Restriction Enzymes: Interference & Impacts on DNA

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Discussion Overview

The discussion centers around the interaction of different restriction enzymes when used together on DNA, exploring whether they interfere with each other's activity, the conditions under which they operate, and potential issues that may arise during double digests.

Discussion Character

  • Technical explanation
  • Debate/contested

Main Points Raised

  • Some participants propose that two different restriction enzymes can generally function together without interference, provided their recognition sites do not overlap.
  • Others argue that overlapping restriction sites could lead to complications, potentially causing the enzymes to "cancel each other out" or cut each other, leading to undesirable outcomes.
  • It is noted that the buffer conditions are critical for the efficiency of the enzymes, and discrepancies in buffer composition may affect their activity.
  • One participant emphasizes the importance of limiting the amount of enzyme used to avoid inhibition from glycerol, suggesting it should be less than 10% of the reaction volume.
  • Another participant mentions that while double digests are generally safe, there are exceptions that may arise due to specific buffering conditions rather than competition between recognition sequences.

Areas of Agreement / Disagreement

Participants generally agree that restriction enzymes do not cut each other and that double digests can be safe under the right conditions. However, there is disagreement regarding the potential for interference when recognition sites overlap, and the discussion remains unresolved on the specifics of enzyme interactions in such cases.

Contextual Notes

Limitations include the dependence on specific buffer conditions and the need for careful consideration of enzyme concentrations to avoid inhibition. The discussion does not resolve the nuances of enzyme interactions in overlapping scenarios.

MaxNumbers
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I'm wondering if, when put into the DNA together, two different restriction enzymes will interfere with each other, and how. Will two different restriction enzymes cut the DNA as they each would separately, since they are specifically formed to react with it and not each other, or would they disturb each other? Or, is this a case-by-case issue?
 
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There is usually no problem when using two restriction enzyme in the same reaction. It will only be a problem if you restriction site of you two enzymes overlap. The major problem is usually the buffer used. The condition of the reaction will affect the effcienty of the enzyme.
 
You need to be careful that you don't add more enzyme than 10% of the reaction, the glycerol will inhibit the cutting. There shouldn't be interference, though Ian makes a good point that there might be a problem if the two restriction sites overlap, it wouldn't be smart wanting to cut DNA with such like enzymes anyway, so I don't think that will ever be the case :)

Be carefull that the buffer conditions are the same, adjust the amount of enzyme if one enzyme cuts less efficiently in a certain buffer.
 
I agree with Ian, as two restriction enzymes could cancel each other out, or, worse, cut each other up instead, and then you'd have a whole big (relatively :wink: ) mess to clean up. As long as the restriction sites don't overlap or are too near each other, then using two or more different enzymes shouldn't present too much of a problem.









Chaos. Disorder. Widespread panic. My work is done here.
 
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Restriction enzymes don't cut each other. Double digests are perfectly safe if both enzymes work in the supplied buffer. For some reason there are exceptions which can be found on the following site http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/double_digests.asp I think that is because of buffering conditions and not recognition sequence competition.

ps. glycerol should be less than 5% to prevent star activity.
 
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