Microbial metabolites
ANTIBIOTICS (STREPTOMYCIN)
PRESENTED BY:
MINHAZ AHMED
INT. MSC 6TH SEM
BBI11014
Tezpur University
WHAT?
• Primary and Secondary Metabolites: Primary metabolites
are produced during active cell growth, and secondary
metabolites are produced near the onset of stationary phase
• Antibiotics are produced industrially by a process
of fermentation, where the source microorganism is grown in
large containers (100,000 – 150,000 liters or more) containing
a liquid growth medium.
WHERE THEY WORK?
Rifamycins
Cell wall
Penicillins
Cephalosporins
cycloserine
polymyxins
sulfonamides
Chloramphenicol
Streptomycin
tetracyclines
Ribosomes
capsule
cytoplasm
Streptomycin
Secondary metabolite
produced by Streptomyces
griseus.
Change in environment
condition and substrate
availability influence final
product.
In fermentation a soyabean
based medium is used with
glucose as carbon source.
Nitrogen source is combined in
soyabean meal, limits growth.
After growth the antibiotic
levels in the culture begin to
increase.
Source: www.indiamart.com
Source: pubs.rsc.org
Phases during fermentation of
streptomycin
PHASE 1: Rapid growth producing
mycelial biomasss.Little production
of Streptomycin is obtained.
PHASE 2: Additional production of
mycelium.Streptomycin accumulates in
the medium.
PHASE 3: Process has completed.Finally
the mycelium is separated by filtration
and antibiotic recovered.
Proteolytic activity of the microbe
releases NH3 to the medium from the
soybean meal, causing a rise in pH
The glucose and NH3 released are
consumed during this phase.The pH
remains fairly constant-between 7.6
and 9.0.
Indian antibiotic companies:
 Hindustan Antibiotics Limited (HAL)
 Megmus pharmaceutical
Disadvantages of fermentation for antibiotics:
 Complex and Expensive nutrients required
 Isolation of product is difficult
Antibiotic Producing microorganism
Cephalosporin Cephalosporium acrimonium
Chloramphenicol Streptomyces venezuelae
Erythromycin Streptomyces erythreus
Griseofulvin Penicillium griseofulvin
Penicillin Penicillium chrysogenum
Streptomycin Streptomyces griseus
Tetracycline Streptomyces aureofaciens
Gentamicin Micromonospora purpurea
References:
• Industrial enzymes, structure function and
application- julio Poliana and Andrew P.
MacCabe(2007)
THANK YOU

metabolites : antibiotics by fermentation

  • 1.
    Microbial metabolites ANTIBIOTICS (STREPTOMYCIN) PRESENTEDBY: MINHAZ AHMED INT. MSC 6TH SEM BBI11014 Tezpur University
  • 2.
    WHAT? • Primary andSecondary Metabolites: Primary metabolites are produced during active cell growth, and secondary metabolites are produced near the onset of stationary phase • Antibiotics are produced industrially by a process of fermentation, where the source microorganism is grown in large containers (100,000 – 150,000 liters or more) containing a liquid growth medium.
  • 3.
    WHERE THEY WORK? Rifamycins Cellwall Penicillins Cephalosporins cycloserine polymyxins sulfonamides Chloramphenicol Streptomycin tetracyclines Ribosomes capsule cytoplasm
  • 4.
    Streptomycin Secondary metabolite produced byStreptomyces griseus. Change in environment condition and substrate availability influence final product. In fermentation a soyabean based medium is used with glucose as carbon source. Nitrogen source is combined in soyabean meal, limits growth. After growth the antibiotic levels in the culture begin to increase. Source: www.indiamart.com
  • 5.
  • 6.
    Phases during fermentationof streptomycin PHASE 1: Rapid growth producing mycelial biomasss.Little production of Streptomycin is obtained. PHASE 2: Additional production of mycelium.Streptomycin accumulates in the medium. PHASE 3: Process has completed.Finally the mycelium is separated by filtration and antibiotic recovered. Proteolytic activity of the microbe releases NH3 to the medium from the soybean meal, causing a rise in pH The glucose and NH3 released are consumed during this phase.The pH remains fairly constant-between 7.6 and 9.0.
  • 7.
    Indian antibiotic companies: Hindustan Antibiotics Limited (HAL)  Megmus pharmaceutical Disadvantages of fermentation for antibiotics:  Complex and Expensive nutrients required  Isolation of product is difficult Antibiotic Producing microorganism Cephalosporin Cephalosporium acrimonium Chloramphenicol Streptomyces venezuelae Erythromycin Streptomyces erythreus Griseofulvin Penicillium griseofulvin Penicillin Penicillium chrysogenum Streptomycin Streptomyces griseus Tetracycline Streptomyces aureofaciens Gentamicin Micromonospora purpurea
  • 8.
    References: • Industrial enzymes,structure function and application- julio Poliana and Andrew P. MacCabe(2007)
  • 9.