Table of contents
- 1. Introduction to Biology2h 42m
- 2. Chemistry3h 37m
- 3. Water1h 26m
- 4. Biomolecules2h 23m
- 5. Cell Components2h 26m
- 6. The Membrane2h 31m
- 7. Energy and Metabolism2h 0m
- 8. Respiration2h 40m
- 9. Photosynthesis2h 49m
- 10. Cell Signaling59m
- 11. Cell Division2h 47m
- 12. Meiosis2h 0m
- 13. Mendelian Genetics4h 44m
- Introduction to Mendel's Experiments7m
- Genotype vs. Phenotype17m
- Punnett Squares13m
- Mendel's Experiments26m
- Mendel's Laws18m
- Monohybrid Crosses19m
- Test Crosses14m
- Dihybrid Crosses20m
- Punnett Square Probability26m
- Incomplete Dominance vs. Codominance20m
- Epistasis7m
- Non-Mendelian Genetics12m
- Pedigrees6m
- Autosomal Inheritance21m
- Sex-Linked Inheritance43m
- X-Inactivation9m
- 14. DNA Synthesis2h 27m
- 15. Gene Expression3h 6m
- 16. Regulation of Expression3h 31m
- Introduction to Regulation of Gene Expression13m
- Prokaryotic Gene Regulation via Operons27m
- The Lac Operon21m
- Glucose's Impact on Lac Operon25m
- The Trp Operon20m
- Review of the Lac Operon & Trp Operon11m
- Introduction to Eukaryotic Gene Regulation9m
- Eukaryotic Chromatin Modifications16m
- Eukaryotic Transcriptional Control22m
- Eukaryotic Post-Transcriptional Regulation28m
- Eukaryotic Post-Translational Regulation13m
- 17. Viruses37m
- 18. Biotechnology2h 58m
- 19. Genomics17m
- 20. Development1h 5m
- 21. Evolution3h 1m
- 22. Evolution of Populations3h 53m
- 23. Speciation1h 37m
- 24. History of Life on Earth2h 6m
- 25. Phylogeny2h 31m
- 26. Prokaryotes4h 59m
- 27. Protists1h 12m
- 28. Plants1h 22m
- 29. Fungi36m
- 30. Overview of Animals34m
- 31. Invertebrates1h 2m
- 32. Vertebrates50m
- 33. Plant Anatomy1h 3m
- 34. Vascular Plant Transport1h 2m
- 35. Soil37m
- 36. Plant Reproduction47m
- 37. Plant Sensation and Response1h 9m
- 38. Animal Form and Function1h 19m
- 39. Digestive System1h 10m
- 40. Circulatory System1h 49m
- 41. Immune System1h 12m
- 42. Osmoregulation and Excretion50m
- 43. Endocrine System1h 4m
- 44. Animal Reproduction1h 2m
- 45. Nervous System1h 55m
- 46. Sensory Systems46m
- 47. Muscle Systems23m
- 48. Ecology3h 11m
- Introduction to Ecology20m
- Biogeography14m
- Earth's Climate Patterns50m
- Introduction to Terrestrial Biomes10m
- Terrestrial Biomes: Near Equator13m
- Terrestrial Biomes: Temperate Regions10m
- Terrestrial Biomes: Northern Regions15m
- Introduction to Aquatic Biomes27m
- Freshwater Aquatic Biomes14m
- Marine Aquatic Biomes13m
- 49. Animal Behavior28m
- 50. Population Ecology3h 41m
- Introduction to Population Ecology28m
- Population Sampling Methods23m
- Life History12m
- Population Demography17m
- Factors Limiting Population Growth14m
- Introduction to Population Growth Models22m
- Linear Population Growth6m
- Exponential Population Growth29m
- Logistic Population Growth32m
- r/K Selection10m
- The Human Population22m
- 51. Community Ecology2h 46m
- Introduction to Community Ecology2m
- Introduction to Community Interactions9m
- Community Interactions: Competition (-/-)38m
- Community Interactions: Exploitation (+/-)23m
- Community Interactions: Mutualism (+/+) & Commensalism (+/0)9m
- Community Structure35m
- Community Dynamics26m
- Geographic Impact on Communities21m
- 52. Ecosystems2h 36m
- 53. Conservation Biology24m
16. Regulation of Expression
The Lac Operon
Problem 10
Textbook Question
X-gal is a colorless, lactose-like molecule that can be split into two fragments by ββ-galactosidase. One of these product molecules creates a blue color. The photograph here shows E. coli colonies growing in a medium that contains X-gal. Find three colonies whose cells have functioning copies of ββ-galactosidase.
Find three colonies whose cells might have mutations in the lacZ or the lacY genes.
Suppose you analyze the protein-coding sequence of the lacZ and lacY genes of cells from the three mutant colonies and find that these sequences are wild type (normal).
What other region of the lac operon might be altered to account for the mutant phenotype of these colonies?

1
Step 1: Understand the role of X-gal and β-galactosidase. X-gal is a substrate that mimics lactose and is cleaved by the enzyme β-galactosidase. When cleaved, one of the products produces a blue color. Colonies that appear blue have functioning β-galactosidase, while white colonies may indicate a mutation in the lac operon.
Step 2: Identify colonies with functioning β-galactosidase. Look for three blue colonies on the plate, as these indicate that the cells in these colonies have active β-galactosidase and are likely expressing the lacZ gene properly.
Step 3: Identify colonies with potential mutations. Look for three white colonies, as these indicate that the cells in these colonies are not producing functional β-galactosidase. This could be due to mutations in the lacZ or lacY genes, or other regions of the lac operon.
Step 4: Analyze the protein-coding sequences of lacZ and lacY in the mutant colonies. If the sequences are wild type (normal), this suggests that the mutations are not in the coding regions of these genes. Instead, the issue may lie in regulatory regions of the lac operon.
Step 5: Consider other regions of the lac operon that could be altered. The mutation might be in the promoter region (where RNA polymerase binds), the operator region (where the repressor binds), or in the gene encoding the repressor protein (lacI). These mutations could prevent proper transcription or regulation of the lacZ and lacY genes, leading to the observed mutant phenotype.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Lac Operon
The lac operon is a set of genes in E. coli that are involved in the metabolism of lactose. It includes the genes lacZ, lacY, and lacA, which encode proteins necessary for lactose uptake and breakdown. The operon is regulated by the presence or absence of lactose, allowing the bacteria to efficiently use lactose as an energy source when available.
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The Lac Operon
β-galactosidase
β-galactosidase is an enzyme encoded by the lacZ gene that catalyzes the hydrolysis of lactose into glucose and galactose. It also cleaves X-gal, a synthetic substrate, producing a blue pigment as a byproduct. The presence of this enzyme is crucial for E. coli to utilize lactose, and its activity can be used as a marker for the functionality of the lac operon.
Mutations in Regulatory Regions
Mutations can occur not only in the coding regions of genes but also in regulatory regions that control gene expression. In the context of the lac operon, mutations in the promoter or operator regions can prevent the transcription of the lacZ and lacY genes, leading to a lack of β-galactosidase and lactose permease, even if the coding sequences are normal. These regulatory mutations can explain the mutant phenotype observed in the colonies.
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Mutations
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Related Practice
Textbook Question
IPTG is a molecule with a structure much like lactose. IPTG can be transported into cells by galactoside permease and can bind to the lac repressor protein. However, unlike lactose, IPTG is not broken down by ββ-galactosidase. Predict what would occur to lac operon regulation if IPTG were added to E. coli growth medium containing no glucose or lactose.
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