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Veer Narmad South Gujarat University,

Surat
M.Sc. (Microbiology) Syllabus
(Effective from June, 2022)

Page 1 of 20
VEER NARMAD SOUTH GUJARAT UNIVERSITY, SURAT
M.Sc. MICROBIOLOGY SEM I
Academic year 2022 onwards

Theory Paper/ Practical Teaching Exam schedule Total Credit


schedule Duration Internal External marks
Hrs/ (Hrs) marks marks
week
Theory papers:
1: Core Paper -I 4 3 30 70 100 4
(CC-1)
Microbial diversity
2: Core Paper - II 4 3 30 70 100 4
(CC-2)
Molecular biology and
genetic engineering
3: Core Paper - III 4 3 30 70 100 4
(CE-1)
Environmental
microbiology and
biofuels

Inter / multi- 4 3 30 70 100 4


Disciplinary (AECC)
4: Elective Paper –1
Biophysical techniques
and instrumentation

4: Elective Paper –2
Cell chemistry and
molecular interactions

Practicals:
5. Practical based on 12 10-15 50 100 150 6
Core I, II, III &
Elective paper
6. Skill Based elective 2 0 20 30 50 2
paper / swayam/ other
MOOC courses
GE-1
Biosecurity and
Biosafety in Public
Health Laboratories

Page 2 of 20
Veer Narmad South Gujarat University, Surat
Program outcome, Program specific oucome, course outcome
Program name: M. Sc. Microbiology

PO1: Master of Science in Microbiology is designed to develop students for academic and
industrial excellence. The course shall enable the students to develop their career in pharmaceutical
and fermentation industries. The course emphasizes on the applications of microbiology to address
environmental problems and provide microbial remedial measures. The outcome of the study is
the usage of knowledge in developing a sustainable environment. The major areas focused in the
course is microbial diversity, environmental microbiology, molecular biology and genetic
engineering, Biophysical techniques and instrumentations, biochemistry of molecules and
molecular interactions, enzyme kinetics, microbial ecology and physiological adaptations,
molecular pathogenesis, immunology and immunological techniques, fermentation technology,
bioprocess engineering, pharmaceutical microbiology, microbial products and the applied subjects
for the better understanding of the applications of microbiology.
PO2: Students shall be enabled to distinguish, differentiate, identify and classify various types of
microorganisms. They shall be able to use various bioanalytical instrumentations and techniques
to study various aspects of microbiology. The course shall develop capacitance to address
environmental problems with microbial solutions. Students shall gain an understanding of the
molecular pathogenesis of infectious diseases and advances in immunology. The study of
fermentation technology and pharmaceutical microbiology shall prepare the students for various
industries. The study of microbial products and the knowledge of industrial microbiology as well
as microbial technology shall enable the students to envision themselves as bio entrepreneurs.
PO3: Students shall develop aptitude for research, learn to formulate hypothesis and design
experiments to test the hypothesis. The research accomplished in their dissertations shall make
them understand the relevance of microbiology in addressing the environmental problems and
finding out microbial solutions and maintaining sustainable environment. Students shall be
inclined towards research and shall learn to pursue and formulate plan of work to achieve the set
objectives.

Program specific outcome:


PSO1: Student shall gain knowledge and skills aligned to microbial fermentation and microbial
technology. They shall obtain polished skill set for analytical investigations related to microbial
research and allied life sciences field.
PSO2: Student shall be empowered by the curriculum having theoretical, experimental and
dissertation components in M.Sc. Microbiology. Multi-faceted learning approach shall provide
student great chances to acumen in industrial and professional arena.

Page 3 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Semester I
MB 1001: MICROBIAL DIVERSITY

1. Course Code & Title

Course code: Core course 1


Course title: Microbial diversity
Course type: Core
Course credits: 04

2. Course overview and Course Objectives

The main aspect of this course is to study the diverse forms of microorganisms and principles
underlying its classification, study of major phyla of the domain bacteria and archaea. The paper
also includes the study of viruses, fungi and algae.

Course Objectives

 To study classification and identification of prokaryotic organism.


 To learn characteristics of archea and proteobacteria.
 To study structure, replication of viruses and emerging viral diseases.
 To increase understanding of classification and characterization of fungi and algae.

3. Course Content

UNIT 1 PROKARYOTIC TAXONOMY


1.1 Prokaryotic domain
1.2 Classification of prokaryotic organisms
1.3 Identification of prokaryotes
1.4 Numerical and polyphasic taxonomy
1.5 Prokaryotic systematic
1.6 Bacterial nomenclature
1.7 Taxonomic framework for prokaryotic systematic
1.8 Intellectual property of prokaryotes

UNIT 2 ARCHAEA AND PROTEOBACTERIA


2.1 The Archaea
2.1.1 Overview of Archaea
2.1.2 Phylum Creanarchaeota,
2.1.3 Phylum Euarcheaeota
2.2 The Proteobacteria
2.2.1 Alphaproteobacteria

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2.2.2 Betaproteobacteria
2.2.3 Gammaproteobacteria
2.2.4 Deltaproteobacteria
2.2.5 Epsilonproteobacteria

UNIT 3 VIROLOGY
3.1 Principles of virus structure
3.2 virus replication strategies
3.3 Viral conquest of the host cell
3.4 Emerging viral diseases
3.5 Viroids and prions
3.6 Plant phages: TMV
3.7 Protists viruses: Chlorella viruses
3.8 Animal viruses: HIVs and their replication
3.9 Bacteriophages: phage λ, phage Mu-1

UNIT 4 MYCOLOGY AND PHYCOLOGY


4.1 Natural classification of fungi
4.1.1 Members of kingdom Fungi
4.1.2 The species concept in fungi
4.1.3 The untrue fungi
4.1.4 Ecosystem mycology
4.2 Hyphal cell biology: Mycelium: the hyphal mode of growth, Spore germination
and dormancy, The fungal lifestyle: colony formation, Mycelium growth kinetics
4.3 Fungal cell and tissue differentiation: Mycelial differentiation, Making spores
4.4 Arbuscular (AM) endomycorrhizas
4.5 Characteristics of algae
4.5.1 Structure of algal cell
4.5.2 Nutrition of algae
4.5.3 Classification of algae
4.6 Cyanobacteria
4.6.1 Ecology of Cyanobacteria
4.6.2 Classification

4. Course Learning Outcomes/Student’s Learning Outcomes (SLO)

Unit 1: Students shall learn the principles of prokaryotic classification and bacterial nomenclature
as well as the IPR of prokaryotes.
Unit 2: Students shall gain knowledge of few phyla of archea as well as proteobacteria
Unit 3: Students will gain an understanding of virus structure, replication as well as emerging viral
diseases. They shall learn important virus of plant, animal and bacteria.
Unit 4: Students shall develop an understanding of classification and characterization of fungi,
mycorrhiza, algae and cynaobacteria.

Page 5 of 20
Recommended Learning Resources:

 Bergey’s manual of systematic bacteriology, (2009) 2nd edition, vol 1 Springer. (ISBN; 978-0387-
95041-9).
 Wiley J., Sherwood I., (2011), Prescott, Harley and Kleins Microbiology, 9th edition., Mc Graw
Hill. (ISBN; 978-0073402406)
 David M. Knipe, Peter M. Howley, (2007). 5th edition., vol. 1, Fields Virology. (ISBN; 978-07817-
6060-7)
 David Moore, Geoffrey Robson, Anthony Trinci, (2011) 21st century guidebook to fungi,
Cambridge University Press. (ISBN; 978-0-521-18695-7)
 Robert Edward Lee, (2008) Phycology, Cambridge University Press. (ISBN; 978-0-521-
14144-4).

Page 6 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Semester I
MB 1002: MOLECULAR BIOLOGY AND GENETIC ENGINEERING

1. Course Code & Title

Course code: Core course II


Course title: Molecular biology and genetic engineering
Course type: Core
Course credits: 04

2. Course overview and Course Objectives

The course includes the study of structure of genetic material and molecular mechanisms in
bacteria. It shall include the various tools and technology applied for the construction of rDNA
and the applications of tools and techniques to carry out transfection in plants and animals.

Course Objectives

 To understand the structure and topology of genetic material and its replication.
 To gain an insight on the genetic code and the process of transcription and translation.
 To learn about the tools and techniques used in genetic engineering.
 To increase knowledge of varied application of rDNA technology.

3. Course Content

UNIT 1 GENOME ORGANIZATION AND REPLICATION


1.1 Nucleosomes
1.2 DNA Structure
1.3 DNA topology
1.4 RNA Structure
1.5 The replication fork
1.6 The specialization of DNA polymerases
1.7 DNA replication in prokaryotes
1.7.1 Synthesis at the replication fork
1.7.2 Initiation
1.7.3 Binding and unwinding
1.7.4 Finishing replication

UNIT 2 EXPRESSION OF THE GENOME


2.1 Transcription
2.1.1 RNA polymerase
2.1.2 Features of prokaryotic promoters
2.1.3 The transcription cycle in Bacteria

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2.2 Translation
2.2.1 Messenger RNA
2.2.2 Structure and role of tRNA
2.2.3 Ribosome structure
2.2.4 Genetic code
2.2.5 Initiation, elongation and termination of protein synthesis in prokaryotes

UNIT 3 TOOLS AND TECHNIQUES OF RECOMBINANT DNA TECHNOLOGY


3.1 Enzymes
3.1.1 Enzymes used in Genetic Engineering
3.1.2 Restriction Endonucleases
3.1.3 Ligation of DNA fragments using DNA Ligases
3.2 Vectors: plasmids as vectors in Genetic engineering, λ and M13 bacteriophages as cloning
vehicle, phagemids, cosmids, YAC, BAC, HAC, MAC
3.3 Polymerase Chain Reaction
3.4 Construction of Genomic and cDNA libraries

UNIT 4 APPLICATIONS OF RECOMBINANT DNA TECHNOLOGY


4.1 Nucleic acid as therapeutic agents
4.1.1 Anti-sense RNA
4.1.2 Interference RNA
4.1.3 Nucleic acid delivery
4.2. Transfection of Plants
4.2.1 Plant Transformation with Ti plasmid
4.2.2 Ti plasmid derived vector systems
4.2.3 Plants as Bioreactors
4.3 Methods of Transgenesis in Animals
4.3.1 Retroviral Vector Method for mice
4.3.2 DNA microinjection method
4.3.3 Cre-loxP Recombination System

4. Course Learning Outcomes/Student’s Learning Outcomes (SLO)

Unit 1: Students shall understand the structure, topology and structure of DNA and RNA. It shall also
include the study of DNA replication and role of DNA polymerase in replication.
Unit 2: Students shall gain knowledge of transcription process, importance of genetic code and the
process of translation.
Unit 3: Students shall learn about the various tools and techniques for rDNA technology.
Unit 4: Students shall develop an insight regarding the application of nucleic acids as therapeutic agents
and the methods of plant transfection and animal transgenesis.

Page 8 of 20
Recommended Learning Resources:
 Watson, J. D. et al (2017). Molecular Biology of the Gene. 7th edition., Pearson India
Education Services Pvt. Ltd. (ISBN; 9780321762436)
 Glick B.R. and Patten C.L. (2017, 2018 Indian reprint). Molecular Biotechnology
Principles and Applications of Recombinant DNA. 5th edition, ASM Press Washington DC,
USA. (ISBN; 978-1-555-81936-1)
 Rastogi S. and Pathak N. (2016). Genetic engineering. 7th impression, Oxford University
Press. (ISBN; 978-0195696578)
 Primrose S.B. and Twyman R.M. (2007), Principles of gene manipulation and Genomics.
7th edition. Blackwell Publishing, USA. (ISBN; 978-1-405-13544-3)

Page 9 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Semester I
MB 1003: ENVIRONMENTAL MICROBIOLOGY AND BIOFUELS

1. Course Code & Title

Course code: Core course III / Course elective 1


Course title: Environmental microbiology and biofuels
Course type: Core
Course credits: 04

2. Course overview and Course Objectives

The objective of the course is to enrich the students with the current problems and research being
focused to address environmental problems. The understanding of principles of environmental
microbiology and its application for sustainable development. The course focuses on aspects of
waste water engineering and reuse of water, versatility of microbial ecology, bioremediation and
biodegradation as well as intricacies of microbial fuels.

Course Objectives

 To understand the principles of microbial ecology and its strategic approaches and to learn
microbial ecological phenomena.
 To gain knowledge of constituents of waste water and the treatment and use of wastewater.
 To learn about biodegradation and bioremediation by microorganisms and microbial
transformations of pesticides and heavy metals.
 To understand the use of cellulose for ethanol technology and algal fuels.

3. Course Content

UNIT 1 MICROBIAL ECOLOGY


1.1 Principles of microbial ecology
1.2 Strategic approach to study microbial ecology
1.3 Microbial mats
1.4 Biofilms
1.5 Algal blooms
1.6 Endophytic microbes
1.7 Quorum sensing

UNIT 2 WASTEWATER TREATMENT AND REUSE


2.1 Constituents in wastewater treatment, sampling, analysis methods
2.2 Aggregate organic constituents
2.3 Types of biological processes for wastewater treatment
2.4 Biological nitrification, denitrification and phosphorus removal

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2.5 Guidelines for planning and designing treatment plants and CETPs

UNIT 3 BIODEGRADATION AND BIOREMEDIATION


3.1 Biodegradation and Bioremediation
3.2 Bioremediation technologies
3.3 Biodesulfurization
3.4 Biotreatment of pharmaceuticals and nuclear wastes
3.5 Biotreatment of textile effluent, food and dairy industry
3.6 Biodegradation of dyes
3.7 Biodegradation of polymers
3.8 Microbial transformation of pesticides
3.9 Microbial transformation of heavy metals

UNIT 4 BIOFUELS AND BIOENERGY


4.1 Cellulosic ethanol technology
4.1.1 Enzymatic processes
4.1.2 Cellulosic hydrolysis and fermentation
4.1.3 Ethanol extraction
4.1.4 Process economics
4.2 Algal fuels
4.2.1 Microalgae: growth and harvesting
4.2.2 Algae oil extraction
4.2.3 Transesterification for biodiesel
4.2.4 Prospects and economics
4. Course Learning Outcomes/Student’s Learning Outcomes (SLO)

Unit 1: Students shall learn the principles of microbial ecology and gain knowledge of microbial mats,
biofilms, algal blooms, endophytes and quorum sensing by microorganisms.
Unit 2: Students shall gain insight on the constituents of waste water and the treatment of waste
water and working of CETPs.
Unit 3: Students shall learn microbial degradation of dyes, polymers, biotreatment of pharmaceuticals,
nuclear wastes, textile effluents, food and dairy as well as microbial transformations.
Unit 4: Students shall learn cellulosic ethanol technology, algal fuels and its economics.

Recommended Learning Resources


 T. M. Schmidt and M. Schaechter, (2012). Topics in ecological and environmental microbiology.
edited by Academic press. (ISBN; 978-0-12-383878-0)
 Metcaff & Eddy Inc, (2002). Wastewater engineering: Treatment and Reuse, 4th edition, McGraw
Hill higher education. (ISBN; 9780070495395)
 Doble, M. & Anil kumar. (2005). Biotreatment of industrial effluents. Butterworth Heinemannan
imprint of Elsevier. (ISBN; 9780080456218)
 Mohapatra P.K. (2010). Environmental Biotechnology, I.K. International. (ISBN 9788188237548)
 Sungyu Lee and Shah Y.T., (2013). Biofuels and Bioenergy Processes and Technologies, CRC
Press. (ISBN 978-1-4200-8955-4)

Page 11 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Semester I
Elective paper 1
MB 1004: BIOPHYSICAL TECHNIQUES AND INSTRUMENTATION

1. Course Code & Title

Course code: Elective paper 1


Course title: Biophysical techniques and instrumentation
Course type: Elective (AECC)
Course credits: 04

2. Course overview and Course Objectives

This course is to learn the principles of detection and measurement systems and principles of the
major molecular techniques to study the prokaryotes. The study also emphasizes the study of the
various separation techniques and the spectroscopic techniques for the detection of bio-analytes.

Course Objectives

 To learn molecular techniques based on non-amplified and amplified nucleic acids and genetic
fingerprinting methods.
 To study principle and different types of chromatographic techniques and electrophoresis.
 To understand UV/vis, IR and Mass spectroscopic techniques.
 To study NMR and X-ray spectrometers and its applications.

3. Course Content

UNIT 1 MOLECULAR TECHNIQUES


1.1 Non-amplified nucleic acid probes
1.2 Amplified nucleic acid technique
1.2.1 Signal Amplification technique
1.2.2 Target amplification technique
1.2.3 Probe Amplification technique
1.3 Genetic fingerprinting methods
1.3.1 RFLP to analyze lower eukaryotic pathogens and prokaryotes.
1.3.2 RFEL
1.3.3 RAPD
1.3.4 Other PCR-Based method for DNA fingerprinting.

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UNIT 2 SEPARATION TECHNIQUES
2.1 Chromatographic techniques
2.1.1 Principles of chromatography
2.1.2 Chromatographic performance parameters
2.1.3 Partition chromatography
2.1.4 Adsorption chromatography
2.1.5 Thin layer chromatography
2.1.6 Gel permeation chromatography
2.1.7 Ion exchange chromatography
2.1.8 Affinity chromatography
2.1.9 High-Performance Liquid chromatography
2.1.10 Gas chromatography
2.2 Electrophoresis
2.2.1 Principle
2.2.2 Modes of electrophoresis
2.2.3 Support media
2.2.4 Different types of electrophoresis
2.2.5 Electrophoresis of DNA
2.2.6 Immuno-electrophoresis

UNIT 3 SPECTROSCOPIC TECHNIQUES


3.1 3.1.1 General properties of electromagnetic radiation
3.1.2 The electromagnetic spectrum
3.1.3 Interactions of radiation and matter
3.1.4 Transmittance, Absorbance & Beer’s law
3.1.5 Measurement of Transmittance and Absorbance
3.2 UV/Vis Spectrometry
3.2.1 Instrument component
3.2.2 Types of instruments
3.2.3 Some typical instruments: Photometers & Spectrophotometers
3.2.4 Qualitative Applications of UV/Vis Spectroscopy
3.3 IR Spectrometry
3.3.1 Theory of IR absorption spectrometry
3.3.2 IR instrumentation
3.3.3 IR sources and transducers
3.3.4 Sample handling for IR spectrometry
3.3.5 Application of IR spectrometry
3.4 Mass spectrometer
3.4.1 Molecular mass spectra
3.4.2 Ion Sources
3.4.3 Mass Spectrometers: Instrument components
3.4.4 Mass Analyzers
3.4.5 Tandem Mass Spectrometry
3.4.6 Application of Mass spectrometry

Page 13 of 20
UNIT 4 BIOPHYSICAL TECHNIQUES
4.1 Nuclear Magnetic Resonance spectrometers
4.1.1 Theory of NMR: Quantum & Classical Description
4.1.2 Types of NMR Spectrometers
4.1.3 Theory of chemical shift
4.1.4 NMR Spectrometers: Instrumentation
4.1.5 Application of NMR
4.2 X-Ray Spectrometers
4.2.1 X-Ray Spectrum
4.2.2 Instrumentation for X-Ray Spectrometry
4.2.3 X-Ray Diffractometers
4.2.4 X-Ray Absorption meter
4.2.5 X-Ray Fluorescent spectrometer
4.2.6 Electron probe microanalyzer

4. Course Learning Outcomes/Student’s Learning Outcomes (SLO)

Unit 1: Students shall gain an understanding of amplified nucleic acid techniques and applications
of genetic fingerprinting methods.
Unit 2: Students shall learn the principle of chromatography and electrophoresis, types and
application of separation techniques.
Unit 3: Students shall develop insight of principle of spectroscopic techniques and applications of
IR and Mass spectrometer.
Unit 4: Students shall learn theory and applications of NMR and X-ray spectrometers.

Recommended Learning Resources:


 Murray, P. R., Baron, E. J., Pfaller, M. A., Tenover, F. C., & Yolken, R. H. (2005). Manual of
clinical microbiology. 9th edition, Vol.2, American Society of Microbiology Press, Washington DC,
(ISBN; 1-55581-255-4)
 Wilson, K. and Walker, J., (2010). Principles and Techniques of Biochemistry and Molecular
Biology, 7th edition, Cambrige University Press (Low price edition), New York. (ISBN;
9780521731676)
 Ghosal, S., & AVASTHI, A. S. (2018). Fundamentals of bioanalytical techniques and
instrumentation. PHI Learning Pvt. Ltd. (ISBN; 978-8120338555)
 Skoog, D. A., Holler, F. J., & Crouch, S. R. (2017). Instrumental analysis. Cengage learning.
(ISBN; 978-8131505427)
 Khandpur, R. S., (2008). Handbook of analytical instruments. 2nd edition, Tata McGraw-Hill
Publishing Company Limited (New Delhi). (ISBN; 978-0070604605)

Page 14 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Semester I
Elective Paper 2
MB 1004: CELL CHEMISTRY AND MOLECULAR INTERACTIONS

1. Course Code & Title

Course code: Elective paper 2


Course title: Cell chemistry and molecular interactions
Course type: Elective (AECC)
Course credits: 04

2. Course overview and Course Objectives

This course is to learn the principles governing the structure and function of cell defined at cellular,
chemical, physical, genetic and evolutionary level. It includes the understanding of interaction in
these biomolecules so as to understand its structure and function. It gives an understanding of law
of thermodynamics and energy generation as well as cell signaling pathways for the functioning
of cell.

Course Objectives

 To learn the biochemistry of cell structure and function.


 To study principle of molecular interactions and its role in determining cell structure and
function.
 To understand the laws of thermodynamics and principles underlying energy generation.
 To study cell signaling pathways.

3. Course Content

UNIT 1 CELL CHEMISTRY


1.1 Cellular foundations
1.2 Chemical foundations
1.3 Physical foundations
1.4 Genetic foundations
1.5 Evolutionary foundations

UNIT 2 MOLECULAR INTERACTIONS


2.1 Weak interactions in aqueous systems
2.2 Ionization of water, weak acids and weak bases
2.3 Separation, purification and characterization of proteins by electrophoresis
2.4 Determination of protein structure: primary, secondary and tertiary
2.5 Determination of protein structure: DNA based methods

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2.6 Extraction, separation and determination of lipid structure

UNIT 3 BIOENERGETICS
3.1 Bioenergetics and thermodynamics
3.3.1 Laws of thermodynamics
3,3,2 Free –energy changes
3.2 Phosphoryl group transfers and ATP
3.3 Biological oxidation-reduction reactions
3.3.1 Half reactions and dehydrogenation
3.3.2 Reduction potentials
3.3.3 Universal and soluble electron carriers

UNIT 4 BIOSIGNALING
4.1 G protein coupled receptors and second messengers
4.2 Receptor Tyrosine kinases
4.3 Gated Ion channels
4.4 Nuclear Hormone receptors
4,5 Signaling in microorganisms
4.6 Regulation of cell cycle
4.7 Programmed cell death

4. Course Learning Outcomes/Student’s Learning Outcomes (SLO)

Unit 1: Students shall gain an understanding of cell chemistry at varied levels.


Unit 2: Students shall develop insight regarding molecular interactions underlying the determination
of cell structure and function.
Unit 3: Students shall gain knowledge of laws of thermodynamics and the principle governing
energy generation in cell
Unit 4: Students shall learn the varied ways of a cell in signaling in cellular structure and
functioning.

Recommended Learning Resources:


 Nelson, D. L., Lehninger, A. L., & Cox, M. M. (2008). Lehninger principles of
biochemistry. Macmillan.
 Voet, D., Voet, J. G., & Pratt, C. W. (2016). Fundamentals of biochemistry: life at the
molecular level. John Wiley & Sons.
 Champe, P. C., Harvey, R. A., & Ferrier, D. R. (2005). Biochemistry. Lippincott Williams
& Wilkins.
 Garrett, R. H., & Grisham, C. M. (2012). Biochemistry. Cengage Learning.
 White, A. (1954). Principles of biochemistry. McGraw-Hill Book.

Page 16 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Microbiology Semester-I
MBP-1005: PRACTICALS
1. Determination of burst size of coliphage lysate by One-step growth curve.
2. Extraction and detection (Electrophoretic & spectrophotometric) of bacterial genomic DNA.
3. Ligation of DNA fragments.
4. Amplification of gene by PCR.
5. Study of RFLP
6. Study of bacterial transformation
7. Extraction of total RNA from yeast.
8. Extraction of plasmid DNA from bacteria
9. Thin layer chromatography of sugars and amino acids.
10. Analysis of physico-chemical analysis of domestic water and wastewater.
• Acidity
• Alkalinity
• Hardness –EDTA titrimetric method
• Solids: TDS and TSS
• Chlorine demand
• Chloride
11. Analysis of aggregate organic constituents
• Biochemical oxygen demand
• Chemical oxygen demand
12. Enzyme substrate coliform test for drinking water.
13. Isolation and cultivation of cyanobacteria.
14. Study of bacterial growth curve.
15. Study of fungal growth by slide culture technique.
16. Decontamination of disposable and reusable lab materials.
17. Disinfection and validation test of laminar air flow cabinet.
18. Monitoring and validation of sterilization in autoclave.
 Note: A report has to be prepared for the industrial field visit/ educational tour undertaken
during the semester.

Page 17 of 20
Veer Narmad South Gujarat University, Surat
M. Sc. Semester I
MB 1006: Skill based Elective paper
BIOSECURITY AND BIOSAFETY IN PUBLIC HEALTH LABORATORIES

1. Course Code & Title

Course code: General Elective 1


Course title: Biosecurity and Biosafety in Public Health Laboratories
Course type: Skill based Elective paper
Course credits: 02

2. Course overview and Course Objectives

The course shall include the importance of biosafety in laboratories, biosafety level, risk
assessment, preparations of samples for shipment and biosecurity program. It includes the good
microbiological techniques and safe laboratory procedures. The course gives an understanding of
health care waste management, including segregation, collection, transport, treatment and waste
disposal, is fundamental to wider efforts to provide safe and quality health care. Student’s will
have an insight on biosecurity, biosafety and biomedical waste management.

Course Objectives

 To study the routes of exposure for a pathogen to a human being.


 To demonstrate and assess the proper use of PPE, best practices, biological containment, and
be prepared to safely conduct research.
 To study and identify the role of the Biosafety Professional in Biomedical Research
Laboratories.

3. Course Content

UNIT 1 Introduction to Biosafety and Biosecurity in Laboratories.


1.1 General Principles of Biosafety.
1.2 Different elements of containment.
1.3 Various Biosafety Levels.
1.4 Risk assessment in Biosafety.
1.5 Practices followed at various biosafety levels.
1.6 Biosecurity and Biosafety.
1.7 Laboratory biosecurity programme.
1.8 General preparation of shipments for transport.

Page 18 of 20
UNIT 2 Safety equipment and safe laboratory procedures
2.1 Biosafety cabinets and its types.
2.2 Use of Biosafety cabinets in work practices and procedures.
2.3 Cleaning and Disinfection of Work Surfaces.
2.4 Decontamination of equipment.
2.5 Certification of Biosafety cabinet.
2.6 Good Microbiological Techniques-Safe laboratory procedures

UNIT 3 Biosafety precautions and Biomedical Waste Management


3.1 Specimen collection and handling.
3.2 Handling of lyophilized biological material.
3.3 General biosafety instructions for lab workers.
3.4 National Rules/Regulatory mechanisms for BMW management in India.
3.5 Biological Hazards, Asphyxiation Hazards, Explosion Hazards.

UNIT 4 Sterilization, disinfection and transport of infectious substances


4.1 Methods of sterilization.
4.2 Decontamination and Disinfectants.
4.3 Washing of laboratory glassware.
4.4 Quality Control
4.5 Classification of infectious substances.

Course Learning Outcomes/Student’s Learning Outcomes (SLO)

 Students shall learn the principles related to biosafety in research and clinical laboratories,
various biosafety levels, risk assessment and laboratory biosecurity program.
 Students shall gain knowledge of various types of biosafety cabinets used in laboratory and
its use at various biosafety levels. Students shall learn the use of different disinfection
procedures at work places that will help the researcher/student for effective result.
 Students shall understand the handling of infected specimens and waste generated in the
laboratory. Students shall gain awareness of hazards and rules/regulatory mechanisms for
Biomedical waste management.
 Students shall learn about basic aspects of various sterilization and disinfection methods
used in laboratory and classification of infectious substances.

Recommended Learning Resources

Page 19 of 20
 Government of India Ministry of Health. Biosafety Manual for Public Health Laboratories.
(https://ncdc.gov.in/WriteReadData/l892s/File608.pdf)
 Training Manual on Biomedical-waste management for doctors, nurses, nodal officers and
waste managers. Training component of the project “Environmentally sound management
of medical wastes of India” Endeavour of GEF, UNIDO, MoEFCC and State Government
of Gujarat, Karnataka, Maharashtra, Odisha and Punjab, 2018.
https://www.biomedicalwastemanagementinindia.in/Resurces/5_Waste_handlers_manual
_FLIP_CHART.pdf
 https://www.researchgate.net/publication/235990567_Biomedical_Waste_Management_
Manual_for_Healthcare_Personnel_in_Grenada
 Laboratory biosafety manual Third edition. World Health Organization Geneva 2004.
https://www.who.int/publications-detail-redirect/9241546506

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