Skip to main content

Fourth Semester M.Sc. Degree Examination, March 2021BotanySpecial Paper II----ElectiveBIOTECHNOLOGY(2019 Admission)

(5474)
Reg. No.....
Name:..........
Fourth Semester M.Sc. Degree Examination, March 2021
Botany
Special Paper II----Elective
BIOTECHNOLOGY
(2019 Admission)

Max. Marks: 75


Instructions: Draw diagrams and illustrate with examples wherever necessary.

1.Answer the following questions.
1.What is antisense technology?
2. EPSPS Pathway.
3. Ri Plasmid.
4.Binary vector.
5. Monoclonal antibody.
6. Vitrification.
7.Hardening of tissue culture raised plants.
8. Vertical resistance.
9.a-amylases.
10. Embryo rescue.


(10 x 1 =10 Marks)

1II. Answer all the following questions in not more than 50 words.

11. (a) Explain the strategies used in making a disarmed Ti plasmid.
Or
(b) What is a frame shift mutation?

12. (a) Explain the utility of adapters in gene cloning.
Or 
(b) What are marker genes?

13. (a) Explain pyrosequencing.
OR

(b) Differentiate between RFLP and RAPD.

14. (a) Explain the process of developing a gene knockout.
OR
(b) What is a cybrid? How is it used in plant breeding?

15. (a) Explain bulbosum method.
OR
(b) What is biotransformation?
(5 x 2 = 10 Marks)
III. Answer all the following questions in not more than 150 words.

16. (a) Explain the encapsulation dehydration method of cryopreservation.
OR
(b) How does bioaugmention of microbial products achieved?


17. (a) Explain the role of transposable elements in plant improvement.
OR
(b) Explain the strategies for developing pulses with essential aminoacids.

18. (a) Describe two important variants of PCR.
OR
(b) Explain Callus. How somatic embryos are formed.

19. (a) What is buffer zone in transgenic science? How is it related to biological containment?
OR
(b) Explain northern-western blotting with its applications.

20. (a) Explain the process of electroporation for introducing a new gene fragment into a protoplast.
OR
(b) What are PR proteins? Explain its application in agriculture.

21. (a) What are reporter genes? Name two and explain their mode of action.
OR
(b) What are edible vaccines? What are its advantage and disadvantages?

22. (a) Explain molecular farming with examples.
OR
(b) Explain with example viral coat-protein mediated immunity in plants.

(7 x 5= 35 Marks)

IV. Answer all the following questions in not more than 250 words.

23. (a) Explain the mechanism of inducing salt tolerance in plants.
OR
(b) Explain different techniques for developing a transgenic plant.

24. (a) What are single cell proteins? How the eukaryotic cells are engineered to get overexpress valuable proteins?
OR
(b) What is herbicide resistance? Explain the strategies used in developing
herbicide tolerant plants.


(2 x 10 = 20 Marks)


Comments

Popular Posts

••CLASSIFICATION OF ALGAE - FRITSCH

      MODULE -1       PHYCOLOGY  CLASSIFICATION OF ALGAE - FRITSCH  ❖F.E. Fritsch (1935, 1945) in his book“The Structure and  Reproduction of the Algae”proposed a system of classification of  algae. He treated algae giving rank of division and divided it into 11  classes. His classification of algae is mainly based upon characters of  pigments, flagella and reserve food material.     Classification of Fritsch was based on the following criteria o Pigmentation. o Types of flagella  o Assimilatory products  o Thallus structure  o Method of reproduction          Fritsch divided algae into the following 11 classes  1. Chlorophyceae  2. Xanthophyceae  3. Chrysophyceae  4. Bacillariophyceae  5. Cryptophyceae  6. Dinophyceae  7. Chloromonadineae  8. Euglenineae    9. Phaeophyceae  10. Rhodophyceae  11. Myxophyce...

Mapping of DNA

DNA MAPPING   1. Introduction DNA mapping refers to the process of determining the relative positions of genes or DNA sequences on a chromosome. It provides information about the organization, structure, and distance between genetic markers in a genome. DNA mapping is an essential step toward genome sequencing, gene identification, disease diagnosis, and genetic engineering. DNA maps serve as roadmaps that guide researchers to locate specific genes associated with traits or diseases. 2. Objectives of DNA Mapping To locate genes on chromosomes To determine the order of genes To estimate distances between genes or markers To study genome organization To assist in genome sequencing projects. 3. Principles of DNA Mapping DNA mapping is based on: Recombination frequency Physical distance between DNA fragments Hybridization of complementary DNA Restriction enzyme digestion Use of genetic markers The closer two genes are, the less frequently they recombine during meiosis. 4 . Types of DNA...

Biological Databases – Types of Data and DatabasesNucleotide Sequence Databases (EMBL, GenBank, DDBJ)

Biological Databases – Types of Data and Databases Nucleotide Sequence Databases (EMBL, GenBank, DDBJ) 1. Introduction Biological databases are systematic, computerized collections of biological information that allow efficient storage, retrieval, updating, and analysis of large volumes of biological data. With the advent of genome sequencing, molecular biology, and bioinformatics, biological databases have become essential tools in biological research. These databases support studies in genomics, proteomics, evolutionary biology, taxonomy, medicine, agriculture, and biotechnology. 2. Types of Data Stored in Biological Databases Biological databases store diverse types of biological information, including: 1. Sequence Data DNA sequences RNA sequences Protein sequences 2. Structural Data Three-dimensional structures of proteins Nucleic acid structures 3. Functional Data Gene functions Enzyme activity Regulatory elements 4. Genomic Annotation Data Gene location Exons, introns Promoters a...

Agrobacterium & CaMV-Mediated Gene Transfer –

Agrobacterium and CaMV-Mediated Gene Transfer – Detailed Notes 1. Introduction Gene transfer in plants is often achieved by exploiting natural genetic mechanisms of Agrobacterium tumefaciens and Cauliflower Mosaic Virus (CaMV). These systems allow stable introduction of foreign genes into plant genomes for transgenic plant development. 2. Agrobacterium-Mediated Gene Transfer 2.1 Definition Agrobacterium-mediated gene transfer uses the natural ability of Agrobacterium tumefaciens, a soil bacterium, to transfer a part of its DNA (T-DNA) into plant cells. T-DNA integrates into the plant nuclear genome, enabling stable transformation. 2.2 Mechanism Recognition and attachment Agrobacterium detects phenolic compounds secreted by wounded plant cells. These compounds activate virulence (vir) genes on the Ti (tumor-inducing) plasmid. Activation of vir genes VirA (sensor kinase) and VirG (response regulator) induce expression of other vir genes (VirB, VirC, VirD, VirE). T-DNA processing and tran...

❃HPLC – High Performance Liquid Chromatography

HPLC – High Performance Liquid Chromatography ┏━━━━━ •❃°•°❀°•°❃•━━━━•━━━┓  1. Introduction High Performance Liquid Chromatography (HPLC) is an advanced analytical technique used for the separation, identification, and quantification of components present in a mixture. It is based on the differential distribution of analytes between a stationary phase and a liquid mobile phase under high pressure. HPLC is widely used in biochemistry, biotechnology, pharmaceuticals, food analysis, environmental studies, and clinical diagnostics. 2. Principle of HPLC The principle of HPLC is based on partition, adsorption, ion-exchange, or size-exclusion mechanisms, depending on the type of column used. A liquid mobile phase is pumped at high pressure through a column packed with fine stationary phase particles Sample components interact differently with the stationary phase Components with stronger interaction elute slower Components with weaker interaction elute faster Separated components are detec...

❃HPTLC (HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY) DETAILED NOTES

HPTLC (HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY) DETAILED NOTES ┏━━━━━ •❃°•°❀°•°❃•━━━━•━━━┓ 1. INTRODUCTION HPTLC is an advanced form of Thin Layer Chromatography (TLC) that allows high-resolution separation and quantitative analysis of chemical compounds. It combines classical TLC principles with automation, precise sample application, and densitometric detection. HPTLC is widely used in pharmaceuticals, herbal medicine, food analysis, and chemical research. Compared to TLC, HPTLC offers: Better resolution Higher sensitivity Quantitative capabilities Example: Fingerprinting of plant extracts, identification of drugs in mixtures, detection of contaminants in food. 2. PRINCIPLE HPTLC separates compounds based on differential migration on a stationary phase under the influence of a mobile phase. Principle: Adsorption chromatography Compounds interact with the stationary phase (silica gel, alumina, or cellulose) differently depending on polarity, molecular size, or functional groups. Mo...

❃LC-MS (LIQUID CHROMATOGRAPHY – MASS SPECTROMETRY)

LC-MS (LIQUID CHROMATOGRAPHY – MASS SPECTROMETRY)  ┏━━━━━ •❃°•°❀°•°❃•━━━━•━━━┓ 1. INTRODUCTION LC-MS is a hyphenated analytical technique combining Liquid Chromatography (LC) and Mass Spectrometry (MS). It is used for separation, identification, and quantification of compounds in complex mixtures. LC separates analytes based on polarity, size, or charge, while MS detects molecules based on mass-to-charge ratio (m/z). Developed in the 1970s–1980s, LC-MS is now widely used in pharmaceutical, clinical, environmental, and food analysis. Importance : Detects trace levels of compounds (ng–pg range) Analyzes non-volatile, thermally labile compounds that cannot be analyzed by GC-MS Provides structural information through mass fragmentation Example: Detection of drugs in plasma, protein identification in proteomics, pesticide residue analysis in food. 2. COMPONENTS OF LC-MS The LC-MS system has three main parts: A. Liquid Chromatograph (LC) Function: Separates components of a mixture befor...