Restriction Enzymes: Interference & Impacts on DNA

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SUMMARY

The discussion centers on the interaction of restriction enzymes during DNA digestion. It is established that two different restriction enzymes can be used together in a reaction without interference, provided their recognition sites do not overlap. The efficiency of the enzymes is influenced by the buffer conditions, and it is critical to maintain consistent buffer environments. Additionally, the concentration of glycerol should be kept below 5% to prevent star activity, which can hinder enzyme performance.

PREREQUISITES
  • Understanding of restriction enzymes and their function in DNA manipulation
  • Familiarity with buffer systems used in molecular biology
  • Knowledge of enzyme kinetics and reaction conditions
  • Experience with double digest techniques in DNA analysis
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  • Research the effects of buffer conditions on restriction enzyme activity
  • Learn about the principles of double digests in molecular cloning
  • Investigate the significance of recognition site overlap in restriction enzyme applications
  • Explore the concept of star activity and its impact on enzyme efficiency
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This discussion is beneficial for molecular biologists, genetic engineers, and laboratory technicians involved in DNA manipulation and cloning techniques.

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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