CBSE Class 12 Biotechnology Previous Year Question Paper 2014 Compartment Outside Delhi Set-1

Question Papers Class 12 PDF

This is the CBSE Class 12 Biotechnology Previous Year Question Paper for the 2014 Compartment examination, Outside Delhi, Set-1. The paper is divided into four sections: A, B, C, and D. It includes very short answer questions (1 mark each), short answer questions (2 and 3 marks each), and long answer questions (5 marks each). While there is no overall choice, internal choices are provided in some questions of 3 and 5 marks, requiring students to attempt only one option. Calculators are not permitted, but log tables may be used if necessary. Solving this board question paper helps students familiarize themselves with the exam structure, question types, and marking scheme, which is crucial for effective preparation and achieving better results in their board exams.

Quick info

BoardCBSE
Class12
SubjectBiotechnology
Session2014
LanguageEnglish
TypePrevious Year Question Paper
Exam typeBoard Exam

Paper pattern

The question paper contains four sections (A, B, C, D) with questions ranging from 1 to 5 marks. Internal choices are provided in some 3-mark and 5-mark questions.

Topics covered

Paper topics

  • Fruit ripening gene mutation
  • DNA sequencing
  • Crop yield improvement
  • Microbial cell culture
  • Antibiotic downstream processing
  • Restriction mapping
  • DNA fragment size
  • SDS and protein structure
  • Molecular mass determination
  • Database retrieval tools
  • E. coli growth rate
  • Generation time
  • Monoclonal antibodies
  • Hybridoma technology
  • Therapeutic monoclonal antibodies
  • Sanger's dideoxy method
  • Protein separation
  • Isoelectric point (pI)
  • Genome vs Proteome

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Question paper text

Question Paper 2014 Comp. Outside Delhi set 1 CBSE Class 12 Biotechnology

General Instructions:

All questions are compulsory.

There is no overall choice. However, an internal choice has been provided in one question of three marks and two questions of five marks. You have

to attempt only one of the choices in such questions. Question paper contains four sections ¾ A, B, C and D.

Questions No. 1 to 5 are very short answer questions, carrying 1 mark each.

Questions No. 6 to 15 are short answer questions, carrying 2 marks each.

Questions No. 16 to 25 are also short answer questions, carrying 3 marks each.

Questions No. 26 to 28 are long answer questions, carrying 5 marks each.

  • Use of calculators is not permitted. However, you may use log tables, if necessary.

SECTION A

  1. If the genes involved in fruit ripening are selectively mutated, what commercial importance can this serve?
  2. Is it necessary to use a thermostable form of DNA polymerase in dideoxy DNA sequencing? Why or why not?
  3. Environmentalists advocate the disuse of chemical insecticides. Suggest an alternative way to improve crop yields.
  4. Why is strain preservation important in microbial cell culture?
  5. Two laboratories have developed a procedure for downstream processing of an antibiotic. The major difference lies in the number of steps involved. Which one would you prefer and why?

SECTION B

1/4

6.Restriction mapping of a linear piece of DNA reveals the following EcoRI restriction sites:

EcoRI site 1 EcoRI site 2

<math>0 \text{ kb}</math> <math>1 \mathrm{\,kb}</math> <math>2 \, \mathrm{kb}</math> <math>3 \text{ kb}</math> 4 kb <math>6 \text{ kb}</math> <math>5 \text{ kb}</math>

  1. This piece of DNA is cut by EcoRI, the resulting fragments are separated by gel

electrophoresis and the gel is stained. What is the size of the fragments obtained?

  1. If a 1000 bp of DNA were inserted between the two restriction sites, what will be the size of fragments when step (a) is repeated?
  1. What is the effect of SDS on protein structure? How does it facilitate the determination of molecular mass?
  2. Name two database retrieval tools. What is their purpose?
  3. In a culture of E. coli, the cell population increases from <math>2.0 \times 10^6</math> cells/ml

to <math>16 \times 10^6</math> cells/ml in 30 minutes. What is the generation time of the given culture?

  1. Why is the technique for the production of monoclonal antibodies called hybridoma technology? Give an example of a therapeutic monoclonal antibody for breast cancer patients.
  2. If Sanger's dideoxy method shows that the template strand sequence is: 5' – TGCAATGCC – 3' sketch the gel pattern that would lead to this conclusion.
  1. You have been provided with a mixture of proteins (A, B, C and D) in a buffer of pH 6.5.

Protein A has a pI of 5.0 and all other proteins have a pI <math>></math> 7.0. Based on this information, how will you separate protein A from the mixture? Indicate the principle involved also.

  1. A scientist determines the complete genome and proteome of a liver cell and a muscle cell

from the same person. Would you expect bigger differences in the genome or proteome of 2/4

Frequently asked questions

What is this document?

This is the CBSE Class 12 Biotechnology Previous Year Question Paper from the 2014 Compartment examination, Outside Delhi, Set-1.

What is the structure of the Biotechnology 2014 Compartment paper?

The paper has four sections (A, B, C, D) with questions carrying 1, 2, 3, and 5 marks. Internal choices are available in some questions.

Can I use a calculator for this paper?

No, the use of calculators is not permitted. However, you may use log tables if necessary.

How does solving previous year papers help?

Solving previous year question papers helps students understand the board exam pattern, question types, and marking scheme, leading to better preparation and improved scores.

What is the importance of this paper for Class 12 Biotechnology students?

This paper provides essential practice for the CBSE Class 12 Biotechnology board exam, allowing students to test their knowledge and refine their exam-taking strategies.

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