrial matrix
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What is the Krebs cycle? State which two-carbon molecule enters it coming from the oxidation of pyruvate and which gas is released in its reactions.

What is the Krebs cycle? State which two-carbon molecule enters it coming from the oxidation of pyruvate and which gas is released in its reactions.

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Draw or describe a mitochondrion, pointing out its outer membrane, its inner membrane with the cristae and the matrix, and state in which zones the Krebs cycle and the…

Draw or describe a mitochondrion, pointing out its outer membrane, its inner membrane with the cristae and the matrix, and state in which zones the Krebs cycle and the electron transport chain occur.

You can do it on paper and send a photo with your answer.

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In the diagram of aerobic respiration, state which stage corresponds to each numbered box (1, 2, and 3), name the molecules labeled A and B, and indicate where in the…

In the diagram of aerobic respiration, state which stage corresponds to each numbered box (1, 2, and 3), name the molecules labeled A and B, and indicate where in the cell each stage takes place.

glucose 1 2 3 A CO₂ O₂ B ATP
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In the Krebs cycle, acetyl-CoA joins oxaloacetate and, after a series of reactions, the oxaloacetate is regenerated. Explain why this pathway is called a "cycle" and…

In the Krebs cycle, acetyl-CoA joins oxaloacetate and, after a series of reactions, the oxaloacetate is regenerated. Explain why this pathway is called a "cycle" and detail what energy products and what waste product are generated per turn.

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The electron transport chain and oxidative phosphorylation

Animation of the respiratory chain: an electron travels from NADH through complexes I, III and IV to oxygen; at each complex a proton H⁺ is raised into the intermembrane space, and then all three return to the matrix through ATP synthase, which spins. inner membrane I III IV ATP synthase NADH → e⁻ O₂ + 4H⁺ → 2H₂O pumping of H⁺ H⁺ returns → ATP
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State which molecule acts as the final electron acceptor in the electron transport chain and what substance is formed when that molecule is reduced.

State which molecule acts as the final electron acceptor in the electron transport chain and what substance is formed when that molecule is reduced.

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Explain the role played by $\text{NAD}^+$ and FAD in cellular respiration and what happens to their reduced forms (NADH and $\text{FADH}2$) in the electron transport…

Explain the role played by $\text{NAD}^+$ and FAD in cellular respiration and what happens to their reduced forms (NADH and $\text{FADH}_2$) in the electron transport chain.

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ATP synthase works like a rotary molecular motor. Explain what makes it spin, what reaction it catalyzes and in which membrane it is located in the mitochondrion.

ATP synthase works like a rotary molecular motor. Explain what makes it spin, what reaction it catalyzes and in which membrane it is located in the mitochondrion.

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Mitochondria possess their own DNA, their own ribosomes and divide by binary fission. Explain what evolutionary origin these data suggest (the endosymbiotic theory) and…

Mitochondria possess their own DNA, their own ribosomes and divide by binary fission. Explain what evolutionary origin these data suggest (the endosymbiotic theory) and why these organelles are the right place to house cellular respiration.

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Assays are performed with isolated mitochondria supplied with different respiratory substrates: when malate is provided (which generates intramitochondrial NADH),…

Assays are performed with isolated mitochondria supplied with different respiratory substrates: when malate is provided (which generates intramitochondrial NADH), $\text{O}_2$ consumption is recorded along with a synthesis ratio of about $2.5\ \text{ATP}$ per electron pair; when rotenone (an inhibitor of Complex I) is added, $\text{O}_2$ consumption ceases, but it is restored upon supplying succinate (which reduces FAD to $\text{FADH}_2$), yielding only about $1.5\ \text{ATP}$ per electron pair. a) Justify at the molecular and chemiosmotic level the biophysical cause of this difference in energy yield between both substrates. b) Reasonably deduce what would happen to $\text{O}_2$ consumption and ATP synthesis from succinate if a specific inhibitor of Complex IV (cytochrome c oxidase) is added. c) In skeletal muscle, electrons from glycolytic NADH enter the respiratory chain via the glycerol-3-phosphate shuttle, whereas in the myocardium they do so through the malate-aspartate shuttle. Calculate the difference in the total net ATP yield per mole of fully oxidized glucose between both tissues and justify the metabolic cause of this discrepancy.

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Poisons and uncouplers: when the chain fails

This section goes beyond the course standards for this level.

Inner mitochondrial membrane with the respiratory chain and ATP synthase in two cases: A, cyanide binds to complex IV, electrons do not reach oxygen and no ATP is formed; B, the uncoupler DNP returns protons to the matrix without passing through ATP synthase and the energy is lost as heat. A. Cyanide: blocks complex IV Qc IIIIIV NADH → NAD⁺e⁻ ATP synthase intermembranespaceinnermembranematrix ½ O₂ H₂O CN⁻ With no final acceptor, the complexes do not pump H⁺: there is no gradientand ATP synthase stops → no ATP is formed even if O₂ is present. B. DNP (uncoupler): H⁺ leak without ATP Qc IIIIIV NADH → NAD⁺e⁻ ATP synthase intermembranespaceinnermembranematrix ½ O₂ H₂O H⁺H⁺H⁺ H⁺H⁺H⁺H⁺H⁺ H⁺ heat DNP The H⁺ return to the matrix without passing through ATP synthase:O₂ is consumed, but the energy of the gradient is lost as heat.
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To experimentally test the chemiosmotic hypothesis, intact mitochondria are isolated and suspended in a medium at pH 8.0 without ADP or oxidizable substrates. After…

To experimentally test the chemiosmotic hypothesis, intact mitochondria are isolated and suspended in a medium at pH 8.0 without ADP or oxidizable substrates. After allowing the matrix to reach this pH, they are abruptly transferred to a medium at pH 4.0 containing ADP and $\text{P}_i$, in the total absence of oxygen and electron donors. a) Predict with justification whether ATP will be synthesized under these artificial conditions and describe the biophysical mechanism through which ATP synthase exploits this situation. b) What would happen to ATP synthesis if the inner mitochondrial membrane had previously been treated with an ionophore substance that allows the free passage of protons? Justify your answer. c) Reason why, under normal physiological conditions, oxygen depletion halts oxidative phosphorylation.

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Cyanide blocks the last complex of the respiratory chain (cytochrome c oxidase). Predict what will happen to oxygen consumption, ATP synthesis, and the fate of pyruvate…

Cyanide blocks the last complex of the respiratory chain (cytochrome c oxidase). Predict what will happen to oxygen consumption, ATP synthesis, and the fate of pyruvate in a poisoned cell, and explain why cyanide is lethal even if glucose is available.

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2.4-Dinitrophenol (DNP) is an uncoupler: it makes the inner mitochondrial membrane permeable to protons without ATP being produced. Predict, with reasoning, what will…

2.4-Dinitrophenol (DNP) is an uncoupler: it makes the inner mitochondrial membrane permeable to protons without ATP being produced. Predict, with reasoning, what will happen to oxygen consumption, to ATP synthesis and to the body temperature of someone who ingests it, and explain why it came to be used as a weight-loss drug with deadly consequences.

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Carbon monoxide binds to hemoglobin with more affinity than oxygen. a) Explain what effect it has on the transport of $\text{O}2$ to the tissues. b) Reason which stages…

Carbon monoxide binds to hemoglobin with more affinity than oxygen. a) Explain what effect it has on the transport of $\text{O}_2$ to the tissues. b) Reason which stages of cellular respiration will be affected and why cells switch to fermentation even when they have glucose. c) Compare the toxicity mechanism of carbon monoxide with that of cyanide.

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Back to the beginning: By breaking glucose down step by step instead of burning it all at once, the cell avoids an uncontrolled combustion that would destroy its structures and manages to convert about $30\%$ of that chemical energy into 30-32 ATP bonds that can be used directly.

Summary

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