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Science Olympiad Material for Microbe Mission
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National Event Supervisor National Rules Committee Chairman – Life Science DISCLAIMER - This presentation was prepared using draft rules. There may be some changes in the final copy of the rules. The rules which will be in your Coaches Manual and Student Manuals will be the official rules. BE SURE TO CHECK THE 201 8 EVENT RULES for EVENT PARAMETERS and TOPICS FOR EACH COMPETITION LEVEL TRAINING MATERIALS:
CELLULAR LIFE - All cells have the following
Organelles of Microbial Origin
Measuring bacterial growth: Optical Density: using a spectrophotometer to measure the turbidity (cloudiness) of a bacterial culture Plate counts: dilute and plate bacterial cultures, count the number of colonies that form to determine Colony Forming Units per mL (CFU/mL) Quantifying DNA or Protein: extract DNA and protein from bacterial culture and quantify using laboratory assays Isolation of bacteria Streaking for isolation: spread a heavy streak of cells with a sterile stick or loop; re-sterilize stick or loop with flame, pull cells from previous streak, and dilute by dragging stick or loop across plate; repeat until cells sufficiently diluted to form isolated colonies. Serial dilution and plating: dilute culture 10-fold (ex: 1mL of culture into 9mL of fresh medium); transfer same volume of first dilution to a second tube with the same amount of fresh media, generating a 100-fold dilution, continue until 10 6 dilution has been made; spread volumes of each dilution on plates; count colonies that form; determine Colony Forming Units per mL of medium (CFU/mL). Streaking for isolation: Serial dilution and plating:
Gram positive bacteria
Amoeba
2018 MICROBIAL DISEASES – 5 - 21 - 2017 (New in red bold) VIRAL DISEASES