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Chapter 6, part A Microbial Growth
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Microbial Growth Microbial growth = increase in number of cells, not cell size
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The Requirements for Growth: Physical Requirements
Temperature Minimum growth temperature Optimum growth temperature Maximum growth temperature
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Temperature Figure 6.1
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Psychrotrophs Grow between 0°C and 20-30°C Cause food spoilage
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Psychrotrophs Figure 6.2
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The Requirements for Growth: Physical Requirements
Most bacteria grow between pH 6.5 and 7.5 Molds and yeasts grow between pH 5 and 6 Acidophiles grow in acidic environments
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The Requirements for Growth: Physical Requirements
Osmotic Pressure Hypertonic environments, increase salt or sugar, cause plasmolysis Extreme or obligate halophiles require high osmotic pressure Facultative halophiles tolerate high osmotic pressure
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The Requirements for Growth: Physical Requirements
Figure 6.4
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The Requirements for Growth: Chemical Requirements
Carbon Structural organic molecules, energy source Chemoheterotrophs use organic carbon sources Autotrophs use CO2
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The Requirements for Growth: Chemical Requirements
Nitrogen In amino acids, proteins Most bacteria decompose proteins Some bacteria use NH4+ or NO3 A few bacteria use N2 in nitrogen fixation Sulfur In amino acids, thiamine, biotin Some bacteria use SO42 or H2S Phosphorus In DNA, RNA, ATP, and membranes PO43 is a source of phosphorus
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The Requirements for Growth: Chemical Requirements
Trace Elements Inorganic elements required in small amounts Usually as enzyme cofactors
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The Requirements for Growth: Chemical Requirements
Oxygen (O2) obligate aerobes Faultative anaerobes Obligate anaerobes Aerotolerant anaerobes Microaerophiles
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Toxic Forms of Oxygen Singlet oxygen: O2 boosted to a higher-energy state Superoxide free radicals: O2 Peroxide anion: O22 Hydroxyl radical (OH)
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The Requirements for Growth: Chemical Requirements
Organic Growth Factors Organic compounds obtained from the environment Vitamins, amino acids, purines, pyrimidines
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Culture Media Culture Medium: Nutrients prepared for microbial growth
Sterile: No living microbes Inoculum: Introduction of microbes into medium Culture: Microbes growing in/on culture medium
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Agar Complex polysaccharide
Used as solidifying agent for culture media in Petri plates, slants, and deeps Generally not metabolized by microbes Liquefies at 100°C Solidifies ~40°C
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Culture Media Chemically Defined Media: Exact chemical composition is known Complex Media: Extracts and digests of yeasts, meat, or plants Nutrient broth Nutrient agar
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Culture Media Table 6.2 & 6.4
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Anaerobic Culture Methods
Reducing media Contain chemicals (thioglycollate or oxyrase) that combine O2 Heated to drive off O2
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Anaerobic Culture Methods
Anaerobic jar Figure 6.5
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Anaerobic Culture Methods
Anaerobic chamber Figure 6.6
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Capnophiles require high CO2
Candle jar CO2-packet Figure 6.7
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Selective Media Suppress unwanted microbes and encourage desired microbes. Figure 6.9b, c
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Differential Media Make it easy to distinguish colonies of different microbes. Figure 6.9a
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Enrichment Media Encourages growth of desired microbe
Assume a soil sample contains a few phenol-degrading bacteria and thousands of other bacteria Inoculate phenol-containing culture medium with the soil and incubate Transfer 1 ml to another flask of the phenol medium and incubate Only phenol-metabolizing bacteria will be growing
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A pure culture contains only one species or strain
A colony is a population of cells arising from a single cell or spore or from a group of attached cells A colony is often called a colony-forming unit (CFU)
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Streak Plate Figure 6.10a, b
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Preserving Bacteria Cultures
Deep-freezing: -50°to -95°C Lyophilization (freeze-drying): Frozen (-54° to -72°C) and dehydrated in a vacuum
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Reproduction in Prokaryotes
Binary fission Budding Conidiospores (actinomycetes) Fragmentation of filaments
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Binary Fission Figure 6.11
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Figure 6.12b
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If 100 cells growing for 5 hours produced 1,720,320 cells:
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Figure 6.13
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Figure 6.14
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Direct Measurements of Microbial Growth
Plate Counts: Perform serial dilutions of a sample Figure 6.15, top portion
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Plate Count Inoculate Petri plates from serial dilutions Figure 6.16
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Plate Count After incubation, count colonies on plates that have colonies (CFUs) Figure 6.15
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Direct Measurements of Microbial Growth
Filtration Figure 6.17a, b
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Direct Measurements of Microbial Growth
Multiple tube MPN test Count positive tubes and compare to statistical MPN table. Figure 6.18b
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Direct Measurements of Microbial Growth
Direct Microscopic Count
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Direct Measurements of Microbial Growth
Figure 6.19
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Estimating Bacterial Numbers by Indirect Methods
Turbidity Figure 620
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Estimating Bacterial Numbers by Indirect methods
Metabolic activity Dry weight
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