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MICROBIAL NUTRITION

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Photoautotrophs use CO2 and sunlight energy. Photoheterotrophs use ... (2) Coulter method - a machine determines the number of cells that are present in ... – PowerPoint PPT presentation

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Title: MICROBIAL NUTRITION


1
  • MICROBIAL NUTRITION

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  • All living organisms require nutrients
  • Micronutrients
  • Macronutrients

3
How organisms acquire food
  • Photoautotrophs use CO2 and sunlight energy
  • Photoheterotrophs use sunlight and C in an
    organic form
  • Chemoautotrophs use chemical energy from
    reactions
  • Chemoheterotrophs use energy from autotrophs or
    other heterotrophs

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Nitrogen
  • Makes up 79 of atmosphere
  • Most organisms cannot use gaseous nitrogen so
    they are dependent on organisms that can fix
    nitrogen

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Bacterial nutrition
  • Different species of bacteria can differ in the
    nutrients that are required
  • Some bacteria are picky or fastidious

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  • ECOLOGY

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Microbes ( other organisms) are influenced by
  • 1. limited resources (e.g., food or nutrients)
  • 2. intraspecific interactions
  • 3. interspecific interactions
  • 4. abiotic factors such as temperature, pH,
    salinity etc.

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  • ENVIRONMENTAL FACTORS

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  • A. In general, organisms including microbes are
    influenced by
  • 1. limited resources (e.g., food or nutrients)
  • 2. intraspecific interactions
  • 3. interspecific interactions
  • 4. abiotic factors such as temperature, pH,
    salinity etc.

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  • Graphs will be drawn on the board

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Quantifying Bacteria
  • Methods include but are not limited to
  • a. Measuring turbidity (cloudiness) in a liquid
    culture.
  • (1) an increase in turbidity indicates an
    increase in the number of bacterial cells
    present. We can qualitatively estimate bacterial
    numbers by looking at the degree of turbidity.
  • (2) spectrophotometric methods . We can use a
    spectrophotometer to measure the amount of light
    absorbed by a tube containing broth and bacteria
    (or the amount of light that is transmitted).
    This absorbence (or transmittance) can be
    compared to a standard.
  • b. Colony counts. Bacteria are plated on agar
    and then the number of colonies that are present
    are counted. If necessary the solution
    containing the bacteria is diluted prior to
    plating by serial dilution
  • c. Cell counts
  • (1) microscopic - the number of bacterial cells
    in a sample is counted
  • (2) Coulter method - a machine determines the
    number of cells that are present in a sample

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  • How to maintain microbes in the laboratory

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Types (physical) of media
  • a. liquid (e.g., broth)
  • b. semisolid with a gelatinous consistency
  • c. solid or firm containing agar (a solidifying
    agent, a complex polysaccharide derived from red
    algae).

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  • Properties of agar
  • (1) solid at room temperature
  • (2) liquid at the boiling point of water (100oC)
  • (3) resolidifies at 42oC
  • (4) because of this, agar can be melted (and
    sterilized) and then poured into individual petri
    dishes. Prior to the inoculation of microbes
    media must be sterilized.

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Functional types of media
  • a. general purpose media for the growth of many
    different species of microbes
  • b. enriched (AKA Complex) media contain extra
    ingredients e.g., blood,
  • c. selective and differential media are designed
    for the growth of certain bacterial species. A
    selective medium contains one or more agents that
    inhibit the growth of certain species while not
    inhibiting the growth of other species. Thus the
    latter is selected for. A differential medium
    supports the growth of several species of
    bacteria but these bacterial species appear
    different.
  • d. Misc. media such as reducing media that
    reduce the reduction-oxidation potential

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