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All I get is supercoiled DNA...

cloning supercoiled dna digestion e coli

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#1 Michelle F

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Posted 10 November 2014 - 11:40 AM

Hi all,

 

I have been having a problem with the cloning of a synthesized construct (6.7kb, provided in pUC57 from Genscript company) into my desired vector (~8kb).  I first cut the synthesized construct and desired vector with BamHI/EcoRI.  Then run the agarose gel and elute the appropriate fragments. I always get the expected band sizes from the first digestion, so I do not think this is an issue.

 

After elution of bands from the gel using Promega's "Wizard SV Gel Clean-Up Kit", I check the concentration of DNA by Nanodrop and use a 1:5 or 1:3 ratio of vector:insert, with about 10ng of vector for the ligation reaction in a 20uL total volume.  We use Invitrogen's T4 DNA ligase at 14C overnight for the ligations. I also do a control reaction with no insert, and do not get resulting transformants (or minimal, only 1-3 per plate).

 

Then, heat inactivate the ligase at 65C for 20 minutes - or not... sometimes I don't, and I'm not sure it matters.  After chilling the DNA on ice, I use 10uL of the ligation reaction to transform homemade DH5alpha chemically competent cells.  I culture these cells on solid LB+spectinomycin and streptomycin.  The following day, single colonies are cultured in liquid LB media + spec/strep for 16 hours, and then DNA extraction by Sigma-Aldrich's "GenElute Plasmid Miniprep Kit".  

 

All is well until I extract DNA from the cultured colonies:  all I seem to get is supercoiled DNA.  See the attached picture as an example of the resulting colony DNA extractions. The last two lanes on that gel are the initial construct and desired vector digested with EcoRI/BamHI.  The red box denotes the size of the fragments that were eluted and ligated.  

 

For colony DNA digested, I use 10uL of extracted DNA, 1uL each BamHI and EcoRI, 3uL Cutsmart buffer, and 15uL H2O for a total of 30uL.  

 

Why do I get such "random" banding pattern?  Any help is appreciated!

 

 

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  • cloning1.jpg


#2 bob1

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Posted 10 November 2014 - 05:06 PM

The forms you are getting are not only supercoiled DNA, but also nicked and linear forms of the plasmid DNA. You need to screen the extracts for your insert (and sequence it if you want to be sure) , but by the looks of it you have nice DNA so this shouldn't be a problem.



#3 Michelle F

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Posted 11 November 2014 - 11:56 AM

Any explanation why I get such a "random" banding pattern from the ligation of two distinct fragments?  This should be easy stuff, it's just a sticky end ligation after all...



#4 bob1

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Posted 11 November 2014 - 01:30 PM

The "random" bands are not random - they are the supercoiled, nicked circular (i.e. unwound/no longer supercoiled) and linear forms of the plasmid respectively.



#5 Michelle F

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Posted 12 November 2014 - 09:41 AM

I meant "random" as in why when I ligate two fragments of 6.7 and 8kb, do I get a multitude of different band sizes as product? I've decided to have the company do the cloning service for me, no sense wasting any more time or money!



#6 bob1

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Posted 12 November 2014 - 12:00 PM

I see what you mean now - this could be through failed PCR products (there will be some in every PCR, no matter how good you are at PCR), self-ligation of partially cut plasmid, self ligation of the insert.

 

I would say that you have what you are looking for, you just need to sequence a few.







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