Which of the following statements is not correct for Restriction enzymes?
Ligases join sticky ends of DNA together.
In molecular biology, several enzymes play crucial roles in manipulating DNA, especially in processes like recombinant DNA technology. Restriction enzymes are among the most important tools, but other enzymes like exonucleases, endonucleases, and ligases are also essential. This question asks us to identify the statement that is not correct regarding these enzymes.
This statement describes the function of exonucleases accurately. Exonucleases are enzymes that cleave nucleotides one at a time from the end (either 5' or 3') of a polynucleotide chain. They work on the terminal part of the DNA or RNA molecule.
Analysis: This statement is correct.
This statement accurately describes endonucleases. Endonucleases are enzymes that cleave phosphodiester bonds within a polynucleotide chain. Restriction endonucleases, often simply called restriction enzymes, are a specific type of endonuclease that recognizes and cuts DNA at specific nucleotide sequences, known as recognition sites.
Analysis: This statement is correct.
DNA ligase is an enzyme that repairs single-strand breaks (nicks) in double-stranded DNA and joins DNA fragments together by catalyzing the formation of phosphodiester bonds. Ligases can join DNA fragments with complementary "sticky ends" (overhangs) where base pairing occurs, facilitating the joining process. They can also join fragments with "blunt ends" (no overhangs), although this process is less efficient.
While it is true that ligases join sticky ends of DNA together, this statement might be considered 'not correct' in the context of this question possibly because it is an incomplete description of ligase activity (they also join blunt ends and repair nicks) or because, compared to the other statements which are precise definitions or facts, this description might be seen as less precise or potentially misleading if interpreted as their sole function. However, ligases indeed perform the function of joining sticky ends.
Analysis: This statement describes a specific action of ligases, which is joining sticky ends. While ligases also join blunt ends and repair nicks, the statement itself is a true action they perform. Let's compare with other options.
Historical research confirms that HindII was the first restriction endonuclease to be isolated and characterized. It was isolated from the bacterium Haemophilus influenzae serotype d and was shown to cut DNA at a specific recognition sequence.
Analysis: This statement is correct.
Comparing the statements, Statements 1, 2, and 4 are widely accepted correct facts about the respective enzymes or history. Statement 3, "Ligases join sticky ends of DNA together," while true, is a specific instance of ligase function and might be considered incomplete or potentially 'not correct' in comparison if the question seeks the least accurate statement among the options. Based on the options provided and common understanding in molecular biology, if only one statement is incorrect, it points to Statement 3 being the intended incorrect option, likely due to the perceived incompleteness or potential implication that this is their only joining function.
Therefore, the statement that is not correct among the given options is "Ligases join sticky ends of DNA together," when interpreted as the statement that deviates most from a complete or universally precise description compared to the others.
| Enzyme Type | Primary Function | Specificity |
|---|---|---|
| Exonuclease | Remove nucleotides from DNA/RNA ends | Acts on ends (5' or 3') |
| Endonuclease | Cut DNA/RNA internally | Acts within the strand |
| Restriction Endonuclease (Restriction Enzyme) | Cut DNA internally at specific recognition sequences | Specific nucleotide sequences |
| DNA Ligase | Join DNA fragments by forming phosphodiester bonds; repair nicks | Joins blunt ends, sticky ends, and single-strand breaks |
Restriction Enzymes: These are natural enzymes found in bacteria, where they serve as a defense mechanism against invading viruses (bacteriophages). They cut the viral DNA, rendering it harmless. Bacteria protect their own DNA from being cut by modifying their recognition sites, usually by methylation.
Restriction enzymes are categorized into different types (e.g., Type I, Type II, Type III) based on their structure, recognition site, and cleavage position. Type II restriction enzymes are the most commonly used in molecular biology because they cut DNA at specific recognition sites and the cleavage site is typically within or very close to the recognition site.
DNA Ligases: These enzymes are essential for many biological processes, including DNA replication, repair, and recombination. In recombinant DNA technology, ligase is used to join the DNA fragment of interest (like a gene) into a vector (like a plasmid) after both have been cut with restriction enzymes. This joining step is often referred to as ligation.
The ability of restriction enzymes to create specific DNA fragments and ligases to join them together forms the foundation of genetic engineering and the creation of recombinant DNA molecules.
Which of the following is not a step of Polymerase Chain Reaction?
Given below are two statements:
Statement I: In a bioreactor, small volumes of cultures are developed in which useful bio-products are produced.
Statement II: In downstream processing, the products formulated with suitable preservatives are ready for marketing without testing of their quality.
In the light of the above statements, choose the correct answer from the options given below:
A thermostable DNA polymerase is isolated from:
Which one of the following is not a process of DNA recombinant technology?
Downstream processing method involves:
Arrange the following steps involved in the transformation of bacteria in a sequence from initiation to end:
(A) Incubation of rDNA with bacterial cell on ice
(B) Treatment with divalent cations
(C) Heat shock treatment
(D) Selection on antibiotic-containing agar plate
(E) Placed them again on ice
Which of the following statements are incorrect?
(A) Fragments of DNA can be separated by ELISA.
(B) Transformation is a procedure through which a piece of DNA is introduced into a host bacterium.
(C) Recombinant DNA technology does not involve isolation of a desired DNA fragment.
(D) DNA ligases are used for stitching DNA fragments into a vector.
The first restriction endonuclease to be isolated was:
Arrange the following steps of PCR in correct sequence:
Choose the correct answer from the options given below:
The process of cutting out DNA fragments from agarose gel and their extraction from gel piece is known as:
Arrange the following steps of rDNA technology in correct sequence.
(A) Amplification of gene by PCR
(B) Insertion of rDNA into host cell using vector
(C) Isolation of the genetic material from the cell
(D) Cutting the DNA at specific location
In biolistic method, the cells are bombarded with high velocity microparticles of: