Process of Recombinant DNA Technology

IMPORTANT

Process of Recombinant DNA Technology: Overview

This topic covers concepts such as Recombinant DNA Technology, Tools of Recombinant DNA Technology, Enzymes Used in Recombinant DNA Technology, Lysing Enzymes, Cleaving Enzymes, Synthesizing Enzymes, Restriction Enzymes, etc.

Important Questions on Process of Recombinant DNA Technology

EASY
IMPORTANT

Choose the option that is showing the correct sequence of events occurring in each cycle of polymerase chain reaction (PCR).

MEDIUM
IMPORTANT

A recombinant DNA is formed when sticky ends of vector DNA and foreign DNA join. The sticky ends are formed by which of the following enzymes:

EASY
IMPORTANT

Agrobacterium mediated genetic transformation described as natured genetic engineering is used to resist plants from:

EASY
IMPORTANT

Which of the following technique is used for separating the fragments of DNA cut by restriction endonucleases?

HARD
IMPORTANT

Biotechnologists refer to which of the following bacteria as a natural genetic engineer of plants.

EASY
IMPORTANT

Which of the following feature of a vector is required to identify the transformed cell?

EASY
IMPORTANT

In recombinant DNA technology, ‘molecular scissors’ are:

EASY
IMPORTANT

The source organisms that possess Taq polymerase are

EASY
IMPORTANT

An extra-chromosomal, self-replicating part of the cell that has proven to be a boon to biotechnology is:

EASY
IMPORTANT

In which of the following technique the bacterium Thermus aquatics is used:

MEDIUM
IMPORTANT

Colonies of recombinant bacteria appear white in contrast to non-recombinant bacteria because of 

HARD
IMPORTANT

The genes (a) ori, (b) ampR and (c) rop are associated with which of the following vectors:

EASY
IMPORTANT

Fragments of DNA segments can be separated by:

EASY
IMPORTANT

In genetic engineering, which of the following is used?

MEDIUM
IMPORTANT

In four separate experiments (Table), a vector DNA pBxyz6000bp and a DNA-X 1500 bp fragment was digested with the indicated restriction enzymes. Both, the digested vector and DNA-X were purified and ligated. Ampr represents the ampicillin resistant gene and Ori is the origin of replication. The resultant recombinant vector was transformed into Escherichia coli cells and incubated in a liquid nutrient medium with ampicillin for 24 hours at 37°C. Based on the restriction enzymes used for cloning, choose the correct option.

Experiment No. Restriction enzymes used
1 BamHI and SalI
2 EcoRI and SalI
3 KpnI and HindIII
4 KpnI and SalI

Question Image 

MEDIUM
IMPORTANT

A pure culture of Escherichia coli was streaked on a plate to get single isolated colonies. The plasmid DNA from two such colonies was individually isolated. The DNA were then individually treated with EcoRI ( P and Q ) or double digested with EcoRI + HindIII (P' and Q'). The digested DNA were electrophoresed on an agarose gel and the pattern of the linear DNA so obtained is depicted in the figure below. Patterns P and P' are obtained for DNA from colony 1 and are as expected for the original DNA sequence of the plasmid. The best reason for the differing pattern in Q' is because the plasmid DNA from colony 2 has a mutation

Question Image

MEDIUM
IMPORTANT

As indicated in the gel image, lanes X and Y represent samples obtained from a circular plasmid DNA after complete digestion using restriction enzyme X or Y with different recognition sites, respectively. How many sites for X and Y are present in the plasmid (sizes of the bands in kilo base pairs (kb) is shown)?

Question Image  

EASY
IMPORTANT

Bacterial plasmids are genetic entities that

HARD
IMPORTANT

Provided below are recognition sequences for restriction enzymes 1 (RE1), 2 (RE2) and 3 (RE3). Arrows indicate the positions where the enzymes digest on the two strands. Which of the following can the RE1 digested DNA ligate to?

Question Image