Tag: cutting, insertion and ligation of dna

Questions Related to cutting, insertion and ligation of dna

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

PCR proceeds in three distinct steps governed by temperature. The order of the steps is 

  1. Denaturation, Synthesis, Annealing

  2. Annealing, Synthesis, Denaturation

  3. Synthesis, Annealing, Denaturation

  4. Denaturation, Annealing, Synthesis

Reveal answer Fill a bubble to check yourself
D Correct answer
Explanation

The three steps of PCR are: 1) Denaturation (high heat to separate strands), 2) Annealing (cooling to allow primers to bind), and 3) Extension/Synthesis (optimal temperature for polymerase to build the new strand).

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

What is true about DNA polymerase used in PCR?

  1. It is used to ligate introduced DNA in recipient cells.

  2. It serves as selectable marker.

  3. It is isolated from a virus.

  4. It is active at high temperature.

Reveal answer Fill a bubble to check yourself
D Correct answer
Explanation

The DNA polymerase used in PCR (like Taq) is derived from thermophilic bacteria, making it heat-stable and capable of remaining active through the repeated high-temperature denaturation cycles.

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

Melting of DNA at 70$^o$ C is due to breakdown of

  1. Phosphodiester bonds

  2. Hydrogen bonds

  3. Glycosidic bonds

  4. Disulphide bonds

Reveal answer Fill a bubble to check yourself
B Correct answer
Explanation

DNA denaturation involves the separation of the two strands of the double helix. This process is driven by the breaking of hydrogen bonds between complementary nitrogenous bases.

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

Amplification of gene of interest by using PCR may go upto

  1. 0.1 million

  2. 1.0 million

  3. 1.0 billion

  4. 1.0 trillion

Reveal answer Fill a bubble to check yourself
C Correct answer
Explanation

PCR is a powerful technique for amplifying DNA sequences. Through repeated cycles of denaturation, annealing, and extension, a single DNA molecule can be amplified to approximately 1 billion copies.

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

At which temperature a DNA molecule is denatured by heat in PCR

  1. 70$^o$ - 80$^o$C
  2. 90$^o$ - 95$^o$C
  3. 42$^o$C
  4. 50$^o$ - 65$^o$C
Reveal answer Fill a bubble to check yourself
B Correct answer
Explanation

In the PCR process, the denaturation step requires high temperatures to break the hydrogen bonds between DNA strands. This typically occurs between 90 and 95 degrees Celsius.

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

Taq polymerase is isolated from which bacteria?

  1. E. coli

  2. Bacillus thuringiensis

  3. Thermus aquaticus

  4. Agrobacterium

Reveal answer Fill a bubble to check yourself
C Correct answer
Explanation

Taq polymerase is named after the bacterium Thermus aquaticus, which lives in hot springs and provides a heat-stable enzyme necessary for PCR.

Multiple choice bio-chemistry applications of biotechnology pcr cutting, insertion and ligation of dna gene cloning procedure biotechnological regulations asexual modes of reproduction

Polymerase chain reaction (PCR) is used for

  1. In vivo replication of specific DNA sequence using thermostable DNA polymerase

  2. In vitro synthesis of mRNAIn vivo synthesis of mRNA

  3. In vitro replication of specific DNA sequence using thermostable DNA polymerase

  4. Separation of DNA fragments according to their size

Reveal answer Fill a bubble to check yourself
C Correct answer
Explanation

PCR is an in vitro technique used to amplify specific DNA sequences. It utilizes a thermostable DNA polymerase to synthesize multiple copies of the target DNA.