Restriction Enzymes. Molecular Scissors Restriction enzymes are molecular scissors.

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Presentation transcript:

Restriction Enzymes

Molecular Scissors Restriction enzymes are molecular scissors

Restriction Enzymes scan the DNA code Find a very specific set of nucleotides Make a specific cut

Picking a palindrome Words that read the same forwards as backwards Hannah Level Madam hannaH leveL madaM

Palindromes in DNA sequences Genetic palindromes are similar to verbal palindromes. A palindromic sequence in DNA is one in which the 5’ to 3’ base pair sequence is identical on both strands (the 5’ and 3’ ends refers to the chemical structure of the DNA).

Each of the double strands of the DNA molecule is complimentary to the other; thus adenine pairs with thymine, and guanine with cytosine.

Restriction enzymes recognize and make a cut within specific palindromic sequences, known as restriction sites, in the genetic code. This is usually a 4- or 6 base pair sequence. Example?

HaeIII HaeIII is a restriction enzyme that searches the DNA molecule until it finds this sequence of four nitrogen bases. 5’ TGACGGGTTCGAGGCCAG 3’ 3’ ACTGCCCAAGGTCCGGTC 5’ 5’ TGACGGGTTCGA GGCC AG 3’ 3’ ACTGCCCAAGGT CCGG TC 5’

Once the recognition site was found HaeIII could go to work cutting (cleaving) the DNA 5’ TGACGGGTTCGA GGCC AG 3’ 3’ ACTGCCCAAGGT CCGG TC 5’

These cuts produce what scientists call “blunt ends” 5’ TGACGGGTTCGA GGCC AG 3’ 3’ ACTGCCCAAGGT CCGG TC 5’

The names for restriction enzymes come from: the type of bacteria in which the enzyme is found the order in which the restriction enzyme was identified and isolated. EcoRI for example R strain of E.coli bacteria I as it is was the first E.coli restriction enzyme to be discovered.

“blunt ends” and “sticky ends” Remember how HaeIII produced a “blunt end”? EcoRI, for instance, makes a staggered cut and produces a “sticky end” 5’ GAATTC 3’ 3’ CTTAAG 5’ 5’ GA ATTC 3’ 3’ CTTA AG 5’ 5’ GAATTC 3’ 3’ CTTAAG 5’

blunt end sticky end

Some more examples of restriction sites of restriction enzymes with their cut sites: HindIII: 5’ AAGCTT 3’ 3’ TTCGAA 5’ BamHI: 5’ GGATCC 3’ 3’ CCTAGG 5’ AluI: 5’ AGCT 3’ 3’ TCGA 5’

“sticky ends” are useful DNA fragments with complimentary sticky ends can be combined to create new molecules which allows the creation and manipulation of DNA sequences from different sources. Think about how this could be used and abused in the medical field