/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 2 Net Equation for Glycolysis and ... [FREE SOLUTION] | 91影视

91影视

Net Equation for Glycolysis and the Citric Acid Cycle Write the net biochemical equation for the metabolism of a molecule of glucose by glycolysis and the citric acid cycle, including all cofactors.

Short Answer

Expert verified
The net equation is: \(C_6H_{12}O_6 + 10 \text{NAD}^+ + 2 \text{FAD} + 4 \text{ADP} + 4 \text{P}_i + 2 \text{H}_2O \rightarrow 6 \text{CO}_2 + 10 \text{NADH} + 10 \text{H}^+ + 2 \text{FADH}_2 + 4 \text{ATP}\).

Step by step solution

01

Understand Glycolysis Overview

Glycolysis is the process where one molecule of glucose (C6H12O6) is broken down in the cytoplasm to produce two molecules of pyruvate. This process generates 2 ATP molecules and reduces 2 NAD+ to 2 NADH.
02

Identify Glycolysis Net Equation

The net equation for glycolysis starting with glucose is:\[ C_6H_{12}O_6 + 2 ext{ADP} + 2 ext{P}_i + 2 ext{NAD}^+ ightarrow 2 ext{C}_3H_4O_3 (pyruvate) + 2 ext{ATP} + 2 ext{NADH} + 2 ext{H}^+ + 2 ext{H}_2O \]
03

Understand Citric Acid Cycle Overview

The citric acid cycle, also known as the Krebs cycle, takes place in the mitochondria. Each pyruvate is converted into acetyl-CoA and enters the cycle, producing ATP, NADH, FADH2, and CO2.
04

Identify Citric Acid Cycle Net Equation

For each glucose molecule, two pyruvate molecules are metabolized through the cycle:\[ 2 ext{C}_3H_4O_3 + 8 ext{NAD}^+ + 2 ext{FAD} + 2 ext{ADP} + 2 ext{P}_i + 2 ext{H}_2O ightarrow 6 ext{CO}_2 + 8 ext{NADH} + 8 ext{H}^+ + 2 ext{FADH}_2 + 2 ext{ATP} + 2 ext{CoA} \]
05

Combine Glycolysis and Citric Acid Cycle Equations

Add the net equations of glycolysis and the citric acid cycle to get the overall equation:\[ C_6H_{12}O_6 + 10 ext{NAD}^+ + 2 ext{FAD} + 4 ext{ADP} + 4 ext{P}_i + 2 ext{H}_2O ightarrow 6 ext{CO}_2 + 10 ext{NADH} + 10 ext{H}^+ + 2 ext{FADH}_2 + 4 ext{ATP} \]
06

Confirm the Biochemical Changes

Check that all molecules and ions are balanced on both sides of the equation, ensuring that mass, charge, and atom counts are equal. This confirms all reactants have clearly turned into products.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Citric Acid Cycle
The Citric Acid Cycle, often referred to as the Krebs cycle or TCA cycle, is a crucial metabolic pathway that takes place in the mitochondria. It plays a vital role in cellular respiration, helping to generate energy from carbohydrates, proteins, and fats. When glucose is metabolized through glycolysis, it produces two molecules of pyruvate, which then enter the mitochondria. Here, each pyruvate is converted into acetyl-CoA, which is a key component required to start the Citric Acid Cycle.

In this cycle, for each acetyl-CoA molecule, a series of reactions occur which:
  • Release two molecules of carbon dioxide (CO鈧).
  • Generate three NADH and one FADH鈧, which are vital electron carriers.
  • Produce one ATP (or GTP, depending on the organism) molecule, which serves as a direct energy source for cells.
The cycle works to convert these energy carriers, NADH and FADH鈧, into ATP in the next stage of cellular respiration known as oxidative phosphorylation.

Completing this cycle twice for every glucose molecule (since it produces two pyruvate molecules) is essential for maximizing energy yield within a cell.
Glucose Metabolism
Glucose metabolism is a fundamental process that provides energy to cells throughout the body. It begins with glycolysis, an anaerobic process occurring in the cytoplasm, where a single glucose molecule (C鈧咹鈧佲倐O鈧) is split into two pyruvate molecules. This process yields a small amount of energy: 2 molecules of ATP and 2 NADH molecules, which are used in the mitochondria for further energy production.

Following glycolysis, the resulting pyruvate enters the mitochondria. Here, it is transformed into acetyl-CoA to enter the Citric Acid Cycle where even more energy is extracted. This transition from glycolysis to the citric acid cycle is vital to provide a continuous flow of fuel for high-energy activities.

The complete metabolism of glucose includes:
  • Glycolysis - breaking down glucose to pyruvate.
  • Pyruvate conversion to acetyl-CoA.
  • Citric Acid Cycle - further processing to extract energy-rich NADH and FADH鈧.
  • Electron transport chain and oxidative phosphorylation - the final step where ATP is generated.
This network of reactions ensures that glucose is efficiently metabolized to maintain energy needs across different tissues in the body.
Biochemical Equation
Biochemical equations are important representations to understand chemical processes within living organisms. These equations help illustrate the transformation of molecules through metabolic pathways, highlighting the conversion of reactants to products. For glucose metabolism, the net biochemical equation combines reactions from both glycolysis and the Citric Acid Cycle.

The full net reaction for glucose metabolism through these pathways is summarized as:\[ C_6H_{12}O_6 + 10 \text{NAD}^+ + 2 \text{FAD} + 4 \text{ADP} + 4 \text{P}_i + 2 \text{H}_2O \rightarrow 6 \text{CO}_2 + 10 \text{NADH} + 10 \text{H}^+ + 2 \text{FADH}_2 + 4 \text{ATP} \]

This equation indicates that a single glucose molecule is converted into carbon dioxide and water, while simultaneously capturing energy in the form of ATP. Additionally, electrons are transferred to the carriers NADH and FADH鈧, which play pivotal roles in further energy conversion processes.
Biochemical equations ensure mass, charge, and atom counts are balanced, providing meaningful insights into the efficiency and regulation of cellular metabolic activities.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Thermodynamics of Citrate Synthase Reaction in Cells Citrate is formed by the condensation of acetyl-CoA with oxaloacetate, catalyzed by citrate synthase: Oxaloacetate \(+\) acetyl-CoA \(+\mathrm{H}_{2} \mathrm{O} \rightleftharpoons\) citrate \(+\mathrm{CoA}+\mathrm{H}^{+}\) In rat heart mitochondria at \(\mathrm{pH} 7.0\) and \(25^{\circ} \mathrm{C}\), the concentrations of reactants and products are oxaloacetate, \(1 \mu \mathrm{M}\); acetyl-CoA, \(1 \mu \mathrm{M}\); citrate, \(220 \mu \mathrm{m}\); and CoA, \(65 \mu \mathrm{M}\). The standard free-energy change for the citrate synthase reaction is \(-32.2 \mathrm{~kJ} / \mathrm{mol}\). What is the direction of metabolite flow through the citrate synthase reaction in rat heart cells? Explain.

Oxaloacetate Pool What factors might decrease the pool of oxaloacetate available for the activity of the citric acid cycle? How can the pool of oxaloacetate be replenished?

Oxaloacetate Depletion Mammalian liver can carry out gluconeogenesis using oxaloacetate as the starting material (Chapter 14). Would the extensive use of oxaloacetate for gluconeogenesis affect the operation of the citric acid cycle? Explain your answer.

How the Citric Acid Cycle Was Discovered The detailed biochemistry of the citric acid cycle was determined by several researchers over a period of decades. In a 1937 article, Krebs and Johnson summarized their work and the work of others in the first published description of this pathway. The methods used by these researchers were very different from those of modern biochemistry. Radioactive tracers were not commonly available until the 1940 s, so Krebs and other researchers had to use nontracer techniques to work out the pathway. Using freshly prepared samples of pigeon breast muscle, they determined oxygen consumption by suspending minced muscle in buffer in a sealed flask and measuring the volume (in \(\mu \mathrm{L}\) ) of oxygen consumed under different conditions. They measured levels of substrates (intermediates) by treating samples with acid to remove contaminating proteins, then assaying the quantities of various small organic molecules. The two key observations that led Krebs and colleagues to propose a citric acid cycle as opposed to a linear pathway (like that of glycolysis) were made in the following experiments. Experiment I: They incubated \(460 \mathrm{mg}\) of minced muscle in 3 \(\mathrm{mL}\) of buffer at \(40^{\circ} \mathrm{C}\) for 150 minutes. Addition of citrate increased \(\mathrm{O}_{2}\) consumption by \(893 \mu \mathrm{L}\) compared with samples without added citrate. They calculated, based on the \(\mathrm{O}_{2}\) consumed during respiration of other carbon-containing compounds, that the expected \(\mathrm{O}_{2}\) consumption for complete respiration of this quantity of citrate was only \(302 \mu \mathrm{L}\). Experiment II: They measured \(\mathrm{O}_{2}\) consumption by \(460 \mathrm{mg}\) of minced muscle in \(3 \mathrm{~mL}\) of buffer when incubated with citrate and/or with 1-phosphoglycerol (glycerol 1-phosphate; this was known to be readily oxidized by cellular respiration) at \(40^{\circ} \mathrm{C}\) for 140 minutes. The results are shown in the table. \begin{tabular}{llc} 1 & No extra & 342 \\ \hline 2 & \(0.3 \mathrm{~mL} 0.2 \mathrm{M}\) 1-phosphoglycerol & 757 \\ \hline 3 & \(0.15 \mathrm{~mL} 0.02 \mathrm{M}\) citrate & 431 \\ \hline 4 & \(0.3 \mathrm{~mL} 0.2 \mathrm{M}\) 1-phosphoglycerol and \(0.15 \mathrm{~mL} 0.02\) & 1,385 \\ & M citrate & \\ \hline \end{tabular} a. Why is \(\mathrm{O}_{2}\) consumption a good measure of cellular respiration? b. Why does sample 1 (unsupplemented muscle tissue) consume some oxygen? c. Based on the results for samples 2 and 3 , can you conclude that 1-phosphoglycerol and citrate serve as substrates for cellular respiration in this system? Explain your reasoning. d. Krebs and colleagues used the results from these experiments to argue that citrate was "catalytic"that it helped the muscle tissue samples metabolize 1 phosphoglycerol more completely. How would you use their data to make this argument? e. Krebs and colleagues further argued that citrate was not simply consumed by these reactions, but had to be regenerated. Therefore, the reactions had to be a cycle rather than a linear pathway. How would you make this argument? Other researchers had found that arsenate \(\left(\mathrm{AsO}_{4}^{3-}\right)\) inhibits \(a\)-ketoglutarate dehydrogenase and that malonate inhibits succinate dehydrogenase. f. Krebs and coworkers found that muscle tissue samples treated with arsenate and citrate would consume citrate only in the presence of oxygen; under these conditions, oxygen was consumed. Based on the pathway in Figure 16-7, what was the citrate converted to in this experiment, and why did the samples consume oxygen? In their article, Krebs and Johnson further reported the following: (1) In the presence of arsenate, \(5.48\) mmol of citrate was converted to \(5.07 \mathrm{mmol}\) of \(a\) ketoglutarate. (2) In the presence of malonate, citrate was quantitatively converted to large amounts of succinate and small amounts of \(a\)-ketoglutarate. (3) Addition of oxaloacetate in the absence of oxygen led to production of a large amount of citrate; the amount was increased if glucose was also added. Other workers had found the following pathway in similar muscle tissue preparations: Succinate \(\rightarrow\) fumarate \(\rightarrow\) malate \(\rightarrow\) oxaloacetate \(\longrightarrow \mathrm{p}\) g. Based only on the data presented in this problem, what is the order of the intermediates in the citric acid cycle? How does this compare with Figure 16-7? Explain your reasoning.

Mode of Action of the Rodenticide Fluoroacetate Fluoroacetate, prepared commercially for rodent control, is also produced by a South African plant. After entering a cell, fluoroacetate is converted to fluoroacetyl-CoA in a reaction catalyzed by the enzyme acetate thiokinase: You perform a perfusion experiment to study the toxic effect of fluoroacetate using intact isolated rat heart. After perfusing the heart with \(0.22 \mathrm{~mm}\) fluoroacetate, you see a decrease in the measured rate of glucose uptake and glycolysis as well as an accumulation of glucose 6-phosphate and fructose 6-phosphate. Examination of the citric acid cycle intermediates reveals that their concentrations are below normal, except for citrate, which has a concentration 10 times higher than normal. a. Where did the block in the citric acid cycle occur? What causcd citrate to accumulate and the other cycle intermediates to be depleted? b. Fluoroacetyl-CoA is enzymatically transformed in the citric acid cycle. What is the structure of the end product of fluoroacetate metabolism? Why does it block the citric acid cycle? How might the inhibition be overcome? c. In the heart perfusion experiments, why did glucose uptake and glycolysis decrease? Why did hexose monophosphates accumulate? d. Why is fluoroacetate poisoning fatal?

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.