Production of penicillin

Similar documents

Chapter 20: Antimicrobial Drugs

Methods of Grading S/N Style of grading Percentage Score 1 Attendance, class work and assignment 10 2 Test 20 3 Examination 70 Total 100

Fungi and Industry. Can you think of any products that depend on the use of fungi at any stage during manufacture?

Respiration Worksheet. Respiration is the controlled release of energy from food. Types of Respiration. Aerobic Respiration

Enzymes. Chapter Enzymes and catalysts. Vital mistake. What is an enzyme?

PHOTOSYNTHESIS AND CELLULAR RESPIRATION

Medical Microbiology Culture Media :

LAB 4. Cultivation of Bacteria INTRODUCTION

INTRODUCTION TO BACTERIA

ANTIBIOTIC INHIBITION OF BACTERIA

DP419 RNAsimple Total RNA Kit. RNAprep pure Series. DP501 mircute mirna Isolation Kit. DP438 MagGene Viral DNA / RNA Kit. DP405 TRNzol Reagent

Expression and Purification of Recombinant Protein in bacteria and Yeast. Presented By: Puspa pandey, Mohit sachdeva & Ming yu

Cells are tiny building blocks that make up all living things. Cells are so small that you need a microscope to see them.

PRESTWICK ACADEMY NATIONAL 5 BIOLOGY CELL BIOLOGY SUMMARY

FACULTY OF MEDICAL SCIENCE

What affects an enzyme s activity? General environmental factors, such as temperature and ph. Chemicals that specifically influence the enzyme.

Beneficial Microflora in Honey Bee Colonies

What happens to the food we eat? It gets broken down!

General Properties Protein Nature of Enzymes Folded Shape of Enzymes H-bonds complementary

NUTRITION AND GROWTH OF BACTERIA

1. The diagram below represents a biological process

Biological Sciences Initiative

Effects of Antibiotics on Bacterial Growth and Protein Synthesis: Student Laboratory Manual

Get It Right. Answers. Chapter 1: The Science of Life. A biologist studies all living things.

WHY IS THIS IMPORTANT?

The growth of Mos are effected by Chemical and Physical surroundings:

Topic 3: Nutrition, Photosynthesis, and Respiration

Microbial Nutrition And bacterial Classification Microbiology Unit-I. Muhammad Iqbal Lecturer KMU

Cellular Respiration: Practice Questions #1

Lecture 3: Biodegradable Polymers

1. Enzymes. Biochemical Reactions. Chapter 5: Microbial Metabolism. 1. Enzymes. 2. ATP Production. 3. Autotrophic Processes

Nutrient Removal at Wastewater Treatment Facilities. Nitrogen and Phosphorus. Gary M. Grey HydroQual, Inc X 7167

The design of fermenter

Bacteria: The good, the bad, and the ugly. SEPA BioScience Montana Module 2

- Oxygen is needed for cellular respiration [OVERHEAD, fig. 6.2, p. 90 / 4th: 6.1] - lungs provide oxygen to blood, blood brings oxygen to the cells.

Module 3 Questions. 7. Chemotaxis is an example of signal transduction. Explain, with the use of diagrams.

BIOLOGY HIGHER LEVEL

Metabolism Dr.kareema Amine Al-Khafaji Assistant professor in microbiology, and dermatologist Babylon University, College of Medicine, Department of

Lecture 1 MODULE 3 GENE EXPRESSION AND REGULATION OF GENE EXPRESSION. Professor Bharat Patel Office: Science 2, b.patel@griffith.edu.

Chemical Basis of Life Module A Anchor 2

Keystone Review Practice Test Module A Cells and Cell Processes. 1. Which characteristic is shared by all prokaryotes and eukaryotes?

Gas and Solute Exchange

Laboratory Exercise # 11: Differentiation of the Species Staphylococcus and Streptococcus

How antifungal drugs kill fungi and cure disease

Biotechnology and Recombinant DNA (Chapter 9) Lecture Materials for Amy Warenda Czura, Ph.D. Suffolk County Community College

Cellular Respiration Worksheet What are the 3 phases of the cellular respiration process? Glycolysis, Krebs Cycle, Electron Transport Chain.

Development of low-cost culture media for effective biosurfactant production

Bioremediation. Biodegradation

Welcome to Implementing Inquirybased Microbial Project. Veronica Ardi, PhD

Chapter 4: A Tour of the Cell. 1. Cell Basics. Limits to Cell Size. 1. Cell Basics. 2. Prokaryotic Cells. 3. Eukaryotic Cells

Bacterial Transformation and Plasmid Purification. Chapter 5: Background

Disc Diffusion Susceptibility Methods

Anabolic and Catabolic Reactions are Linked by ATP in Living Organisms

Multiple Choice Questions

Chapter 2. The Chemistry of Life Worksheets

Control of fermentation of lignocellulosic hydrolysates

HighPure Maxi Plasmid Kit

Microbial Metabolism. Biochemical diversity

GENE CLONING AND RECOMBINANT DNA TECHNOLOGY

Draw one line from each structure in List A to the correct information about the structure in List B.

CONTROLLING MICROBIAL GROWTH IN WINE

Define conversion and space time. Write the mole balances in terms of conversion for a batch reactor, CSTR, PFR, and PBR.

1. A covalent bond between two atoms represents what kind of energy? a. Kinetic energy b. Potential energy c. Mechanical energy d.

Figure 5. Energy of activation with and without an enzyme.

CONTROLLING MICROBIAL GROWTH IN WINE

Overview on EFSA data requirements for the safety evaluation of food enzymes applications

Chapter 5: The Structure and Function of Large Biological Molecules

7. A selectively permeable membrane only allows certain molecules to pass through.

Cells & Cell Organelles

Introduction to Beneficial Bacteria

Chapter 2: Cell Structure and Function pg

Enzymes. A. a lipid B. a protein C. a carbohydrate D. a mineral

General Trends in Infectious Disease

Name Date Period. Keystone Review Enzymes

-Loss of energy -Loss of hydrogen from carbons. -Gain of energy -Gain of hydrogen to carbons

Gymnázium, Brno, Slovanské nám. 7, WORKBOOK - Biology WORKBOOK.

OPTIMIZING BIOLOGICAL PHOSPHORUS REMOVAL FROM AN SBR SYSTEM MIDDLEBURY, VT. Paul Klebs, Senior Applications Engineer Aqua-Aerobic Systems, Inc.

Penicillin. Nobel Lecture, December 11, 1945

3.0 Treatment of Infection

Respiration occurs in the mitochondria in cells.

Beer Styles for the Novice Your Brew Day Sanitation

B2 Revision. Subject Module Date Biology B2 13 TH May (am)

Vancomycin. Beta-lactams. Beta-lactams. Vancomycin (Glycopeptide) Rifamycins (rifampin) MID 4

Visualizing Cell Processes

Gene Transcription in Prokaryotes

AP BIOLOGY 2006 SCORING GUIDELINES. Question 1

Introduction to Microbiology The Microbial World and You (Chapter 1) Lecture Materials for Amy Warenda Czura, Ph.D. Suffolk County Community College

Balancing chemical reaction equations (stoichiometry)

CELL/ PHOTOSYNTHESIS/ CELLULAR RESPIRATION Test 2011 ANSWER 250 POINTS ANY WAY IN WHICH YOU WANT

Microbiology BIOL 275 DILUTIONS

10.1 The function of Digestion pg. 402

Genetics Lecture Notes Lectures 1 2

DIGESTION is the physical and

Physical Methods Of Microbial Control: 1. Heat: denatures proteins (enzymes) = death

Chemistry 20 Chapters 15 Enzymes

UTILIZATION of PLASMA ACTIVATED WATER in Biotechnology, Pharmacology and Medicine. JSC TECHNOSYSTEM-ECO Moscow, Russia April, 2009

Experiment 8 Synthesis of Aspirin

008 Chapter 8. Student:

1942b), activity in vivo (Metzger, Waksman, Pugh, 1943; Robinson, 1943),

Transcription:

Production of penicillin Learning objective: To be able to identify useful products from microorganisms To be able to identify the microorganisms used and the main stages in the production of penicillin. To be able to describe how Downstream processing is carried out to extract and purify the end product of fermentation.

UNIT II PENCILLIN PRODUCTION R.KAVITHA,M.PHARM LECTURER, DEPARTMENT OF PHARMACUTICS SRM COLEGE OF PHARMACY SRMUNIVERITY

Downstream Processing Products in a fermenter are impure and dilute, so need to be purified by downstream processing. This usually involves filtration to separate the microbial cells from the liquid medium, followed by chemical purification and concentration of the product Downstream processing can account for 50% of the cost of a process.

Antibiotics are antimicrobial agents produced naturally by other microbes (usually fungi or bacteria). The first antibiotic was discovered in 1896 by Ernest Duchesne and "rediscovered" byalexander Flemming in 1928 from the filamentous fungus Penicilium notatum.

The antibiotic substance, named penicillin, was not purified until the 1940s (by Florey and Chain), just in time to be used at the end of the second world war. Penicillin was the first important commercial product produced by an aerobic, submerged fermentation

When penicillin was first made at the end of the second world war using the fungus Penicilium notatum, the process made 1 mg dm 3. Today, using a different species (P. chrysogenum) and a better extraction procedures the yield is 50 g dm 3. There is a constant search to improve the yield.

Antibiotics can be selectively toxic by targeting such features as the bacterial cell wall, 70S ribosomes, and enzymes that are specific to bacteria. In this way the human eukaryotic cells are unaffected.

For example: penicillin, ampicillin, amoxycillin, methicillin Inhibits enzymes involved in synthesis of peptidoglycan for bacterial cell wall, causing cell lysis. Bacteriocidal Narrow spectrum little effect on Gram negative cells.

Other antibiotics MO may affect: Cell membrane DNA replication Transcription Translation

Antibiotic production There are over 10 000 different antibiotics known, but only about 200 in commercial use, since most new antibiotics are no better than existing ones. There is a constant search for new antibiotics. Antibiotics are the most prescribed drugs and are big business. Finding a new antibiotic and getting it on to the market is a very long process and can take 15 years.

Antibiotic Production Methods Antibiotics are produced on an industrial scale using a variety of fungi and bacteria. Penicillin is produced by the fungus Penicillium chrysogenum which requires lactose, other sugars, and a source of nitrogen (in this case a yeast extract) in the medium to grow well. Like all antibiotics, penicillin is a secondary metabolite, so is only produced in the stationary phase. What sort of fermenter does it require? It requires a batch fermenter, and a fed batch process is normally used to prolong the stationary period and so increase production.

Downstream processing is relatively easy since penicillin is secreted into the medium (to kill other cells), so there is no need to break open the fungal cells. However, the product needs to be very pure, since it being used as a therapeutic medical drug, so it is dissolved and then precipitated as a potassium salt to separate it from other substances in the medium.

The resulting penicillin (called penicillin G) can be chemically and enzymatically modified to make a variety of penicillins with slightly different properties. These semi synthetic penicillins include penicillin V, penicillin O, ampicillin and amoxycillin.

1. What is the Carbon source? lactose 2. What is the nitrogen source? yeast 3. What is the energy source? glucose 4. Is the fermentation aerobic or anaerobic? aerobic 5. What is the optimum temperature? 25-27ºC 6. Is penicillin a primary or secondary metabolite? 7. What volume fermenter is used? 8. Why isn't a larger fermenter used? 9. When is penicillin produced? 10. How long can it be produced for? 11. What was the first fungus known to produce penicillin? 12. What species produces about 60mg/dm3 of penicillin? 13. How did scientists improve the yield still further? 14. What is the substrate? 15. Why is batch culture used? secondary 40 200 dm 3 To difficult to aerate 40 hours after main increase in fungal mass 140 hours (180 40 hours) Genetic modification 16. What are the processes involved Corn steep in down stream liquor processing? a) Secondary metabolite b) c) Filtration of liquid 17. Why Extraction can't penicillin from be filtrate taken orally? by counter current of butylacetate 18. Name Precipitation the form of penicillin by potassium which can salts be taken orally. 19. How does Penicillin kill bacteria? Destroyed by stomach acid 20. Why are Gram negative bacteria not killed by penicillin? Penicillin notatum Penicillin chrysogenum Penicillin V, ampicillin Stops production of cell wall Different cell wall