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proteobacteria, Gamma proteobacteria, Delta proteobacteria, Epsilon proteobacteria, Zeta proteobacteria, Gram Positive: Low G+
          C (Firmicutes), High G+C (Actinobacteria). Cyanobacteria.
          References:
               1.  S.C. Rastogi.  Cell Biology, Tata McGraw Hill Pub. Co. New Delhi, 2010.
               2.  P. K. Gupta. A Text Book of Cell and Molecular Biology, Rastogi Publications, Meerut, 2019.
                                                                                                   th
               3.  J. Willey, L. Sherwood and C. J. Woolverton. Prescott’s Microbiology, Tata McGraw Hill Publishing, 10  Edition, 2017.
               4.  B. Alberts, D. Bray, J. Lewis, M. Raff and J.D. Watson. Molecular Biology of the Cell, Garland Publishing Inc. New York,
                  2017.
               5.  D. Robertis, Cell and Molecular Biology, Waverly International, New York, 2011.
               6.  H. Lodish, A. Berk, S.L. Zipursky, P. Matsudiara, D. Baltimore, and J. Darnell, Molecular Cell Biology, WH Freeman & Co.,
                  New York, 2013.

          BT1212: MICROBIAL NUTRITION AND GROWTH [2 1 0 3]
          Microbial Nutritional Types and Requirements: Carbon, Oxygen, Hydrogen, Nitrogen, Phosphorus, Sulphur and Growth factors.
          Nutrient uptake mechanisms. Types of culture media. Isolation, pure culture and preservation techniques of microorganisms and
          pure  culture  techniques  of  microorganisms.  Microbial  Growth:  Definition  of  growth,  growth  curve  and  kinetics,  cultivation  of
          anaerobic  bacteria.  Measurement  of  Growth:  Direct  Microscopic  count-Petroff-Hausser  counting  chamber,  haemocytometer,
          spread  plate  and  pour  plate  techniques,  membrane  filtration,  cell  mass  and  turbidity  measurement.  Synchronous  growth,
          Continuous growth (chemostat and turbidostat), Diauxic growth and Growth Yield. Influence of environmental factors on growth.
          Viable non-culturable organisms. Control of Microorganisms: Pattern/Rate of Microbial Death.
          References:
                                                              th
               1.  M.J. Pelczar, E.C.S. Chan and N.R. Krieg. Microbiology. 5 edition. McGraw Hill Book Company, 1993.
               2.  S. Srivastava and P.S. Srivastava. Understanding Bacteria. Kluwer Academic Publishers, Dordrecht, 2003.
                                                                                                   th
               3.  J. Willey, L. Sherwood and C. J. Woolverton. Prescott’s Microbiology, Tata McGraw Hill Publishing, 10  Edition, 2017.
                                                                                    th
               4.  R.Y. Stanier, J.L. Ingraham, M.L. Wheelis, and P.R. Painter.General Microbiology. 5 edition. McMillan, 2005.
                                                                           th
               5.  G.J. Tortora, B.R. Funke, and C.L. Case. Microbiology: An Introduction. 9  edition Pearson Education, 2008.
                                                                                                                   th
               6.  M.T. Madigen, J.M. Martinko, K.S. Bender, D.H. Buckley, D. A. Stahl and T. Brock. Brock Biology of Microorganisms. 15
                  edition, Benjamin Cunnings-Pearson, 2018.

          BT1232: CELL BIOLOGY AND BIOCHEMISTRY LABORATORY [0 0 4 2]
          To study the morphology of different bacterial samples suing simple staining, negative staining, Gram’s staining, acid fast staining,
          Capsule staining, Spore staining, Isolation of pure cultures of bacteria by streaking method, Estimation of CFU count by spread
          plate method, Motility by hanging drop method. Study of specimens of lichens such as Lecidia, Graphis, Parmelia, Usnea, Cladonia,
          Ramalina. Observation of disease symptoms in different hosts. Study and microscopic preparation of slides of the following fungi:
          Albugo, Aspergillus, Puccinia. Field visit and study of some locally available plant diseases caused by viruses, mycoplasma, bacteria
          and fungi. Preparation of posters of following diseases: green ear disease of Bajra, rust of Crucifers, rusts and smuts of Wheat, red
          rot of sugarcane. Study of specimens and permanent slides of all above mentioned course material. Demonstration of mushroom
          cultivation.

          BT1233: MICROBIOLOGY LABORATORY - II [0 0 4 2]
          Physiological  differentiation  of  microorganisms  on  different  media.  Demonstration  of  fermentation  of  carbohydrates,
          determination of effect of pH, substrate concentration and temperature on bacterial growth, determination of microbial growth,
          determination  of  bacterial  growth  by  turbidimetric  method,  determination  of  photosynthetic  pigments  in  cyanobacteria,
          demonstration of the thermal death time and decimal reduction time of E. coli. Preparation of buffers, Biochemical tests for the
          following- carbohydrate, starch, proteins, fats, tannins, ascorbic acid and anthocyanins, estimation of sugar by anthrone method,
          DNS method, Biuret method, estimation of protein by Lowry’s method.

                                                     THIRD SEMESTER

          BT2101: FUNDAMENTALS OF BIOINFORMATICS [2 1 0 3]
          Introduction to Bioinformatics: Historical background. Scope of bioinformatics. Applications of bioinformatics. Biological databases
          and data analysis: nucleotide databanks (NCBI, EMBL, DDBJ), protein databanks: sequence databanks: PIR, SWISSPROT, TrEMBL;
          structural databases: PDB, SCOP, CATH. Sequence relationship and alignment: Similarity, identity and homology. Alignment – local
          and global alignment, pairwise and multiple sequence alignments, alignment algorithms, amino acid substitution matrices (PAM
          and  BLOSUM),  BLAST  and  CLUSTALW.  Phylogenetic  Analysis:  Construction  of  phylogenetic  tree,  dendrograms,  methods  of
          construction of phylogenetic trees - maximum parsimony, maximum likelihood and distance methods. Protein structure prediction
          and  analysis:  Levels  of  protein  structure.  Protein  tertiary  structure  prediction  methods.  Significance  of  Ramachandran  map.
          Genomics:  Information  flow  in  biology;  DNA  sequence  data,  experimental  approaches,  genome  information  resources-UCSC
          genome browser, GENSCAN.

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