Biochemistry, The Molecular Basis of Life, 6th Edition
6th Edition
ISBN: 9780190259204
Author: Trudy McKee, James R. McKee
Publisher: Oxford University Press
expand_more
expand_more
format_list_bulleted
Question
Chapter 11, Problem 63TQ
Summary Introduction
Introduction:
Lipids are the macromolecular complexes made up of fatty acids and polyhydroxy alcohols. These molecules can be saturated or unsaturated, depending on the nature of bonding of fatty acids. In case of saturated fatty acids, single covalent bonds are present throughout the hydrocarbon chain. Unsaturated fatty acids, on the other hand, have at least a single double bond in the hydrocarbon chain.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Discuss the differences between eukaryotic and prokaryotic cells with regards to their genetic materials. Including in your discussion the structure and organisation of genetic material, as well as any implications these differences may have on cellular functions and evolution.
Rubric
Understanding of genetic material differences (provides a comprehensive and accurate explanation of the differences between eukaryotic and prokaryotic cells in terms of their genetic material, including the structure, organisation and function of genetic material in each cell type. Demonstrates a thorough understanding of the topic)
Analysis of implications (analyze the differences between eukaryotic and prokaryotic cells in terms of their genetic material with depth and insight, discussing the implications of these differences on cellular functions and evolution. Provides specific examples and explanations.)
When was the dihydropyridine calcium channel blocker isradipine first patented and by whom? Please provide information on the origin and history of isradipine and who owns it/manufactures it.
9) Below, there is a representation of an SDS-PAGE gel. Assuming the samples in the
MW standard have masses of: 66 kDa, 45 kDa, 36 kDa, 29 kDa, 24 kDa, 20.1 kDa, and
14.2 kDa,
a) Figure 4: indicate where each of the measurements were taken and label as in II.6.
figure 2 above.
b) As in II.7. Table 1 above create Table 2 using the data below. Determine the r.f.
values for the MW standards, plot the relative mobility versus the log of the mass
for the standards, and use the best fit straight line to determine the molecular
weights of the proteins in the whey, peak 1, and peak 2 lanes. (5 pts—this will be
scaled up appropriately if your gel did not develop properly)
dye
MW
Whey
Peak 1 Peak 2
Chapter 11 Solutions
Biochemistry, The Molecular Basis of Life, 6th Edition
Ch. 11 - Prob. 1QCh. 11 - Prob. 2QCh. 11 - Prob. 3QCh. 11 - Prob. 4QCh. 11 - Prob. 5QCh. 11 - Prob. 6QCh. 11 - Prob. 7QCh. 11 - Prob. 8QCh. 11 - Prob. 9QCh. 11 - Prob. 1RQ
Ch. 11 - Prob. 2RQCh. 11 - Prob. 3RQCh. 11 - Prob. 4RQCh. 11 - Prob. 5RQCh. 11 - Prob. 6RQCh. 11 - Prob. 7RQCh. 11 - Prob. 8RQCh. 11 - Prob. 9RQCh. 11 - Prob. 10RQCh. 11 - Prob. 11RQCh. 11 - Prob. 12RQCh. 11 - Prob. 13RQCh. 11 - Prob. 14RQCh. 11 - Prob. 15RQCh. 11 - Prob. 16RQCh. 11 - Prob. 17RQCh. 11 - Prob. 18RQCh. 11 - Prob. 19RQCh. 11 - Prob. 20RQCh. 11 - Prob. 21RQCh. 11 - Prob. 22RQCh. 11 - Prob. 23RQCh. 11 - Prob. 24RQCh. 11 - Prob. 25RQCh. 11 - Prob. 26RQCh. 11 - Prob. 27RQCh. 11 - Prob. 28RQCh. 11 - Prob. 29RQCh. 11 - Prob. 30RQCh. 11 - Prob. 31RQCh. 11 - Prob. 32RQCh. 11 - Prob. 33RQCh. 11 - Prob. 34RQCh. 11 - Prob. 35RQCh. 11 - Prob. 36RQCh. 11 - Prob. 37RQCh. 11 - Prob. 38RQCh. 11 - Prob. 39RQCh. 11 - Prob. 40RQCh. 11 - Prob. 41RQCh. 11 - Prob. 42RQCh. 11 - Prob. 43RQCh. 11 - Prob. 44FBCh. 11 - Prob. 45FBCh. 11 - Prob. 46FBCh. 11 - Prob. 47FBCh. 11 - Prob. 48FBCh. 11 - Prob. 49FBCh. 11 - Prob. 50FBCh. 11 - Prob. 51FBCh. 11 - Prob. 52FBCh. 11 - Prob. 53FBCh. 11 - Prob. 54SACh. 11 - Prob. 55SACh. 11 - Prob. 56SACh. 11 - Prob. 57SACh. 11 - Prob. 58SACh. 11 - Prob. 59TQCh. 11 - Prob. 60TQCh. 11 - Prob. 61TQCh. 11 - Prob. 62TQCh. 11 - Prob. 63TQCh. 11 - Prob. 64TQCh. 11 - Prob. 65TQCh. 11 - Prob. 66TQCh. 11 - Prob. 67TQCh. 11 - Prob. 68TQCh. 11 - Prob. 69TQCh. 11 - Prob. 70TQ
Knowledge Booster
Similar questions
- what are the different classes and some examples of neuroprotectants that can be used to treat, prevent, or combat neurotoxicity/a neurotoxicant...for example, antioxidants, nutraceuticals, etc.,..?arrow_forwardImagine that aldolase can react with the seven carbon molecule Sedoheptulose-1,7-bisphosphate (below). Use the mechanism to predict the two products generated. Please draw out the stereochemistry in a fischer projection.arrow_forwardSodium borohydride (NaBH4) is a potent inhibitor of aldolase. It is known to ONLY inhibit theenzyme when it is complexed with substrate. Treatment of the enzyme alone has no effect.What is the mechanism for this inhibition? Please draw out the mechanism and show how it inhibits this.arrow_forward
- Show the fate of the proton on the 4-Oxygen molecule of F-1,6-BP. Please include a drawing showing the electron flow that occurs.arrow_forward1. Which one is the major organic product obtained from the following aldol condensation? O NaOH, H₂O heat A B C D Earrow_forwardAn organic chemist ordered the wrong item. She wanted to obtain 1-hydroxy-2-butanone, butinstead ordered 2-hydroxybutyraldehyde. As a good biochemist, show how the organic chemistcould use biological catalysis to make her desired compound. Please show the mechanism by drawing.arrow_forward
- Show the fate of the hydrogen on carbon-2 of glucose. Please draw out the structure using curve arrows to show electron flow.arrow_forward3. Which one of the compounds below is the major product formed by the reaction sequence shown here? CH3 + CH3NO2 NaOH H2, Ni ? nitromethane acetophenone OH OH HO HN- u x x x x Ph A HO -NH2 HO H Ph Ph Ph N- H B Ph NH2 D Earrow_forward4. Only ONE of the five compounds below can be prepared by an aldol condensation in which a single carbonyl compound is treated with base. Which one is it? To solve this problem, reverse the aldol condensation that formed each of these molecules to find out what two molecules came together to make the products. The one in which the two molecules are identical is the answer. Ph Ph ཚིག གནས ག ནཱ ཀ ན ཀནཱ A Ph H B Ph Ph H D Ph. Ph Ph E Harrow_forward
- 5. Which one is the major organic product obtained from the following reaction sequence? First, equimolar amounts of cyclopentanone and LDA are mixed at -78°C. Then propionaldehyde (propanal) is added. Addition of aqueous acid completes the process. LDA, -78°C. 1. 2. H₂O* H A B H 0 D H H Earrow_forward2. Which one is the major organic product obtained from the following reaction? NaOH, H₂O heat A B C D Earrow_forwardCH3CH2CHO + propanal PhCH2CHO 2-phenylacetaldehyde mixture of four products NaOH 10. In the crossed aldol reaction of propanal and 2-phenylacetaldehyde shown above, a mixture of four products will be formed. Which ONE of the compounds below will NOT be formed in this crossed aldol reaction? OH Ph A H OH OH Ph H B OH OH H H H Ph Ph C Ph D Earrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Human Physiology: From Cells to Systems (MindTap ...BiologyISBN:9781285866932Author:Lauralee SherwoodPublisher:Cengage Learning
Essentials of Pharmacology for Health ProfessionsNursingISBN:9781305441620Author:WOODROWPublisher:Cengage
Human Physiology: From Cells to Systems (MindTap ...
Biology
ISBN:9781285866932
Author:Lauralee Sherwood
Publisher:Cengage Learning
Essentials of Pharmacology for Health Professions
Nursing
ISBN:9781305441620
Author:WOODROW
Publisher:Cengage