Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
5. Genetics of Bacteria and Viruses
Working with Microorganisms
Problem 4a
Textbook Question
Fifteen bacterial colonies growing on a complete medium are transferred to a minimal medium. Twelve of the colonies grow on minimal medium.
The serine biosynthetic pathway is a three-step pathway in which each step is catalyzed by the enzyme product of a different gene, identified as enzymes A, B, and C in the diagram below.
Mutant 1 grows only on In addition to growth on , mutant 2 also grows on and . Mutant 3 grows on and . Identify the step of the serine biosynthesis pathway at which each mutant is defective.


1
Identify the compounds that each mutant can grow on, as these will help determine which step in the pathway is defective.
For Mutant 1, since it grows only on a specific compound, it indicates a defect in the first step catalyzed by Enzyme A, as it cannot convert 3-Phosphoglycerate to 3-Phospho-hydroxypyruvate.
For Mutant 2, since it grows on two compounds, it suggests a defect in the second step catalyzed by Enzyme B, as it cannot convert 3-Phospho-hydroxypyruvate to 3-Phosphoserine.
For Mutant 3, since it grows on two compounds, it indicates a defect in the third step catalyzed by Enzyme C, as it cannot convert 3-Phosphoserine to Serine.
Match each mutant to the corresponding enzyme defect based on the growth patterns on the specific compounds.

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