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Veterinary Medicine
Brawijaya University
 The growth of a population is an increase in
the number of cells
 The requirements for microbial growth are
both physical and chemical
Temperature
 Psychrophiles (cold loving)
 Mesophiles (moderate-temperature loving)
 Thermophiles (heat-loving)
pH
 Most bacteria grow best at pH 6.5 - 7.5
 Acidophiles  tolerant to acidity
Osmotic pressure
 They require water for growth and made up of 80-90%
water
 In hypertonic solution,most microbes undergo plasmolysis
 In hypotonic solution wrinkle
 Halophiles, can tolerate high salt concentrations
Carbon
 Carbon is the structural back-bone of living matter
 Half the dry weight of bacterial cell is carbon
 Chemoheterotrophs, use an organic molecule
 Autotroph (chemoautotroph or photoautotroph) derive
their carbon from carbon dioxide
Nitrogen
 Nitrogen is needed for protein and nucleic acid
synthesis
 Nitrogen can be obtained from the decomposition of
proteins or from NH4
+ or NO3
-
 A few bacteria are capable of nitrogen (N2) fixation
Oxygen
 On the basis of oxygen requirements, organisms are
classified as
obligate aerobes
facultative anaerobes
aerotolerant anaerobes
microaerophilic
capnophilic
 Aerobes, facultative anaerobes, and aerotolerant
anaerobes must have the enzymes superoxide dismutase
(2O2
- + 2H+  O2 + H2O2) and either catalase (2H2O2 
2H2O + O2) or peroxidase (H2O2 + 2H2  2H2O)
Other chemicals required for microbial growth include
sulfur, phosphorus, trace elements, and, for some
organisms, organic growth factors
 A culture medium is any material prepared for the
growth of bacteria in a laboratory
 Microbes that grow and multiply in or on a culture
medium known as a culture
- Agar is a common solidifying agent for a
culture medium
- Broth medium is a liquid medium
- Semisolid medium
TYPE PURPOSE
Chemically defined media Growth of chemoautotrophs and
photoautotrophs, and microbiolo-
gical assay
Complex media, made up of
nutrient such as extract from
yeast, meat, or digest of protein
exp: nutrient agar or nutrient broth
Most heterotrophic bacteria and
fungi are routinely grown on
complex media
Reducing media Cultivation of anaerobic bacteria
Contain ingredients, such as
sodium thioglycholate, that
chemically combine with
dissolved oxygen and depleted
the oxygen in the culture medium
TYPE PURPOSE
Differential media
McConkey, Urease medium,
Salmonella Shigella Agar (SSA),
BloodAgar Plate (BAP)
Differentiation of colonies of
desired microbes from others
Selective media
Bismuth Sulfite Agar (BSA), Eosin
Methylene Blue (EMB),
Thiosulphate Citrate Bile Salt
Sucrose(TCBS)
Suppression of unwanted
microbes; encouraging
desired microbes
Enrichment media
Selenite broth
Alkali PeptonWater (APW)
Similar to selective media but
designed to increase numbers
of desired microbes to
detectable level
Enriched media
BAP, Chocolate Agar Plate (CAP),
Brain Heart Infusion (BHI)
For fastidious bacteria
Transport media
Cary-Blair (V. cholerae)
Amis (Nesseria gonorrhoe)
It was needed if the specimens
was taken from far places
Bacterial Division
 Bacteria normally reproduce by binary fission, in which a
single cell divides into two identical cells
 Fungi reproduce by budding, aerial spore formation, or
fragmentation
 Bacterial division occurs according to a logarithmic
progression : 2 cells  4 cells  8 cells  etc.
GenerationTime
 The time required for a cell to divide or a population to
double is known as the generation time
 Most bacteria have generation time 1 – 3 hours; other require
more than 24 hours per generation
Pathogenic Mycobacterium require > 8 weeks
 During the lag phase, there is little or no change in
the number of cells, but metabolic activity is high
 During the log phase (exponential growth phase),
bacteria multiply at the fastest rate possible under
the conditions provided
 During the stationary phase, there is equilibrium
between cell division and death
 During the death phase, the number of deaths
exceeds the number of new cells formed
 A standard plate count reflects the number of viable
microbes and assumes that each bacterium grows into a
single colony; plate count are reported as number of
colony forming units (CFU)
 In filtration, bacteria are retained on the surface of a
membrane filter and then transferred to a culture
medium to grow and subsequently be counted
 The most probable number (MPN) method can be used
for microbes that will grow in a liquid medium; it is
statistically estimation
 In a direct microscopic count, the microbes in a
measured volume of a bacterial suspension are counted
with the use of a specially designed slide Petroff-
Hausser cell counter
Turbidity
 A spectrophotometer is used to determine turbidity
by measuring the amount of light that passes
through a suspension of cells
 McFarland standard
Metabolic Activity
 Acid production or oxygen consumption
DryWeight
 For filamentous organisms such as fungi, measuring
dry weight is a convenient method of growth
measurement
-Thank You For Your
Attention-

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Microbial growth3

  • 2.  The growth of a population is an increase in the number of cells  The requirements for microbial growth are both physical and chemical
  • 3. Temperature  Psychrophiles (cold loving)  Mesophiles (moderate-temperature loving)  Thermophiles (heat-loving) pH  Most bacteria grow best at pH 6.5 - 7.5  Acidophiles  tolerant to acidity Osmotic pressure  They require water for growth and made up of 80-90% water  In hypertonic solution,most microbes undergo plasmolysis  In hypotonic solution wrinkle  Halophiles, can tolerate high salt concentrations
  • 4. Carbon  Carbon is the structural back-bone of living matter  Half the dry weight of bacterial cell is carbon  Chemoheterotrophs, use an organic molecule  Autotroph (chemoautotroph or photoautotroph) derive their carbon from carbon dioxide Nitrogen  Nitrogen is needed for protein and nucleic acid synthesis  Nitrogen can be obtained from the decomposition of proteins or from NH4 + or NO3 -  A few bacteria are capable of nitrogen (N2) fixation
  • 5. Oxygen  On the basis of oxygen requirements, organisms are classified as obligate aerobes facultative anaerobes aerotolerant anaerobes microaerophilic capnophilic  Aerobes, facultative anaerobes, and aerotolerant anaerobes must have the enzymes superoxide dismutase (2O2 - + 2H+  O2 + H2O2) and either catalase (2H2O2  2H2O + O2) or peroxidase (H2O2 + 2H2  2H2O) Other chemicals required for microbial growth include sulfur, phosphorus, trace elements, and, for some organisms, organic growth factors
  • 6.  A culture medium is any material prepared for the growth of bacteria in a laboratory  Microbes that grow and multiply in or on a culture medium known as a culture - Agar is a common solidifying agent for a culture medium - Broth medium is a liquid medium - Semisolid medium
  • 7. TYPE PURPOSE Chemically defined media Growth of chemoautotrophs and photoautotrophs, and microbiolo- gical assay Complex media, made up of nutrient such as extract from yeast, meat, or digest of protein exp: nutrient agar or nutrient broth Most heterotrophic bacteria and fungi are routinely grown on complex media Reducing media Cultivation of anaerobic bacteria Contain ingredients, such as sodium thioglycholate, that chemically combine with dissolved oxygen and depleted the oxygen in the culture medium
  • 8. TYPE PURPOSE Differential media McConkey, Urease medium, Salmonella Shigella Agar (SSA), BloodAgar Plate (BAP) Differentiation of colonies of desired microbes from others Selective media Bismuth Sulfite Agar (BSA), Eosin Methylene Blue (EMB), Thiosulphate Citrate Bile Salt Sucrose(TCBS) Suppression of unwanted microbes; encouraging desired microbes
  • 9. Enrichment media Selenite broth Alkali PeptonWater (APW) Similar to selective media but designed to increase numbers of desired microbes to detectable level Enriched media BAP, Chocolate Agar Plate (CAP), Brain Heart Infusion (BHI) For fastidious bacteria Transport media Cary-Blair (V. cholerae) Amis (Nesseria gonorrhoe) It was needed if the specimens was taken from far places
  • 10. Bacterial Division  Bacteria normally reproduce by binary fission, in which a single cell divides into two identical cells  Fungi reproduce by budding, aerial spore formation, or fragmentation  Bacterial division occurs according to a logarithmic progression : 2 cells  4 cells  8 cells  etc. GenerationTime  The time required for a cell to divide or a population to double is known as the generation time  Most bacteria have generation time 1 – 3 hours; other require more than 24 hours per generation Pathogenic Mycobacterium require > 8 weeks
  • 11.
  • 12.
  • 13.  During the lag phase, there is little or no change in the number of cells, but metabolic activity is high  During the log phase (exponential growth phase), bacteria multiply at the fastest rate possible under the conditions provided  During the stationary phase, there is equilibrium between cell division and death  During the death phase, the number of deaths exceeds the number of new cells formed
  • 14.  A standard plate count reflects the number of viable microbes and assumes that each bacterium grows into a single colony; plate count are reported as number of colony forming units (CFU)  In filtration, bacteria are retained on the surface of a membrane filter and then transferred to a culture medium to grow and subsequently be counted  The most probable number (MPN) method can be used for microbes that will grow in a liquid medium; it is statistically estimation  In a direct microscopic count, the microbes in a measured volume of a bacterial suspension are counted with the use of a specially designed slide Petroff- Hausser cell counter
  • 15. Turbidity  A spectrophotometer is used to determine turbidity by measuring the amount of light that passes through a suspension of cells  McFarland standard Metabolic Activity  Acid production or oxygen consumption DryWeight  For filamentous organisms such as fungi, measuring dry weight is a convenient method of growth measurement
  • 16. -Thank You For Your Attention-