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What is restriction enzyme sequence?

What is restriction enzyme sequence?

A restriction enzyme is a protein that recognizes a specific, short nucleotide sequence and cuts the DNA only at that specific site, which is known as restriction site or target sequence. In live bacteria, restriction enzymes function to defend the cell against invading viral bacteriophages.

What sequence does the restriction enzyme recognize?

They recognize and bind to specific sequences of DNA, called restriction sites. Each restriction enzyme recognizes just one or a few restriction sites. When it finds its target sequence, a restriction enzyme will make a double-stranded cut in the DNA molecule.

What enzyme matches the codon sequence?

The ribosome is the site of this action, just as RNA polymerase was the site of mRNA synthesis. The ribosome matches the base sequence on the mRNA in sets of three bases (called codons) to tRNA molecules that have the three complementary bases in their anticodon regions.

What are Isoschizomers and Neoschizomers?

Isoschizomers are restriction enzymes that have the same recognition sequence and the same specificity. Neoschizomers recognize the same nucleotide sequence but cleave DNA at different positions.

Which DNA sequence would most likely be recognized by a restriction enzyme?

A recognition sequence of a restriction endonuclease must be a palindromic sequence. The palindromic arrangement represents the same nucleotide from the 5′- 3′ end of one strand with the 3′-5′ end of the opposite DNA strand. Therefore, the correct options are (A) and (D).

Why do restriction enzymes recognize palindromic sequences?

Explanation: Enzymes such as restriction enzymes have to recognize a very specific sequence in order to carry out its task. It binds to the DNA only in one specific configuration. A palindromic sequence also increases the chance that both strands of DNA are cut.

How many amino acids are coded by a set of codons that share the same first two nucleotide bases?

The nucleotide triplet that encodes an amino acid is called a codon. Each group of three nucleotides encodes one amino acid. Since there are 64 combinations of 4 nucleotides taken three at a time and only 20 amino acids, the code is degenerate (more than one codon per amino acid, in most cases).

Which two enzymes are examples of isoschizomers?

Isoschizomers are pairs of restriction enzymes specific to the same recognition sequence. For example, SphI (CGTAC/G) and BbuI (CGTAC/G) are isoschizomers of each other.

What is a restriction enzyme that is an isoschizomer of Psti?

It is also an isoschizomer restriction enzyme SalPI from Streptomyces albus P.

What is palindrome sequence example?

So if a sequence is palindromic, the nucleotide sequence of one strand would be the same as its reverse complementary strand. An example of a palindromic sequence is 5′-GGATCC-3′, which has a complementary strand, 3′-CCTAGG-5′.

How is the structure of an enzyme related to its function?

Enzymes are a linear chain of amino acids that generate the three-dimensional structure. The sequence of amino acids enumerates the structure which in turn identifies the catalytic activity of the enzyme. The structure of the enzyme denatures when heated, leading to loss of enzyme activity, which is typically connected to the temperature.

How is site complexity used in enzyme recognition?

Site Complexity: Used to reject enzymes that cut too frequently. Enter the minimum number of basepairs in the enzyme recognition sequence, adjusted for ambiguity.

What is the role of repeated sequence in DNA?

Repeated sequence (DNA) Sequence repeats are a common feature of amyloid-forming proteins and assume the role of self-assembling building blocks (Gilead and Gazit, 2005; Gazit, 2007a).

Which is a favourable model of enzyme-substrate interaction?

The favourable model of enzyme-substrate interaction is called the induced-fit model. This model states that the interaction between substrate and enzyme is weak, and these weak interactions induce conformational changes rapidly and strengthen binding and bring catalytic sites close enough to substrate bonds.