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Stages of Downstream Processing

The document discusses downstream processing in fermentation technology. Downstream processing refers to the recovery and purification of fermentation products after production. It involves multiple stages including removal of insoluble materials, product isolation, purification, and polishing. Some key techniques used are centrifugation, filtration, precipitation, chromatography, and drying. The goal is to recover the product in high yields and purity at low cost. Choosing appropriate recovery methods requires considering factors like product properties, costs, scale of production, and quality standards.

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Nitin Khodifad
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0% found this document useful (0 votes)
851 views7 pages

Stages of Downstream Processing

The document discusses downstream processing in fermentation technology. Downstream processing refers to the recovery and purification of fermentation products after production. It involves multiple stages including removal of insoluble materials, product isolation, purification, and polishing. Some key techniques used are centrifugation, filtration, precipitation, chromatography, and drying. The goal is to recover the product in high yields and purity at low cost. Choosing appropriate recovery methods requires considering factors like product properties, costs, scale of production, and quality standards.

Uploaded by

Nitin Khodifad
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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NMEICT-MHRD (Govt.

of India) Project on - Creation of e-Contents on Fermentation Technology

Module-24: Introduction to Product Recovery & Purification

 After the production of the desired fermentation product,the next most important step
includes product recovery and purification.
 The recovery and purification of fermentation products refers Downstream
Processing.
 Downstream processing includes many technologies for laboratory& industrial-scale
separation of biological products.
 The Downstream Processing of fermentation products may be difficult and costly.
 Main purpose of this is to obtain a high-quality product as fast as possible at an
effectiverecovery rate using least costs.
 The recovery costs of microbial products may vary from 15% to 70% of the total
costs.
 It is an essential step in the manufacture of many products such as,
1. antibiotics,
2. hormones,
3. industrial enzymes,
4. natural fragrance and
5. flavor compounds.
 At the time of harvesting, the product concentration may be low in an aqueous
solution, which may containmicro-organisms, cell debris, soluble and insoluble media
components and other metabolic products.
 The product may also be intracellular, heat labile and easily damagedbycontaminating
micro-organisms which increase the difficulties of product recovery.
 If product is heat labile,speed of operation may be the dominant factor in noble
product recovery.
 To ensure the proper processing of harvested broth within a reasonable time
limitprocessing equipment must be of the correct type andof correct size.
 The choice of recovery process is based on the following criteria:
1. The location of the product: Intracellular or Extracellular
2. The quantity of the product in the fermentation broth.
3. The proposed use of the product.

Project control No: RE-02091011297, Christ College, Rajkot, Gujarat, India


NMEICT-MHRD (Govt. of India) Project on - Creation of e-Contents on Fermentation Technology

4. The marginal acceptable standard of purity.


5. The physical and chemical nature of the desired product.
6. The magnitude of bio-hazard
7. The impurities in the fermented broth.
8. The market potential of the product.

Stages of downstream processing

Stage – 1 Removal of Insoluble

 The first stage for the recovery of an extracellular product aims to remove large solid
particles and microbial cells.
 It is possible by various measures like by centrifugation, filtration, sedimentation,
precipitation, flocculation, electro-precipitation, and gravity settling.

Stage – 2ProductIsolation

 In this stage, the broth is extracted into major fractions using various techniques
likeultrafiltration, reverse osmosis, adsorption/ion-exchange/ gel filtration or affinity
chromatography, liquid- liquid extraction, two phase aqueous extraction, precipitation
etc.
 It allows the removal of unnecessary components whose properties differdistinctly
from that of the desired product.

Stage – 3 Product Purification

 Once, the product-containing fraction is purified by fractional precipitation, further


more precise chromatographic techniques and crystallization is used to obtain a highly
concentrated product which is essentially free from impurities.
 Steps in this stage are expensive because itrequires sensitive and sophisticated
equipment which contributes a majorsection of the entire downstream processing
expenditure.

Project control No: RE-02091011297, Christ College, Rajkot, Gujarat, India


NMEICT-MHRD (Govt. of India) Project on - Creation of e-Contents on Fermentation Technology

Stage – 4 Product Polishing

 It is the last processing steps which end with packaging of the product.
 It includes Crystallization, desiccation and spray drying.
 Sometime it alsoincludes operationsto sterilize the product by removing contaminants
which otherwise affect product safety.
 In short the downstream processing involves the following major procedures:

i. Removal of microbial cells and other solid matter:Charged properties of


microbial cells to be exploited by electrophoresis and dielectrophoresis&
flocculation characteristics and magnetic separations to beimproved byultrasonic
treatment
ii. Foam separation:It exploits differences in surface activity of materials. The
material is selectively adsorbed to the surface of gas bubbles rising through a
liquid.Then it separated and finally removed.
iii. Precipitation:This is thechemical process in which solid gets formed in a
solution or inside another solid.Various agentscan be used in precipitation like
acids, bases, salts of sodium and ammonium, organic solvents, non-ionic
polymers (polyethylene glycol), protein binding dyes etc.
iv. Filtration: it is commonly used method which separate suspended particles from
liquid or gas. It uses a porous medium that retain the suspended particles by
allowing the liquid or gas to pass through.So it allows separation of solids by
interfering a medium through which only the fluid can pass.
v. Centrifugation:Centrifuge works using the sedimentation principle, where the
centripetal speed causes separation of denser substances along the radial
direction.Various types of centrifuges are used like the basket centrifuge, the
tubular-bowl centrifuge, the solid-bowl scroll centrifuge etc.
vi. Cell disruption:It is a method for releasing intracellular molecules. To release
the cellular contents from their extremely tough cell wall a number of methods
have been established. For examplephysico mechanical methods such as liquid
shear, solid shear, freeze thawing, agitation with abrasives, and ultra-sonication.
The chemical methods includeosmotic shock, usage of detergents, alkali
treatment, and enzyme treatment.

Project control No: RE-02091011297, Christ College, Rajkot, Gujarat, India


NMEICT-MHRD (Govt. of India) Project on - Creation of e-Contents on Fermentation Technology

vii. Liquid- liquid extraction:It is a method to separate compounds on the basis of


their relative solubilities in two different immiscible liquids.So, an extraction of a
substance from one to another liquid phase in which the desired product is
preferentially soluble is known as liquid-liquid extraction. It is also known as
solvent extraction and partitioning.
viii. Solvent recovery:Distillation is the best method for solvent recovery
whichincludes three stages evaporation, vapour-liquid separation in a column and
condensation.
ix. Chromatography: In chromatography separation is based on differential
partitioning between two phases that is mobile and stationary. Different types of
chromatography techniques are used like adsorption chromatography, ion-
exchange chromatography, gel permeation chromatography, affinity
chromatography, reverse-phase chromatography and high-performance liquid
chromatography.
x. Drying:To allow minimum loss in viability, activity and nutritional value drying
is necessary.It removes water from a heat-sensitive material assuringleast
damage.
xi. Crystallization:It is used for final purification of a diverse range of compounds
including the recovery of organic acids and amino acids.

 It must be remembered that the upstream and downstream processing are integral
parts of an overall process.
 As they are interconnected, neither stage should be developed independently, as this
might result in problems and unnecessary expenditure.
 So, by taking care of some steps in the upstream process productrecovery may be
made easier. i.e.
1. Selection of test strain: By selecting test microorganisms that do not produce any
pigment and/or undesirable metabolites.
2. Environmental setup: By adjusting the production environments to allow least
production of undesirable secondarymetabolites.
 Beside this some process parameters should be checked and maintained like:
1. Time of harvesting
2. pHmaintenance during fermentation and harvesting

Project control No: RE-02091011297, Christ College, Rajkot, Gujarat, India


NMEICT-MHRD (Govt. of India) Project on - Creation of e-Contents on Fermentation Technology

3. Temperature maintenance
4. Use of suitable chemicals for flocculation and separation
 The recovery and purification of many compounds may be achieved by a number of
alternative ways.
 The decision to follow a particular way involves study of the following factors:
1. Capital expenses
2. Processing expenses
3. Probable yield
4. Product quality
5. Availability oftechnical skill
6. Requirements of waste disposal
7. Type of Processing: Continuous or batch
8. Automation
9. Health and safety
 There are so many problems associated with the product recovery program.
 For example, the recovery of extra cellular enzymes might be difficult as it needs
immediate processing.
 One another problem is pigment production by test organisms because some time the
pigment binds to the same resin as the enzyme.
 At the time of foam separation, selection of antifoam should be proper otherwise it
affect ultrafiltration or ion exchange resins used in recovery stages.
 In short it should always be remembered that good recovery starts in the fermentation
by the selection of proper upstream processing like the correct media and proper time
of harvesting.
 The major problem currently faced in product recovery is transfer of small-scale
preparative methods to the production scale without disturbingyield of the process,
quality of the product and purity levelof the product.

Project control No: RE-02091011297, Christ College, Rajkot, Gujarat, India


NMEICT-MHRD (Govt. of India) Project on - Creation of e-Contents on Fermentation Technology

References

 Principles of Fermentation Technology: (2nd edition, by Peter F. Stanbury, Allan Whitaker and
Stephen J. Hall, Butterworth-Heinemann, An imprint of Elsevier Science.)
 Industrial Microbiology: (By Casida L. E.New Age international (P) ltd publications)
 A Text Book of Industrial Microbiology: (2nd edition By WulfCrueger&AnnelieseCrueger)
 Biotechnology: Food Fermentation Microbiology, Biochemistry & Technology Vol. 1 & 2:(By V.K.
Joshi & Ashok Pandey)
 Manual of Industrial Microbiology and Biotechnology: (2nd Edition by Arnold L. Demain and Julian
E. Davies, Ronald M. Atlas, Gerald Cohen, Charles L. Hershberger, Wei-Shou Hu, David H. Sherman,
Richard C. Willson and J. H. David Wu)
 Industrial Microbiology-An introduction: By Michael J. Waites, Neil L. Morgan, John S. Rockey and
Gary Higton)
 Comprehensive Biotechnology-The Principles, Applications and Rugulations of Biotechnology in
Industry, Agriculture and Medicine: (By Mrray Moo Young)
 Fermentation Technology : Up Stream Fermentation Technology- Vol-I: (By H. A. Modi-Pointer
Publications)
 Fermentation Technology : Down Stream Fermentation Technology- Vol-II: (By H. A. Modi-Pointer
Publications)
 Industrial Microbiology by Prescott and Dunn's: (4th edition, edited by Gerald Reed, CBR
publications)
 Fermentation Technology: (By M.L. Srivastava, NAROSA publications)
 Industrial Microbiology: (By A.H. Patel)
 International student edition: Microbiology- A laboratory Manual: (4th edition. By James G.
Chappuccino& Natalie Sherman)
 Bacteriological Techniques: (By F.J. Baker)
 Introduction to Microbial Techniques: (By Gunasekaran)
 Mannual of Industrial Microbiology and Biotechnology: (2nd Edition by Arnold L. Demain and Julian
E. Davies, Ronald M. Atlas, Gerald Cohen, Charles L. Hershberger, Wei-Shou Hu, David H. Sherman,
Richard C. Willson and J. H. David Wu)

Web references

 http://www.homebrew.net/ferment/
 http://www.soyinfocenter.com/HSS/fermentation.php
 http://www.ensymm.com/pdf/ensymm_fermentation_abstract.pdf
 http://scialert.net/fulltext/?doi=jm.2007.201.208
 http://aem.asm.org/content/7/1/57.full.pdf
 http://www.slideshare.net/yongkangbirdnest/lecture-4-sterilization
 http://www.ars.usda.gov/research/publications/publications.htm?seq_no_115=140721
 http://www.scribd.com/doc/30706834/Fermentation-Design
 http://www.wiley-vch.de/books/sample/3527318194_c01.pdf
 http://www.engineersirelandcork.ie/downloads/Biopharmaceuticals%2020Jan09%20-%202%20-
%20Ian%20Marison%20DCU.pdf
 www.yobrew.co.uk/fermentation.php
 http://bioscipub.com/journals/bbb/pdf/19-24.pdf
 http://gertrude-old.case.edu/276/materials/web/immobilizedenzymereview.pdf
 http://download.bioon.com.cn/upload/month_0902/20090223_b809d1c59ba2a6e2abfdJtWiJOiFDm02.att
ach.pdf
 http://bioprocess-maulik.blogspot.in/2007/07/design-of-industrial-fermentation.html

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NMEICT-MHRD (Govt. of India) Project on - Creation of e-Contents on Fermentation Technology

 http://hsc.csu.edu.au/biology/options/biotechnology/3051/biotechnologyPart3.html
 http://www.rsc.org/ebooks/archive/free/BK9780854046065/BK9780854046065-00001.pdf
 http://www.biotech.upm.edu.my/academics/On%20Line%20Note/Bioprocess/BTK%205301/Lect6%28I
noculum%20Preparation%20and%20Development%29.pdf
 http://www.biotechresources.com/services-strain.shtml
 http://www.idosi.org/wjc/4%281%2909/14.pdf
 http://cheserver.ent.ohiou.edu/Paper-gu/DualFeed.pdf

Project control No: RE-02091011297, Christ College, Rajkot, Gujarat, India

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