Exam 3: Bioenergetics,enzymes and Metabolism
Exam 1: Introduction to the Study of Cell and Molecular Biology72 Questions
Exam 2: The Chemical Basis of Life60 Questions
Exam 3: Bioenergetics,enzymes and Metabolism54 Questions
Exam 4: The Structure and Function of the Plasma Membrane114 Questions
Exam 5: Aerobic Respiration and the Mitochondrion98 Questions
Exam 6: Photosynthesis and the Chloroplast98 Questions
Exam 7: Interactions Between Cells and Their Environment97 Questions
Exam 8: Cytoplasmic Membrane Systems: Structure, function, and Membrane Trafficking208 Questions
Exam 9: The Cytoskeleton and Cell Motility136 Questions
Exam 10: The Nature of the Gene and the Genome94 Questions
Exam 11: Gene Expression: From Transcription to Translation109 Questions
Exam 12: Control of Gene Expression96 Questions
Exam 13: Dna Replication and Repair86 Questions
Exam 14: Cellular Reproduction100 Questions
Exam 15: Cell Signaling and Signal Transduction: Communication Between Cells106 Questions
Exam 16: Cancer74 Questions
Exam 17: The Immune Response95 Questions
Exam 18: Techniques in Cell and Molecular Biology144 Questions
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Why are alcoholic beverages often made in airtight containers?
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The alcohol in these beverages is produced by fermentation,which only occurs in the absence of oxygen.
You isolate the enzyme that synthesizes folic acid in bacteria and conduct some enzyme kinetics experiments.You find,not surprisingly,that sulfa drugs inhibit the enzyme's activity.What happens to the Vmax and KM of this enzyme when it is treated with sulfa drugs? Why do sulfa drugs have no effect on human metabolism?
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Since the sulfa drugs are competitive inhibitors,the Vmax should stay the same and the KM should increase.Sulfa drugs work by acting as a competitive inhibitor of an enzyme that converts p-aminobenzoic acid (PABA)to the essential coenzyme folic acid.Since humans lack a folic-acid synthesizing enzyme,they must obtain this essential coenzyme in their diet and,consequently,sulfa drugs have no effect on human metabolism.
The energy stored in ATP is converted to mechanical energy that moves organelles around within the cell.This is an example of __________.
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C
Given the equation G = H - T S,which set of conditions would result in a reaction that is unambiguously nonspontaneous?
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There have been two new classes of antibiotics developed and approved since 1963.One of these antibiotics acts specifically on bacterial ribosomes.What is it? Another new group of antibiotics is the cyclic lipopeptides.What is a representative of this group and how does this group of antibiotics work?
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What is the effect of a competitive inhibitor on an enzyme-mediated reaction?
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Metabolic pathways that make available raw materials from which other molecules can be synthesized and that provide chemical energy required for many cell activities are known as ______.
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How are new compounds typically screened for their effectiveness as antibiotics?
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What kind of enzyme adds phosphate groups to enzymes for the purpose of activating or deactivating them?
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If mice are maintained on very strict diets with reduced caloric intake,what happens to their life span as compared to littermates fed diets with normal caloric content? What is a possible explanation for the effect of this diet on these animals?
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Proteins are dynamic molecules that are capable of ________ motion that can have important functional relevance.The existence of this type of motion has suggested that enzymes are capable - even in the absence of substrate - of many of the same movements that can be detected during their catalytic cycle.
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Why has the pharmaceutical industry drastically cut resources devoted to the development of new antibiotics?
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Below is a segment of a cell's collection of biochemical pathways.M is a product of one series of these reactions.It is also a regulatory molecule.Look at the pathway below and indicate the position(s)at which M is most likely to act as a feedback inhibitor when its concentration gets too high.


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What strategies are employed to combat the ability of the AIDS (HIV)virus to develop drug-resistant variants?
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An enzyme has a KM of 20 µM and a Vmax of 50 mmoles of product/minute/µg of enzyme.After exposure to an inhibitor and analysis on a Lineweaver - Burk plot the following values are obtained: -1/ KM = - 0.05 liters/µmole and 1/ Vmax = 0.04 (mmoles of product/minute/µg of enzyme)-1.What kind of inhibitor was used in the experiment?
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Which reaction below might be a suitable coupled reaction for the reaction A + B <-> C + D ( G = -8.7 kcal/mole)?
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Penicillin is an irreversible inhibitor of the transpeptidases,enzymes that cross-link components of the bacterial cell wall.The cell wall is thus fragile and the bacteria die.Penicillin and its derivatives are structural analogs of the natural substrates of these enzymes.Why doesn't penicillin normally kill humans,unless a severe allergic reaction (anaphylaxis)develops? How does penicillin inhibit transpeptidase?
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What appears to be the effect of reduced calorie intake on rhesus monkeys?
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