Biotechnology And Its Applications MCQs With Answers – Part 2 (Class 12 Biology)
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Biotechnology and its Applications MCQs with Answers – Part 2 (Class 12 Biology)

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111. Crop P controls a susceptible insect by expressing a Bt toxin, while transgenic tobacco Q resists Meloidogyne incognita by producing complementary RNA related to a nematode gene. The most important mechanistic distinction is that:
ⓐ. both systems depend on identical pore-forming proteins
ⓑ. both systems silence parasite mRNA through complementary dsRNA formed inside susceptible insect cells
ⓒ. Bt resistance requires Agrobacterium to remain permanently inside the pest
ⓓ. Bt acts through an insecticidal protein, whereas RNAi acts through sequence-specific gene silencing
112. Two groups of tobacco cells are transformed. Group P receives the complete nematode-specific construct through Agrobacterium and later produces the expected complementary transcripts. In Group Q, transfer of the construct fails completely. After regeneration and nematode challenge, protection is seen only in plants from P. The result most strongly supports the conclusion that:
ⓐ. Agrobacterium must survive permanently in the mature tobacco plant to kill nematodes
ⓑ. nematode infection itself automatically creates the engineered RNAi construct
ⓒ. successful introduction of the nematode-specific sequences is required to establish this transgenic RNAi protection
ⓓ. failure of transformation converts the tobacco plant into a Bt crop
113. Assess the statements below comparing Bt-mediated resistance with RNAi-mediated resistance. I. Bt resistance can involve a bacterial toxin protein expressed by a crop. II. RNAi resistance depends on sequence complementarity to a target mRNA. III. Bt toxin action and RNAi both protect plants through exactly the same molecular pathway. IV. RNAi against Meloidogyne incognita can interfere with parasite survival without using the Bt pore-forming mechanism. Which combination is valid?
ⓐ. I, II and IV only
ⓑ. I and III only
ⓒ. II, III and IV only
ⓓ. I, II and III only
114. A biotechnology company needs a therapeutic molecule in quantities much larger than can be obtained conveniently from its natural source. Which advantage of recombinant DNA technology is most relevant?
ⓐ. It converts every therapeutic molecule into an antibiotic
ⓑ. It enables large-scale production of selected therapeutic products
ⓒ. It eliminates all downstream purification requirements
ⓓ. It restricts therapeutic production to animal tissues
115. Four statements are given below about recombinant therapeutics. I. Recombinant DNA technology can support large-scale production of therapeutic molecules. II. Recombinant products may provide therapeutics compatible with human use. III. Recombinant production guarantees that purification is unnecessary. IV. Recombinant therapeutics can form an important application of medical biotechnology. Which combination is valid?
ⓐ. I and III only
ⓑ. II and III only
ⓒ. I, III and IV only
ⓓ. I, II and IV only
116. A therapeutic protein isolated from a non-human source causes unwanted immune reactions in some patients. A recombinant form corresponding closely to the human protein is introduced instead. The most direct expected advantage is:
ⓐ. reduced likelihood of reactions caused by recognition of a foreign protein
ⓑ. conversion of the therapeutic protein into a carbohydrate
ⓒ. complete removal of the need for dosage control
ⓓ. automatic correction of the patient's defective gene
117. Patient P receives a therapeutic protein purified from a non-human animal source and develops a foreign-protein reaction. Patient Q receives a recombinant human-compatible form with the same therapeutic function and shows no such reaction. The comparison most strongly supports the conclusion that:
ⓐ. all non-human proteins are completely inactive in humans
ⓑ. recombinant therapeutics work only by altering patient DNA
ⓒ. human-compatible recombinant products can reduce some immunological problems associated with non-human preparations
ⓓ. recombinant proteins cannot be recognised by the immune system under any condition
118. The following values are given as historical reference data for recombinant therapeutics.
ContextApproximate number stated
Approved worldwide for human use\(30\)
Marketed in India\(12\)
Which interpretation is most appropriate?
ⓐ. The values prove the current global pharmaceutical totals today
ⓑ. The values imply that exactly \(18\) therapeutics were permanently unavailable in India
ⓒ. The values should be treated as historical reference figures rather than a present-day market census
ⓓ. The values show that recombinant therapeutics are no longer used
119. A student reads that about \(30\) recombinant therapeutics were approved worldwide and \(12\) were marketed in India in the historical reference. Which use of these numbers is scientifically appropriate?
ⓐ. Use them as contextual evidence that recombinant therapeutics had reached practical medical use
ⓑ. Treat them as permanent values that cannot change over time
ⓒ. Infer that every approved product was identical in function
ⓓ. Conclude that only \(12\) recombinant therapeutics can ever be marketed in India under any circumstances
120. Before recombinant human insulin became available, insulin used for treatment was commonly obtained from:
ⓐ. plant meristems and fungal cultures
ⓑ. transgenic tobacco roots
ⓒ. human lymphocyte cultures
ⓓ. pancreas of cattle and pigs
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