The Arabinose (Ara) Genetic Marker

Background

The Escherichia coli B strain REL606 has a mutation in the araA gene that renders it unable to utilize the sugar L-arabinose. Strain REL607 is a spontaneous revertant of REL606 containing a single point mutation that restores the ability to metabolize L-arabinose. This marker is selectively neutral in a variety of conditions and can be used to determine the relative frequencies of Ara (REL606-derived) and Ara+ (REL607-derived) cells in a mixture for competition assays or marker divergence experiments. Ara and Ara+ cells form red and white colonies, respectively, on tetrazolium arabinose (TA) plates, because utilization of the sugar rather than only the tryptone and yeast extract components of this medium causes the excretion of acetic acid which acidifies the area surrounding the colony, changing the tetrazolium indicator color from red to white.

strain marker araA sequence
REL606 Ara 92D (GAC)
REL607 Ara+ 92G (GGC)

Selection for arabinose utilization from REL606 is known to also produce, more rarely, neutral Ara+ revertants that have an araA 92A (GCC) sequence.

Selection of Ara+ Revertants from Ara Strains Derived from REL606

General Procedure

For a non-mutator strain. Grow several 10 ml cultures in DM1000 media (LB is also fine in most situations). Spin down to concentrate cells and plate them all on separate minimal arabinose (MA) plates. Grow for 48 hours, pick one colony from each plate (it has to be an Ara+ revertant to grow). Streak each candidate colony on a new MA plate and grow overnight to verify that it is Ara+ and a clone. Then, grow an overnight culture in DM1000 (or LB( and store frozen. For a mutator strain, you can plate 1/10 to 1/100th as many cells and expect to get the same number of Ara+ revertant candidates.

Detailed Procedure

Supplies

supply per strain
MA plates 6
50 ml Erlenmeyer flasks 5
9.9 ml saline dilution tubes 6
DM1000 50 ml

All quantities are approximate amounts per Ara strain where Ara+ revertants are desired. They assume three replicates.

Day 1: Revive

  1. Revive strains to be tested from the freezer in DM1000 in 5 ml cultures in test tubes or 10 ml cultures in 50 ml Erlenmeyer flasks.
  2. Incubate shaking at 120 RPM at 37C overnight.

Day 2: Grow replicates

  1. Take each strain you revived (which reaches a density of approximately 5×109 cells/ml after overnight growth) and make a 106-fold dilution by transferring 10 l to 10 ml saline in one dilution tube, vortexing, and then transferring 10 l to 10 ml saline in a second dilution tube.
  2. Vortex again to mix and inoculate 100 l of this into 10 ml of DM1000 in a 50 ml Erlenmeyer. (You have added approximately 500 cells). Do this step 3 times (inoculate three separate flasks) for each of your test strains.
  3. Incubate flasks shaking at 120 RPM at 37C overnight.

Explanation: Why is it important to inoculate with so few cells? At this stage we are trying to establish evolutionary independence between the different replicate cultures, so that any Ara+ revertants that we find are sure to be derived from independent mutational events, and most importantly, we want to establish that they don't share any deleterious mutations that will prevent them all from being neutral with respect to the Ara strain we started with.

Day 3: Plate on Selective Media

  1. Pour each DM1000 culture into a 15 ml Falcon tube.
  2. Pellet cells by spinning for 15 minutes at 4,000 rpm in the Eppendorf 5810R with the swinging bucket rotor.
  3. Carefully pour the supernatant out of each tube, leaving a few hundred l of liquid at the bottom.
  4. Using a 1 ml pipetor, pipet up and down to re-suspend the cells in the remaining liquid into a dense milkshake.
  5. Plate this entire volume on one Minimal Arabinose (MA) plate. You may need to incubate it agar side down if you have a lot of liquid.
  6. Incubate MA plates at 37C for 3648 hours.

Variant: This procedure is for a strain with a normal wild-type mutation rate. For a mutator strain it is generally sufficient to plate 100200 l of a dense overnight culture directly on the MA plates.

Day 5:

  1. At this point, you should have several colonies on most plates. They might appear as small colonies after only 24 hrs of growth, but it's safer to wait two days before proceeding. Sometimes a plate will have zero cells. Sometimes it might have hundreds or thousands (a jackpot). For more about this distribution, read about fluctuation tests.
  2. Pick ONE colony from each plate and streak it out on a new MA plate. This extra step ensures that you have isolated your new strain from the hazy background of Ara cells and that it is not a mixture of two Ara+ revertants. Store the old plates at 4C until you are sure your new streaks have grown.
  3. Incubate new MA plates at 37C for 2448 hours.

Day 6:

  1. Pick a single colony from each plate into a test tube filled with 5 ml of DM1000. Store the MA streak plates at 4C until you are sure your new cultures have grown without contamination.
  2. Incubate cultures shaking at 120 RPM at 37C overnight.

Day 7:

  1. Freeze down each strain. Label these cryovials with a temporary strain designation, something like "JEB592 Ara+ #3". Only once a clone passes the PCR-RFLP test to be sure it has the appropriate mutation AND a co-culture competition test for fitness neutrality should the strain be given a permanent designation and entered in the strain database.

PCR-RFLP Assay for Verifying the REL607 Mutation

To verify that you have the precise reversion present in REL607 in your new Ara+ revertant candidate, you can use PCR followed by digestion with a restriction enzyme that cuts only when the REL607 allele is present.

Perform a standard PCR reaction from whole cells using these two primers. Always include REL606 (Ara+) and REL607 (Ara) controls when doing this assay. You can use cells from a freezer stock.

Primer Coordinates Sequence
REL256 REL606/70660-70683 5'-CCGATACGCTCATGGGCTTGTTTA-3'
REL257 REL606/71177-71154 5'-CTGCCCAGGCCGTTGCGACTCTAT-3'

Use a 1 minute extension time. This PCR produces a 495 bp product.

Next, cut the PCR product with the restriction enzyme HaeIII (Blunt cutter: GG^CC). It is not necessary to use a PCR cleanup kit before this step. To do this, make a master mix consisting of 3.8 l dH2O, 1 l 10x NEBuffer 4, 0.1 l 100x BSA (10 mg/ml), and 0.1 l of HaeIII (20,000 U/ml). Add 5 l of this master mix to 5 l of PCR sample. The amount of enzyme per reaction comes out to 2 U. Incubate samples in a water bath or PCR machine block at 37C for >1 hr.

Run the products on a 3% agarose gel. Load all 10 l of each sample (adding an appropriate amount of load buffer to them). You will need good resolution of small fragments to see the results. Ara+ with the REL607 reversion mutation will show a shift of the 226 bp band down into the composite ~200 bp band because this mutation creates an additional copy of the restriction site.

Strain Marker RFLP Fragment Sizes
REL606 Ara 226, 197, 72 (bp)
REL607 Ara+ 207, 197, 72, 19 (bp)

The expected result is that a majority (>50%) of selected Ara+ revertants have this exact mutation.

 Barrick Lab  >  ProtocolList  >  ProtocolsAraMarker

Topic revision: r14 - 26 Jun 2013 - 02:22:48 - JeffreyBarrick
Lab.ProtocolsAraMarker moved from Lab.ProceduresSelectingArabinoseMarkerRevertants on 10 Jun 2010 - 18:13 by JeffreyBarrick - put it back
 
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