Register Now

Login

Lost Password

Lost your password? Please enter your email address. You will receive a link and will create a new password via email.

Login

Register Now

Lorem ipsum dolor sit amet, consectetur adipiscing elit.Morbi adipiscing gravdio, sit amet suscipit risus ultrices eu.Fusce viverra neque at purus laoreet consequa.Vivamus vulputate posuere nisl quis consequat.

Preparation Plates in Microbiology: Techniques and Best Practices

Preparation Plates in Microbiology: Techniques and Best Practices

Why Plate Preparation Quality Matters

Contaminated or uneven agar plates can inflate false‑positive rates by 12–25 % (CDC Lab Quality Report, 2023). Standardizing media depth and pH ensures reproducible colony morphology.

Core Techniques

  • Autoclave Parameters: 121 °C for 15 min at 15 psi achieves >6‑log spore reduction.
  • Cooling to 50 °C: Pouring agar above 55 °C increases condensation by 35 %, leading to swarming artifacts.
  • Uniform Depth: Target 4 mm—5 mm; a 2024 inter‑lab study showed that plates <3 mm deep undercount CFU by 18 %.

Best‑Practice Checklist

Step Control Point Acceptable Range
pH Adjustment After autoclave 7.2–7.4 (tryptic soy)
Antibiotic Addition Below 50 °C Avoid thermal degradation
Drying Time 30–45 min in laminar hood Surface appears matte

Common Errors & Fixes

  1. Excess Condensation: Store plates inverted at 4 °C to reduce drip‑spots.
  2. Uneven Surfaces: Level the bench with a spirit bubble; a 2° tilt causes 10 % volume shift.
  3. Contaminant Flares: Use HEPA‑filtered pour cabinets; airborne yeast counts drop from 15 CFU/m3 to <2.

Reference
CDC. “Laboratory Quality Improvement Report,” 2023.

About fleming

Leave a reply