Multiple colony types from streaking 1 E.coli colony
Posted 10 February 2009 - 03:35 AM
I have some really puzzling results when I tried to transform pGEM-3z into DH5-alpha E. coli.
I transformed 1ul of pGEM-3z (all that we had left!) into DH5-alpha and spread it on LB-agar with ampicillin.
The next day there were clearly 2 colony types - a few big and many small (at least 100x more small). I miniprepped plasmid DNA from both and the small colony grew very slowly in liquid and gave much less DNA but the plasmid was correct in both cases.
I wanted to check that it would be OK to do blue/white screening so I streaked 2 of each colony type onto LB-agar + ampicillin with IPTG and X-gal.
The big colonies gave rise to BOTH big/white and small/blue colonies (~100x more small than big).
The small colonies also gave rise to both colony types (~1000x more small than big), but there were about 3 big colonies which were also kind of blue. These big blue colonies also contained the correct plasmid.
I have no idea what is going on here, please let me know if you have seen this before! I need to be sure that white colonies result from insertional inactivation later on when I use the pGEM3z for cloning, so having white colonies with the empty vector is not good.
Posted 10 February 2009 - 03:42 AM
Posted 10 February 2009 - 07:05 AM
Also, I was very careful not to touch surrounding colonies when I was picking the colonies for secondary streaking.
Edited by microphobe, 10 February 2009 - 07:07 AM.
Posted 10 February 2009 - 07:20 AM
Posted 10 February 2009 - 08:43 AM
I once experience something similar but not on the scale you are experiencing. Upon transformation of my empty vector into e coli with X-gal, i found a few white colonies... when all should be blue. One of these white colonies (there were only about 10 when I have 100s, maybe 1000s of colonies that were blue), contained a plasmid that was being worked on in the lab. I assumes it was a contamination problem, more so as my lab reused electroporation cuvettes.
Posted 07 March 2014 - 09:49 AM
Hi!, I have the same problem and I don't know what to do. I tried to isolate a positive colony, get plasmid of it and transform, but the two populations appear again.
How do you solved the problem?