5.3 Measuring Bacterial Growth

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Last updated 3:28 AM on 6/19/26
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15 Terms

1
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What is the range of time it takes for a cell to divide?

20 minutes to 3 hours

2
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How do bacteria grow?

Bacteria grow through binary fission

3
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Describe the bacterial growth curve

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4
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How can we measure turbidity?

We can measure turbidity through a spectrophotometer

<p>We can measure turbidity through a <strong>spectrophotometer</strong></p>
5
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What are the advantages of using a spectrophotometer?

Advantage: Results are obtained right away

6
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What are the disadvantages of using a spectrophotometer?

Disadvantages: Cannot be used for very dilute cultures, dead cells are also counted

7
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What is the Petroff Hausser Chamber?

The Petroff Hausser Chamber observed a very small liquid sample under a microscope

<p>The Petroff Hausser Chamber observed a very small liquid sample under a microscope</p>
8
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What are the advantages of the Petroff Hausser Chamber?

Advantage: Results are obtained right away

9
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What are the disadvantages of the Petroff Hausser Chamber?

Disadvantages: Cannot be used for very dilute cultures, dead cells are also counted

10
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What does CFU mean?

CFU means colony forming units

11
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What are the advantages of plating?

Advantages: Counts only live cells, more accurate

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What are the disadvantages of plating?

Disadvantages: Incubations are required, so obtaining the results are after a few days

  • Dilutions are also required, as plating a sample will lead to a lawn of growth (TNTC)

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How many colonies are considered countable on plating?

Ideally 20 to 200 colonies

14
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What is the process of serial dilutions?

  1. A sample is mixed with a diluent (usually water)

  2. That sample with the diluent is further mixed with more diluent, repeating several times

15
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What is the formula for counting colonies in serial dilutions?

CFU / plating factor x 1 / dilution factor