Microbial Growth and Forensics
Microorganisms are cultured on agar or in broth using aseptic technique. A growth curve has a lag phase (enzymes being made), log (exponential) phase (doubling each generation), stationary phase (births = deaths; nutrients limited, waste builds up) and death phase. . Counting: serial dilution then plate count (colonies × dilution factor ÷ volume plated); haemocytometer; turbidity (colorimeter). Forensics: time of death is estimated from body temperature (falls ~1.5 °C per hour to surroundings), rigor mortis (starts 2–6 h, lasts ~36 h, as ATP runs out), decomposition by bacteria and enzymes, and forensic entomology (blowfly larvae stages), plus a predictable succession of insects on the body. DNA profiling identifies victims and suspects.
Learning objectives
- Describe culturing and counting microorganisms.
- Explain the phases of a growth curve.
- Calculate population size from growth and dilution data.
- Describe methods to estimate time of death.
Why do bacteria stop growing exponentially in a flask?
Core idea
A single bacterium dividing every 20 minutes could produce millions of cells by teatime.
Bacterial populations grow exponentially until resources run out; forensic scientists use biology to estimate time of death.
Several clues combined.
45 colonies from 0.1 cm³ of a 10⁻⁵ dilution.
- Goal
- Cells per cm³ originally.
- Strategy
- Colonies ÷ volume × dilution factor.
- In the diluted sample.
- Undo the dilution.
Summary
- Growth curve phases.
- N = N₀ × 2ⁿ.
- Time of death evidence.
- Generation time
- Time for a bacterial population to double.
- Forensic entomology
- Using insects to estimate time of death.
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