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Sarita Aggarwal solutions for Biology [English] Class 12 ISC chapter 15 - Biotechnology: Principles and Processes [null edition]

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Sarita Aggarwal solutions for Biology [English] Class 12 ISC chapter 15 - Biotechnology: Principles and Processes - Shaalaa.com
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Solutions for Chapter 15: Biotechnology: Principles and Processes

Below listed, you can find solutions for Chapter 15 of CISCE Sarita Aggarwal for Biology [English] Class 12 ISC.


EXERCISES
EXERCISES [Pages 790 - 802]

Sarita Aggarwal solutions for Biology [English] Class 12 ISC 15 Biotechnology: Principles and Processes EXERCISES [Pages 790 - 802]

A. OBJECTIVE QUESTIONS I. Multiple choice questions Choose the correct answer:

I. 1.Page 790

Which one of the following is not required for rDNA technology?

  • DNA polymerase

  • DNA ligase

  • restriction endonuclease

  • reverse transcriptase

I. 2.Page 790

Which one of the following is not a cloning vector in genetic engineering?

  • transposons

  • plasmids

  • bacteriophages

  • protozoans

I. 3.Page 790

Gene transfer through vectors can be done by ______.

  • plasmids

  • microinjections

  • tungsten particles coated with DNA

  • electroporation

I. 4.Page 790

An animal containing a foreign gene is called a ______.

  • plasmid

  • transgenic

  • surrogate mother

  • probe

I. 5.Page 790

The role of restriction endonucleases is ______.

  • to cut DNA fragment at specific sites

  • to join DNA fragments

  • to introduce DNA into plasmid

  • none of the above

I. 6.Page 790

The function of DNA ligase is ______.

  • to break DNA into fragments

  • to seal DNA fragments

  • to introduce DNA into plasmid

  • to produce desired protein

I. 7.Page 790

Identify the plasmid.

  • EcoRI

  • pBR322

  • AIUI

  • HindIII

I. 8.Page 790

Restriction endonucleases used in recombinant rDNA technology are obtained from ______.

  • bacteriophages

  • bacterial cells

  • plasmids

  • all prokaryotic cells

I. 9.Page 790

Plasmids are ______.

  • cDNA

  • mitochondrial DNA

  • circular extrachromosomal DNA in bacteria

  • viral RNA

I. 10.Page 790

One of the key factors, which makes the plasmid the vector in genetic engineering is that ______.

  • it is resistant to antibiotics

  • it is resistant to restriction enzymes

  • its ability to carry a foreign gene

  • its ability to cause infection in host

I. 11.Page 791

Which of the following is used as a best genetic vector in plants?

  • Bacillus thuringiensis

  • Agrobacterium tumefaciens

  • Pseudomonas putida

  • All of these

I. 12.Page 791

The tumour-inducing capacity of Agrobacterium tumefaciens is located in large extrachromosomal plasmids called ______.

  • Ri plasmid

  • lambda phage

  • pBR322

  • Ti plasmid

I. 13.Page 791

The construction of the first recombinant DNA was done by using the native plasmid of ______.

  • E. coli

  • Salmonella typhimurium

  • B. thuringiensis

  • yeast

I. 14.Page 791

The linking of antibiotic resistancе gene with the plasmid vector became possible with ______.

  • DNA polymerase

  • exonuclease

  • DNA ligase

  • endonucleases

I. 15.Page 791

Gel electrophoresis is used for ______.

  • construction of recombinant DNA by joining with cloning

  • isolation of DNA molecules

  • cutting of DNA into fragments

  • separation of DNA fragments according to their size

Fill in the blanks

II. 1.Page 791

A segment of DNA or a desired gene can be cut and isolated with the help of ______ enzyme.

II. 2.Page 791

The process of making multiple identical copies of any piece of DNA is called ______ of DNA.

II. 3.Page 791

The endonuclease used by scientists Cohen and Boyer was ______.

II. 4.Page 791

Plasmid-free E. coli are treated with chemical ______ to make their membranes more permeable to insert the recombinant plasmid.

II. 5.Page 791

The sequences recognised by endonucleases are typically 4-6 nucleotides long and are ______ nucleotide sequences.

II. 6.Page 791

In the plasmid named pSC101, S and C refer to ______.

II. 7.Page 791

DNA fragments can be separated by a technique called ______.

II. 8.Page 791

______ and ______ are natural vectors for cloning of genes in plants and animals.

II. 9.Page 791

Agrobacterium contains tumourinducing plasmids called ______.

II. 10.Page 791

Electroporation produces ______ in the plasma membrane of the host cells.

III. 1.Page 791

State whether the following is true or false.

rDNA involves combining of DNA from two different organisms to generate a recombinant DNA.

III. 2.Page 791

State whether the following is true or false.

Cutting of a DNA fragment is done with the help of enzyme DNA ligase.

III. 3.Page 791

State whether the following is true or false.

Cohen and Boyer used a restriction endonuclease which was obtained from bacteria Agrobacterium.

III. 4.Page 791

State whether the following is true or false.

Plasmid DNA acts as vector as it can transfer the piece of desired DNA to the host cell.

III. 5.Page 791

State whether the following is true or false.

EcoRI is the name of a plasmid obtained from bacteria E. coli.

III. 6.Page 791

State whether the following is true or false.

The sequences recognised by restriction endonucleases are palindrome nucleotide sequences.

III. 7.Page 791

State whether the following is true or false.

Chitinases are used to break open the fungal cells.

III. 8.Page 791

State whether the following is true or false.

DNA fragments being positively charged move towards the negative electrode during electrophoresis.

III. 9.Page 791

Annealing means amplification of genes.

III. 10.Page 791

State whether the following is true or false.

A bioreactor has an agitator and an oxygen delivery system along with pH control.

IV.Page 792

Match the following.

Column I Column II
1. Restriction endonuclease (a) Joining DNA fragments together
2. DNA ligase (b) Movement of DNA fragments towards anode
3. Electrophoresis (c) Production of desired gene product on large scale
4. Electroporation (d) Cutting a DNA fragment from plasmid
5. Bioreactor (e) Treatment of cells with CaCl2
V. 1.Page 792

Answer the following in one or two words.

A technique in which microparticles of gold or tungsten coated with foreign DNA are bombarded into target host cells.

V. 2.Page 792

Answer the following in one or two words.

Scientific name of the organism whose plasmid was used by Cohen and Boyer.

V. 3.Page 792

Answer the following in one or two words.

A plant pathogenic bacteria that is known as natural genetic 'engineer' as it can transfer part of its plasmid into the host plant.

V. 4.Page 792

Answer the following in one or two words.

A technique to make multiple copies of desired gene by using DNA polymerase.

V. 5.Page 792

Answer the following in one or two words.

A large vessel in which the large amount of culture can be processed and gene products can be produced on a large scale.

In the questions given below, there are two statements marked as Assertion (A) and Reason (R). Read the statements and choose the correct option

VI. 1.Page 792

Assertion (A): Restriction enzymes cut the strand of DNA to produce sticky ends.

Reason (R): Stickiness of the ends facilitates the action of the enzyme DNA polymerase.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 2.Page 792

Assertion (A): Plasmids are extrachromosomal DNA.

Reason (R): Plasmids are found in bacteria and are useful in genetic engineering.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 3.Page 792

Assertion (A): Plasmids are single-stranded extra chromosomal DNA.

Reason (R): Plasmids are usually present in eukaryotic cells.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 4.Page 792

Assertion(A): Restriction endonucleases function by 'inspecting' the length of a DNA sequence to find the specific recognition sequence.

Reason (R): The sequences recognised by endonucleases are typically 4-6 nucleotides long and are palindromes, also called palindromic nucleotide sequences.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 5.Page 792

Assertion (A): E. coli having pBR322 with DNA insert at BamHI site cannot grow in medium containing tetracycline.

Reason (R): Recognition site for BamHI is present in tetr region of pBR322.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 6.Page 792

Assertion (A): For amplification of gene, DNA polymerase is used to copy the identified gene by polymerase chain reaction.

Reason (R): Amplification of a gene can be done by inserting it into a bacterium and allowing a bacterium to undergo repeated cell divisions.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 7.Page 792

Assertion (A): Ori is a sequence from where replication starts.

Reason (R): A prokaryotic DNA has a single origin of replication.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 8.Page 793

Assertion (A): Electroporation makes a bacterial cell a competent host to take up DNA.

Reason (R): This technique induces temporary pores in the plasma membrane of the host cell to facilitate entry of foreign DNA.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 9.Page 793

Assertion (A): Agrobacterium tumefaciens is commonly used in genetic engineering because this bacterium is associated with roots of all cereals and pulse crops.

Reason (R): A gene incorporated in the bacterial chromosomal genome gets automatically transferred to the crop with which the bacterium is associated.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VI. 10.Page 793

Assertion (A): In a bioreactor, the desired gene products are biologically converted into specific products like proteins and enzymes.

Reason (R): A bioreactor provides the optimal growth conditions like temperature, pH, salts, vitamins and oxygen.

  • Both assertion (A) and reason (R) are true, and reason is the correct explanation of assertion.

  • Both assertion (A) and reason (R) are true, but reason is not the correct explanation of assertion.

  • Assertion (A) is true but reason (R) is false.

  • Both assertion (A) and reason (R) are false.

VII. A.Page 793

Read the sources given and answer any four from the questions given below:

A plasmid is a small, extrachromosomal DNA molecule within a cell that is physically separated and distinct from chromosomal DNA and can replicate independently. They are most commonly found as small circular, double-stranded DNA molecules.

Plasmids naturally exist in all bacterial cells but can be seen in some archaebacteria and eukaryotes. Often, the genes carried in plasmids provide bacteria with genetic advantages, such as antibiotic resistance.

The most commonly used cloning vectors are E. coli plasmids which include three functional regions: (1) an origin of replication (Ori), (2) a drug-resistance gene and (3) a region where DNA can be inserted without interfering with plasmid replication or expression of the drug-resistance gene. The replication origin (Ori) is a specific DNA sequence of 50-100 base pairs that must be present in a plasmid for it to replicate

  1. Where are plasmids in bacteria located?
    1. inside the nucleus of bacteria
    2. outside the nuclear matter of bacteria
    3. as a part of chromosomal segment of bacteria
    4. on the surface of bacteria
  2. How many origins of replication are present in a bacterial plasmid
    1. one
    2. two
    3. three
    4. many
  3. Most bacterial plasmids have the following structure.
    1. large circular DNA molecule
    2. small circular DNA molecule
    3. large circular RNA molecule
    4. linear DNA molecule
  4. Most commonly used cloning vector E. coli plasmid has the following functional regions.
    1. a drug resistance gene
    2. a region where DNA can be inserted
    3. both (a) and (b)
    4. Ori having specific RNA sequence
  5. Plasmids can be seen in
    1. all bacteria
    2. all eukaryotes
    3. all viruses
    4. both (a) and (b)
VII. B.Page 793

Read the sources given and answer any four from the questions given below:

Restriction endonucleases are enzymes that are produced by bacteria and cut the double-stranded DNA molecule at specific recognition sequences known as restriction sites. The sequences recognised by endonucleases are typically 4–6 nucleotides long and are palindromes called palindromic nucleotide sequences. A palindrome is a base sequence that reads the same on two strands but in the opposite direction, for example, 5' GAATТС 3', 3' СТТАAG 5'.

After cleavage, each DNA strand has a little single-stranded hanging portion at the end. These are called sticky ends. When cut by the same restriction enzyme, the resultant DNA fragments have the same kind of sticky ends which can be joined together by DNA ligases.

  1. The function of restriction endonuclease is to
    1. cut RNA at specific restriction sites
    2. cut DNA at specific recognition sequences
    3. form rDNA
    4. cut double-stranded RNA
  2. Which of the following sequence is a palindrome?
    1. 5' GAATTC 3', 3' GAATTC 5'
    2. 5' CCATGG 3', 3' GGTACC 5'
    3. 5'AAGCTT 3', 3' GAATTC 5'
    4. 5' GGATCC 3', 5' CCAAGG 3'
  3. The overhanging parts of two strands of DNA of cut DNA
    1. are called sticky ends
    2. have single strands of RNA
    3. are of no use for rDNA
    4. are cut and deleted from DNA
  4. Function of DNA ligase is to
    1. cut and join DNA
    2. form sticky ends
    3. join fragments of DNA
    4. recognise restriction sites
  5. Restriction endonucleases are present in the following
    1. eukaryotes
    2. bacteria
    3. humans
    4. higher plants
VII. C.Page 794

Read the sources given and answer any four from the questions given below:

Agrobacterium tumefaciens is a plant pathogenic bacterium that can naturally transfer part of its plasmid DNA as it infects the host plant. The bacterium Agrobacterium contains large tumourinducing plasmids, Ti-plasmids and passes on this tumour-causing gene into the genome of the host plant. The host plant could be any dicotyledonous plant. Ti-plasmids are used as gene vectors to transfer foreign genes into target host cells.

Vector-less methods involvethe transfer of gene, i.e., rDNA containing foreign gene by a direct method without any vector. These can be done by electroporation, microinjection and biolistic guns. In electroporation, temporary holes are produced in the plasma membrane of the host cell to facilitate the entry of foreign DNA. This is done by treating the bacterial cells with specific concentration of divalent cations like CaCl2. In microinjection foreign genes (rDNA) are introduced directly into the nucleus of plant or animal cells by using micropipettes. By using biolistic or gene particle gun, the microparticles of gold or tungsten particles coated with foreign DNA are bombarded into the target host cells with high velocity.

  1. Agrobacterium is used as a vector because it
    1. infects dicot plants
    2. contains plasmid
    3. is easily available bacteria
    4. can transfer foreign gene into target host cell
  2. Which of the following statements are true for T1 plasmid?
    1. has a tumour-causing gene
    2. has foreign gene
    3. used in electroporation technique
    4. contains chromosomal DNA of bacteria
  3. Microparticles of gold coated with rDNA are used in the following technique:
    1. electroporation
    2. biolistic gun
    3. microinjection
    4. T1 plasmid
  4. What is done in the electroporation technique?
    1. Cells are treated with divalent cations
    2. Temporary holes are created in the plasma membrane
    3. both (a) and (b)
    4. plasmids are used
  5. rDNA are introduced directly into the nucleus of a plant by fine pipettes in the following technique:
    1. Agrobacterium
    2. microinjection
    3. electroporation
    4. gene particle gun

B. SUBJECTIVE QUESTIONS Very short answer type questions (1 mark)

I. 1.Page 796

Name the enzyme used to cut a segment of DNA in rDNA technology.

I. 2.Page 796

What is another term given for a genetically modified organism?

I. 3.Page 796

What is the work of DNA Ligase?

I. 4.Page 796

Which enzyme is used to isolate a desired gene?

I. 5.Page 796

What is the extra-chromosomal circular DNA in bacteria called as?

I. 6.Page 796

What is the role of a plasmid in rDNA technology?

I. 7.Page 796

Name the enzymes involved in rDNA technology.

I. 8.Page 796

Which enzyme is used to insert, isolate gene into the plasmid?

I. 9.Page 796

Which mechanism helps in insertion of plasmid into bacteria E. coli?

I. 10.Page 796

Name a few cloning vectors.

I. 11.Page 796

What is the term used for the pairs of sequence of nucleotide that read the same on two strands of DNA in their 5'-3' direction?

I. 12.Page 796

What is the meaning of sticky ends?

I. 13.Page 796

Name the bacteria which is a natural vector and transfers its Ti plasmid to the plant cells to produce cancerous cells.

I. 14.Page 796

Name a few vector less or direct methods of gene transfer.

I. 15.Page 796

Scientific term for a foreign gene that is inserted in rDNA.

Short answer type questions (2 marks)

II. 1.Page 797

What is recombinant DNA?

II. 2.Page 797

Give the basic tools required for the formation of rDNА.

II. 3.Page 797

Name important enzymes essential for rDNA technology.

II. 4.Page 797

What is a cloning vector?

II. 5.Page 797

Name a few cloning vectors used in rDNA technology.

II. 6.Page 797

What is the role of restriction endonuclease?

II. 7.Page 797

Name two important enzymes used in the formation of recombinant DNA.

II. 8.Page 797

Study the linking of DNA fragments shown below.

(i) Name 'a' DNA and 'b' DNA.

(ii) Name the restriction enzyme that recognises this palindrome.

(iii) Name the enzyme that can link these two DNA fragments.

II. 9. (i) (a)Page 797

What are ‘molecular scissors’?

I. 9. (i) (b)Page 797

Give one example of 'molecular scissors'.

II. 9. (ii)Page 797

Explain 'molecular scissors' role in recombinant DNA technology.

II. 10.Page 797

Why is Agrobacterium tumefaciens a good cloning vector? Explain.

II. 11.Page 797

DNA being hydrophilic cannot pass through the cell membranes of a host cell. Explain how does recombinant DNA get introduced into the host cell to transform the latter.

II. 12. (i)Page 797

Mention the role of vectors in recombinant DNA technology.

II. 12. (ii)Page 797

Give any two examples of vectors in recombinant DNA technology.

II. 13.Page 797

With the help of diagrammatic representation only, show the steps of recombinant DNA technology.

Short answer type questions (3 marks)

III. 1.Page 797

What are the two basic steps in rDNA technology? Name the enzymes involved in these steps.

III. 2. (i)Page 797

Explain the following steps in rDNA technology.

Isolation of desired gene

III. 2. (ii)Page 797

Explain the following steps in rDNA technology.

Role of plasmid

III. 2. (iii)Page 797

Explain the following steps in rDNA technology.

Cloning of gene

III. 3. (i)Page 797

Give the role of following enzyme in formation of transgenic cell.

Restriction endonuclease

III. 3. (ii)Page 797

Give the role of following enzyme in formation of transgenic cell.

DNA ligase

III. 3. (iii)Page 797

Give the role of following enzyme in formation of transgenic cell.

DNA polymerase

III. 4.Page 797

How do restriction endonucleases cut DNA? Explain with one example.

III. 5. (i)Page 797

How is a plasmid named?

III. 5. (ii)Page 797

Give one example of plasmid.

III. 5. (iii)Page 797

What is EcoRI?

III. 5. (iv)Page 797

What does the name EcoRI signify?

III. 6. (i)Page 797

What is the significance of Ori?

III. 6. (ii)Page 797

What is the significance of selectable marker?

III. 6. (iii)Page 797

What is the significance of cloning site in rDNA technology?

III. 7. (i)Page 797

What is the meaning of indirect method of gene transfer?

III. 7. (ii)Page 797

Give one example of indirect method of gene transfer.

III. 7. (iii)Page 797

List some direct methods also.

III. 8.Page 797

How can the product of a gene be obtained at a large scale? What is its significance?

III. 9. (i)Page 797

What is the need for a downstream processing?

III. 9. (ii)Page 797

Give basic important systems present in a bioreactor.

III. 10.Page 797

List various steps in the process of recombinant DNA technology.

III. 10. (i)Page 797

Explain amplification.

III. 10. (ii)Page 797

Explain annealing.

IV. 1.Page 797

Distinguish between plasmid DNA and chromosomal DNA.

IV. 2.Page 797

Distinguish between exonuclease and endonuclease.

IV. 3.Page 797

Differentiate between the following:

DNA ligase and DNA polymerase

IV. 4.Page 797

Differentiate between the following:

Normal cell and a Transgenic cell

IV. 5.Page 797

Differentiate between the following:

Indirect and Direct methods of gene transfer

Long answer type questions (5 marks)

V. 1.Page 798

Give the tools needed for genetic engineering.

V. 2.Page 798

Explain various steps involved in rDNA technique.

V. 3.Page 798

What are the various ways by which the desired genes can be transferred?

V. 4.Page 798

Explain the contribution of Thermus aquaticus in the amplification of a gene of interest.

V. 5.Page 798

Name and explain the techniques used in the separation and isolation of DNA fragments to be used in recombinant DNA technology.

V. 6.Page 798

Plasmid is a boon to biotechnology. Justify this statement quoting the production of human insulin as an example.

V. 7.Page 798

(a) Identify the selectable markers in the diagram of E. coli vector shown above.

(b) How is the coding sequence of beta-galactosidase considered a better marker than the ones identified by you in the diagram? Explain.

E. BOARD QUESTIONS 1 mark

1.Page 802

Give a reason for the following:

DNA cannot enter directly into the host cell.

2 marks

2.Page 802

Write a short note on Electrophoresis.

3 marks

1. (i)Page 802

What is a bioreactor?

1. (ii)Page 802

Explain important features of a stirred tank bioreactor.

2.Page 802

Name and explain the technique used for separating DNA fragments and making them available for biotechnology experiments.

5 marks

1.Page 802

Explain the various steps involved in recombinant DNA technology.

2. (i)Page 802

What are the restriction endonucleases? Give the rules of their nomenclature.

2. (ii)Page 802

Explain the mechanism of action of restriction endonucleases that makes them suitable for genetic engineering.

3. (i)Page 802

Explain what are the desirable characteristics of an ideal cloning vector used in rDNA technology.

3. (ii)Page 802

Describe two vectors less methods of gene transfer used in rDNA technology.

4. (i)Page 802

What does PCR stand for?

4. (ii)Page 802

Describe the steps of PCR technique.

Solutions for 15: Biotechnology: Principles and Processes

EXERCISES
Sarita Aggarwal solutions for Biology [English] Class 12 ISC chapter 15 - Biotechnology: Principles and Processes - Shaalaa.com

Sarita Aggarwal solutions for Biology [English] Class 12 ISC chapter 15 - Biotechnology: Principles and Processes

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