<div style="text-align:justify"> ---+ Gene Gorging Marker Mutations For competitive fitness assays, one must be able to distinguish two _E. coli_ subpopulations in a mixed culture. One way this can be accomplished is by mutating genes required for sugar fermentation to create a genetic marker (Ara, Mal, Lac, etc.). Plating a – version of these strains will produce red colonies and plating the + version will produce pinkish white colonies on tetrazolium indicator agar containing a rich media base plus the sugar of interest (TA, TM, etc). This procedure has been used to create defined Ara<sup>+</sup> and Ara<sup>–</sup> versions of Escherichia coli B (REL606) and Mal<sup>-</sup> derivatives of Escherichia coli K12 (Keio collection strains) with the _malF_ Keio deletion. For a more detailed description of the Ara genetic marker, see also: [[ProtocolsAraMarker][Ara Marker]]. %TOC% ---++ Materials <div style="float: right; display:inline; margin:10px;"> %TABLE{valign="bottom"}% | *Plasmid* | *Marker* | | pJEB11 | →Ara<sup>–</sup> | | pJEB12 | →Ara<sup>+</sup> | | pJEB15 | →Mal<sup>–</sup> | </div> * [[ProtocolsAntibioticStockSolutions][Antibiotic stock solutions]] of Chloramphenicol (Cam) and Kanamycin (Kan). * Final concentrations of antibiotics in all media (liquid or plates) are 25 µg/ml Cam and 50 µg/ml Kan. * [[ProtocolsMediaRecipes][LB and TA plates]] with antibiotic. You will need LB + Cam + Kan, TA + Cam, TA + Kan, and TA plates. * Note: The protocol refers to TA plates throughout. If you are not using the Ara marker, substitute the proper sugar, e.g. make TM plates if using the maltose marker. * 20% L-Arabinose stock. Dissolve 10 g in 50 ml of ddH<sub>2</sub>0 and filter sterilize or autoclave. * [[ProtocolsElectrocompetentCells][Electrocompetent cells]] of the parent strain. * pACBSR (the _gene-gorging_ plasmid) * Donor plasmid for desired mutation (see Table). * Typically this is a pCR3.1-derived plasmid generated by TOPO cloning a ~1000 bp DNA fragment PCR amplified from a strain containing the marker mutation. <div style="clear:both;"></div> ---++Day 1: Transform Gene-Gorging and Donor Plasmid 1 Thaw one 1.7 ml microfuge tube of electrocompetent cells for each parent strain on ice. 1 While waiting for this to thaw, place one electroporation cuvette on ice for each parent strain. 1 Add 1 µl of pACBSR and 1 µl of the donor plasmid to each tube of electrocompetent cells on ice. Mix by flicking the tube with your finger. Do not pipette up and down or vortex to mix. 1 [[ProtocolsElectrocompetentCells#TransformingElectroporation][Electroporate]] 1 Pipette sample out of cuvette into original microfuge tube on ice. Add 500 µl of room temperature SOC medium. 1 Grow at 37°C for 1 hr in a shaking incubator to induce antiobiotic expression. 1 Plate 100 µl and 10 µl + 90 µl saline on two separate LB + Cam + Kan plates. 1 Grow plates overnight at 37°C. ---++ Day 2: Induce Gene-Gorging 1 Pick three colonies from each successful transformation into separate test tubes containing 5 ml of LB medium supplemented with 0.2% L-Arabinose and 20 µg/ml Chloramphenicol (Cam). The arabinose is to induce expression of the λ Red genes from the gene-gorging plasmid. Use arabinose regardless of which sugar marker you are changing. 1 Grow cultures overnight at 37°C, shaking at 120 rpm. ---++ Day 3: Screen or Select for Desired Mutation 1 Make a 10<sup>4</sup>-fold dilution of each overnight culture with two 100 µl transfers through dilution tubes containing 10 ml of saline. Note that the cell density achieved after induction is considerably lower than that usually achieved during growth in LB. 1 A. If you are gene gorging the – version of the the marker you must *screen* for successful mutations. Plate 200 µl of a 10<sup>4</sup> dilution of each culture on tetrazolium arabinose (TA), tetrazolium maltose (TM), or other suitable indicator agar containing 20 µg/ml Chloramphenicol (Cam). Successful mutants will be red.<br> B. If you are gene gorging the + version of the the marker you could *screen* for successful mutations as above, but it is easier to *select* for them by plating 100 µl of a 10<sup>2</sup> dilution on minimal arabinose (MA) or minimal maltose (MM). 1 Grow plates overnight at 37°C. ---++ Day 4: Screen for Gene-Gorging Plasmid Loss Expected results are 0-10 colonies with the marker change per 200 colonies of the other color. 1 Pick one colony from each plate into 5 ml of LB medium in a test tube. Give each picked colony an isolate designation. Colonies from the same plate are not necessarily independent isolates, they may share undesired second-dite mutations. Picking individual isolated 1 Grow cultures overnight at 37°C, shaking at 120 rpm. 1 Grow plates overnight at 37°C. ---++ Day 5: Plate to Single Colonies 1 Plate 100 µl of a 10<sup>6</sup> dilution of each culture on tetrazolium arabinose (TA, blue stripe) or tetrazolium maltose (TM, purple stripe). The dilution can be made with three 100 µl transfers through dilution tubes containing 10 ml of saline. 1 Grow plates overnight at 37°C. ---++ Day 6: Patch for Plasmid Loss 1 Patch 6-12 colonies from each plate on three LB (or TA/TM) plates with 20 µg/ml Chloramphenicol, with Kanamycin, and - last - with no antibiotic. 1 Grow plates overnight at 37°C. ---++ Day 7: Save a Freezer Stock of the New Strain 1 Pick from a patch that grows without antibiotic and not with either antibiotic present. Usually a majority of patched colonies have successfully lost both plasmids. 1 Grow cultures overnight at 37°C and archive 2 × 1 ml frozen copies in 10% glycerol. ---++ Test for Marker Neutrality Competitive fitness assays should be used to test for non-neutral mutations that sometimes occur during strain construction by this method. Testing three independent isolates usually assures one success. ---++ References 1 Herring, C.D., Glasner, J.D., and Blattner, F.R. (2003) Gene replacement without selection: regulated suppression of amber mutations in Escherichia coli. _Gene_ *311*, 153-163. 1 Sean Sleight's Detailed Procedure. </div>
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Topic revision: r9 - 2010-05-11 - JeffreyBarrick