Why do typical Gram-positive cells retain purple dye during correct decolorization?
- Safranin makes complexes that stay in the wall
- Thick peptidoglycan retains the dye complexes
- The outer membrane keeps dye inside the cell
What is the order of the four Gram stain reagents?
- Iodine, safranin, crystal violet, decolorizer
- Decolorizer, crystal violet, safranin, iodine
- Crystal violet, iodine, decolorizer, safranin
During correct decolorization, thick peptidoglycan helps Gram-positive cells retain dye complexes, while thin peptidoglycan fails to retain them after the Gram-negative outer membrane is disrupted.
Circle one: True False
Which layer is absent from the usual Gram-positive envelope but can restrict antibiotic entry in Gram-negative cells?
- The inner membrane
- The peptidoglycan wall
- The outer membrane
A fresh Gram-positive culture receives too much decolorizer and then safranin. Which misleading result can occur?
- Some cells lose both dyes and remain colourless
- Some cells lose purple dye and then stain pink
- Some cells retain more purple dye after the wash
A susceptible bacterium is growing in dilute surroundings. A beta-lactam blocks new peptidoglycan cross-links. Which outcome can follow?
- The cell may shrink as water moves out of its cytoplasm
- The cell may burst as water enters and internal pressure rises
- The cell wall may strengthen as fewer cross-links are made
Two bacterial isolates both stain pink. What is needed to assess whether a particular antibiotic inhibits each isolate?
- Compare each isolate's response in susceptibility testing
- Compare the isolates' shades of pink after counterstaining
- Compare the isolates' peptidoglycan thickness in their walls
A Gram-negative cell loses purple dye during decolorization. Lee says its outer membrane must let antibiotics enter freely. Which reply explains the problem?
- Alcohol leaves the outer membrane intact, so purple dye loss measures antibiotic entry.
- Safranin tests membrane channels, so its colour predicts antibiotic entry.
- Alcohol disrupts the membrane, so dye loss does not test intact-cell drug entry.