Biochemistry Chapter: Electron Transport Chain
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Questions and Answers

Which of the following represents the reduced form of coenzyme Q?

  • FMNH2
  • QH2 (correct)
  • NAD+
  • Q

Complex II is responsible for transferring hydrogen from NADH.

False (B)

What is formed when NADH donates electrons to FMN?

FMNH2

At Complex I, NADH is converted to ________ during the electron transport chain.

<p>NAD+</p> Signup and view all the answers

Match the following complexes with their corresponding electron carriers:

<p>Complex I = FMN Complex II = FADH2 Complex III = Cytochrome c Complex IV = Oxygen</p> Signup and view all the answers

What is the final product formed when electrons from the electron transport chain combine with oxygen?

<p>H2O (B)</p> Signup and view all the answers

Electron transport does not produce ATP energy.

<p>False (B)</p> Signup and view all the answers

What are the hydrogen ions and electrons transferred from NADH and FADH2 used for in the electron transport chain?

<p>To form water and produce ATP energy.</p> Signup and view all the answers

What is the primary function of ATP synthase?

<p>To convert ADP and Pi into ATP (C)</p> Signup and view all the answers

What compound is formed by the hydrolysis of succinyl CoA?

<p>GTP (C)</p> Signup and view all the answers

The F1 complex of ATP synthase contains the channel for proton flow.

<p>False (B)</p> Signup and view all the answers

Succinate undergoes hydration in the process of forming fumarate.

<p>False (B)</p> Signup and view all the answers

What occurs in the T site of the F1 complex during ATP synthesis?

<p>ATP is formed and remains strongly bound.</p> Signup and view all the answers

Which of the following describes catabolic reactions?

<p>Metabolic reactions that break down large molecules to smaller molecules + energy. (D)</p> Signup and view all the answers

The flow of protons through the _____ complex provides the energy for ATP synthesis.

<p>F0</p> Signup and view all the answers

What is the result of the dehydrogenation of malate?

<p>Oxaloacetate</p> Signup and view all the answers

Match the following sites in the F1 complex with their functions:

<p>L site = Binds ADP and Pi T site = ATP formation O site = Releases ATP</p> Signup and view all the answers

The citric acid cycle can operate under both aerobic and anaerobic conditions.

<p>False (B)</p> Signup and view all the answers

Succinyl CoA provides energy to add phosphate to GDP and form _____ .

<p>GTP</p> Signup and view all the answers

How many ATP are synthesized from the energy provided by one NADH in Complex I?

<p>2.5 ATP (D)</p> Signup and view all the answers

Match the following reactions with their product:

<p>Hydrolysis of Succinyl CoA = GTP Dehydrogenation of Succinate = Fumarate Hydration of Fumarate = Malate Dehydrogenation of Malate = Oxaloacetate</p> Signup and view all the answers

What is produced during anaerobic conditions?

<p>Lactate</p> Signup and view all the answers

The citric acid cycle oxidizes the acetyl group in acetyl CoA to produce ________.

<p>CO2</p> Signup and view all the answers

What change occurs to the L site of the F1 complex after the center subunit turns?

<p>It changes to a T conformation.</p> Signup and view all the answers

Which molecule is reduced during the dehydrogenation of succinate?

<p>FAD (D)</p> Signup and view all the answers

The F0 complex contains the protein subunits where ATP forms.

<p>False (B)</p> Signup and view all the answers

Water is added to fumarate to produce malate.

<p>True (A)</p> Signup and view all the answers

Match the following terms with their descriptions:

<p>Glycolysis = Reaction series that converts glucose to pyruvate. Lactate = Produced during anaerobic conditions. Catabolic Reactions = Metabolic reactions that break down large molecules to smaller molecules + energy. Coenzymes = Substances that remove or add H atoms in oxidation and reduction reactions.</p> Signup and view all the answers

What is the first product formed when oxaloacetate combines with acetyl CoA?

<p>Citrate (A)</p> Signup and view all the answers

The process through which succinate loses two H to form a double bond is known as _____ .

<p>dehydrogenation</p> Signup and view all the answers

Isomerization is a process that changes a molecule from one isomer to another.

<p>True (A)</p> Signup and view all the answers

What does the citric acid cycle generate that is essential for further energy production?

<p>NADH and FADH2</p> Signup and view all the answers

What is the main product of the transamination reaction involving aspartate and alpha-ketoglutarate?

<p>Oxaloacetate (A), Glutamate (C)</p> Signup and view all the answers

The urea cycle converts ammonium ion to urea in the liver.

<p>True (A)</p> Signup and view all the answers

Name one enzyme involved in the transamination reaction.

<p>Aminotransferase</p> Signup and view all the answers

The products of transamination are _____ and glutamate.

<p>oxaloacetate</p> Signup and view all the answers

Match the following processes with their products:

<p>Transamination of aspartate = Oxaloacetate and glutamate Oxidative deamination of glutamate = Alpha-ketoglutarate and ammonium ion Urea cycle = Urea Carbamoyl phosphate formation = Carbamoyl phosphate</p> Signup and view all the answers

Which molecule provides the amino group for the formation of glutamate in a transamination reaction?

<p>Aspartate (C)</p> Signup and view all the answers

Carbamoyl phosphate is formed in the cytoplasm during the reaction of ammonium ion and CO2.

<p>False (B)</p> Signup and view all the answers

How much urea does the body typically produce daily for urine formation?

<p>25-30 g</p> Signup and view all the answers

What is the product of the urea cycle that is formed from ammonium ion?

<p>Urea (C)</p> Signup and view all the answers

The formation of carbamoyl phosphate occurs in the cytosol.

<p>False (B)</p> Signup and view all the answers

Which group is transferred to ornithine to form citrulline?

<p>Carbamoyl group</p> Signup and view all the answers

During the urea cycle, ______________ is cleaved from argininosuccinate.

<p>Fumarate</p> Signup and view all the answers

Match the following steps of the urea cycle with their corresponding sites:

<p>Formation of carbamoyl phosphate = Mitochondrion Aspartate combines with citrulline = Cytosol Hydrolysis forms urea = Cytosol Fumarate is cleaved = Cytosol</p> Signup and view all the answers

Which energy molecule is used when citrulline combines with aspartate?

<p>AMP (C)</p> Signup and view all the answers

The urea cycle converts aspartate into glucose.

<p>False (B)</p> Signup and view all the answers

What accompanies the conversion of 3 ATP during the urea cycle?

<p>2 ADP, 1 AMP, 4 Pi</p> Signup and view all the answers

Flashcards

Catabolic Reactions

Metabolic reactions that break down large molecules into smaller molecules, releasing energy in the process.

Coenzymes

Substances that assist enzymes in chemical reactions by accepting or donating electrons (H atoms) during oxidation and reduction.

Glycolysis

A metabolic pathway that breaks down glucose into pyruvate, generating ATP and reducing NAD+ to NADH.

Lactate

A product of anaerobic fermentation, formed when pyruvate is reduced by NADH under oxygen-limited conditions.

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Citric Acid Cycle

A series of reactions that completely oxidizes acetyl CoA to CO2, producing ATP, NADH, and FADH2.

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What bonds with oxaloacetate in the citric acid cycle?

Acetyl (a 2-carbon unit) from acetyl CoA combines with oxaloacetate (a 4-carbon molecule) to form citrate (a 6-carbon molecule).

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How is citrate converted back to oxaloacetate in the citric acid cycle?

A series of oxidation and decarboxylation reactions transform citrate into oxaloacetate, releasing CO2 and generating reduced coenzymes (NADH and FADH2).

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What happens after oxaloacetate is regenerated in the citric acid cycle?

The regenerated oxaloacetate can combine with another acetyl group, starting the cycle again.

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Succinyl CoA Hydrolysis

The breaking of the thioester bond in succinyl CoA releases energy used to convert GDP to GTP, a high-energy compound.

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GTP: A High-Energy Compound

GTP is a molecule similar to ATP that carries a lot of energy, often used in reactions requiring energy.

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Succinate Dehydrogenation

Succinate loses two hydrogen atoms (H) and forms a double bond, producing fumarate. FAD picks up these hydrogen atoms and becomes FADH2.

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FADH2: A Reduced Electron Carrier

FADH2 is a reduced form of FAD, carrying electrons (and potential energy) to the electron transport chain.

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Fumarate Hydration

Fumarate gains a water molecule (H2O), breaking the double bond and forming malate.

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Malate Dehydrogenation

Malate gets oxidized, losing two hydrogen atoms and forming oxaloacetate with a carbonyl group (C=O). NAD+ takes these hydrogen atoms and converts to NADH + H+.

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NADH + H+: Reduced Electron Carrier

NADH + H+ is a reduced form of NAD+, carrying electrons (and potential energy) to the electron transport chain.

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Oxaloacetate: The Starting Point

Oxaloacetate is the final product of the citric acid cycle, ready to combine with acetyl-CoA to start another cycle.

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Electron Transport

A process that uses electron carriers to transfer electrons from NADH and FADH2 to oxygen, producing water and ATP energy.

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Electron Carriers

Molecules that transport electrons between different components of the electron transport chain.

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Oxidative Phosphorylation

The process of generating ATP using energy from the electron transport chain.

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What does NADH do in electron transport?

NADH donates electrons and protons to Complex I, initiating the electron transport chain.

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What does FADH2 do in electron transport?

FADH2 donates electrons and protons to Complex II, contributing to the electron flow.

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ATP Synthase

A protein complex embedded in the inner mitochondrial membrane that synthesizes ATP using proton motive force.

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Proton Motive Force

The potential energy stored in the concentration gradient of protons across the inner mitochondrial membrane.

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What is QH2 and why is it important?

QH2 is a mobile electron carrier that transfers electrons from Complex I or II to Complex III.

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F0 Complex

The part of ATP synthase embedded in the mitochondrial membrane that provides a channel for proton flow.

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What is Complex I?

Complex I (NADH dehydrogenase) accepts electrons from NADH, transferring them to FMN and eventually to coenzyme Q.

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What is Complex II?

Complex II (Succinate dehydrogenase) accepts electrons from FADH2, transferring them to coenzyme Q.

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F1 Complex

The part of ATP synthase that protrudes into the mitochondrial matrix and contains the catalytic sites for ATP synthesis.

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L Site

The subunit in F1 complex that binds ADP and Pi.

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What is coenzyme Q?

Coenzyme Q (ubiquinone) is a mobile electron carrier that accepts electrons from Complex I and II and delivers them to Complex III.

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T Site

The subunit in F1 complex where ATP is formed.

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O Site

The subunit in F1 complex that releases ATP.

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Transamination

A chemical reaction that transfers an amino group from an amino acid to an α-keto acid, forming a new amino acid and a new α-keto acid.

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α-ketoglutarate

A five-carbon α-keto acid involved in both the citric acid cycle and amino acid metabolism.

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Pyruvate

A three-carbon α-keto acid produced from the breakdown of glucose in glycolysis.

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Glutamate

A non-essential amino acid that plays a crucial role in nitrogen metabolism and neurotransmission.

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Oxidative Deamination

A metabolic process that removes the amino group from glutamate, producing α-ketoglutarate and ammonium ion.

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Urea Cycle

A metabolic pathway that detoxifies ammonium ions from amino acid breakdown by converting it to urea in the liver.

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Carbamoyl Phosphate

A high-energy molecule formed in the mitochondria from ammonium ion and carbon dioxide, involved in the urea cycle.

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Urea

A nitrogenous waste product produced in the urea cycle and excreted by the kidneys.

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Carbamoyl Phosphate Synthetase I

An enzyme that catalyzes the synthesis of carbamoyl phosphate from ammonia, carbon dioxide, and ATP.

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What does carbamoyl phosphate synthetase I do?

It catalyzes the synthesis of carbamoyl phosphate from ammonia, carbon dioxide, and ATP in the first step of the urea cycle.

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Where does carbamoyl phosphate synthesis occur?

Carbamoyl phosphate synthesis occurs in the mitochondria.

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What happens in the urea cycle?

The urea cycle is a metabolic pathway that converts ammonia into urea for excretion.

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Reaction 1 of the urea cycle

The carbamoyl group from carbamoyl phosphate is transferred to ornithine to form citrulline.

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What is citrulline?

A non-protein amino acid produced in the urea cycle.

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Reaction 2 of the urea cycle

Citrulline combines with aspartate to form argininosuccinate in the cytosol.

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What is argininosuccinate?

An intermediate in the urea cycle, formed by the condensation of citrulline and aspartate.

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Study Notes

Metabolic Pathways and Energy Production

  • Metabolism encompasses all chemical reactions in cells, breaking down (catabolism) or building (anabolism) molecules.
  • A metabolic pathway is a series of linked reactions, each catalyzed by a specific enzyme.
  • Pathways can be linear (a series of reactions yielding a final product) or cyclic (reactions regenerate the first reactant).
  • Digestion breaks down complex molecules like polysaccharides, lipids, and proteins into smaller components (e.g., glucose, fatty acids, amino acids).
  • Cells store energy from food as ATP (adenosine triphosphate).
  • Catabolism breaks down large molecules into smaller molecules, releasing energy.
  • Anabolism uses ATP energy to build larger molecules.

Stages of Metabolism

  • Stage 1: Digestion and hydrolysis. Large molecules are broken down into smaller molecules, which enter the bloodstream.
  • Stage 2: Degradation. Molecules are broken down further into two- and three-carbon compounds.
  • Stage 3: Oxidation. Small molecules are oxidized in the citric acid cycle and electron transport, producing ATP.

Metabolism and ATP Energy

  • Catabolic reactions break down large compounds, producing energy and smaller molecules.
  • Anabolic reactions use ATP to synthesize larger molecules consuming energy.
  • ATP is crucial for cellular processes like muscle contraction, synthesis of large molecules, sending nerve impulses, and transporting substances across cell membranes.
  • The hydrolysis of ATP to ADP releases energy.
  • 7.3 kcal/mol is required to convert ADP + P; to ATP.

Coenzymes in Metabolic Pathways

  • Oxidation involves the loss of hydrogen atoms, while reduction involves the gain.
  • Coenzymes like NAD+ and FAD carry hydrogen ions and electrons from or to the reacting substrate.
  • NAD+ (nicotinamide adenine dinucleotide) is involved in reactions producing carbon-oxygen double bonds.
  • FAD (flavin adenine dinucleotide) participates in reactions forming carbon-carbon double bonds.

Important Nucleotide-Containing Compounds

  • ATP is the primary energy currency for cells.
  • ATP consists of adenine (nitrogenous base), ribose (sugar), and three phosphate groups.
  • Hydrolysis of ATP releases energy (7.3 kcal/mol).
  • Hydrolysis of ADP further releases energy.

Mitochondria

  • Mitochondria are sausage-shaped organelles.
  • Contain outer and inner membranes.
  • Inner membrane folds into cristae, increasing surface area.
  • The inner membrane is impermeable to most substances.
  • The intermembrane space and the matrix are the compartments created by the inner membrane.

Glycolysis

  • Glycolysis is a metabolic pathway using glucose to break it down to pyruvate (3C) molecules.
  • It is an anaerobic process (occurs without oxygen).
  • It takes place in the cytoplasm.

Glycolysis: Energy-Investment Phase

  • In reactions 1-5 of glycolysis, energy is required to add phosphate groups to glucose.
  • Glucose is converted to two three-carbon molecules.

Glycolysis: Energy-Production Phase

  • In reactions 6-10 of glycolysis, energy is generated as sugar phosphates are cleaved to triose phosphates.
  • Four ATP molecules are produced for each glucose.

Pathways for Pyruvate

  • Pyruvate, under aerobic conditions, is converted to Acetyl CoA, CO2, and NADH in the mitochondria.
  • Under anaerobic conditions, pyruvate is converted to lactate in the cytosol.
  • In some microorganisms, pyruvate can be further converted into ethanol through fermentation.

Citric Acid Cycle

  • The citric acid cycle (stage 3) operates under aerobic conditions only.
  • Oxidizes the two-carbon acetyl group in acetyl-CoA to 2 CO₂.
  • Produces reduced coenzymes NADH and FADH₂ and one ATP directly

Electron Transport Chain

  • Electron carriers are oxidized and reduced to transfer hydrogen atoms and electrons from NADH and FADH₂ to oxygen.
  • Transfers hydrogen ions and electrons, forming water.
  • Produces ATP through oxidative phosphorylation.

ATP Synthase

  • Proton flow through ATP synthase provides energy for ATP synthesis.
  • The F₁ complex of ATP synthase turns the subunit (y) as protons flow through F₀.
  • The shape (conformation) of the three subunits changes in the process.

ATP from Glucose

  • Complete oxidation of glucose yields 32 ATP molecules.

Fatty Acid Activation

  • Fatty acid activation occurs in the cytosol.
  • A fatty acid combines with CoA and ATP to form fatty acyl-CoA, then combines with carnitine.

Transport of Fatty Acyl-CoA

  • Fatty acyl-CoA forms fatty acylcarnitine, which transports the fatty acyl group into the matrix.
  • The fatty acyl group recombines with CoA for oxidation.

Summary of Fatty Acid Activation

  • Fatty acid activation is complex but it regulates the degradation and synthesis of fatty acids.

Beta-Oxidation of Fatty Acids

  • The length of a fatty acid determines the number of acetyl CoA groups produced.
  • Reactions involved in the breakdown are dehydrogenation, hydration, and thiolysis.

ATP from Beta-Oxidation

  • Activation of a fatty acid requires 2 ATP.
  • One cycle of fatty acid Beta-oxidation produces 1 NADH, 1 FADH2, and 1 Acetyl CoA.
  • 1 Acetyl CoA can produce 10 ATP in the citric acid cycle.

Ketogenesis and Ketone Bodies

  • Ketogenesis occurs when there is insufficient carbohydrate to meet energy needs.
  • Large amounts of acetyl CoA accumulate, leading to the formation of ketone bodies (acetoacetate, beta-hydroxybutyrate, acetone).

Transamination

  • Amino acids are degraded in the liver to transfer an amino group to an a-keto acid (usually a-ketoglutarate).

Oxidative Deamination

  • The amino group is removed from glutamate as an ammonium ion, providing a-ketoglutarate for transamination.

Urea Cycle

  • Converts ammonium ions from amino acid degradation to urea in the liver.
  • Urea is excreted in the urine.
  • The cycle utilizes multiple enzymes and reactions in the mitochondria and cytoplasm.

Fates of the Carbon Atoms from Amino Acids

  • Carbon skeletons of amino acids can be used to generate energy by forming intermediates of the citric acid cycle.
  • The breakdown products vary; the carbon-skeletons are categorized for their fates as glucogenic or ketogenic.

Glucogenic and Ketogenic Amino Acid

  • Glucogenic amino acids generate pyruvate or oxaloacetate to synthesize glucose.
  • Ketogenic amino acids generate acetoacetate or acetyl CoA to form ketone bodies or fatty acids.

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Test your knowledge on the Electron Transport Chain, a critical component of cellular respiration. This quiz covers key concepts such as coenzyme Q, NADH oxidation, and ATP synthesis through ATP synthase. Challenge yourself and discover how well you understand these biochemical processes!

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