Microbiology Ch 06 lecture_presentation
Transcript of Microbiology Ch 06 lecture_presentation
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Chapter 6
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Growth Requirements
• Microbial Growth • Increase in a population of microbes
• Due to reproduction of individual microbes
• Results in discrete colony or biofilm
• Colony — aggregation of cells arising from single parent
cell
• Biofilm — collection of microbes living on a surface in a
complex community
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Growth Requirements
• Organisms use a variety of nutrients for their
energy needs and to build organic molecules and
cellular structures
• Most common nutrients contain necessary
elements such as carbon, oxygen, nitrogen, and
hydrogen
• Microbes obtain nutrients from variety of sources
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Sources of carbon, energy, and electrons
• Organisms classified into two groups based on source of
carbon
• Autotrophs
• Heterotrophs
• Organisms classified into two groups based on source of
energy
• Chemotrophs
• Phototrophs
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Figure 6.1 Four basic groups of organisms based on their carbon and energy sources.
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Sources of carbon, energy, and electrons
• Organisms classified into two groups based on source of
electrons
• Organotrophs — heterotrophs acquire electrons from
same organic molecules that provide them carbon
• Lithotrophs — autrotrophs acquire electrons from
inorganic molecules
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Oxygen requirements
• Oxygen is essential for obligate aerobes
• Oxygen is deadly for obligate anaerobes
• How can this be true?
• Toxic forms of oxygen are highly reactive and
excellent oxidizing agents
• Resulting oxidation causes irreparable damage to
cells
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Oxygen requirements
• Four toxic forms of oxygen
• Singlet oxygen — molecular oxygen with electrons in
higher energy state
• Superoxide radicals — form from the incomplete
reduction of O2
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Oxygen requirements
• Four toxic forms of oxygen
• Peroxide anion — formed during reactions catalyzed
by superoxide dismutase
• Hydroxyl radical — result from ionizing radiation and
incomplete reduction of hydrogen peroxide
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Figure 6.2 Catalase test.
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Oxygen requirements
• Aerobes
• Anaerobes
• Facultative anaerobes
• Aerotolerant anaerobes
• Microaerophiles
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Figure 6.3 Using a liquid thioglycollate growth medium to identify the oxygen requirements of organisms.
Loose-fittingcap
OxygenconcentrationHigh
Low Obligateaerobes
Obligateanaerobes
Facultativeanaerobes
Aerotolerantanaerobes
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Nitrogen requirements
• Anabolism often ceases because of insufficient nitrogen
• Nitrogen acquired from organic and inorganic nutrients
• All cells recycle nitrogen from amino acids and
nucleotides
• Nitrogen fixation by certain bacteria is essential to life on
Earth
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Growth Requirements
• Nutrients: Chemical and Energy Requirements• Other chemical requirements
• Phosphorus
• Sulfur
• Trace elements
• Required only in small amounts
• Growth factors
• Necessary organic chemicals that cannot be
synthesized by certain organisms
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Growth Requirements
• Physical Requirements• Temperature
• Temperature affects three-dimensional structure of
proteins
• Lipid-containing membranes of cells and organelles are
temperature sensitive
• If too low, membranes become rigid and fragile
• If too high, membranes become too fluid
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Figure 6.4 The effects of temperature on microbial growth.
Maximum
Optimum
Minimum
37ºC30ºC22ºC
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Figure 6.5 Four categories of microbes based on temperature ranges for growth.
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Figure 6.6 An example of a psychrophile.
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Growth Requirements
• Physical Requirements• pH
• Organisms are sensitive to changes in acidity
• H+ and OH– interfere with H bonding
• Neutrophiles grow best in a narrow range around neutral pH
• Acidophiles grow best in acidic habitats
• Many microbes produce acidic waste products that can accumulate and inhibit their growth
• Alkalinophiles live in alkaline soils and water
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Growth Requirements
• Physical Requirements• Physical effects of water
• Microbes require water to dissolve enzymes and nutrients
• Water is important reactant in many metabolic reactions
• Most cells die in absence of water
• Some have cell walls that retain water
• Endospores and cysts cease most metabolic activity
• Two physical effects of water
• Osmotic pressure
• Hydrostatic pressure
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Growth Requirements
• Physical Requirements• Physical effects of water
• Osmotic pressure
• Pressure exerted on a semipermeable membrane by a solution containing solutes that cannot freely cross membrane
• Hypotonic solutions have lower solute concentrations
• Cell placed in hypotonic solution swells
• Hypertonic solutions have greater solute concentrations
• Cell placed in hypertonic solution shrivels
• Restricts organisms to certain environments
• Obligate and facultative halophiles
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Growth Requirements
• Physical Requirements• Physical effects of water
• Hydrostatic pressure
• Water exerts pressure in proportion to its depth
• Barophiles live under extreme pressure
• Their membranes and enzymes depend on
pressure to maintain their three-dimensional,
functional shape
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Growth Requirements
• Associations and Biofilms• Organisms live in association with different species
• Antagonistic relationships — a microbe harms another
organism
• Synergistic relationships — members of an association
receive benefits that exceed those that would result if
each lived by itself
• Symbiotic relationships — organisms become
interdependent and rarely live outside the relationship
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Growth Requirements
• Associations and Biofilms• Biofilms
• Complex relationships among numerous microorganisms
• Form on surfaces, medical devices, mucous membranes
of digestive system
• Form as a result of quorum sensing
• Many microorganisms more harmful as part of a biofilm
• Dental plaque is a biofilm that can lead to cavities
• Scientists seeking ways to prevent biofilm formation
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Figure 6.7 Biofilm development.
Free-swimming microbes are vulnerable to environmentalstresses.
Bacteria
Some microbes land on a surface, such as a tooth, and attach.
The cells begin producing an intracellular matrix and secrete quorum-sensing molecules.
Quorum sensing triggers cells to change their biochemistry and shape.
New cells arrive, possibly including new species, and water channels form in the biofilm.
Some microbes escape from the biofilm to resume a free-living existence and, perhaps, to form a new biofilm on another surface.
Chemical structure of one type of quorum-sensing molecule
Matrix
Water flow
Water channel
Escapingmicrobes
1
2 3 4 5 6
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Growth Requirements
• Tell Me Why• Why should cardiac nurses and respiratory therapists
care about biofilms?
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Culturing Microorganisms
• Inoculum introduced into nutrients called media
• Inocula obtained from various sources
• Environmental specimens
• Clinical specimens
• Stored specimens
• Culture
• Act of cultivating microorganisms or the microorganisms
that are cultivated
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Figure 6.8 Characteristics of bacterial colonies.
ShapeCircular Rhizoid Irregular Filamentous Spindle
Margin
Elevation
Size
Texture
Pigmenta-tion
Opticalproperty
Entire Undulate Lobate Curled Filiform
Flat Raised Convex Pulvinate Umbonate
Punctiform Small Moderate
Glistening (shiny) or dull
Nonpigmented (e.g., cream, tan, white)Pigmented (e.g., purple, red, yellow)
Opaque, translucent, transparent
Colony
Appearance
Large
Smooth or rough
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Culturing Microorganisms
• Obtaining Pure Cultures• Pure cultures are composed of cells arising from a
single progenitor
• Progenitor is termed a colony-forming unit (CFU)
• Aseptic technique prevents contamination of sterile
substances or objects
• Two common isolation techniques
• Streak plates
• Pour plates
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Figure 6.9 The streak-plate method of isolation.
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Figure 6.10 The pour-plate method of isolation.
Sequential inoculations
1.0 ml
Initialsample
9 mlbroth
Colonies Fewer colonies
1.0 ml to eachPetri dish, add9 ml warm agar,swirl gently to mix
1.0 ml 1.0 ml
9 mlbroth
9 mlbroth
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Culturing Microorganisms
• Obtaining Pure Cultures• Other isolation techniques
• Some fungi are isolated with streak and pour plates
• Protozoa and motile unicellular algae are isolated through
dilution of broth cultures
• Can individually pick single cell of some large
microorganisms and use to establish a culture
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Culturing Microorganisms
• Culture Media• Majority of prokaryotes have not been grown in culture
medium
• Nutrient broth is common medium
• Agar is a common addition to many media
• Complex polysaccharide derived from certain red algae
• Produces a solid surface for colonial growth
• Most microbes cannot digest agar
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Culturing Microorganisms
• Culture Media• Six types of general culture media
• Defined media
• Complex media
• Selective media
• Differential media
• Anaerobic media
• Transport media
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Figure 6.11 Slant tubes containing solid media.
Slant
Butt
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Culturing Microorganisms
• Culture Media• Defined media
• Medium in which the exact chemical composition is known
• Fastidious organisms require the addition of a large
number of growth factors
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Culturing Microorganisms
• Culture Media• Complex media
• Exact chemical composition is unknown
• Contain nutrients released by partial digestion of yeast,
beef, soy, or proteins
• Support growth of wide variety of microorganisms
• Used to culture organisms with unknown nutritional needs
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Figure 6.12 An example of the use of a selective medium.
Bacterial colonies Fungal colonies
pH 7.3 pH 5.6
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Culturing Microorganisms
• Culture Media• Enrichment media
• Use of a selective medium to increase the numbers of a
chosen microbe to observable levels
• May require a series of cultures to enrich for the desired
microbe
• Cold enrichment used to enrich a culture with cold-
tolerant species
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Figure 6.13 The use of blood agar as a differential medium.
Beta-hemolysisAlpha-hemolysis
No hemolysis(gamma-hemolysis)
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Figure 6.14 The use of carbohydrate utilization tubes as differential media.
Durham tube(inverted tubeto trap gas)
Acid fermentationwith gas
No fermentation
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Figure 6.15 The use of MacConkey agar as a selective and differential medium.
Escherichia coli Escherichia coli Escherichia coli
Staphylococcusaureus
Staphylococcusaureus (no growth)
Salmonella entericaserotype Choleraesuis
MacConkey agar MacConkey agarNutrient agar
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Culturing Microorganisms
• Culture Media• Anaerobic media
• Obligate anaerobes must be cultured in the absence of
free oxygen
• Reducing media contain compounds that combine with
free oxygen and remove it from the medium
• Petri plates are incubated in anaerobic culture vessels
• Sealable containers that contain reducing
chemicals
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Figure 6.16 An anaerobic culture system.
Airtight lid
Palladium pelletsto catalyze reactionremoving O2
Methylene blue(anaerobicindicator)
Envelopecontainingchemicals torelease CO2and H2
Petri plates
Chamber
Clamp
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Culturing Microorganisms
• Culture Media• Transport media
• Used by hospital personnel to ensure clinical specimens
are not contaminated and to protect people from infection
• Rapid transport of samples is important
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Culturing Microorganisms
• Special Culture Techniques• Techniques developed for culturing microorganisms
• Animal and cell culture
• Used when artificial media are inadequate
• Required for growth of viruses and other obligate
intracellular parasite
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Culturing Microorganisms
• Special Culture Techniques• Techniques developed for culturing microorganisms
• Low-oxygen culture
• Many organisms prefer intermediate oxygen levels
• Carbon dioxide incubators mimic the environment of
many body tissues
• Candle jars are a low cost alternative
• Ideal for the growth of capnophiles —
microbes that grow best in high carbon dioxide
levels
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Culturing Microorganisms
• Preserving Cultures• Refrigeration
• Stores for short periods of time
• Deep-freezing
• Stores for years
• Lyophilization
• Stores for decades
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Culturing Microorganisms
• Tell Me Why• Why do clinical laboratory scientists keep many different
kinds of culture media on hand?
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Bacterial Growth: Overview
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Binary Fission
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Figure 6.17 Binary fission.Cytoplasmic membraneChromosomeCell wall
Replicatedchromosome
Septum
Completedseptum
30 minutes
60 minutes
90 minutes
120 minutes
Septum
1
2
3
4
5
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Growth of Microbial Populations
• Generation Time• Time required for a bacterial cell to grow and divide
• Dependent on chemical and physical conditions
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Figure 6.18 A comparison of arithmetic and logarithmic growth.
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Figure 6.19 Two growth curves of logarithmic growth.
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Figure 6.20 A typical microbial growth curve.
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Bacterial Growth Curve
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Growth of Microbial Populations
• Continuous Culture in a Chemostat• Chemostat is used to maintain a microbial population in
a particular phase of growth
• Open system
• Requires addition of fresh medium and removal of old
medium
• Allows the study of microbial populations in steady but
low nutrient levels
• Used in several industrial settings
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Figure 6.21 Schematic of chemostat.
Fresh medium witha limiting amountof a nutrient
Sterile airor othergas
Flow-rateregulator
Culturevessel
Overflowtube
Culture
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Growth of Microbial Populations
• Measuring Microbial Reproduction• Direct methods not requiring incubation
• Microscopic counts
• Count microorganisms directly through a microscope
• Suitable for stained prokaryotes and large eukaryotes
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Figure 6.22 The use of a cell counter for estimating microbial numbers.Cover slip
Location ofgrid
Bacterialsuspension
Overflow troughs
Place underoil immersion
Bacterialsuspension
Pipette
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Growth of Microbial Populations
• Measuring Microbial Reproduction• Direct methods not requiring incubation
• Electronic counters
• Coulter counters
• Counts cells as they interrupt an electrical current
flowing in front of an electronic detector
• Flow cytometry
• A light-sensitive detector records changes in light
transmission as cells pass through a tube
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Growth of Microbial Populations
• Measuring Microbial Reproduction• Direct methods requiring incubation
• Serial dilution and viable plate counts
• Membrane filtration
• Most probable number
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Figure 6.23 A serial dilution and viable plate count for estimating microbial population size.
1 ml of originalculture
9 ml of broth +1 ml of originalculture
0.1 ml of eachtransferred toa plate
Incubation period
1.0 ml
1:10dilution(10-1)
Too numerous to count(TNTC)
TNTC 65 colonies 6 colonies 0 colonies
1:100dilution(10-2)
1:1000dilution(10-3)
1:10,000dilution(10-4)
1:100,000dilution(10-5)
1.0 ml 1.0 ml 1.0 ml
0.1 ml0.1 ml0.1 ml0.1 ml
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Figure 6.24 The use of membrane filtration to estimate microbial population size.
Membrane transferredto culture mediumSample to be filtered
Colonies
Membrane filterretains cells
To vacuum
Incubation
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Figure 6.25 The most probable number (MPN) method for estimating microbial numbers.
1:1001:10Undiluted
1.0 ml1.0 ml
Inoculate 1.0 ml intoeach of 5 tubes
Phenol red, pHcolor indicator,added
Incubate
Results
4 tubes positive 2 tubes positive 1 tube positive
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Growth of Microbial Populations
• Measuring Microbial Growth• Indirect methods
• Turbidity
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Figure 6.26 Turbidity and the use of spectrophotometry in indirectly measuring population size.
Direct light
Light source Uninoculatedtube
Light-sensitivedetector
Light source Inoculatedbroth culture
Scattered lightthat does notreach reflector
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Growth of Microbial Populations
• Measuring Microbial Growth• Indirect methods
• Metabolic activity
• Using changes in nutrient utilization, waste production,
or pH to estimate number of cells in a culture
• Dry weight
• Organisms are filtered from media, dried, and weighed
• Genetic methods
• Isolate DNA sequences of unculturable prokaryotes
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Growth of Microbial Populations
• Tell Me Why• Students transfer some "gunk" from a two-week-old
bacterial culture into new media. Why shouldn't they be
surprised when this "death-phase" sample grows?
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Important topics
• Growth in microbiology• Stages of microbial growth• Classification of microorganisms based on carbon and energy source• Different extremophile archaea (halophile, thermophile, …)