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1. Questions and Problems, 19.1 How can inducible and repressible enzymes of microorganisms be distinguished? Ans: By studying the synthesis or lack of synthesis of the enzyme in cells grown on chemically defined media. If the enzyme is synthesized only in the presence of a certain metabolite or a particular set of metabolites, it is probably inducible. If it is synthesized in the absence but not in the presence of a particular metabolite or group of metabolites, it is probably repressible. Feedback: 19.1 Difficulty: medium 2. Questions and Problems, 19.2 Distinguish between (a) repression and (b) feedback inhibition caused by the end product of a biosynthetic pathway. How do these two regulatory phenomena complement each other to provide for the efficient regulation of metabolism? Ans: Repression occurs at the level of transcription during enzyme synthesis. The end-product, or a derivative of the end-product, of a repressible system acts as an effector molecule that usually, if not always, combines with the product of one or more regulator genes to turn off the synthesis of the enzymes in the biosynthetic pathway. Feedback inhibition occurs at the level of enzyme activity; it usually involved the first enzyme of the biosynthetic pathway. Feedback inhibition thus brings about an immediate arrest of the biosynthesis of the end-product. Together, feedback inhibition and repssion rapidly and efficiently turn off the synthesis of both the enzymes and the end-products that no longer need to be synthesized by the cell. Feedback: 19.1 Difficulty: easy 3. Questions and Problems, 19.3 In the lactose operon of E. coli, what is the function of each of the following genes or sites: (a) regulator, (b) operator, (c) promoter, (d) structural gene Z, and (e) structural gene Y? Ans: Gene or Regulatory Element Function (a) Regulator gene Codes for repressor (b) Operator (c) Promoter (d) Structural gene Z (e) Structural gene Y Feedback: 19.4 Difficulty: easy Binding site of repressor Binding site of RNA polymerase and CAP-cAMP complex Encodes -galactosidase Encodes -galactoside permease 4. Questions and Problems, 19.4 What would be the result of inactivation by mutation of the following genes or sites in the E. coli lactose operon: (a) regulator, (b) operator, (c) promoter, (d) structural gene Z, and (e) structural gene Y? Ans: (a) Constitutive synthesis of the lac enzymes. (b) Constitutive synthesis of the lac enzymes. (c) Uninducibility of the lac enzymes. (d) No -galactosidase activity. (e) No -galactosidase permease activity. Feedback: 19.4 Difficulty: medium 5. Questions and Problems, 19.5 Groups of alleles associated with the lactose operon are as follows (in order of dominance for each allelic series): repressor, Is (superrepressor), I+ (inducible), and I (constitutive); operator, Oc (constitutive, cis dominant) and O+ (inducible, cis-dominant); structural, Z+ and Y+. (a) Which of the following genotypes will produce -galactosidase and -galactoside permease if lactose is present: (1) I+O+Z+Y+, (2) I OcZ+Y+, (3) IsOcZ+Y+, (4) IsO+Z+Y+, and (5) I O+Z+Y+? (b) Which of the above genotypes will produce -galactosidase and -galactoside permease if lactose is absent? Why? Ans: (a) 1, 2, 3, and 5. Genotype 1 is wildtype and inducible, whereas genotypes 2, 3, and 5 are consitutive; all will produce structural genes in the presence of lactose. However, genotype 4 has a superrepressor mutation (Is) and is uninducible with normal levels of lactose. (b) 2, 3, and 5. In genotypes, 2 and 3, the repressor cannot bind to Oc and in genotype 5, no repressor is made; both situations render the operon constituitve. Feedback: 19.4 Difficulty: medium 6. Questions and Problems, 19.6 Assume that you have discovered a new strain of E. coli that has a mutation in the lac operator region that causes the wild-type repressor protein to bind irreversibly to the operator. You have named this operator mutant Osb for “superbinding” operator. (a) What phenotype would a partial diploid of genotype I+OsbZ Y+/I+O+Z+Y have with respect to the synthesis of the enzymes -galactosidase and 2 -galactoside permease? (b) Does your new Osb mutation exhibit cis or trans dominance in its effects on the regulation of the lac operon? Ans: (a) -Galactosidase will be produced only when lactose is present. Permease will not be produced at all. (b) Cis dominance. Feedback: 19.5 Difficulty: medium 7. Questions and Problems, 19.7 Why is the Oc mutation in the E. coli lac operon epistatic to the Is mutation? Ans: The Oc mutant prevents the repressor from binding to the operator. The Is mutant repressor cannot bind to Oc. The Is mutant protein has a defect in the allosteric site that binds allolactose, but has a normal operator binding site. Therefore, because the single Oc mutant would have the same phenotype as the Oc Is double mutant, the Oc mutation is, by definition, epistatic to Is. Feedback: 19.4 Difficulty: medium 8. Questions and Problems, 19.8 For each of the following partial diploids indicate whether enzyme synthesis is constitutive or inducible (see Problem 19.5 for dominance relationships): (a) I+O+Z+Y+/I+O+Z+Y+, (b) I+O+Z+Y+/I+OcZ+Y+, + c + + + c + + (c) I O Z Y /I O Z Y , (d) I+O+Z+Y+/I O+Z+Y+, (e) I O+Z+Y+/I O+Z+Y+. Why? Ans: (a) Inducible, this is the wild-type genotype and phenotype. (b) Constitutive, the Oc mutation produces an operator that is not recognized by the lac repressor. (c) Constitutive, same as for (b). (d) Inducible, I+ is dominant to I-. (e) Constitutive, no active repressor is synthesized in this bacterium. Feedback: 19.1 Difficulty: medium 9. Questions and Problems, 19.9 Write the partial diploid genotype for a strain that will (a) produce -galactosidase constitutively and permease inducibly and (b) produce -galactosidase constitutively but not permease either constitutively or inducibly, even though a Y+ gene is known to be present. Ans: (a) I+OcZ+Y-/I+O+Z+Y+ (b) I+OcZ+Y-/IsO+Z+Y+ Feedback: 19.1 Difficulty: medium 3 10. Questions and Problems, 19.10 As a genetics historian, you are repeating some of the classic experiments conducted by Jacob and Monod with the lactose operon in E. coli. You use an F plasmid to construct several E. coli strains that are partially diploid for the lac operon. You construct strains with the following genotypes: (1) I+OcZ+Y /I+O+Z Y+, (2) I+OcZ Y+/I+O+Z+Y , (3) I O+Z+Y+/I+O+Z Y , (4) IsO+Z Y /I+O+Z+Y+, and (5) I+OcZ+Y+/IsO+Z Y+. (a) Which of these strains will produce functional -galactosidase in both the presence and absence of lactose? (b) Which of these strains will exhibit constitutive synthesis of functional -galactoside permease? (c) Which of these strains will express both gene Z and gene Y constitutively and will produce functional products ( -galactosidase and -galactoside permease) of both genes? (d) Which of these strains will show cis dominance of lac operon regulatory elements? (e) Which of these strains will exhibit trans dominance of lac operon regulatory elements? Ans: (a) 1, 5. (b) 2, 5. (c) 5. (d) 1, 2, 5. (e) 3, 4 Feedback: 19.4 Difficulty: hard 11. Questions and Problems, 19.11 Constitutive mutations produce elevated enzyme levels at all times; they may be of two types: Oc or I . Assume that all other DNA present is wild-type. Outline how the two constitutive mutants can be distinguished with respect to (a) map position, (b) regulation of enzyme levels in Oc/O+ versus I /I+ partial diploids, and (c) the position of the structural genes affected by an Oc mutation versus the genes affected by an I mutation in a partial diploid. Ans: (a) The Oc mutations map very close to the Z structural gene; I- mutations map slightly farther from the structural gene (but still very close by; see Figure 19.5). (b) An I+O+Z+Y+ / I+OcZ+Y+ partial diploid would exhibit constitutive synthesis of -galactosidase and -galactoside permease, whereas an I+O+Z+Y+ / I-O+Z+Y+ partial diploid would be inducible for the synthesis of these enzymes. (c) The Oc mutation is cis-dominant; the I- mutation is trans-recessive. Feedback: 19.1 Difficulty: medium 12. Questions and Problems, 19.12 How could the tryptophan operon in E. coli have developed and been maintained by evolution? 4 Ans: The system could have developed from a series of tandem duplications of a single ancestral gene. Mutational changes that make the system more efficient and, therefore, favored in selection could have brought the system to its present level of efficiency. Feedback: 19.5 Difficulty: medium 13. Questions and Problems, 19.13 Of what biological significance is the phenomenon of catabolite repression? Ans: Catabolite repression has apparently evolved to assure the use of glucose as a carbon source when this carbohydrate is available, rather than less efficient energy sources. Feedback: 19.4 Difficulty: easy 14. Questions and Problems, 19.14 How might the concentration of glucose in the medium in which an E. coli cell is growing regulate the intracellular level of cyclic AMP? Ans: Possibly by directly or indirectly inhibiting the enzyme adenylcyclase, which catalyzes the synthesis of cyclic AMP from ATP. Feedback: 19.4 Difficulty: easy 15. Questions and Problems, 19.15 Is the CAP–cAMP effect on the transcription of the lac operon an example of positive or negative regulation? Why? Ans: Positive regulation; the CAP-cAMP complex has a positive effect on the expression of the lac operon. It functions in turning on the transcription of the structural genes in the operon. Feedback: 19.4 Difficulty: easy 16. Questions and Problems, 19.16 Would it be possible to isolate E. coli mutants in which the transcription of the lac operon is not sensitive to catabolite repression? If so, in what genes might the mutations be located? Ans: Yes; in the gene coding for CAP. Some mutations in this gene might result in a CAP that binds to the promoter in the absence of cAMP. Also, mutations in the gene (or genes) coding for the protein (or proteins) that regulate the cAMP level as a function of glucose concentration. 5 Feedback: 19.4 Difficulty: medium 17. Questions and Problems, 19.17 Using examples, distinguish between negative regulatory mechanisms and positive regulatory mechanisms. Ans: Negative regulatory mechanisms, such as that involving the repressor in the lactose operon, block the transcription of the structural genes of the operon, whereas positive mechanisms, such as the CAP-cAMP complex in the lac operon, promote the transcription of the structural genes of the operon. Feedback: 19.2 Difficulty: medium 18. Questions and Problems, 19.18 The following table gives the relative activities of the enzymes -galactosidase and -galactoside permease in cells with different genotypes at the lac locus in E. coli. The level of activity of each enzyme in wild-type E. coli not carrying F’s was arbitrarily set at 100; all other values are relative to the observed levels of activity in these wild-type bacteria. Based on the data given in the table for genotypes 1 through 4, fill in the levels of enzyme activity that would be expected for the fifth genotype. Genotype Inducer + + + + 1. I O Z Y 0.1 2. I O+Z+Y+ 100 3. I+OcZ+Y+ 25 + + + + + 4. I O Z Y /F I O Z Y 200 c + + + + + 5. I O Z Y /F I O Z Y —— -Galactoside -Galactosidase Permease +Inducer Inducer +Inducer 100 0.1 100 100 100 100 100 25 100 200 100 100 —— —— —— Ans: 0.1; 100; 25.1; 200. Feedback: 19.2 Difficulty: hard 19. Questions and Problems, 19.19 The rate of transcription of the trp operon in E. coli is controlled by both (1) repression/derepression and (2) attenuation. By what mechanisms do these two regulatory processes modulate trp operon transcript levels? Ans: Repression/derepression of the trp operon occurs at the level of transcription initiation, modulating the frequency at which RNA polymerase initiates transcription from the trp operon 6 promoters. Attenuation modulates trp transcript levels by altering the frequency of termination of transcription within the trp operon leader region (trpL). Feedback: 19.5 Difficulty: easy 20. Questions and Problems, 19.20 What effect will deletion of the trpL region of the trp operon have on the rates of synthesis of the enzymes encoded by the five genes in the trp operon in E. coli cells growing in the presence of tryptophan? Ans: Deletion of the trpL region would result in the levels of the tryptophan biosynthetic enzymes in cells growing in the presence of tryptophan being increased about tenfold because attenuation would no longer occur if this region were absent. Feedback: 19.5 Difficulty: easy 21. Questions and Problems, 19.21 By what mechanism does the presence of tryptophan in the medium in which E. coli cells are growing result in premature termination or attenuation of transcription of the trp operon? Ans: First, remember that transcription and translation are coupled in prokaryotes. When tryptophan is present in cells, tryptophan-charged tRNATrp is produced. This allows translation of the trp leader sequence through the two UGG Trp codons to the trp leader sequence UGA termination codon. This translation of the trp leader region prevents base-pairing between the partially complementary mRNA leader sequences 75–83 and 110–121 (see Figure 19.13b), which in turn permits formation of the transcription-termination “hairpin” involving leader sequences 110–121 and 126–134 (see Figure 19.13c). Feedback: 19.5 Difficulty: easy 22. Questions and Problems, 19.22 Suppose that you used site-specific mutagenesis to modify the trpL sequence such that the two UGG Trp codons at positions 54–56 and 57–60 (see Figure 19.12) in the mRNA leader sequence were changed to GGG Gly codons. Will attenuation of the trp operon still be regulated by the presence or absence of tryptophan in the medium in which the E. coli cells are growing? Ans: No. Attentuation of the trp operon would now be controlled by the presence or absence of GlytRNAGly. Feedback: 19.5 Difficulty: medium 7 23. Questions and Problems, 19.23 What is a prophage? In what ways does the phage prophage differ from the chromosome present during lytic infections? Ans: A prophage is a chromosome of a bacteriophage after it has become integrated into the chromosome of the host bacterium. The lambda prophage is present as a transcriptionally inactive linear structure in the E. coli chromosome. During lytic infections, the lambda chromosome begins its reproductive cycle by replicating as a transcriptionally active circular DNA molecule. Feedback: 19.6 Difficulty: easy 24. Questions and Problems, 19.24 What is the major structural difference between the operator region in the lac operon of E. coli and the phage operators OL and OR? Ans: The operator region of the lac operon in E. coli contains a single repressor binding site, whereas the lambda operators OL and OR each contain three repressor binding sites that are differentially occupied under different conditions. The differential affinity of lambda repressor for the three binding sites in these operators plays an important role in the maintenance of the lysogenic state of a lambda prophage in E. coli. Feedback: 19.4, 19.6 Difficulty: medium 25. Questions and Problems, 19.25 A lambda phage has a UAG chain-termination mutation in the middle of the CI gene. What phenotype will result from this mutation? Ans: The mutation will produce the so-called clear-plaque phenotype. In the absence of functional repressor, lambda phage can only reproduce lytically. Lysogeny requires the lambda repressor to be present to keep the lytic genes of the lambda prophage repressed. Thus all infected cells will be killed and lysed during the lambda lytic cycle, resulting in clear plaques rather than the turbid plaques formed by wild-type lambda. Feedback: 19.6 Difficulty: medium 26. Questions and Problems, 19.26 Would attenuation of the type that regulates the level of trp transcripts in E. coli be likely to occur in eukaryotic organisms? 8 Ans: No. Since transcription (nucleus) and translation (cytoplasm) are no coupled in eurkaryotes, attenuation of the type occurring in prokaryotes would not be possible. Feedback: 19.6 Difficulty: medium 9