Microbes found to be very useful in genetic engineering are:
Escherichia coli and Agrobacterium tumefaciens
Vibrio cholerae and a tailed bacteriophage
Diplococcus sp. and Pseudomonas sp.
Crown gall bacterium and Caenorhabditis elegans
Restriction endonuclease :
cuts the DNA molecule-randomly
cuts the DNA molecule at specific sites
restricts the synthesis of DNA inside the nucleus,
synthesizes DNA
Which of these are most widely used in genetic engineering?
Plastid
Plasmid
Mitochondrion
Ribosome
Which of the following is a cloning vector?
DNA of Salmonella typhimurium
Ti plasmid
Amp' and Tet' loci
Ori minus PBR322
Which of the following is a palindromic sequence?
3'-CGAATG-5'
3'-GCATAC-5'
3'-CTTAAG-5'
5'-CGTATG-3'
5'-CGAATG-3'
5'-GAATTC-3'
5'-GACTAC-3'
How are transformants selected from nontransformants?
Presence of more than one recognition site in the vector DNA.
Presence of alien DNA into the vector DNA results into insertional inactivation of selectable marker.
Antibiotic resistance gene gets inactivated due to insertion of alien DNA.
Both 2 and 3.
Which of the following is not a characteristic of pBR322 vector?
It is the first artificial cloning vector constructed in 1977 by Boliver and Rodriguez.
It is the most widely used, versatile and easily manipulated vector.
It has two antibiotic resistance genes, tetR and ampR.
It does not have restriction site for Sal I.
Select the correct order of processing of PCR.
Extension, primer annealing, denaturation
Denaturation, primer annealing, extension
Denaturation, extension, primer annealing
Primer annealing, denaturation, extension
Plasmid vector in DNA recombinant technology means
a virus that transfers gene to bacteria
extra-chromosomal autonomously replicating circular DNA
sticky end of DNA
any fragment of DNA carrying desirable gene
Which organism is used to transfer T-DNA?
Streplomyces hygroscopicus
Agrobacterium tumefaciens
Salmonella typhi
Escherichia coli
Match the following column I with column II.
Column I Column II
A. Agrostology 1. Earth
B. Smallest flowering plant 2. Genetic engineering
C. Tectonic 3.Migration
D. Ecesis 4.Wolffia
E. Euphanix 5.Grass
Codes
A B C D E
(c) 2 3 1 5 4
(d) 5 4 3 2 1
(b) 1 2 3 4 5
(a) 5 4 1 3 2
Biolistic (gene gun) is suitable for
disarming pathogen vectors
transformation of plant cell
constructing recombinant DNA by joining with vectors
DNA fingerprinting
A mixture containing DNA fragments, a, b, c and d, with molecular weights of a+b = c, a > b and d>c, was subjected to agarose gel electrophoresis. The positions of these fragments from anode to cathode sides of the gel would be
b, a, c, d
a, b, c, d
c, b, a, d
b, a, d, c
Which of the following DNA sequences qualifies to be designated as a palindrome?
5 - GACCAG - 3’ in one strand
3’- GACCAG - 5’ in one strand
5’- GACGAG- 3’ 3’- CTGGTC - 5’
5’- AGCGCT - 3’ 3’- TCGCGA - 5’
The source of taq polymerase used in PCR is a
thermophilic fungus
mesophilic fungus
thermophilic bacterium
halophilic bacterium
pBR322, which is frequently used as a vector for cloning gene in E. coli is a/an
original bacterial plasmid
modified bacterial plasmid
viral genome
transposon
Which of the following statement is not true:
Transformation is a procedure through which a piece of DNA is introduced in a host bacterium
Normally, the genes encoding resistance to antibiotics are considered useful selectable markers for E.coli
The normal E.coli cells do not carry resistance against antibiotics such as ampicillin, chloramphenicol, tetracycline or kanamycin
Presence of one recognition sites within the vector will generate several fragments, which will complicate the gene cloning
Go through the statements:
A. During the processing of the prohormone "proinsulin" into the mature "insulin", C-peptide is removed from proinsulin.
B. In hydridoma technology, B-cells are fused with myeloma cells.
C. Genetic engineering has been successfully used for producing transgenic mice for testing safety of polio vaccine before use in humans.
D. Some of the characteristics of Bt cotton are high yield and resistance to bollworms.
E. An improved variety of transgenic basmati rice gives high yield and is rich in vitamin A.
F. Gray biotechnology' is referred to industrial process.
G. The polymerase chain reaction is a technique that is used for in vivo replication of DNA.
How many statement(s) is wrong?
One
Two
Four
Six
Molecular probes used for identification of recombinant clone carrying the desired DNA insert can be:
A. Denatured double stranded DNA probes
B. doubles stranded RNA probes
C. Protein probes
D. Single stranded DNA probes.
A, B
B, C
A, D
A, B, C, D
Which is a natural genetic engineer of the plants?
E.coli
A. tumefaciens
Rhizobium
Pseudomonas
The thermostable enzyme Taq polymerase used in PCR technique was discovered by
Alec Jeffrey
Karry Mullis
Temin
Baltimore
To be useful in genetic engineering a vector must have
In 1960’s two enzymes were discovered in bacteria that were responsible for providing immunity against bacteriophages. One was Restriction Endonuclease and the other was
Methylase
Exonuclease
Aminotransferase
Terminal Transferase
E.coli is a commonly used host for gene cloning because
It is free from elements that interfere with replication and recombination of DNA
It is easy to transform
It supports replication of inserted DNA.
All of these
A gene has been inserted into a vector for the purpose of cloning the sequence only. This vector is called
. Suppression vector
. Expression vector
. Cloning vector
. None of these
Electroporation facilitates insertion of foreign DNA into the cell by
Changing the porocity of the membrane
Changing the electrical potential of the membrane
Lysing the cell wall
Active transport
The names associated with construction of first Recombinant DNA are
. Arber, Nathans, Smith
. Annie Chang, Boyer, Berg, Cohen
. Howard Temin, Brenner, Sharp
. Tim Hunt, Hartwell, Nurse
The restriction enzymes most commonly used in rDNA technology are
Type 1 Restriction enzymes
Type II Restriction enzymes
Type III Restriction enzymes
Type IV Restriction enzymes
Restriction enzymes do not act on the the DNA of the Host cell in which they are produced because
A protein is not expressed properly in a diseased tissue. To find out whether the defect is at the level of translation or post translational modifications which techniques would you use ?
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