Biochemistry I MCAT Biology Diagnostic Exam 1A Flashcards
Which of the following situations would NOT stimulate gluconeogenesis? A. High glucagon levels B. High levels of AMP C. High levels of citrate D. High levels of acetyl-CoA
B. Gluconeogenesis will be stimulated when energy charge is high and glycolytic and Krebs cycle intermediates are high. If energy is low, and/or Krebs cycle intermediates are low, then glycolysis will be stimulated. High levels of AMP indicate that energy charge is low and that ATP needs to be made. AMP inhibits the enzyme fructose-1,6-bisphosphatase, keeping levels of fructose-1,6-bisphosphate high and driving the cell towards glycolysis (choice B would not stimulate gluconeogenesis and is the correct answer choice). High levels of citrate and acetyl-CoA indicate that the Krebs cycle is active and does not need more precursors, so will shift the cell away from glycolysis and toward gluconeogenesis. Think of it as taking these biosynthetic precursors and stashing them for future use. They aren’t needed if the Krebs cycle is operating at capacity (choices C and D would stimulate gluconeogenesis and can be eliminated). Glucagon is released when blood glucose levels are low and drives pathways toward gluconeogenesis to keep blood glucose levels stable (choice A would stimulate gluconeogenesis and can be eliminated).
Concepts tested
Biochemistry: Carbohydrate Metabolism
Proteins are macromolecules formed by joining together individual amino acids. Which of the following is true?
A. Protein synthesis proceeds in the NRight arrowC direction, joining the carboxyl group carbon of the first amino acid to the amino group nitrogen of the second amino acid.
B. Protein synthesis proceeds in the NRight arrowC direction, joining the amino group nitrogen of the first amino acid to the carboxyl group carbon of the second amino acid.
C. Protein synthesis proceeds in the CRight arrowN direction, joining the carboxyl group carbon of the first amino acid to the amino group nitrogen of the second amino acid.
D. Protein synthesis proceeds in the CRight arrowN direction, joining the amino group nitrogen of the first amino acid to the carboxyl group carbon of the second amino acid.
A. Protein synthesis proceeds in the NRight arrow.C direction; the next amino acid in the sequence is added to the free carboxy terminus of the growing peptide (choices C and D are wrong). The carbon of the carboxyl group on the first amino acid (or on the polypeptide) is joined to the nitrogen of the amino group on the incoming amino acid (choice A is correct and choice B is wrong).
Concepts tested
Biochemistry: Biomolecules: Amino Acids and Proteins Molecular Biology: Translation
In prokaryotic cellular respiration, which of the following processes occur in the cytoplasm?
Glycolysis Pyruvate decarboxylation (via the PDC) Krebs cycle A. I only B. I and II only C. II and III only D. I, II, and III
D. Since prokaryotes (bacteria) lack cellular organelles, all of cellular respiration takes place in the cytoplasm. Electron transport occurs across the cell membrane. Statements I, II, and III are all true.
Concepts tested
Biochemistry: Glycolysis/Cellular Respiration
In the translation of a fifty-amino acid peptide, which of the following steps requires the greatest overall amount of energy?
A. tRNA loading
B. Initiation
C. Translocation
D. Termination
A. The most energy-intensive process in translation involves the attachment of amino acids to their corresponding tRNAs, also known as tRNA loading (or tRNA charging, or amino acid activation). This requires two high-energy phosphate bonds per aa-tRNA pair (choice A is correct). Initiation requires only 1 GTP (choice B is wrong). Elongation includes A-site binding and translocation (for amino acid number two and onwards); one GTP is hydrolyzed to bring an aa-tRNA into the A site, and one GTP is required for translocation (choice C is wrong). Termination involves the binding of a release factor to a stop codon and does not directly require any energy (choice D is wrong). In this example, it would require 100 ATP to charge a sufficient number of tRNAs to generate the peptide, 1 GTP for initiation, 49 GTP for A-site binding, and 49 GTP for translocation, but note that the answer to this question does not depend upon the number of amino acids in the peptide.
A non-competitive inhibitor:
binds to an allosteric site. reduces the Vmax of a reaction. can be overcome by adding more substrate. A. I only B. I and II only C. II and III only D. I, II, and III
B. Item I is true: non-competitive inhibitors do not bind at the active site, they bind at allosteric sites and prevent the enzyme from catalyzing the reaction (choice C can be eliminated). Item II is true: by “turning off” the enzymes to which it is bound, the inhibitor lowers the effective enzyme concentration, and lowering the enzyme concentration lowers Vmax (choice A can be eliminated). Item III is false: non-competitive inhibition cannot be overcome by adding more substrate. This is only true of competitive inhibition, where the inhibitor and substrate both bind to the active site (choice D can be eliminated and choice B is correct).
Concepts tested
Biochemistry: Enzymes and Enzyme Inhibition
Which of the following alterations to the lac operon in E. coli would negatively impact the cell’s ability to utilize lactose as an energy source?
A. A single amino acid substitution in the repressor’s lactose binding site, preventing lactose binding
B. A single nucleotide mutation in the operator, blocking repressor association
C. A mutation in the DNA binding site of the repressor, markedly reducing its ability to bind to DNA
D. A mutation resulting in the constitutive expression of the repressor
A. Any alteration that would decrease the expression of the genes necessary for lactose transport and breakdown would negatively impact the cell’s ability to utilize lactose as an energy source. If the lactose binding site on the repressor could no longer bind lactose, the repressor would be able to bind to the operator region on DNA, but the presence of lactose would no longer cause dissociation of the repressor, and transcription of the necessary genes would not occur (choice A is correct). If a mutation occurred in the operator which prevented repressor binding, transcription of the lac operon genes would always occur (choice B is wrong). Similarly, a mutation in the DNA binding site of the repressor that prevented it from binding to DNA would lead to constitutive gene expression (choice C is wrong). Increased expression of the repressor itself would not necessarily decrease transcription of the lac operon genes, assuming that the regulation of the repressor by lactose is not affected (choice D is wrong).
Concepts tested
Molecular Biology: Mutations and DNA Repair Molecular Biology: Regulation of Gene Expression
A reaction with a negative ΔG is:
A. spontaneous and has a rapid rate.
B. non-spontaneous and has a slow rate.
C. spontaneous and may or may not have a rapid rate.
D. non-spontaneous and may or may not have a rapid rate.
C. Reactions with a negative ΔG are spontaneous (choices B and D are wrong), but ΔG does not provide any information about the rate of the reaction. Spontaneous reactions can move forward slowly or rapidly (choice A is wrong and choice C is correct). The thermodynamics of a reaction says nothing about rates; to know something about rates, you must consider the kinetics of the reaction.
Concepts tested
Biochemistry: Thermodynamics/Kinetics
Hexokinase catalyzes the first step in glycolysis, the phosphorylation of glucose to form glucose-6-P. High levels of glucose-6-P inhibit hexokinase. This is most accurately described as:
A. positive feedback.
B. negative feedback.
C. feedforward inhibition.
D. non-competitive inhibition.
B. When the product of a reaction inhibits the enzyme running the reaction, it is most accurately termed negative feedback. Positive feedback occurs when an end product stimulates the enzyme running the reaction (choice A is wrong). Feedforward implies that an end product of one reaction affects an enzyme further on in the series of reactions, and that is not the case here (choice C is wrong). Non-competitive inhibition occurs when a molecule distinct from the substrate binds to an allosteric site on the enzyme, turning it off. This may or may not be the case here, although it seems unlikely; if anything this might be competitive inhibition, since glucose and glucose-6-P are structurally similar (choice B is better than choice D).
Concepts tested
Biochemistry: Enzymes and Enzyme Inhibition
Which of the following is true about enzymes?
A. Enzymes stabilize the transition state of a reaction, thereby lowering the energy of activation for the reaction.
B. Enzymes convert non-spontaneous reactions into spontaneous ones.
C. By increasing the energy of activation for a reaction, enzymes make it easier to get to the transition state, thus increasing the rate of the reaction.
D. A single enzyme can catalyze a wide variety of reactions.
A. By stabilizing the transition state of a reaction, the energy required to produce the transition state (energy of activation) is lowered (choice C is false), and the reaction can proceed more quickly (choice A is correct). Enzymes do not affect the thermodynamics of a reaction; they cannot convert a non-spontaneous reaction into a spontaneous one, all they can do is take an already-spontaneous reaction and make it go faster (choice B is false). Enzymes are highly specific for a particular reaction (choice D is false).
Concepts tested
Biochemistry: Enzymes and Enzyme Inhibition
Which of the following is a difference observed between prokaryotic and eukaryotic replication?
A. Polyadenylation is observed in eukaryotes only.
B. Genes in prokaryotes can be polycistronic.
C. Multiple origins of replication are present in the eukaryotic genome.
D. Eukaryotic replication occurs around a single circular chromosome.
C. In order to ensure that replication is completed in a reasonable length of time, eukaryotes possess multiple origins of replication on each chromosome (choice C is correct). Eukaryotes utilize polyadenylation of RNA transcripts and prokaryotic genes are frequently polycistronic. However, neither of these statements (while true), answer the question because they are about transcription instead of DNA replication (choices A and B can be eliminated). Eukaryotic cells have multiple linear chromosomes while prokaryotic cells have a single circular chromosome (choice D is wrong).
Concepts tested
Molecular Biology: DNA Replication
During the oxidative phase of the pentose phosphate pathway:
A. ribulose-5-phosphate is converted into glycolytic intermediates.
B. ribulose-5-phosphate is converted into ribose-5-phosphate for incorporation into nucleic acids.
C. glucose-6-phosphate is oxidized to ribulose-5-phosphate and 2 NADPH are generated.
D. glucose-6-phosphate is oxidized to ribulose-5-phosphate and 2 NADH are generated.
C. During the oxidative phase of the pentose phosphate pathway (PPP), glu-6-P is oxidized while NADP+ is reduced to NADPH (choice C is correct); NADPH is then used in other biosynthetic pathways as a reducing agent. NADH is generated during glycolysis and the Krebs cycle, not the PPP (choice D is wrong). The interconversion of ribulose-5-P to glycolytic intermediates or into ribose-5-P is not oxidative (choices A and B are wrong).
Concepts tested
Biochemistry: Carbohydrate Metabolism
How many NADH molecules are produced from a single glucose molecule during cellular respiration?
A. 6
B. 8
C. 10
D. 12
C. A single glucose molecule generates a total of 10 NADH during cellular respiration. 2 NADH are made in glycolysis, 2 NADH at the pyruvate dehydrogenase complex, and 6 NADH in the Krebs cycle (choice C is correct and choices A, B, and D are wrong).
Concepts tested
Biochemistry: Glycolysis/Cellular Respiration
Vmax is the maximum rate of product formation for a given enzyme. Which of the following would NOT affect Vmax?
Decreasing the substrate concentration Adding a competitive inhibitor Increasing the enzyme concentration A. I only B. I and II only C. II and III only D. I, II, and III
B. Vmax depends only on the enzyme and the concentration of the enzyme. Item I would not affect Vmax: decreasing the substrate concentration would decrease V (the rate of product formation), but would not affect Vmax, which is a theoretical maximum rate of product formation, assuming you have enough substrate to get there (choice C can be eliminated). Item II would not affect Vmax: competitive inhibitors reduce V, but given enough substrate the reaction will ultimately reach the same Vmax as an uninhibited reaction (choice A can be eliminated). Item III would definitely affect Vmax (and can therefore be eliminated): more enzyme means that more product can be formed, and Vmax would increase (choice D is wrong and choice B is correct).
Concepts tested
Biochemistry: Enzymes and Enzyme Inhibition
Which of the following is true of the template strand in transcription?
A. The template strand possesses a sequence nearly identical to the RNA transcript.
B. Another name for the template strand is the coding strand.
C. The template strand possesses distinct codons necessary for transcription initiation.
D. RNA polymerase binds directly to the template strand.
D. The template strand is bound directly by the RNA polymerase and functions as a template for RNA transcript generation (choice D is correct). The template strand’s sequence is complementary to the transcript, not identical (choice A is wrong). The coding strand is the complementary strand of DNA (the strand opposite the template strand) and it is nearly identical in sequence to the RNA transcript (T in the coding strand and U in the RNA transcript, choice B is wrong). Transcription initiation is dictated largely by the promoter, which is found on the DNA, not codons which would be found on RNA and are necessary for translation (choice C is wrong).
Concepts tested
Molecular Biology: Transcription
Both fats and carbohydrates can be used as energy storage molecules. Lipids are a more efficient means of energy storage because:
fats can be easily converted to glucose molecules during times of starvation.
fats ultimately generate more ATP per carbon than do carbohydrates.
fats are hydrophilic, thus bringing along a lot of water molecules.
A. I only
B. I and II only
C. II only
D. II and III only
C. Statement I is false: humans cannot convert fats to glucose because we lack the necessary enzymes to do so. Rather than convert the fat to sugar, we just metabolize the fat directly (choices A and B can be eliminated). Note that both remaining choices include Statement II, so Statement II must be true: fats are broken down into acetyl-CoA molecules through beta oxidation, producing NADH and FADH2. These ultimately go through the electron transport chain (ETC) to generate ATP. The acetyl-CoA molecules from beta oxidation then go through the Krebs cycle, generating even more NADH and FADH2, that generate even more ATP when they go through the ETC. Statement III is false: fats are hydrophobic. This is an advantage because more fat can be packed into a given space than glycogen, which, because it is polar, comes with a lot of water molecules (choice D is wrong and choice C is correct).
Concepts tested
Biochemistry: Protein/Fat Metabolism Biochemistry: Biomolecules: Lipids