Biotechnology and its ApplicationsClass 12 Biology NCERT Solutions
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Q1EXERCISES
Which part of the plant is best suited for making virus-free plants and why?
Solution
The meristem (apical and axillary) is the best part of the plant for making virus-free plants. This is because the meristematic tissue is a region of actively dividing cells and has a high metabolic rate, which is believed to interfere with virus multiplication. Consequently, even if the rest of the plant is infected with a virus, the meristem often remains virus-free. By excising the meristem and growing it in vitro through tissue culture, a whole, healthy, and virus-free plant can be regenerated.
Q2EXERCISES
What is the major advantage of producing plants by micropropagation?
Solution
The major advantage of producing plants by micropropagation (tissue culture) is the ability to produce a very large number of plants from a single parent plant in a very short duration. All the plants produced through this method are genetically identical to the original plant from which they were grown, and are known as somaclones. This ensures the propagation and preservation of desirable traits, such as high yield or disease resistance, uniformly across a large population of plants.
Q3EXERCISES
Find out what the various components of the medium used for propagation of an explant in vitro are?
Solution
The nutrient medium used for the in vitro propagation of an explant is a sterile, gel-based medium containing various components essential for plant growth. These components are:
- Carbon Source: A source of energy, typically sucrose.
- Inorganic Salts: Provides essential macronutrients (like nitrogen, phosphorus, potassium) and micronutrients (like iron, manganese, zinc).
- Vitamins: Organic compounds that act as co-factors for enzymes, such as thiamine and nicotinic acid.
- Amino Acids: Such as glycine, which are the building blocks for proteins.
- Growth Regulators: Plant hormones like auxins (to promote root growth) and cytokinins (to promote shoot growth) are critical for controlling cell division and differentiation.
- Water: High-purity water is used as a solvent for all the components.
- Gelling Agent: A substance like agar is used to solidify the medium, providing physical support to the explant.
Q4EXERCISES
Crystals of Bt toxin produced by some bacteria do not kill the bacteria themselves because -
(a)
bacteria are resistant to the toxin
(b)
toxin is immature;
(c)
toxin is inactive;
(d)
bacteria encloses toxin in a special sac.
Solution
The correct answer is (c) toxin is inactive.
Explanation:
The Bt toxin is produced by the bacterium Bacillus thuringiensis in an inactive form called a protoxin. This protoxin only becomes active under the specific alkaline pH conditions found in the midgut of certain insects. Since the internal environment of the bacterium is not alkaline, the toxin remains in its inactive state and is therefore harmless to the bacterium itself.
Q5EXERCISES
What are transgenic bacteria? Illustrate using any one example.
Solution
Transgenic bacteria are bacteria whose genetic material has been altered by the introduction and expression of a foreign gene from another organism using recombinant DNA technology. These are a type of Genetically Modified Organism (GMO).
Example: Production of Human Insulin
A prominent example is the use of the bacterium Escherichia coli (E. coli) to produce human insulin.
- The human gene responsible for producing insulin is isolated.
- This gene is inserted into a plasmid (a small, circular DNA molecule) from E. coli.
- This recombinant plasmid is then introduced back into E. coli bacteria.
- The transformed bacteria, now containing the human insulin gene, are cultured in large industrial fermenters.
- The bacteria multiply and use their cellular machinery to express the foreign gene, producing human insulin.
- This insulin, called 'humulin', is then extracted, purified, and used as a therapeutic drug for treating diabetes.
Q6EXERCISES
Compare and contrast the advantages and disadvantages of production of genetically modified crops.
Solution
Advantages of Genetically Modified (GM) Crops:
- Pest Resistance: GM crops like Bt cotton produce their own insecticide, reducing the need for chemical pesticides and increasing crop yield.
- Enhanced Nutritional Value: Crops can be fortified with essential nutrients. For example, Golden Rice is engineered to contain beta-carotene, a precursor to Vitamin A, to combat deficiency.
- Tolerance to Abiotic Stresses: Plants can be made more resistant to environmental stresses like drought, salinity, and extreme temperatures, allowing agriculture in previously unsuitable lands.
- Reduced Post-Harvest Loss: Genetic modification can improve the shelf life of produce, reducing spoilage and waste.
- Increased Mineral Usage Efficiency: Some GM plants can absorb and use minerals from the soil more efficiently, which helps in preserving soil fertility.
Disadvantages of Genetically Modified (GM) Crops:
- Environmental Risks: There is a concern that genes from GM crops could transfer to wild relatives, creating herbicide-resistant 'superweeds'. They can also have unforeseen negative impacts on the ecosystem.
- Harm to Non-Target Organisms: The toxins produced by GM crops might harm beneficial insects (like pollinators) or other organisms in the ecosystem.
- Ethical and Social Concerns: There are ethical objections to altering the genetic makeup of living organisms. Additionally, patents on GM seeds held by large corporations can create economic dependency for farmers.
- Potential for Allergic Reactions: Introducing new genes and proteins into food sources carries a theoretical risk of creating new allergens.
Q7EXERCISES
What are Cry proteins? Name an organism that produce it. How has man exploited this protein to his benefit?
Solution
Cry Proteins: Cry proteins are a class of toxic, insecticidal crystal proteins. They are produced in an inactive form (protoxin) and become active only in the alkaline gut of certain insects.
Organism: The organism that produces Cry proteins is the soil bacterium Bacillus thuringiensis (Bt).
Exploitation by Humans: Humans have exploited this protein for agricultural benefit by creating pest-resistant genetically modified (GM) crops. The process is as follows:
- The gene that codes for the Cry protein (the cry gene) is isolated from Bacillus thuringiensis.
- Using recombinant DNA technology, this gene is incorporated into the genome of crop plants like cotton, corn, potato, and tomato.
- These transgenic plants now produce the Cry protein in their tissues.
- When a target insect pest (e.g., the cotton bollworm) feeds on the plant, it ingests the inactive Cry protein.
- The alkaline pH of the insect's gut activates the toxin, which binds to the gut wall, creates pores, and causes cell lysis, leading to the death of the insect. This has created a 'bio-pesticide' within the plant, significantly reducing crop damage and decreasing the reliance on chemical insecticides.
Q8EXERCISES
What is gene therapy? Illustrate using the example of adenosine deaminase (ADA) deficiency.
Solution
Gene Therapy: Gene therapy is a collection of methods aimed at correcting a genetic defect to treat a disease. It typically involves inserting a normal, functional gene into an individual's cells to compensate for a non-functional or missing gene.
Illustration with Adenosine Deaminase (ADA) Deficiency:
ADA deficiency is a severe immunodeficiency disorder caused by the deletion or mutation of the gene that codes for the enzyme adenosine deaminase. This enzyme is essential for the functioning of the immune system.
Gene therapy for ADA deficiency involves the following steps:
- Isolation of Cells: Lymphocytes (a type of white blood cell) are extracted from the patient's blood.
- Genetic Modification: These lymphocytes are grown in a culture outside the body. A functional ADA cDNA (complementary DNA) is then introduced into these cells using a retroviral vector. The vector acts as a vehicle to deliver the correct gene into the lymphocyte's genome.
- Reinfusion: The genetically engineered lymphocytes, which can now produce the functional ADA enzyme, are returned to the patient's bloodstream through an infusion.
This method is not a permanent cure because lymphocytes are not immortal and have a limited lifespan. Therefore, the patient requires periodic infusions of the modified cells. A permanent cure could potentially be achieved if the gene is introduced into hematopoietic stem cells from the bone marrow at an early embryonic stage.
Q9EXERCISES
Digrammatically represent the experimental steps in cloning and expressing an human gene (say the gene for growth hormone) into a bacterium like E. coli?
Solution
While a diagram cannot be drawn here, the experimental steps for cloning and expressing the human growth hormone gene in E. coli are as follows. A diagram would visually represent this process:
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Isolation of Gene and Vector:
- The human DNA is extracted from human cells, and the gene for growth hormone is isolated.
- A plasmid vector is isolated from the bacterium E. coli.
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Cutting with Restriction Enzyme:
- Both the human growth hormone gene and the plasmid DNA are cut with the same restriction enzyme. This creates complementary 'sticky ends' on both DNA fragments.
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Ligation:
- The isolated growth hormone gene is mixed with the cut plasmids. The sticky ends of the gene anneal (base-pair) with the sticky ends of the plasmid.
- The enzyme DNA ligase is added to form permanent phosphodiester bonds, creating a recombinant DNA molecule (a plasmid containing the human gene).
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Transformation:
- The recombinant plasmids are introduced into a host E. coli bacteria. This process is called transformation. The bacteria are treated to make their cell walls permeable to the plasmids.
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Selection of Transformed Cells:
- The plasmid vector also carries a selectable marker, such as a gene for antibiotic resistance.
- The bacteria are grown on a medium containing that antibiotic. Only the bacteria that have successfully taken up the recombinant plasmid will survive and multiply.
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Expression and Production:
- The selected transformed bacteria are grown in large quantities in a bioreactor under optimal conditions (temperature, pH, nutrients).
- The bacteria express the inserted human gene, synthesizing the human growth hormone protein.
-
Downstream Processing:
- The growth hormone is extracted from the bacterial culture and purified to obtain a pure product ready for therapeutic use.
Q10EXERCISES
Can you suggest a method to remove oil (hydrocarbon) from seeds based on your understanding of rDNA technology and chemistry of oil?
Solution
Yes, a method based on recombinant DNA (rDNA) technology, specifically RNA interference (RNAi), can be used to create seeds with reduced or no oil content. Oil synthesis in seeds is a metabolic pathway controlled by specific enzymes, which are encoded by genes.
The method would involve these steps:
- Identify a Key Gene: The first step is to identify a crucial gene in the oil (fatty acid) synthesis pathway of the target plant. For example, a gene coding for an essential enzyme like acetyl-CoA carboxylase.
- Create a Gene-Silencing Construct: Using rDNA technology, a DNA construct is created that will produce a double-stranded RNA (dsRNA) molecule complementary to the mRNA of the target gene. This is often done by introducing DNA that transcribes both 'sense' and 'anti-sense' RNA strands of the target gene.
- Plant Transformation: This construct is introduced into the plant's cells using a vector, such as an Agrobacterium vector. The transformed cells are then cultured to regenerate a whole transgenic plant.
- Initiation of RNAi: In the cells of the transgenic plant, the introduced DNA produces the dsRNA. This dsRNA triggers the RNAi pathway, a natural cellular defense mechanism.
- Gene Silencing: The plant's cellular machinery uses the dsRNA to identify and degrade the target mRNA molecule produced by the plant's own oil-synthesis gene.
- Result: By destroying the mRNA, the translation of the essential enzyme is blocked. Without this enzyme, the oil synthesis pathway is disrupted, and the plant produces seeds with significantly less or no oil.
Q11EXERCISES
Find out from internet what is golden rice.
Solution
Golden Rice is a variety of rice (Oryza sativa) that has been genetically engineered to biosynthesize beta-carotene, a precursor of Vitamin A, in the edible part of the grain. Normal rice does not produce beta-carotene, which is why its grains are white. The presence of beta-carotene gives Golden Rice its characteristic yellow-orange color.
The primary goal for developing Golden Rice is to address Vitamin A deficiency, a significant public health issue in many parts of the developing world where rice is a staple food. Vitamin A deficiency can lead to severe health problems, including blindness in children and a weakened immune system. By providing a source of Vitamin A in a commonly consumed food, Golden Rice is intended to be a cost-effective and sustainable way to improve nutrition and health in these populations.
Q12EXERCISES
Does our blood have proteases and nucleases?
Solution
Yes, our blood does contain both proteases and nucleases, but their activity is tightly regulated to prevent damage to the body's own tissues and essential molecules.
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Proteases: These are enzymes that digest proteins. The blood contains many proteases as part of critical systems like the blood clotting cascade (e.g., thrombin) and the complement system (part of the immune response). They typically circulate as inactive precursors (zymogens) and are activated only when and where they are needed, such as at the site of an injury.
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Nucleases: These are enzymes that break down nucleic acids (DNA and RNA). Nucleases are present in blood plasma to degrade foreign genetic material from pathogens or the nucleic acids released from the body's own dead and dying cells. This is an important cleanup and defense mechanism.
Q13EXERCISES
Consult internet and find out how to make orally active protein pharmaceutical. What is the major problem to be encountered?
Solution
Making a protein-based pharmaceutical (like insulin or growth hormone) orally active is a major challenge in drug development. Several strategies are being researched to achieve this:
Methods to make protein pharmaceuticals orally active:
- Enteric Coating: Encapsulating the protein drug in a polymer coating that resists the acidic environment of the stomach but dissolves in the alkaline pH of the small intestine. This protects the protein until it reaches the site of absorption.
- Use of Protease Inhibitors: Co-administering the protein drug with molecules that inhibit the function of digestive enzymes (proteases) in the stomach and intestine.
- Encapsulation in Nanoparticles: Enclosing the protein in tiny nanoparticles made of biodegradable polymers. These nanoparticles can protect the protein from degradation and are designed to be absorbed through the intestinal wall.
The Major Problem to be Encountered:
The primary obstacle to the oral administration of protein drugs is their degradation in the gastrointestinal (GI) tract and their poor absorption into the bloodstream.
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Degradation:
- Acidic Environment: The highly acidic condition of the stomach (low pH) denatures proteins, causing them to lose their functional three-dimensional structure.
- Enzymatic Digestion: The GI tract is filled with powerful digestive enzymes called proteases (like pepsin and trypsin) that are designed to break down proteins. These enzymes readily digest the protein drug, destroying it before it can be absorbed.
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Poor Absorption: Proteins are large and generally water-soluble molecules. This makes it extremely difficult for them to pass through the lipid-based cell membranes of the intestinal lining to enter the bloodstream.