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Microbial Growth P.2 Ch.6
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Microbial Growth P.2 Ch.6
Requirements of Growth:
- Culture Media:
- Obtaining Pure Cultures:
- Preserving Bacterial Cultures:
- Deep Freezing: -50 to -95 C
- Lyophilization(Freeze drying): Frozen -54 to -72/dehydrated in a vacuum
- Deep Freezing: -50 to -95 C
- Preserving Bacterial Cultures:
- Measurement of Microbial Growth:
- Plate Counts
- Filtration
- Most Probable Number (MPN)
- Direct Microscopic Count
- Indirect Methods:
- Turbity
- Metabolic Activity
- Dry weight
- Metabolic Activity
- Indirect: Metabolic activities: measure amount of metabolic such as acid
- Dry Weight: for mold
- Turbity
- Direct Microscopic Advantages: No incubation Time
- Disadvantage: Motile microbes difficult to count
- Dead cells counted
- High cell concentration required to count
- Dead cells counted
- Disadvantage: Motile microbes difficult to count
- Indirect Methods:
- Multiple tube MPN test
- Count positive tubes
- Useful for microbes that wont grow on solids
- Useful for using different medium to ID microbes
- Useful for microbes that wont grow on solids
- Count positive tubes
- Direct Microscopic Count
- Membrane Filtration:
- Advantages: Can study in diluted samples
- Disadvantages:
- Breaks up cells
- Does not catch all cells
- Breaks up cells
- Disadvantages:
- Advantages: Can study in diluted samples
- Most Probable Number (MPN)
- Advantages: Measures Viable # of cells
- Disadvantages: Take time for incubation
- Bacteria Grow in Clumps
- CFU mesures
- Too many to count
- CFU mesures
- Bacteria Grow in Clumps
- Disadvantages: Take time for incubation
- Filtration
- Plate Counts
- Obtaining Pure Cultures:
- Bacterial division/Binary Fission
- Budding
- Condispores(actinomycetes
- Fragmentation of filaments
- Condispores(actinomycetes
- Budding
- Culture Media:
Growth of Bacterial Cultures:
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- Mind Map on Microbial Growth P.2 Ch.6, created by sunygarcia20 on 25/02/2016.
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