Team:Cambridge/Protocols/Restriction Enzyme Digestion

From 2011.igem.org

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(Practice)
(Practice)
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* '''Master mix preparation'''
* '''Master mix preparation'''
For 2.0μl of DNA solution add:  
For 2.0μl of DNA solution add:  
-
: 0.5μl of each restriction enzyme (or the respective amount of water for the control with uncut plasmids)  
+
:* 0.5μl of each restriction enzyme (or the respective amount of water for the control with uncut plasmids)  
-
: 0.1μl of BSA - ''acetylated Bovine Serum Albumin enhances the performance of restriction enzymes''
+
:* 0.1μl of BSA - ''acetylated Bovine Serum Albumin enhances the performance of restriction enzymes''
-
: 5.9μl of water
+
:* 5.9μl of water
-
: 1.0μl of 2×NEBuffer
+
:* 1.0μl of 2×NEBuffer
* '''Procedure'''
* '''Procedure'''

Revision as of 15:17, 15 July 2011

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OVERVIEW
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Restriction Enzyme Digestion

A method that allows to create a restriction map of a given DNA fragment. Widely used to test for the correct integration of a cloned sequence into a vector.

Theory

Restriction enzymes, also called restriction endonucleases, are enzymes naturally found in bacteria which serve as a protection against foreign DNA found in a cell which usually implies a phage infection. The enzymes introduce a double-strand cuts in the DNA leaving either blunt or sticky single-strand ends, recognizing specific, usually 4bp or 6bp palindromic sequences.

Practice

  • Master mix preparation

For 2.0μl of DNA solution add:

  • 0.5μl of each restriction enzyme (or the respective amount of water for the control with uncut plasmids)
  • 0.1μl of BSA - acetylated Bovine Serum Albumin enhances the performance of restriction enzymes
  • 5.9μl of water
  • 1.0μl of 2×NEBuffer
  • Procedure
  1. Mix DNA solution with the suitable amount of the master mix. As a control, repeat the same procedure with uncut plasmid
  2. incubate at 37°C for 2 hours
  3. perform gel electrophoresis (10μl of DNA-restriction enzyme mixture in each well)
  4. compare with predicted fragment sizes
  5. remember about molecular weight markers
  • Tips on Restriction Enzyme Usage
  • Store restriction enzymes in the freezer, at around -20°C.
  • Never make up restriction digests with the restriction enzyme composing more than 1/10 of the final volume. The reason is that restriction enzymes are stored in glycerol, and at concentrations above 10%, glycerol not only inhibits the digestion but also changes enzyme specificity (star activity).
  • Check for the compatibility of the restriction enzymes chosen.
To check if the two selected restriction enzymes can perform effective catalysis in the same solution, go to the website of [http://www.neb.com New England Biolabs] → select [http://www.neb.com/nebecomm/DoubleDigestCalculator.asp? Double Digest Finder] → choose which restriction enzymes you want to use → follow the digest recommendations.

Safety

The safety implication of the procedure.