Biochemistry
6th Edition
ISBN: 9781305577206
Author: Reginald H. Garrett, Charles M. Grisham
Publisher: Cengage Learning
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 25, Problem 12P
Interpretation Introduction
Interpretation:
To propose the reaction mechanism for the mammalian branched-chain a-keto acid dehydrogenase complex from the information provided.
Concept Introduction:
BCKAD complex- the multi-subunit enzyme complex which is seen in the mitochondrial inner membrane catalyze the branched, short-chain alpha-ketoacids oxidative decarboxylation.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Palmitoleic acid, 16:1Δ⁹ hexadecaenoic acid, (16 carbon FA with one double bond )is an important fatty acid component of TAGs and cell membranes. Briefly explain the process of beta oxidation of this fatty acid and the number (only) of FADH, NADH and acetyl CoA outcome. What is the total ATP (only number) generated from this fatty acid after beta oxidation.
The conversion of glucose-6-phosphate to fructose-6-phosphate in the glycolytic pathway (Choose
all that apply)
O positions a carbonyl group on carbon 2 of fructose-1-phosphate
O positions an amino group NH2 on carbon 3 of fructose-1-phosphate
O positions a carbonyl group on carbon 3 of fructose-1-phosphate
O is an aldose-keto isomerization
O positions a primary alcohol function at carbon C-1 that facilitates phosphorylation of fructose-6-phosphate
O is a keto-aldose isomerization
O positions an amino group NH2 on carbon 2 of fructose-1-phosphate
Biosynthesis of fatty acid 20:D6 from acetyl-CoA occurs in the __________ of mammalian cells.
Cytosol
Endoplasmic reticulum
Both A and B
Neither A nor B
Assuming all three carbon atoms of glycerol are labeled as C14 radioisotopes and the radioisotope-labeled glycerol undergoes metabolism in animals. All of the following molecules in the animal maycontain C14 radioisotopes EXCEPT:
Pyruvate
Acetyl-CoA
Glutamine
Fatty acids
Oxaloacetate
All of the above molecules may contain C14 radioisotope
Chapter 25 Solutions
Biochemistry
Ch. 25 - Prob. 1PCh. 25 - Prob. 2PCh. 25 - Regulation of Glutamine Synthetase by Covalent...Ch. 25 - The Energetic Cost of Nitrogen Excretion via the...Ch. 25 - Prob. 5PCh. 25 - Prob. 6PCh. 25 - Prob. 7PCh. 25 - Prob. 8PCh. 25 - Prob. 9PCh. 25 - Prob. 10P
Ch. 25 - Prob. 11PCh. 25 - Prob. 12PCh. 25 - Prob. 13PCh. 25 - Prob. 14PCh. 25 - Prob. 15PCh. 25 - A Deficiency on 3-Phosphogtycerate Dehydrogenase...Ch. 25 - Prob. 17PCh. 25 - Prob. 18PCh. 25 - Prob. 19PCh. 25 - Consider the synthesis and degradation of tyrosine...Ch. 25 - Prob. 21PCh. 25 - Prob. 22P
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biochemistry and related others by exploring similar questions and additional content below.Similar questions
- Extending the Mechanism of Methylmalonyl-CoA Mutase to Similar Reactions Based on the mechanism for the methylmalonyl-CoA mutase (see problem 14), write reasonable mechanisms for the following reactions shown.arrow_forwardUsing the ActiveModel for aldose reductase, describe the structure of the TIM barrel motif and the structure and location of the active site.arrow_forward. Pyruvate can be processed under anaerobic conditions to ethanol (in yeast) or to lactate (in mammals), as shown. Explain the primary purpose of these reactions. Describe the major biochemical features of each reactionarrow_forward
- Considering the complete oxidation of an 18-C fatty acid. Give the answer for the following question.a. How many rounds of beta-oxidation is needed?b. How many NADH molecules are produced in beta-oxidation only?c. How many FADH2 molecules are produced in beta-oxidation only?d. How many Acetyl Co-A are produced?arrow_forwardATP Accounting Upon digestion of starch, maltose, one of its degradation products, is further hydrolyzed into its monosaccharide components prior to intestinal absorption and entry into the glycolysis. Calculate the number of ATP molecules produced from the digestion and complete oxidation of 3 molecules of maltose considering the malate-aspartate shuttle. Answer the following items using numerical value only (e.g. 1, not "1 ATP") which will help you arrive at the final answer for this question. a. Total number of glucose molecules entering glycolysis: b. Total number of pyruvate molecules produced at the end of glycolysis: c. Total number of mitochondrial NADH produced after pyruvate is acted upon by the pyruvate dehydrogenase complex: d. Total number of CO2 released right after the pyruvate dehydrogenase complex reaction: e. Total number of acetyl CoA molecules entering the citric acid cycle: f. Total number of net cytosolic ATP molecules produced right after glycolysis: g. Total…arrow_forwardHelp filling in the blanks: The malate aspartate shuttle plays many roles in carbohydrate and amino acid metabolism. Malate can be transferred into the cytosol and interconverted in one enzymatic step to produce [oxaloacetate/glucose/PEP/pyruvate] for use in the pathway of [glycolysis/gluconeogenesis]. A product of the urea cycle, derived from aspartate, can also be converted to malate in one enzymatic step and shuttled into the mitochondria so that the urea cycle product can be used in [fatty acid synthesis/the citric acid cycle/β-oxidation]. The amino group from aspartate can be transferred to [oxalacetate/malate/fumarate/pyruvate/a- ketoglutarate] to form glutamate, which is then transported into the mitochondria. In fact many amino acids are transaminated in this way to form glutamate in the cytosol. In this way, incoming amino acids from the bloodstream can be shuttled into the liver mitochondria as glutamate for conversion by glutamate dehydrogenase to [glutamate/a-ketoglutarate…arrow_forward
- Give detailed Solution with explanation needed (no need Handwritten answerarrow_forwardM-CSA Mechanism and Catalytic Site Atlas (ebi.ac.uk) (ii) Acyl Carrier Protein S-acetyltransferase (EC 2.3.1.38) is a transferase enzyme that catalyzes the first biosynthetic pathway for fatty acid synthase. It transfers the acyl group (CH3CO) first from coenzyme A to a cysteine residue in the active site. This is similar to what happens in Chymotrypsin, however utilizing a sulfur instead of an oxygen. The acyl group is then transferred to the molecule ACP. Provide the enzyme- catalyzed mechanism for the reaction below, making sure to identify the roles of all key amino acids: i H3C SCOA acetyl COA enzyme + HS i H3C SACP acetyl ACParrow_forwardFirst option (3,6 or 0)arrow_forward
- Draw the product of the dehydration reaction of the B- hydroxyacyl-SACP catalyzed by B-hydroxyacyl-ACP dehydratase (DH) in the third elongation step of fatty acid synthesis. Provide the structure in the protonation state found in physiological conditions. OH B-hydroxyacyl-ACP dehydratase (DH) O Drawing SACP Qarrow_forwardCalculate the total number of ATP that can be generated from the ß-oxidation of paulinic acid? ОН 1. How many ATP expended for activating fatty acid to fatty acyl-CoA? How many rounds of beta oxidation? How many FADH2 per round of beta oxidation? Is there any point in the beta oxidation of an unsaturated fatty acid where we skip over FADH, production? How many FADH, total from beta oxidation? How many NADH per round of beta oxidation? How many NADH total from beta oxidation? How many acetyl-CoA are produced through beta oxidation? 6. 2. 3. 4. 5. How many NADH and FADH, are produced per acetyl-CoA in the citric acid cycle? How many NADH total from all acetyl-CoA running through the citric acid cycle? How many FADH, total from all acetyl-CoA running through the citric acid cycle? How many ATP are produced per acetyl-CoA in the citric acid cycle? How many ATP total from all acetyl-CoA running through the citric acid cycle? How many ATP per NADH,? 9. 7. 1. 8. How many ATP per FADH,? 10.…arrow_forwardCompare and contrast Pyruvate Dehydrogenase with a-ketoglutarate dehydrogenaseOutline the mechanisms of both enzymes. Discuss the functions of the coenzymes. List the similarities and the differences between the 2 enzymes. Both are very large membrane bound complexes. What are the advantages of this strategy?How detailed is the enzyme structure known below(It's Pyruvate Dehydrogenase )? What insight(s) does this structural detail give you about the enzyme mechanism.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- BiochemistryBiochemistryISBN:9781305577206Author:Reginald H. Garrett, Charles M. GrishamPublisher:Cengage Learning
Biochemistry
Biochemistry
ISBN:9781305577206
Author:Reginald H. Garrett, Charles M. Grisham
Publisher:Cengage Learning
Anaerobic Respiration; Author: Bozeman Science;https://www.youtube.com/watch?v=cDC29iBxb3w;License: Standard YouTube License, CC-BY