Table of contents
- 1. Introduction to Biology2h 40m
- 2. Chemistry3h 40m
- 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 41m
- Introduction to Mendel's Experiments7m
- Genotype vs. Phenotype17m
- Punnett Squares13m
- Mendel's Experiments26m
- Mendel's Laws18m
- Monohybrid Crosses16m
- 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 20m
- 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 52m
- 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 Transport2m
- 35. Soil37m
- 36. Plant Reproduction47m
- 37. Plant Sensation and Response1h 9m
- 38. Animal Form and Function1h 19m
- 39. Digestive System10m
- 40. Circulatory System1h 57m
- 41. Immune System1h 12m
- 42. Osmoregulation and Excretion50m
- 43. Endocrine System4m
- 44. Animal Reproduction2m
- 45. Nervous System55m
- 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
15. Gene Expression
Genetic Code
2:39 minutes
Problem 9a
Textbook Question
Textbook QuestionDraw a hypothetical metabolic pathway in Neurospora crassa composed of five substrates, five enzymes, and a product called nirvana. Number the substrates 1–5, and label the enzymes A–E, in order. (For instance, enzyme A catalyzes the reaction between substrates 1 and 2.) (a) Suppose a mutation made the gene for enzyme C nonfunctional. What molecule would accumulate in the affected cells?
Verified step by step guidance
1
Step 1: First, let's draw the metabolic pathway. We have five substrates numbered 1-5, and five enzymes labeled A-E. Substrate 1 is converted to substrate 2 by enzyme A, substrate 2 is converted to substrate 3 by enzyme B, substrate 3 is converted to substrate 4 by enzyme C, substrate 4 is converted to substrate 5 by enzyme D, and finally, substrate 5 is converted to the product nirvana by enzyme E.
Step 2: Now, let's consider the mutation that made the gene for enzyme C nonfunctional. This means that enzyme C is no longer available to catalyze the reaction from substrate 3 to substrate 4.
Step 3: Without enzyme C, the conversion of substrate 3 to substrate 4 cannot occur. This means that substrate 3 cannot be used up in the reaction.
Step 4: As a result, substrate 3 will start to accumulate in the cells because it is being produced by the action of enzyme B but not being used up due to the absence of enzyme C.
Step 5: Therefore, in the cells affected by the mutation that made the gene for enzyme C nonfunctional, the molecule that would accumulate would be substrate 3.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Metabolic Pathway
A metabolic pathway is a series of chemical reactions occurring within a cell, where substrates are converted into products through the action of enzymes. Each step in the pathway is catalyzed by a specific enzyme, which facilitates the transformation of substrates into intermediate compounds and ultimately into the final product. Understanding the sequence and function of these reactions is crucial for analyzing the effects of mutations on metabolic processes.
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Introduction to Metabolism
Enzyme Function and Mutations
Enzymes are biological catalysts that speed up chemical reactions by lowering the activation energy required. A mutation that renders an enzyme nonfunctional can disrupt the entire metabolic pathway, leading to the accumulation of substrates that precede the blocked reaction. In the context of Neurospora crassa, if enzyme C is nonfunctional, the substrate immediately before enzyme C in the pathway will accumulate, as it cannot be converted into the next substrate.
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Functions of Enzymes
Substrate Accumulation
Substrate accumulation occurs when a specific substrate cannot be converted into its product due to a malfunctioning enzyme. This buildup can indicate where in the metabolic pathway the disruption has occurred. In the case of the hypothetical pathway in Neurospora crassa, identifying which substrate accumulates when enzyme C is nonfunctional helps to pinpoint the metabolic block and understand the pathway's dynamics.
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