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Let's start with what aerobic respiration really is. It's the process where glucose is broken down in the presence of oxygen to release energy. Can anyone tell me why oxygen is important for this process?
Oxygen helps in completely oxidizing glucose, right?
Exactly! Oxygen is crucial as it acts like a final electron acceptor in the electron transport chain. What do we get as end products of this process?
Carbon dioxide and water!
Correct! And alongside, we produce ATP, which is the energy currency of the cell. Remember, we can summarize aerobic respiration as glucose plus oxygen, resulting in CO2, H2O, and energy. You might use the acronym 'GOCE' to remember this.
What does 'GOCE' stand for?
'G' for Glucose, 'O' for Oxygen, 'C' for Carbon dioxide, and 'E' for Energy. This can help you recall the main components of aerobic respiration!
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Now, let's focus on the Krebs cycle, also known as the citric acid cycle. Can anyone explain what happens here?
The acetyl CoA from pyruvate enters the cycle and gets transformed, releasing CO2.
Great observation! In addition to CO2, the Krebs cycle also generates high-energy molecules, NADH and FADH2, which are pivotal for ATP synthesis. Let's break down the key steps for clarity.
What do we do with the NADH and FADH2 later on?
Excellent question! They enter the electron transport chain, where their energy is harnessed to produce ATP. Think of NADH and FADH2 as 'energy currency' that powers ATP production in the next steps.
So, itβs all interconnected!
Exactly! Each step of respiration builds on the previous one, ensuring efficient energy extraction from glucose.
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Now that we have a good grasp of the Krebs cycle, let's look at the electron transport chain. Can someone tell me its role in respiration?
It's where most ATP is produced, and it uses the high-energy electrons from NADH and FADH2.
Spot on! Electrons move through a series of proteins in the inner mitochondrial membrane, and as they pass through, they help pump protons across the membrane, creating a gradient. What do we call this process of ATP formation?
Itβs called oxidative phosphorylation!
Correct again! And remember, oxygen combines with electrons and protons at the end of this chain, forming water, essential for the process.
What happens if oxygen isn't present?
Good thinking! Without oxygen, cells may resort to anaerobic processes, like fermentation, which is less efficient in producing ATP.
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In aerobic respiration, pyruvate generated from glycolysis is further processed in the mitochondria, leading to the complete oxidation of carbohydrates. This process is vital for energy production in cells and involves several critical stages, including the Krebs cycle and the electron transport chain, which facilitate ATP synthesis using oxygen as the final electron acceptor.
Aerobic respiration is a vital metabolic pathway that occurs in the mitochondria and is characterized by the complete oxidation of pyruvate, a product of glycolysis, leading to the release of carbon dioxide (CO2) and water (H2O), along with the generation of ATP.
This energy-efficient process yields a maximum of approximately 38 ATP molecules from one glucose molecule, highlighting its importance in cellular respiration.
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For aerobic respiration to take place within the mitochondria, the final product of glycolysis, pyruvate is transported from the cytoplasm into the mitochondria. The crucial events in aerobic respiration are:
Aerobic respiration occurs in the mitochondria after glycolysis. The pyruvate produced during glycolysis is transported into the mitochondria. Here, it undergoes a significant transformation. The process involves the complete breakdown of pyruvate, where all hydrogen atoms are removed step by step, producing carbon dioxide (COβ) as a byproduct. Simultaneously, the electrons released from this breakdown are transferred to oxygen (Oβ), which is necessary for the synthesis of ATP, the energy currency of cells.
Think of pyruvate like a slice of bread that is baked in an oven (the mitochondria). As the bread rises (oxidation), it gives off steam (COβ) and turns golden brown (ATP production). Just like the steam is a byproduct of baking, COβ is produced during aerobic respiration.
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Pyruvate, which is formed by the glycolytic catabolism of carbohydrates in the cytosol, after it enters mitochondrial matrix undergoes oxidative decarboxylation by a complex set of reactions catalysed by pyruvic dehydrogenase. The reactions catalysed by pyruvic dehydrogenase require the participation of several coenzymes, including NADβΊ and Coenzyme A.
Pyruvate + CoA + NADβΊ βΆ Acetyl CoA + COβ + NADH + HβΊ.
Once pyruvate enters the mitochondria, it undergoes a process called oxidative decarboxylation, where it loses a carbon atom in the form of carbon dioxide (COβ). This reaction is catalyzed by the enzyme pyruvic dehydrogenase and also involves coenzymes such as NADβΊ and Coenzyme A. This reaction converts pyruvate into Acetyl CoA, which is essential for the next set of reactions in cellular respiration.
Imagine pyruvate as a Lego block that you need to modify before fitting into a larger structure (Krebs cycle). During this modification, you remove a piece (the carbon atom), which creates space for the altered block (Acetyl CoA) to join the larger structure.
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The acetyl CoA then enters a cyclic pathway, tricarboxylic acid cycle, more commonly called as Krebsβ cycle after the scientist Hans Krebs who first elucidated it. The TCA cycle starts with the condensation of acetyl group with oxaloacetic acid (OAA) and water to yield citric acid (Figure 12.3). The reaction is catalysed by the enzyme citrate synthase and a molecule of CoA is released.
The TCA cycle, also known as the Krebs cycle, begins with Acetyl CoA combining with oxaloacetic acid to form citric acid. This reaction is catalyzed by the enzyme citrate synthase. The cycle involves a series of reactions that lead to the regeneration of oxaloacetic acid, enabling Acetyl CoA to enter and cycle through continuously. Throughout the cycle, various electron carriers like NADH and FADHβ are produced.
Think of the Krebs cycle like a roundabout in a town where cars (Acetyl CoA) enter and exit at various points (intermediate compounds). Each time a car makes a full circle, it exchanges parts (NADH and FADHβ), similar to how cars contribute to the flow of energy around the town.
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The following steps in the respiratory process are to release and utilise the energy stored in NADH + HβΊ and FADHβ. This is accomplished when they are oxidised through the electron transport system and the electrons are passed on to Oβ resulting in the formation of HβO. The metabolic pathway through which the electron passes from one carrier to another, is called the electron transport system (ETS).
The energy stored in NADH and FADHβ is used in the electron transport chain (ETS), a series of protein complexes located in the inner mitochondrial membrane. As electrons are transferred through this chain, they release energy that is used to pump protons across the membrane, creating a proton gradient. This gradient drives ATP synthesis when protons flow back into the mitochondrial matrix through ATP synthase.
You can think of the electron transport chain as a water dam. The flow of water (electrons) spins a turbine (ATP synthase) to produce electricity (ATP). Just as water is essential for generating energy, electrons from NADH and FADHβ are crucial for producing ATP.
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We have till now seen that glucose has been broken down to release COβ and eight molecules of NADH + HβΊ; two of FADHβ have been synthesised besides just two molecules of ATP in TCA cycle. The net gain of ATP during aerobic respiration of one molecule of glucose can be up to 38 ATP molecules.
In summary, aerobic respiration efficiently breaks down glucose, resulting in the production of carbon dioxide and significant amounts of electron carriers (NADH and FADHβ). The total yield of ATP from one glucose molecule can be approximately 38 ATP under optimal conditions, depending on how effectively the electron transport chain functions.
Think of aerobic respiration as running a marathon. While every step burns energy (glucose), the body conserves energy effectively, allowing it to cover long distances (38 ATP molecules) compared to walking slowly (fermentation).
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Key Concepts
Pyruvate Transport: Pyruvate moves from glycolysis into the mitochondria for further processing.
Krebs Cycle: A cyclic series of reactions that produce NADH and FADH2 from acetyl CoA.
Electron Transport Chain: The pathway where NADH and FADH2 donate electrons to produce ATP.
Oxidative Phosphorylation: The process of ATP generation linked to electron transport and oxygen consumption.
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In aerobic respiration, glucose is converted to 2 pyruvate molecules during glycolysis, which then enter the mitochondria for further oxidation.
The complete oxidation of one glucose molecule through aerobic respiration can yield a theoretical maximum of 38 ATP molecules.
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Pyruvate goes in, to breathe, to win; Krebs will spin, ATP will begin!
Once upon a cell, glucose was hungry and needed energy. It journeyed to the mitochondria, where pyruvate was processed, hitting the Krebs cycle, producing ATP, and eventually escaping as carbon dioxide and water.
Krebs Cycle = 'C-A-D-F' (Citric Acid, Acetyl CoA, Decarboxylation, FADH2).
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Review the Definitions for terms.
Term: Aerobic Respiration
Definition:
A metabolic process that converts glucose and oxygen into energy (ATP), carbon dioxide, and water.
Term: Pyruvate
Definition:
A key intermediate in cellular metabolism, formed from glucose during glycolysis.
Term: Acetyl CoA
Definition:
A central molecule in energy metabolism derived from pyruvate that enters the Krebs cycle.
Term: Krebs Cycle
Definition:
A series of enzymatic reactions that produce energy through the oxidation of acetyl CoA.
Term: Electron Transport Chain (ETS)
Definition:
A series of protein complexes in the inner mitochondrial membrane that transfer electrons and pump protons for ATP production.
Term: Oxidative Phosphorylation
Definition:
The process of ATP production using energy from the electron transport chain, coupled with the reduction of oxygen.