PSEB 12th Class Biology Solutions Chapter 11 Biotechnology: Principles and Processes

Punjab State Board PSEB 12th Class Biology Book Solutions Chapter 11 Biotechnology: Principles and Processes Textbook Exercise Questions and Answers.

PSEB Solutions for Class 12 Biology Chapter 11 Biotechnology: Principles and Processes

PSEB 12th Class Biology Guide Biotechnology: Principles and Processes Textbook Questions and Answers
Question 1.
Can you list 10 recombinant proteins which are used in medical ; practice? Find out where they are used as therapeutics (use the internet).
Answer:

Recombinant proteins Therapeutic uses
(a) Insulin Used for diabetes mellitus
(b) OKT-3 Therapeutic antibody, used for reversal
(c) DNase Treatment of cystic fibrosis
(d) Reo Pro Prevention of blood clots
(e) Blood clotting factor VIII Treatment of haemophilia A
(f) Blood clotting factor IX Treatment of haemophilia B
(g) Tissue plasminogen activator For acute myocardial infarction
(h) Interferon alpha (INF alpha) Used for hepatitis C
(i) Interferon beta (INF beta) Used for multiple sclerosis
(j) Interferon gamma (INF gamma) Used for granulomatous disease

Question 2.
Make a chart (with diagrammatic representation) showing a restriction enzyme, the substrate DNA on which it acts, the site at which it cuts DNA and the product it produces.
Answer:
PSEB 12th Class Biology Solutions Chapter 11 Biotechnology Principles and Processes 1

PSEB 12th Class Biology Solutions Chapter 11 Biotechnology: Principles and Processes

Question 3.
From what you have learnt, can you tell whether enzymes are bigger or DNA is bigger in molecular size? How did you know?
Answer:
The molecular size of DNA molecules is more than that of enzymes. It is because an enzyme (protein) is synthesised from a segment of DNA called the gene.

Question 4.
What would be the molar concentration of human DNA in a human cell? Consult your teacher.
Answer:
The molar concentration of human DNA in a human diploid cell is as follows:
Total number of chromosomes × 6.023 × 1023
= 46 × 6.023 × 1023
= 2.77 × 1018moles

Question 5.
Do eukaryotic cells have restriction endonucleases? Justify your answer.
Answer:
No. Eukaryotic cells do not have restriction endonucleases. All the restriction endonucleases have been isolated from the various strains of bacteria and they are also named according to the genus and species of prokaryotes. The first letter of the enzyme comes from the genus and the second two letters come from the species of the prokaryotic cell from which they have been isolated. For example, EcoRI comes from Escherichia coliRY 13. In EcoRI, the letter ‘R’ is derived from the name of the strain. Roman numbers following the names indicate the order in which the enzymes were isolated from that strain of bacteria.

Question 6.
Besides better aeration and mixing properties, what other advantages do stirred tank bioreactors have over shake flasks?
Answer:
Shake flasks are used for growing microbes and mixing the desired materials on a small scale in the laboratory. However, the large-scale production of a desired biotechnological product requires large stirred tank bioreactors.

Besides better aeration and mixing properties, bioreactors have the following advantages:

  • It has an oxygen delivery system.
  • It has a foam control, temperature and pH control system.
  • Small volumes of culture can be withdrawn periodically.

PSEB 12th Class Biology Solutions Chapter 11 Biotechnology: Principles and Processes

Question 7.
Collect 5 examples of palindromic DNA sequences by consulting your teacher. Better try to create a palindromic sequence by following base-pair rules.
Answer:
Some palindromic DNA sequences and the restriction enzymes which act on them are as follows :

  • 5′-AGCT-3′ Alul (Arthrobacter luteus)
    3′-TCGA-5′
  • 5′-GAATTC-3′ EcoRI (Escherichia coli)
    3′-CTTAAG-5′
  • 5′-AAGCTT-3′ Hindlil (Haemophilus influenzae)
    3′-TTCGAA-5′
  • 5′-GTCGAC-3′ Sail (Streptomyces albus)
    3′-CAGCTG-5′
  • 5′-CTGCAG-3′ PstI (Providencia stuartii)
    3′-GACGTC-5′

Question 8.
Can you recall meiosis and indicate at what stage a recombinant DNA is made?
Answer:
A recombinant DNA is made in the pachytene stage of prophase I by f crossing over.

Question 9.
Can you think and answer how a reporter enzyme can be used to
monitor transformation of host cells by foreign DNA in addition to a selectable marker?
Answer:
Reporter enzyme can differentiate recombinants from non-recombinants on the basis of their ability to produce a specific colour in the presence of a chromogenic substrate. DNA is inserted within the coding sequence of the enzyme p-galactosidase. This results into inactivation of the enzyme which is referred to as insertional inactivation.

The presence of a chromogenic substrate gives blue-coloured colonies if the plasmid in the bacteria does not have an insert. The presence of the insert results in insertional inactivation of α-galactosidase and the colonies do not produce any colour. These are identified as recombinant colonies.

Question 10.
Describe briefly the following:
(a) Origin of replication
(b) Bioreactors
(c) Downstream processing
Answer:
(a) Origin of Replication: This is a sequence from where replication starts and any piece of DNA when linked to this sequence can be made to replicate within the host cells. This sequence is also responsible for controlling the copy number of the linked DNA. So, if one wants to recover many copies of the target DNA it should be cloned in a vector whose origin supports a high copy number.

(b) Bioreactors: Bioreactors are vessels in which raw materials are biologically converted into specific products, individual enzymes etc. using microbial plant, animal or human cells. A bioreactor provides the optimal conditions for achieving the desired product by providing optimum growth conditions (temperature, pH, substrate, salts, vitamins, oxygen). The most commonly used bioreactors are of stirring type. A biogas plant is a good example of a bioreactor.

(c) Downstream Processing: After completion of the biosynthetic stage, the product is subjected through a series of processes before it is ready for marketing as a finished product. The processes include separation and purification, which are collectively referred to as downstream processing. The product has to be formulated with suitable preservatives. Such formulation has to undergo thorough clinical trials as in the case of drugs. Strict quality control testing for each product is also required. Downstream processing and quality control testing vary from product to product.

Question 11.
Explain briefly
(a) PCR
(b) Restriction enzymes and DNA
(c) Chitinase
Answer:
(a) PCR: PCR stands for Polymerase Chain Reaction. In this reaction multiple copies of the gene (or DNA) of interest is synthesised in vitro using two sets of primers and the enzyme DNA polymerase. The enzyme extends the primers using the nucleotides provided in the reaction and the genomic DNA as template. The segment of DNA can be amplified to approximately billion times if the process of replication of DNA is repeated many times.

(b) Restriction Enzymes and DNA: Restriction enzymes are synthesised by microbes as a defence mechanism and are specifically endonucleases which cleave the double-stranded DNA with the desired genes. This activity occurs at a limited number of sites depending on the number of recognition sequences in DNA. Lysing enzymes, synthesising enzymes (DNA polymerase and reverse transcriptase) and ligases are also tools of genetic engineering.

(c) Chitinase: During the isolation of DNA in the processes of recombinant DNA technology, the fungal cell is heated with an enzyme called chitinase. The chitinase enzyme dissolves the chitin membrane to open the cell for release of DNA along with other macromolecules such as RNA, proteins, polysaccharides and lipids.

PSEB 12th Class Biology Solutions Chapter 11 Biotechnology: Principles and Processes

Question 12.
Discuss with your teacher and find out how to distinguish between
(a) Plasmid DNA and Chromosomal DNA
(b) RNA and DNA
(c) Exonuclease and Endonuclease
Answer:
(a)

Plasmid DNA Chromosomal DNA
Plasmid DNA is the naked double-stranded DNA which forms a circle with no free ends. It is associated with few proteins but contains RNA polymerase enzyme. They are smaller than the host chromosomes and can be easily separated. Chromosomal DNA is a double-stranded linear DNA molecule associated with large proteins. This DNA exists in relaxed and supercoiled forms and provides a template for replication and transcription. It has free ends represented as 3′-5′.

(b)

DNA RNA
(i) It is mainly confined to the nucleus. A small quantity occurs in mitochondria and chloroplasts. It mainly occurs in the cytoplasm. A small quantity is found in the nucleus.
(ii) Its quantity is constant in each cell of a species. Its quantity varies in different cells.
(iii) It contains deoxyribose sugar. It contains ribose sugar.
(iv) Its pyrimidines are adenine and thymine. Its pyrimidines are adenine and uracil.
(v) The amount of adenine is equal to the amount of thymine. Also, the amount of cytosine is equal to the amount of guanine. Adenine and uracil are not necessarily in equal amounts, nor are cytosine and guanine necessarily in equal amounts.
(vi) It can replicate itself. It cannot replicate itself. It is formed by DNA. Some RNA viruses (paramyxo virus) can produce RNA from an RNA template.

(c) Exonucleases are nucleases which cut off the nucleotides from the 5′ or 3′ ends of a DNA molecule, whereas endonucleases are nucleases which cleave the DNA duplex at any point except at the ends.

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