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Subjects included;
•   Cultivation
•   Medium
•   Inoculation of media
•   The Requirements for Growth
•   Preparation
•   Classification
•   Eplanation of types of media
    functionally.
Cultivation;
  The propagation of living organisms, applied
especially to the growth of microorganisms or other
cells in artificial media.

Medium
 Any preparation that contains nutrients essential
for microorganisms growth.

Culture medium:
 A nutrient substance that is used to grow
micro-organisms .
Inoculation of media
  Introduction of infected material to the medium ,for
cultivation of organisms.

  Agar
 Is 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 at ~40°C
The Requirements for Growth
1.CHEMICAL REQUIREMENTS
(NUTRITIONAL FACTORS)
•   Carbon
•   Nitrogen, sulfur, and phosphorous
•   Trace elements
•   Organic growth factor
•   Vitamins (e.g. folic acid, vitamin B-12, vitamin K)
•   Oxygen
2.PHYSICAL REQUIREMENTS

•   Temperature
•   PH
•   Hydrostatic Pressure
•   Osmotic pressure
Preparation
• Wash hands & wear gloves
• Sterilize all equipments
• Pour D/W in glassware (required amount)
• Add powder ingredients (required amount)
• Heat to dissolve completely
• Autoclave
• Dispense the medium into tubes ,bottles
  &plates
• Store at required temperature
• Sterilizing Culture Media
Classification

  1. Consistency
  2. Nutritional
  3. Functional
1.Consistency
a ) Solid e.g nutrient agar
b ) Semi-solid e.g peptone water.
c ) Liquid medium e.g nutrient broth.
2.Nutritional
 a ) Simple e.g peptone water
 b ) Complex e.g blood agar
 c ) Synthetic e.g Davis /mingioli medium
3.Functional
a) Basic media
b) Selective media
c ) Differential media
d ) Enriched media
e ) Enrichment media
 f ) Transport media
Basic media
• This is an undefined medium because
  the amino acid source contains a
  variety of compounds with the exact
  composition being unknown.
• Nutrient media contain all the
  elements that most bacteria need for
  growth and are non-selective, so they
  are used for the general cultivation and
  maintenance of bacteria kept in
  laboratory culture collections.
Basic media
• This media contains;
 1.A carbon source such as glucose for
  bacterial growth
 2.Water
 3.Various salts needed for bacterial growth
There are two types:
1. nutrient broth which is liquid media
2. nutrient agar which is solid media
Selective media
• culture medium that allows the growth
  of certain types of organisms, while
  inhibiting the growth of other
  organisms
• Any agar media can be made
  selective by addition of certain
  inhibitory agents that
  don’t affect the pathogen.
• Various approaches to make a
  medium selective include addition
  ofantibiotics, dyes, chemicals,
  alteration of pH or a combination of
  these medium
Selective media
• Thiosulphate citrate bile salt sucrose
  (TCBS) which is selective for Vibrio
  cholerae
• MacConkey agar contain bile salt
  which is selective for
  Enterobacteriaceae
Differential media
• distinguishs one microorganism type from
  another based on a difference in colony
  appearance includes (color, shape, or
  growth pattern) on the media.

• uses the biochemical characteristics of a
  microorganism growing in the presence of
  specific nutrients or indicators (such as
  neutral red, phenol red , or methylene blue)
  added to the medium to visibly indicate the
  defining characteristics of a microorganism
Differential media
• is used for the detection of microorganisms
  and by molecular biologists to detect
  recombinant strains of bacteria

• Examples;
 Mannitol salt agar
 Eosin methylene blue
 MacConkey agar
• Mannitol salt agar
 which is differential for mannitol
 fermentation
 Like Staphylococcus aureus change
 the color of agar from pink to yellow


• Eosin methylene blue
 which is differential for lactose
 and sucrose fermentation
• MacConkey agar
 which is differential for lactose fermentation Ex: E.coli
 From non lactose fermentersEx: salmonella,shigella
Enriched media
• Enriched with
   Blood,serum,extrapeptones,egg&
   vitamins
• Used for:
  cultivation of all fastidious organisms,
  (haemophilus influenza&Streptococcus
  spp.)
• Examples:
• Blood agar &chocolate agar
7.Mixing
4.Adding the
 the blood
contentstobottle
  1.agar powders
 with
 molten
 medium              2.Weighing out
 at 45 c             the ingredients
                 5.Autoclaving
                  8.Pouring
                  plates

                             3.Measuring
                             the desired
                             6.Adding
                             volume of
                             blood to the
                             water for
  Preparation of             blood agar out
                               9.Laying
                             medium
  bloodmedia                 base
                               plates to set
                             medium
Chocolate agar

 fastidious respiratory bacteria, such as Haemophilus
• Originally, red growth factors, like NADto a melted
influenzae need blood cells were added and hemin,
which are insideand heatedcells; thus, a prerequisite to
   nutrient base red blood to approximately 75°C
growth is lysis the red blood cells
   which lysed of the red blood cells. The agar is
named for the color and contains no actual chocolate.
Enrichment media
• A liquid culture medium promotes the
  growth of a particular organism and
  prevent the growth of normal
  competitors.
• Prevent non pathogenic bacteria from
  overgrowing the pathogenic bacteria

• Example: selenite-Fbroth
           alkaline-peptone water
SELENITE –F BROTH

• Intended Use :is used for the selective
  enrichment of Salmonella spp.
• Prepared Appearance: Prepared medium is
  clear, with no to light precipitate and very pale
  yellow.
ALKALINE PEPTONE WATER

• Intended use:
  is used for the enrichment of Vibrio cholera
 and Vibrio species from food, water, feces and
 clinical studies.
• Prepared appearance:
  The color is amber
Transport media
• Preserve viability and ratio of
  microbes during its transportation
  over 24_48 hours.
• Example:
  CARY-BLAIR MEDIUM
STUART TRANSPORT MEDIUM
CARY-BLAIR MEDIUM
• Intended use;
• for the collection and transport of fecal and rectal
  samples, maintaining viability of Salmonella and
  Shigella.
• Survival depends upon:
  1. bacterial type &concentration , transport medium
  formulation, transport temperature and duration.
• the color is white opalescent
STUART TRANSPORT MEDIUM
• Intended use:
 is a semisolid medium used in the transport and
  preservation of specimens for the cultivation of
  diverse organisms such as gonococci,
  streptococci, Enterobacteria

The color : is blue in surface.
REFERENCES
http://www.condalab.com/pdf/1518.pdf
http://www.condalab.com/pdf/1529.pdf
http://www.neogen.com/Acumedia/pdf/ProdInfo/7
155_PI.pdf
http://www.condalab.com/pdf/1407.pdf
http://www.neogen.com/Acumedia/pdf/ProdInfo/7
102_PI.pdf

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Culture media in microbiobiolgy

  • 1.
  • 2.
  • 3. Subjects included; • Cultivation • Medium • Inoculation of media • The Requirements for Growth • Preparation • Classification • Eplanation of types of media functionally.
  • 4. Cultivation; The propagation of living organisms, applied especially to the growth of microorganisms or other cells in artificial media. Medium Any preparation that contains nutrients essential for microorganisms growth. Culture medium: A nutrient substance that is used to grow micro-organisms .
  • 5. Inoculation of media Introduction of infected material to the medium ,for cultivation of organisms. Agar Is 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 at ~40°C
  • 6. The Requirements for Growth 1.CHEMICAL REQUIREMENTS (NUTRITIONAL FACTORS) • Carbon • Nitrogen, sulfur, and phosphorous • Trace elements • Organic growth factor • Vitamins (e.g. folic acid, vitamin B-12, vitamin K) • Oxygen
  • 7. 2.PHYSICAL REQUIREMENTS • Temperature • PH • Hydrostatic Pressure • Osmotic pressure
  • 8. Preparation • Wash hands & wear gloves • Sterilize all equipments • Pour D/W in glassware (required amount) • Add powder ingredients (required amount) • Heat to dissolve completely • Autoclave • Dispense the medium into tubes ,bottles &plates • Store at required temperature • Sterilizing Culture Media
  • 9. Classification 1. Consistency 2. Nutritional 3. Functional
  • 10. 1.Consistency a ) Solid e.g nutrient agar b ) Semi-solid e.g peptone water. c ) Liquid medium e.g nutrient broth.
  • 11. 2.Nutritional a ) Simple e.g peptone water b ) Complex e.g blood agar c ) Synthetic e.g Davis /mingioli medium
  • 12. 3.Functional a) Basic media b) Selective media c ) Differential media d ) Enriched media e ) Enrichment media f ) Transport media
  • 13.
  • 14. Basic media • This is an undefined medium because the amino acid source contains a variety of compounds with the exact composition being unknown. • Nutrient media contain all the elements that most bacteria need for growth and are non-selective, so they are used for the general cultivation and maintenance of bacteria kept in laboratory culture collections.
  • 15. Basic media • This media contains; 1.A carbon source such as glucose for bacterial growth 2.Water 3.Various salts needed for bacterial growth
  • 16. There are two types: 1. nutrient broth which is liquid media
  • 17. 2. nutrient agar which is solid media
  • 18. Selective media • culture medium that allows the growth of certain types of organisms, while inhibiting the growth of other organisms • Any agar media can be made selective by addition of certain inhibitory agents that don’t affect the pathogen. • Various approaches to make a medium selective include addition ofantibiotics, dyes, chemicals, alteration of pH or a combination of these medium
  • 19. Selective media • Thiosulphate citrate bile salt sucrose (TCBS) which is selective for Vibrio cholerae • MacConkey agar contain bile salt which is selective for Enterobacteriaceae
  • 20. Differential media • distinguishs one microorganism type from another based on a difference in colony appearance includes (color, shape, or growth pattern) on the media. • uses the biochemical characteristics of a microorganism growing in the presence of specific nutrients or indicators (such as neutral red, phenol red , or methylene blue) added to the medium to visibly indicate the defining characteristics of a microorganism
  • 21. Differential media • is used for the detection of microorganisms and by molecular biologists to detect recombinant strains of bacteria • Examples; Mannitol salt agar Eosin methylene blue MacConkey agar
  • 22. • Mannitol salt agar which is differential for mannitol fermentation Like Staphylococcus aureus change the color of agar from pink to yellow • Eosin methylene blue which is differential for lactose and sucrose fermentation
  • 23. • MacConkey agar which is differential for lactose fermentation Ex: E.coli From non lactose fermentersEx: salmonella,shigella
  • 24. Enriched media • Enriched with Blood,serum,extrapeptones,egg& vitamins • Used for: cultivation of all fastidious organisms, (haemophilus influenza&Streptococcus spp.) • Examples: • Blood agar &chocolate agar
  • 25. 7.Mixing 4.Adding the the blood contentstobottle 1.agar powders with molten medium 2.Weighing out at 45 c the ingredients 5.Autoclaving 8.Pouring plates 3.Measuring the desired 6.Adding volume of blood to the water for Preparation of blood agar out 9.Laying medium bloodmedia base plates to set medium
  • 26. Chocolate agar fastidious respiratory bacteria, such as Haemophilus • Originally, red growth factors, like NADto a melted influenzae need blood cells were added and hemin, which are insideand heatedcells; thus, a prerequisite to nutrient base red blood to approximately 75°C growth is lysis the red blood cells which lysed of the red blood cells. The agar is named for the color and contains no actual chocolate.
  • 27. Enrichment media • A liquid culture medium promotes the growth of a particular organism and prevent the growth of normal competitors. • Prevent non pathogenic bacteria from overgrowing the pathogenic bacteria • Example: selenite-Fbroth alkaline-peptone water
  • 28. SELENITE –F BROTH • Intended Use :is used for the selective enrichment of Salmonella spp. • Prepared Appearance: Prepared medium is clear, with no to light precipitate and very pale yellow.
  • 29. ALKALINE PEPTONE WATER • Intended use: is used for the enrichment of Vibrio cholera and Vibrio species from food, water, feces and clinical studies. • Prepared appearance: The color is amber
  • 30. Transport media • Preserve viability and ratio of microbes during its transportation over 24_48 hours. • Example: CARY-BLAIR MEDIUM STUART TRANSPORT MEDIUM
  • 31. CARY-BLAIR MEDIUM • Intended use; • for the collection and transport of fecal and rectal samples, maintaining viability of Salmonella and Shigella. • Survival depends upon: 1. bacterial type &concentration , transport medium formulation, transport temperature and duration. • the color is white opalescent
  • 32. STUART TRANSPORT MEDIUM • Intended use: is a semisolid medium used in the transport and preservation of specimens for the cultivation of diverse organisms such as gonococci, streptococci, Enterobacteria The color : is blue in surface.