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MICROBIAL BIOTRANSFORMATION
Dr. A. T. Sharma
Assist. Professor
Nanded Pharmacy College, Nanded
Introduction
• Definition: Process which involves microbial
(enzymatic) conversion of a substrate in to a
product with limited number (one or few) of
enzymatic reactions.
• Micro-organisms covert organic compounds in to
structurally related products.
• Fermentation – Large number of reactions
• Maintains the original carbon skeleton in the
products.
• Living cells like bacteria, filamentous fungi,
animals, plants, algae, yeast, actinomycetes are
used
Selection of an Organism
• From natural sources or from available
cultures
• Cultures like growing cultures, resting cells,
immobilized cells, spores, enzymes,
immobilized enzymes
Growing cultures:
o A strain is cultivated in an appropriate culture
medium and a concentrated substrate
solution is added after an appropriate growth
(6-24 hours)
Advantages:
Usage of large inoculum
Maintaining microbes in growth phase
Use of emulsifiers for dissolution of sparingly
soluble substances
Monitoring of product formation by
spectroscopy/ chromatography
Termination of process after optimum product
formation
Resting cells/ Non-growing cells:
o Cells in which division does not occur
o Cells with induced enzymes capable of doing metabolic
reactions, but suspended in non-growth medium and so
can’t make new proteins or cells.
o High cell density due to concentrating large culture volume
in to a small volume – increased productivity and
minimized contamination
Immobilized cells:
o Cells immobilized over a matrix material so that they can be
repeatedly used
Immobilized enzymes:
o Enzymes immobilized by various immobilization
technologies
o Advantages: No cellular transport barriers, Easy and simple
product recovery and isolation
Method of Biotransformation
• Micro-organisms are grown in medium for 12-72 hours at
optimum pH, temperature, aeration, agitation in a stainless
steel tank
• After sufficient growth, substrate is added and incubated –
product formation
• Separation of broth from substrate and product
• During incubation, product samples subjected for analysis
at a regular intervals by TLC, paper chromatography, gas
chromatography, or HPLC
• Extraction of product using solvents like methylene
chloride, chloroform, ethyl acetate, methyl isobutyl ketone
• Conversion time depends upon type of reaction, substrate
conversion and microbes involved (few hours to days)
• Proper aeration, agitation and sterility is to be maintained
Biotransformation Reactions
Applications
Transformation of steroids and sterols:
• Steroids – natural compounds in nature – e.g. bile
salts, adrenocortical and sex hormones,
sapogenins, alkaloids, antibiotics
• All steroids have same basic structure – a
cyclopentanoperhydrophenanthrene – four fused
rings
• Prednisone from cortisone – increased anti-
inflammatory activity
• Production of testosterone and estrogen from
progesterone
Transformation of non-steroid compounds:
• Dihydroxyacetone from glycerol – used in lotions and
cosmetics
• Prostaglandins from unsaturated fatty acids –
contraceptives, congenital heart failure etc
• Production of L-ascorbic acid (Vitamin C) –Reichstein-
Grussner synthesis
Transformation of antibiotics:
• Development of new, modified and improved
antibiotics with reduced toxicity, broad antimicrobial
spectrum, enhanced oral absorption, less allergic
effects etc.
Transformation of pesticides:
• Detoxification of environment by enzymatic conversion
and removal of pesticides
Transformation of pollutants:
• Microbial transformation of environmental
pollutants like polyaromatic hydrocarbons,
pharmaceutical substances, radionucleotides,
hydrocarbons, polychlorinated biphenyls
Petroleum biotransformation:
• Biodegradation of oil spills by breaking down oil
contaminants in to nontoxic forms
Pharmaceutical research:
• During research activities, comparison of
metabolic pathway of drugs in animal models for
pharmacological and toxicological evaluation.
Thank You…!!!
(Disclaimer: The images and diagrams in this presentation
have been downloaded from the google source. I am grateful
to all the publishers & the google.)

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MICROBIAL BIOTRANSFORMATION & ITS APPLICATIONS.pptx

  • 1. MICROBIAL BIOTRANSFORMATION Dr. A. T. Sharma Assist. Professor Nanded Pharmacy College, Nanded
  • 2. Introduction • Definition: Process which involves microbial (enzymatic) conversion of a substrate in to a product with limited number (one or few) of enzymatic reactions. • Micro-organisms covert organic compounds in to structurally related products. • Fermentation – Large number of reactions • Maintains the original carbon skeleton in the products. • Living cells like bacteria, filamentous fungi, animals, plants, algae, yeast, actinomycetes are used
  • 3. Selection of an Organism • From natural sources or from available cultures • Cultures like growing cultures, resting cells, immobilized cells, spores, enzymes, immobilized enzymes Growing cultures: o A strain is cultivated in an appropriate culture medium and a concentrated substrate solution is added after an appropriate growth (6-24 hours)
  • 4. Advantages: Usage of large inoculum Maintaining microbes in growth phase Use of emulsifiers for dissolution of sparingly soluble substances Monitoring of product formation by spectroscopy/ chromatography Termination of process after optimum product formation
  • 5. Resting cells/ Non-growing cells: o Cells in which division does not occur o Cells with induced enzymes capable of doing metabolic reactions, but suspended in non-growth medium and so can’t make new proteins or cells. o High cell density due to concentrating large culture volume in to a small volume – increased productivity and minimized contamination Immobilized cells: o Cells immobilized over a matrix material so that they can be repeatedly used Immobilized enzymes: o Enzymes immobilized by various immobilization technologies o Advantages: No cellular transport barriers, Easy and simple product recovery and isolation
  • 6. Method of Biotransformation • Micro-organisms are grown in medium for 12-72 hours at optimum pH, temperature, aeration, agitation in a stainless steel tank • After sufficient growth, substrate is added and incubated – product formation • Separation of broth from substrate and product • During incubation, product samples subjected for analysis at a regular intervals by TLC, paper chromatography, gas chromatography, or HPLC • Extraction of product using solvents like methylene chloride, chloroform, ethyl acetate, methyl isobutyl ketone • Conversion time depends upon type of reaction, substrate conversion and microbes involved (few hours to days) • Proper aeration, agitation and sterility is to be maintained
  • 8.
  • 9. Applications Transformation of steroids and sterols: • Steroids – natural compounds in nature – e.g. bile salts, adrenocortical and sex hormones, sapogenins, alkaloids, antibiotics • All steroids have same basic structure – a cyclopentanoperhydrophenanthrene – four fused rings • Prednisone from cortisone – increased anti- inflammatory activity • Production of testosterone and estrogen from progesterone
  • 10. Transformation of non-steroid compounds: • Dihydroxyacetone from glycerol – used in lotions and cosmetics • Prostaglandins from unsaturated fatty acids – contraceptives, congenital heart failure etc • Production of L-ascorbic acid (Vitamin C) –Reichstein- Grussner synthesis Transformation of antibiotics: • Development of new, modified and improved antibiotics with reduced toxicity, broad antimicrobial spectrum, enhanced oral absorption, less allergic effects etc. Transformation of pesticides: • Detoxification of environment by enzymatic conversion and removal of pesticides
  • 11. Transformation of pollutants: • Microbial transformation of environmental pollutants like polyaromatic hydrocarbons, pharmaceutical substances, radionucleotides, hydrocarbons, polychlorinated biphenyls Petroleum biotransformation: • Biodegradation of oil spills by breaking down oil contaminants in to nontoxic forms Pharmaceutical research: • During research activities, comparison of metabolic pathway of drugs in animal models for pharmacological and toxicological evaluation.
  • 12. Thank You…!!! (Disclaimer: The images and diagrams in this presentation have been downloaded from the google source. I am grateful to all the publishers & the google.)