Mesoplasma florum: Tn5 Transposase
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* Fig 1, 1.8 Kb transposon reacted at 2.5 ng/ul with Tn5 transposase at 10 ng/ul in 400 ul final volume, 1 hour at 37C | * Fig 1, 1.8 Kb transposon reacted at 2.5 ng/ul with Tn5 transposase at 10 ng/ul in 400 ul final volume, 1 hour at 37C | ||
** this is 181 fmol/ul of DNA and 5.5 pmol/ul transposase, or a 30x molar excess of transposase | ** this is 181 fmol/ul of DNA and 5.5 pmol/ul transposase, or a 30x molar excess of transposase | ||
| - | * Concentrated to 20 ul and run on a 1.2% gel | + | ** Concentrated to 20 ul and run on a 1.2% gel |
| + | * 3.7 Kb transposon reacted at 50 ng/ul with Tn5 transposase at 10 ng/ul in 40 ul volume, 1 hour at 37C | ||
| + | ** this is 1.8 pmol/ul DNA and 5.5 pmol/ul transposase, for a 3x molar excess | ||
===References=== | ===References=== | ||
* [http://www.neb.com/nebecomm/products/productE6900.asp NEB IMPACT-CN web page] | * [http://www.neb.com/nebecomm/products/productE6900.asp NEB IMPACT-CN web page] | ||
* Goryshin00 | * Goryshin00 | ||
Revision as of 17:07, 19 March 2008
Contents |
Tn5 Transposase production
Tn5 transposase is the key enzyme in forming transposomes for random transposon insertions. It is sold by Epicentre at ridiculously high price. Here, we make it from a plasmid provided by Prof. Wolfgang Hillen PMID 16820464. The protocol also builds on the NEB IMPACT-CN protein purification kit.
Materials
Protocol
- Grow BL21(DE3)pLysS cells transformed with pWH1891 in 10 ml culture.
- Inoculate 2 liters of LB/Cm/Amp culture medium with the culture and grow overnight at 23°C
- Induce cultures at OD 0.5 with 50 mM IPTG and grow an additional 5 hours
- Spin down cultures and resuspend in 50 ml TEGX buffer/original liter, transferring to 50 ml centrifuge tubes
- Spin down a second time and resuspend in 10 ml/original liter TEGX + Roche Complete protease inhibitor
- Sonicate 3x pausing 10 minutes between sonications with the cells on ice
- Centrifuge to remove cell debris
- Load a 2 cm diameter column with 20 ml chitin bead suspension (10 ml beads)
- Wash the column with 100 ml TEGX buffer
- Load the cell supernatent onto the column and allow it to flow through
- Flow the supernatent past the column a second time
- Wash the column with 200 ml TEGX buffer
- Add 1 ml of 1M IPTG to 20 ml of TEGX buffer
- Flow the 20 ml IPTG + TEGX into the column
- Cap the column and hold at 4°C overnight
- Recover the protein with 10 ml TEGX buffer flowed through the column
Molarity
- Gel runs at 55 KD, approximately correct for a 450 AA protein.
- Kostner06 uses 100-500 fmol DNA + 5x excess protein, or .5 - 2.5 pmol
- 1 pmol protein = 55000 g/mol * 1e-12 mol = 55 ng
- 1 pmol transposon = 2700 * 660 * 1e-12 = 1.8 ug
- 100 fmol transposon = 180 ng
DNA binding tests
- Use constant 200 ng of DNA (dilute from 1 ug/ul stock)
- Use serial dilutions of protein starting at 8 ug/ul
- 2x dilutions 0, 2, 1, 500, 250, 125, 62.5, 31.25, 15.6, 0 into 20ul TEGX + 200 ng/ul transposon DNA
- Incubate 30 minutes at 37
- Run on 0.8% E-Gel
- DNA mixture 10*200 ng = 2 ug DNA = 2 ul DNA into 200 ul TEGX
Gel images, Goryshin00
- Fig 1, 1.8 Kb transposon reacted at 2.5 ng/ul with Tn5 transposase at 10 ng/ul in 400 ul final volume, 1 hour at 37C
- this is 181 fmol/ul of DNA and 5.5 pmol/ul transposase, or a 30x molar excess of transposase
- Concentrated to 20 ul and run on a 1.2% gel
- 3.7 Kb transposon reacted at 50 ng/ul with Tn5 transposase at 10 ng/ul in 40 ul volume, 1 hour at 37C
- this is 1.8 pmol/ul DNA and 5.5 pmol/ul transposase, for a 3x molar excess
References
- NEB IMPACT-CN web page
- Goryshin00


