Concept explainers
(a)
Interpretation:
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate succinate has to be determined.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. This process is the reverse of the degradation of fatty acid.
The Citric acid cycle is a series of biochemical reactions that use acetyl CoA (produced by oxidation of pyruvate) to produce carbon dioxide, NADH and FADH2 in a series of
(a)
Answer to Problem 25.106EP
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate succinate is butyrate.
Explanation of Solution
Succinic acid is a dicarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the citric acid cycle is a C4 derivative of dicarboxylic acid. The structure of succinic acid is,
Intermediates involved in the lipogenesis are derivatives of C4 molecule butyric acid. Butyric acid is a monocarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the lipogenesis is a C4 derivative of monocarboxylic acid. The structure of butyric acid is,
The structure of succinate is,
The structure of butyrate is,
Butyrate and succinate are saturated acid with four carbon atoms in each molecule. butyrate is a monoacid formed as intermediate in lipogenesis while succinate is a diacid formed as intermediate in the citric acid cycle. Therefore, the lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate succinate is butyrate.
(b)
Interpretation:
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate malate has to be determined.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. This process is the reverse of the degradation of fatty acid.
The Citric acid cycle is a series of biochemical reactions that use acetyl CoA (produced by oxidation of pyruvate) to produce carbon dioxide, NADH and FADH2 in a series of redox reactions.
Intermediates involved in the lipogenesis are derivative of C4 molecule butyric acid. Butyric acid is a monocarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the lipogenesis is a C4 derivative of monocarboxylic acid. The structure of butyric acid is,
Succinic acid is a dicarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the citric acid cycle is a
(b)
Answer to Problem 25.106EP
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate malate is β-hydroxybutyrate.
Explanation of Solution
Malate is the intermediate in the citric acid cycle. The structure of malate is,
β-Hydroxybutyrate is the intermediate in the lipogenesis. The structure of β-hydroxybutyrate is,
Malate and β-hydroxybutyrate are the hydroxy derivatives of saturated acid with four carbon atoms in each molecule. Malate is a hydroxy derivative of dicarboxylic acid that is formed as the intermediate in the citric acid cycle whileβ-hydroxybutyrate is a hydroxy derivative of monocarboxylic acid that is formed as the intermediate in the lipogenesis. The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate malate is β-hydroxybutyrate.
(c)
Interpretation:
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate oxaloacetate has to be determined.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. This process is the reverse of the degradation of fatty acid.
The Citric acid cycle is a series of biochemical reactions that use acetyl CoA (produced by oxidation of pyruvate) to produce carbon dioxide, NADH and FADH2 in a series of redox reactions.
Intermediates involved in the lipogenesis are derivatives of C4 molecule butyric acid. Butyric acid is a monocarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the lipogenesis is a C4 derivative of monocarboxylic acid. The structure of butyric acid is,
Succinic acid is a dicarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the citric acid cycle is a C4 derivative of dicarboxylic acid. The structure of succinic acid is,
(c)
Answer to Problem 25.106EP
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate oxaloacetate is acetoacetate.
Explanation of Solution
Oxaloacetate is the intermediate in the citric acid cycle. The structure of oxaloacetate is,
Acetoacetate is the intermediate in the lipogenesis. The structure of acetoacetate is,
Oxaloacetate and acetoacetate are the keto derivatives of saturated acid with four carbon atoms in each molecule. Oxaloacetate is a keto derivative of dicarboxylic acid that is formed as the intermediate in the citric acid cycle while acetoacetate is a keto derivative of monocarboxylic acid that is formed as the intermediate in the lipogenesis. Therefore, the lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate oxaloacetate is acetoacetate.
(d)
Interpretation:
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate fumarate has to be determined.
Concept introduction:
Lipogenesis is the process employed for the synthesis of fatty acid. The starting precursor for the synthesis is acetyl CoA. The enzyme employed for the process is fatty acid synthase. It is a multienzyme complex that ties the reaction responsible for the synthesis of fatty acid. This process is the reverse of the degradation of fatty acid.
The Citric acid cycle is a series of biochemical reactions that use acetyl CoA (produced by oxidation of pyruvate) to produce carbon dioxide, NADH and FADH2 in a series of redox reactions.
Intermediates involved in the lipogenesis are derivatives of C4 molecule butyric acid. Butyric acid is a monocarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the lipogenesis is a C4 derivative of monocarboxylic acid. The structure of butyric acid is,
Succinic acid is a dicarboxylic acid and has 4 carbon atoms. Thus, each intermediate of the citric acid cycle is a C4 derivative of dicarboxylic acid. The structure of succinic acid is,
(d)
Answer to Problem 25.106EP
The lipogenesis C4-ACP monoacid intermediate counterpart for the citric acid cycle C4-diacid intermediate fumarate is crotonate.
Explanation of Solution
Fumarate is the intermediate in the citric acid cycle. The structure of fumarate is,
Crotonate is the intermediate in the lipogenesis. The structure of crotonate is,
Fumarate and crotonate are the unsaturated derivatives of the
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Chapter 25 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Consider the docosanoic acid, C21H43CO2H a. Label the a and B carbons b. Draw the acyl CoA derived from this fatty acid c. How many acetyl CoA molecules are formed by complete B-oxidation? d. How many cycles of B-oxidation are needed for complete oxidation? e. How many molecules of ATP are formed from the complete catabolism of this fatty acid?arrow_forward1) under intracellular conditions, answer : If G3P-DH is inhibited by Iodoacetic acid, which glycolytic intermediate will accumulate most rapidly and why ? 2) How will increased oxaloacetate level in mitochondria affect fatty acid biosynthesis ?arrow_forwardThe citric acid cycle is shown. The methyl carbon in acetyl CoA is labeled with C14C14 (shown in red). Identify which of the carbons in each intermediate will be labeled in the first round of the cycle by selecting the indicated carbon(s). Each question has multiple options, please choose more than one. Which carbon(s) in α‑ketoglutarate will contain C14? 1 2 3 4 5 Which carbon(s) in succinyl‑CoA will contain C14? 1 2 3 4 Which carbon(s) in succinate will contain C14? 1 2 3 4 Which carbon(s) in fumarate will contain C14? 1 2 3 4 Which carbon(s) in malate will contain C14? 1 2 3 4 Which carbon(s) in oxaloacetate will contain C14? 1 2 3 4arrow_forward
- Under conditions where ketone bodies are being produced in the liver, how many ATPs can be produced from a molecule of palmitic acid if all resulting molecules of acetyl-CoA are converted into β-hydroxybutyrate?arrow_forwardAcetly CoA can quickly enter the citric acid cyle by joining with a C4 compound and forming citrate. Meanwhile, GTP (or ATP) is generated using inorganic phosphate while succinyl CoA is converted to succinate. What is the main reason both acetly CoA and succinyl CoA can perform such work? a. Acetyl CoA and succinyl CoA both contain coenzyme A, which is a high-energy compound. b. Acetyl CoA and succinyl CoA both form an unstable thioester bond with coenzyme A. c. Acetyl CoA and succinyl CoA both bind with inorganic phosphate which is used to generate ATP (or GTP). d. Acetyl CoA and succinyl CoA both transiently form a covalent bond with the enzymes that catalyze the next reaction, pyruvate dehydrogenase and succinyl-CoA synthetase, respectively. e. Acetyl CoA and succinyl CoA use the energy collected from the electron transport chain.arrow_forwardTwo of the steps in the oxidative decarboxylation of pyruvate (steps 4 and 5 in the figure) do not involve any of the three carbons of pyruvate, yet are essential to the operation of the pyruvate dehydrogenase (PDH) complex. CH3 Pyruvate Hydroxyethyl TPP 1 TPP TPP CHOH 1 CH3 2 Pyruvate dehydrogenase, E₁ CH3 SH Acetyl lipoyllysine 515 CoA-SH CH3- C-S-COA Acetyl-CoA Oxidized lipoyllysine. Reduced 3 lipoyllysine Dihydrolipoyl transacetylase, E₂ Lys FAD -SH SH FADH₂ Dihydrolipoyl dehydrogenase, E3 NADH + H+ NAD+arrow_forward
- The citric acid cycle is shown. The methyl carbon in acetyl CoA is labeled with C14C14 (shown in red). Identify which of the carbons in each intermediate will be labeled in the first round of the cycle by selecting the indicated carbon(s). Each question has multiple options, answering with only one option is incorrect. Which carbon(s) in α‑ketoglutarate will contain C14? 1 2 3 4 5 Which carbon(s) in succinyl‑CoA will contain C14? 1 2 3 4 Which carbon(s) in succinate will contain C14? 1 2 3 4 Which carbon(s) in fumarate will contain C14? 1 2 3 4 Which carbon(s) in malate will contain C14? 1 2 3 4 Which carbon(s) in oxaloacetate will contain C14? 1 2 3 4arrow_forwardIf glutamate were labeled with C-14 at the delta-carbon and added via transamination to the citric acid cycle to produce alpha-ketoglutarate, how long would it take for the compounds containing C-14 to be reduced by 25% (assume 10 seconds per turn of the cycle)?arrow_forwardgive five biological effects of disorders of the citric acid cyclearrow_forward
- Consider the fatty acids: (a) Arachidic acid (C20H40O2); molar mass = 312.5 g/mol) (b) Palmitoleic acid(C16H30O2); molar mass = 256.4 g/mol). i. How many cycles of β -oxidation are needed for complete oxidation?ii. How many molecules of acetyl CoA are formed from its complete catabolism?iii. Calculate the number of molecules (moles) of ATP formed (net) by the completecatabolism of each fatty acid (show your calculation).iv. Calculate number of moles of ATP formed per gram of each fatty acid metabolized.arrow_forwardOne of the regulators of the TCA cycle is succinyl CoA. Discuss the rationale for this molecule to be used to regulate the TCA cycle. What is the metabolic role of succinyl CoA?arrow_forwardConsider docosanoic acid C12H43CO2H a. Label the alpha and beta Carbons. Show the beta-oxidation in an EXPANDED structure. b. Draw each acyl CoA derived from this fatty acid. c. How many acetyl Co A molecules are formed by complete beta-oxidation? d. How many cycles of beta-oxidation are needed for complete oxidation? e. How many molecules of ATP are formed from the complete catabolism of this fatty acid? Show the complete computation. f. How many moles of ATP per gram of fatty acid is formed from the complete catabolism of the given fatty acid? g. What is the molar mass of the given fatty acid? Solution: Show here the complete computations, [from a to e]arrow_forward
- BiochemistryBiochemistryISBN:9781305577206Author:Reginald H. Garrett, Charles M. GrishamPublisher:Cengage Learning