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MICROBIAL BASED
PHARMACUTICAL
PRODUCTS
K.SUBASRI
18MBTA19
II M.Sc INDUSTRIAL BIOTECHNOLOGY
BHARATHIYAR UNIVERSITY
INTRODUCTION
 Microbial based pharmaceutical products.
 Antibiotics
 Vitamins
 Probiotics
ANTIBIOTICS
 Chemical compound acting against life(kill or
inhibit the growth of other organism).
 Low molecular weight.
 Produced micro organism.
 Fermentation.
 pencilin
 streptomycin
 tetracycline
PENICILIN
 Penicillium chrysogenum
 Secondary metabolites.
 Most widely used antibiotics
How its works?
O β-Lactam of penicillin.
O Enzyme.
O peptidoglycan cross linking.
O enzyme is inhibited cross linking.
O Cell wall weakened osmotic imbalance in the
cell. This leads to cell death.
How its works?
O UPSTREAM- before fermentor process.
Sterilization,seed culture.
O DOWNSTREAM- after fermentor process.
extraction ,purification , product.
Mediumforpenicillin
1. MgSO4,
2. K3PO4 and
3. sodium nitrates.
Heat sterilization
121°C at 30 psi or twice the atm.
Sterilization machine
Fermentation
 rotation speed of around 200 rpm.
Fermentors
Seed Culture
 liquid medium.
 grown.
 inoculated into the fermenter.
 Aerated & agitated.
 fed-batch style.
 Maintain parameter.
pH,
temperature ,
stirrer speed and
dissolved oxygen concentration,
Removalofbiomass
Filtration
removing impurities
Rotary vacuum filter - large scale
Introduced-
phosphoric acid,
non-oxidising (8.0 to 6.5 pH )
to prevent loss of activity of penicillin.
Rotary vacuum filter
Addition of solvent
amyl acetate / butyl acetate
Centrifugal Extraction
 Disk centrifuge.
 extraction.
 downstream process .
Extraction
 sodium bicarbonate
 phosphate buffer,
 chloroform solution
Batch extraction unit Basket Centrifuge
Fluidbeddrying
 remove moisture
 hot gas is pumped
 powdered salt
 vacuum chamber.
 Drier penicillin.
Powdered penicillinbeing
blown by hot air
Fluid bed drying tube
Storage
dried environment.
Variety of penicillins
semi-synthetic penicillins,
Penicillin V,
Penicillin O,
ampicillin and
amoxycillin
The White Penicillin-Sodium salt
STREPTOMYCIN
 Streptomyces griseus
 First amino glycoside antibiotic
 Against
 gram + & – bacteria,
 tuberculosis bacteria ,
 mycobacterium tuberculosis
 Medium
 soyabean meal
 Glucose
 sodium chloride
 pH 7.3-7.5
 Colourless, odurless,water soluble
 Submerged culture
HOW ITS WORKS?
O Protein synthesis inhibitor.
O 16s rRNA-
O 30s binding
O Codon misreading
O mRNA- frameshift mutation
O Cell death.
O Not affect humans.
(i) The Inoculum Production
 S. griseus
 soil stocks or lyophilized - sterile skimmed
milk.
 liquid culture
 fed to production fermenter.
(ii) Preparation of the Medium:
 A carbon source and nitrogen source.
 Peptones,
 soya extracts,
 meat extract,
 ammonium salts,
 nitrogen source.
 Magnesium,
 calcium,
 potassium,
 sulphates,
 phosphates and
 chlorides.
(iii) Fermentation:
 temperature 25 to 30°C
 pH 7.0 and 8.0.
 volume of inoculum (4-5%)
(a) The First Phase:
i. 24 hours to 48 hours.
ii. Rapid growth mycelium occurs.
iii. pH 8.0 due
iv. proteolytic activity
(b) The Second Phase:
i. Streptomycin production takes place at a rapid rate
without increase in the mycelial growth.
ii. pH to 7.6-8.0.
iii. Glucose and oxygen are required .
(c) Third Phase:
i. Cells lysis,
ii. increase pH,
iii. Requirement of oxygen decreases
(iv) Harvest and Recovery:
i. mycelium is separated from the broth by filtration.
ii. Streptomycin is recovered by several methods.
TETRACYCLIN
• Streptomyces aureofaciens
• S. rimosus
• S. viridofaciens
• Broad – spectrum antibiotics.
• Against-
• Gram + & - bacteria,
• Vibrio cholerae,
• Mycoplasma
• Candida albicans….etc
HOW ITS WORKS?
Inhibit protein synthesis with in bacterial
cells.
O 30s ribosome
O Attach RNA
O Stop Protein synthesis.
O Cell death
O Anti-Inflammatory
O Treatment of skin diseases.
VITAMINS
O Vitamins are organic substance
that essential for the health,
growth, reproduction.
PROBIOTICS
“Live microorganism which
when administered in
adequate amounts confer a
health benefits on the host”.
THANK YOU….

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Microbial based pharmacutical products

  • 1. MICROBIAL BASED PHARMACUTICAL PRODUCTS K.SUBASRI 18MBTA19 II M.Sc INDUSTRIAL BIOTECHNOLOGY BHARATHIYAR UNIVERSITY
  • 2. INTRODUCTION  Microbial based pharmaceutical products.  Antibiotics  Vitamins  Probiotics
  • 3. ANTIBIOTICS  Chemical compound acting against life(kill or inhibit the growth of other organism).  Low molecular weight.  Produced micro organism.  Fermentation.  pencilin  streptomycin  tetracycline
  • 4.
  • 5. PENICILIN  Penicillium chrysogenum  Secondary metabolites.  Most widely used antibiotics
  • 6. How its works? O β-Lactam of penicillin. O Enzyme. O peptidoglycan cross linking. O enzyme is inhibited cross linking. O Cell wall weakened osmotic imbalance in the cell. This leads to cell death.
  • 8.
  • 9. O UPSTREAM- before fermentor process. Sterilization,seed culture. O DOWNSTREAM- after fermentor process. extraction ,purification , product.
  • 10. Mediumforpenicillin 1. MgSO4, 2. K3PO4 and 3. sodium nitrates. Heat sterilization 121°C at 30 psi or twice the atm. Sterilization machine
  • 11. Fermentation  rotation speed of around 200 rpm. Fermentors
  • 12. Seed Culture  liquid medium.  grown.  inoculated into the fermenter.  Aerated & agitated.  fed-batch style.  Maintain parameter. pH, temperature , stirrer speed and dissolved oxygen concentration,
  • 13. Removalofbiomass Filtration removing impurities Rotary vacuum filter - large scale Introduced- phosphoric acid, non-oxidising (8.0 to 6.5 pH ) to prevent loss of activity of penicillin. Rotary vacuum filter Addition of solvent amyl acetate / butyl acetate
  • 14. Centrifugal Extraction  Disk centrifuge.  extraction.  downstream process . Extraction  sodium bicarbonate  phosphate buffer,  chloroform solution Batch extraction unit Basket Centrifuge
  • 15. Fluidbeddrying  remove moisture  hot gas is pumped  powdered salt  vacuum chamber.  Drier penicillin. Powdered penicillinbeing blown by hot air Fluid bed drying tube
  • 16. Storage dried environment. Variety of penicillins semi-synthetic penicillins, Penicillin V, Penicillin O, ampicillin and amoxycillin The White Penicillin-Sodium salt
  • 17. STREPTOMYCIN  Streptomyces griseus  First amino glycoside antibiotic  Against  gram + & – bacteria,  tuberculosis bacteria ,  mycobacterium tuberculosis  Medium  soyabean meal  Glucose  sodium chloride  pH 7.3-7.5  Colourless, odurless,water soluble  Submerged culture
  • 18. HOW ITS WORKS? O Protein synthesis inhibitor. O 16s rRNA- O 30s binding O Codon misreading O mRNA- frameshift mutation O Cell death. O Not affect humans.
  • 19. (i) The Inoculum Production  S. griseus  soil stocks or lyophilized - sterile skimmed milk.  liquid culture  fed to production fermenter.
  • 20. (ii) Preparation of the Medium:  A carbon source and nitrogen source.  Peptones,  soya extracts,  meat extract,  ammonium salts,  nitrogen source.  Magnesium,  calcium,  potassium,  sulphates,  phosphates and  chlorides.
  • 21. (iii) Fermentation:  temperature 25 to 30°C  pH 7.0 and 8.0.  volume of inoculum (4-5%)
  • 22. (a) The First Phase: i. 24 hours to 48 hours. ii. Rapid growth mycelium occurs. iii. pH 8.0 due iv. proteolytic activity (b) The Second Phase: i. Streptomycin production takes place at a rapid rate without increase in the mycelial growth. ii. pH to 7.6-8.0. iii. Glucose and oxygen are required . (c) Third Phase: i. Cells lysis, ii. increase pH, iii. Requirement of oxygen decreases (iv) Harvest and Recovery: i. mycelium is separated from the broth by filtration. ii. Streptomycin is recovered by several methods.
  • 23. TETRACYCLIN • Streptomyces aureofaciens • S. rimosus • S. viridofaciens • Broad – spectrum antibiotics. • Against- • Gram + & - bacteria, • Vibrio cholerae, • Mycoplasma • Candida albicans….etc
  • 24. HOW ITS WORKS? Inhibit protein synthesis with in bacterial cells. O 30s ribosome O Attach RNA O Stop Protein synthesis. O Cell death O Anti-Inflammatory O Treatment of skin diseases.
  • 25.
  • 26. VITAMINS O Vitamins are organic substance that essential for the health, growth, reproduction.
  • 27.
  • 28.
  • 29. PROBIOTICS “Live microorganism which when administered in adequate amounts confer a health benefits on the host”.
  • 30.
  • 31.
  • 32.
  • 33.