Path: utzoo!utgpu!watserv1!watmath!uunet!samsung!zaphod.mps.ohio-state.edu!uwm.edu!ux1.cso.uiuc.edu!midway!quads.uchicago.edu!rout From: rout@quads.uchicago.edu (Mark Routbort) Newsgroups: bionet.molbio.methds-reagnts Subject: Cloning PCR fragents into vector Message-ID: <1990Sep12.143937.7896@midway.uchicago.edu> Date: 12 Sep 90 14:39:37 GMT Sender: news@midway.uchicago.edu (News Administrator) Organization: University of Chicago Lines: 38 I'm looking for someone with experience cloning medium sized (500-1000 bp) PCR fragments into a vector for screening. I'm having troubles getting transformants to screen. I discovered through a control experiment that Bluescript vector that I had cut, blunt-ended with T4 polymerase, phosphatased with CI alkaline phosphatase, and then kinased with T4 polynucletide kinase would NOT yield Amp resistant colonies. Unfortunately I don't have the cut, blunted, unCIAPed vector to determine if the problem lies with blunting or with kinasing (although either is a problem, since I have to both blunt and kinase the PCR fragements). The sequence of steps on the above control was: 1) Cut CsCl-pure DNA (of a clone that has a 3 Kb insertion into SmaI site of Bluescript) with Asp718I, XbaI, and StuI (which cuts not in vector but in insert so I could distinguish vector fragment from insert). phenol/CHCl3/EtOH. 2) T4 polymerase to hopefully blunt. phenol/CHCl3/EtOH. 3) Calf intestinal alkaline phosphatase. Heat inactivate in presence of EDTA (15' at 65 deg C). Prep gel. Cut out and elute 3 Kb Bluescript fragment. Phenol/CHCl3/EtOH. 4) Rephosphorylate with T4 polynuc. kinase. 5) Use 100 ng of DNA in kinase buffer to ligate with 10 units T4 ligase overnight at 12 deg C. 6) Transform into XL-1 competent cells. No colonies next day. I've never had problems ligating or transforming before using cohesive or blunt ends (directly from enzymes), so I think the problem lies either with the kinase or the polymerase (both brand new). Has anyone had similar problems and resolved them? Unfortunately I _can't_ cut the PCR fragment and ligated with cohesive ends on both sides, although I can do so on _one_ side. Thanks for any tips, insights, and sympathetic commiserations. -- Mark Routbort Due to circumstances beyond my control, rout@midway.uchicago.edu There will be no big parade this Sunday. -- Colonel Scheisskopf in Catch-22