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1800-102-2727Chapter 11 of the NCERT Class 12 Biology textbook, Biotechnology: Principles and Processes, introduces students to the fascinating world of biotechnology. It focuses on the fundamental principles and techniques that form the foundation of this field. This chapter covers key concepts such as genetic engineering, recombinant DNA technology, and how these methods are applied to manipulate and alter organisms at the molecular level. Students will learn about the processes involved in isolating genes, cloning, and how specific enzymes like restriction endonucleases and DNA ligases are used in these techniques. It also explains the creation of genetically modified organisms (GMOs) and how they can be applied in agriculture, medicine, and research.
The NCERT solutions for this chapter offer a step-by-step explanation of the exercises, ensuring a clear understanding of complex topics. These solutions help clarify doubts and reinforce learning, making it easier for students to grasp the subject. By practicing these solutions, students can develop a deeper insight into the workings of biotechnology and perform better in exams. This chapter is not only critical for academic success but also lays the foundation for those interested in pursuing careers in genetic research, molecular biology, or bioengineering.
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Q2. 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:
The following chart shows the action of the restriction enzyme EcoRI, the substrate DNA on which it acts and the site where it cuts
Q4. What would be the molar concentration of human DNA in a human cell? Consult Your Teacher.
Answer:
The molar concentration of DNA in human cells will be the total no. of chromosomes multiplied by 10 23 . Hence, the molar concentration DNA in each diploid cell in humans is 2.77 × 10 23 moles.
Q5. Do eukaryotic cells have restriction endonucleases? Justify your answer.
Answer:
No, eukaryotic cells do not possess restriction enzymes. All the restriction endonucleases have been developed and isolated from different strains of bacteria. The bacteria possess these restriction endonucleases as a defence mechanism to restrict the growth of viruses. Their own DNA remains safe from these enzymes because it is methylated. The eukaryotic cell has RNA interference and institutes defense mechanisms against foreign DNA. Thus, eukaryotic cells do not have restriction endonuclease.
Q6. Besides better aeration and mixing properties, what other advantages do stirred tank bioreactors have over shake flasks?Answer:
The advantages of stirred tank bioreactors over shake flasks are as follows:
1. Stirred tank bioreactors are utilised for large-scale production of biotechnological products,unlike the shake flask method which is used for small-scale production of products.
2. In a stirred tank bioreactor, a small sample can be taken out for testing.
3. Stirred tank bioreactors have foam breakers to control the foam.
4.Stirred tank bioreactors have temperature and pH control systems.
Q7. Collect 5 examples of palindromic DNA sequences by consulting your teacher. Better try to create a palindromic sequence by following the base-pair rule.
Answer:
Palindromic sequences in the DNA molecule refer to groups of bases forming the same sequence when read either backwardly or forwardly. The recognition sites of restriction endonucleases are palindromic sequences. Five examples of palindromic DNA sequences are given below;
1.ACTAGT/TGATCA
2.AAGCTT/TTCGAA
3.GGATCC/CCTAGG
4.AGGCCT/TCCGGA
5.ACGCGT/TGCGCA
Q8. Can you recall meiosis and indicate at what stage a recombinant DNA is made?
Answer:
In meiosis,during the pachytene stage of Prophase I, crossing-over takes place and recombinant DNA is formed by combining portions of male and female DNA.
Q9. Can you think about how a reporter enzyme can be used to monitor transformation of host cells by foreign DNA in addition to a selectable marker?
Answer:
In recombinant DNA technology selection of transformed and non transformed cells can be done using reporter genes that encode for reporter enzymes. During the RDT experiment, the foreign gene is joined with a reporter gene. The reporter gene should be such that it produces visible expression. For example, the Lac Z gene which codes for enzyme beta-galactosidase is used as a reporter gene. The activity of this gene is not found in transformed cells as the product formed by its catalyzation is not formed in transformed cells and bacterial colonies appear white. In non-transformed cells, this gene shows its activity and the catalysed product is formed, as a result of this, bacterial colonies appear blue. Thus, reporter enzymes can be used to monitor the transformation of host cells by foreign DNA in addition to a selectable marker.
Q10. Describe briefly the following:
(a) Origin of replication
Answer:
Origin of replication- This refers to the DNA sequence, from where replication of DNA starts. By linking a DNA sequence with the origin of replication, it can be allowed to replicate in the host cells. Origin of replication also controls the copy number of linked DNA sequences.
(b) Bioreactor
Answer:
Bioreactors - These are large vessels (100-1000 litres) that are used for large-scale production of biotechnological products such as proteins, enzymes etc. from raw materials. In a bioreactor, optimum conditions such as temperature, pH, vitamins, oxygen, salts etc. re m int ined. Stirred bioreactors are the most commonly used bioreactors. Stirred bioreactors can be simple stirred tank bioreactors or sparged tank bioreactors.
(c) Downstream processing:
Downstream processing- The process of separation and purification of biotechnological products is called downstream processing. The processes in downstream processing vary depending on the quality of the product. Before the release of the product, it undergoes clinical trials and quality control testing.
Q11. Explain briefly :
(a) PCR
Answer:
Polymerase Chain Reaction (PCR)- The molecular technique to amplify a gene and obtain its several copies is referred to as PCR. The process of PCR has certain requirements i.e. a thermostable enzyme called Taq polymerase ( obtained from Thermus aquaticus ), primers ( short stretches of DNA ), dNTPs, a template strand etc. The process of PCR takes place in these steps.
1.Denaturation- The double- stranded DNA helix is opened up by breaking their H-bonds at high temperature.
2.Annealing- The primers are allowed to hybridise to complementary regions of DNA.This step takes place at 45-55 C temperature.
3.Extension- The primers are extended with the help of Taq polymerase enzyme and the cycle is repeated several times to obtain the desired number of copies.
(b) Restriction enzymes and DNA
Answer:
Restriction enzymes and DNA- Restriction enzymes are those enzymes which cut DNA at particular places. Restriction enzyme first scans the DNA template and looks for its recognition site. Once it finds the recognition site, it binds at that region of DNA and cuts each of the two strands in their sugar-phosphate backbone.The sites at which restriction enzymes cut DNA are called as recognition sites of DNA. These are palindromic sequences i.e. they read similarly from the backward and forward direction.
(c) Chitinase:
Answer:
Chitinase - The enzyme that catalyses the breakdown of chitin polysaccharide which is usually found in the cell wall of fungi. Chitinase is mainly used during DNA isolation from fungi.
Q12. Discuss with your teacher and find out.How to distinguish between
(a) Plasmid DNA and Chromosomal DNA
Answer:
The differences between plasmid DNA and chromosomal DNA are as follows:
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(b) RNA and DNA
Answer:
The differences between RNA and DNA are as follows:
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(c) Exonuclease and Endonuclease
Answer:
The differences between exonuclease and endonuclease are as follows:
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Q1. What is biotechnology in Class 12 Biology Chapter 11?
Answer: Biotechnology refers to the use of biological processes, organisms, or systems to manufacture products intended to improve human life. In Class 12 Biology Chapter 11, it focuses on the principles and processes involved in genetic engineering and molecular biotechnology.
Q2. What are the main techniques discussed in Biotechnology Principles and Processes?
Answer: The main techniques include recombinant DNA technology, gene cloning, the use of restriction enzymes, and the process of creating genetically modified organisms (GMOs).
Q3. What are the key enzymes used in genetic engineering?
Answer: Key enzymes include restriction endonucleases, which cut DNA at specific sites, and DNA ligase, which joins DNA fragments together.
Q4. What is the role of NCERT solutions for Chapter 11?
Answer: NCERT solutions provide clear, step-by-step explanations for the chapter's exercises, helping students understand difficult concepts and prepare effectively for exams.
Q5. How does Chapter 11 of Class 12 Biology help in exam preparation?
Answer: This chapter is crucial for understanding the principles of biotechnology, which frequently appear in board exams and competitive exams like NEET, making it essential for thorough preparation.
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