Team:Minnesota/Project

From 2009.igem.org

(Difference between revisions)
Line 16: Line 16:
[[Image:ANDgate.jpg|400px|right]]
[[Image:ANDgate.jpg|400px|right]]
 +
<h2>AND Gates</h2>
 +
<h3> How it works</h3>
We studied the potential of a synthetic, single promoter AND gate. This helps us understand at a fundamental level what is happening in a network with multiple regulators and opens further research paths. The device consists of parts of the Tet (tetracycline) and Lac (lactose) and responds to commonly used inducers IPTG (Isopropyl β-D-1-thiogalactopyranoside) and aTc. Three or fewer of these operators can be combined to form a promoter and the order and quantity of each operator site result in different constructs, that is, given three blank spots for operators on a promoter and the choice of either -, T or L for each spot, there are a variety of possible promoter designs. We chose to focus on four constructs:
We studied the potential of a synthetic, single promoter AND gate. This helps us understand at a fundamental level what is happening in a network with multiple regulators and opens further research paths. The device consists of parts of the Tet (tetracycline) and Lac (lactose) and responds to commonly used inducers IPTG (Isopropyl β-D-1-thiogalactopyranoside) and aTc. Three or fewer of these operators can be combined to form a promoter and the order and quantity of each operator site result in different constructs, that is, given three blank spots for operators on a promoter and the choice of either -, T or L for each spot, there are a variety of possible promoter designs. We chose to focus on four constructs:

Revision as of 16:27, 16 July 2009

Mnlogo.jpg
Home The Team The Project Parts Submitted to the Registry Modeling Parts Characterization Notebook

Contents

The Project

ANDgate.jpg

AND Gates

How it works

We studied the potential of a synthetic, single promoter AND gate. This helps us understand at a fundamental level what is happening in a network with multiple regulators and opens further research paths. The device consists of parts of the Tet (tetracycline) and Lac (lactose) and responds to commonly used inducers IPTG (Isopropyl β-D-1-thiogalactopyranoside) and aTc. Three or fewer of these operators can be combined to form a promoter and the order and quantity of each operator site result in different constructs, that is, given three blank spots for operators on a promoter and the choice of either -, T or L for each spot, there are a variety of possible promoter designs. We chose to focus on four constructs:

  • T T L
  • T T -
  • T - -
  • - T -

We also examined 4 mutations in the Tet operator site for each construct.




The Experiments



Results


Protocols: Standard techniques that we used in the wet lab

Bacterial Culture

Sterile Technique

  1. Always work around a flame or in the hood
  2. Flame the mouth and cap of any bottle, flask or tube upon uncapping and recapping
  3. Sterilize metal instruments between uses by dipping in 100% ethanol and flaming


Bacterial Culture Maintenance

Culture cells:

  1. At 36 degrees Celsius
  2. Shaking at 220 rpm
  3. At 10% total flask/tube volume
  4. In mid-log phase(0.1 < OD600 <= 0.4) (with OD600 = 1 ->8.8x108cell/ml)


Bacterial Culture For Gene Expression Experiments

  1. Pick and individual colony from a plate and inoculate 2ml LB + amp media
  2. Incubate overnight at 37 C, shaking at 220 rpm
  3. Inoculate fresh media with overnight culture such that new culture has 2.5% inoculum; this is the secondary culture
  4. Incubate at 37 C shaking at 220 rpm until OD600 = 0.4 (~2 hrs)
  5. Inoculate 4 ml LB + amp + inducer (aTc or IPTG) with 100ul secondary culture
  6. Continue cultures as described above in "bacterial culture maintenance" for 9 hrs
  7. Isolate cell samples from cultures at 3, 6, and 9 hour time points
  8. Remove 100ul sample aliquots from cultures
  9. Pellet samples at 5K rpm for 5 minutes
  10. Remove supernatant
  11. Wash cells with 1 ml chilled 1xPBS, pH 7.6
  12. Resuspend cells by vortexing
  13. Re-pellet cells at 5K rpm for 5 minutes
  14. Remove supernatant
  15. Fix cells; resuspend cells in 1 ml 4% PFA (in PBS)
  16. Incubate at RT for 30 minutes
  17. Pellet cells at 5K rpm for 5 minutes
  18. Remove supernatant
  19. Resuspend cells in 1 ml 1xPBS
  20. Store samples at 4 C until analysis by flow cytometry


Transformation of Chemically Competent Cells

  1. Thaw cells and incubate transformant DNA in ice(~15 minutes)
  2. Combine 50 ul cells with ~3uL DNA and mix gently
  3. Incubate samples on ice for 15 minutes
  4. Heat shock cells in 42C water bath of 50 seconds
  5. Incubate samples on ice for 5 minutes
  6. Recover cells in 0.5 ml SOC media, shaking at 37C for 1 hour at 220 rpm
  7. Transfer cells to a 2 ml microfuge tube
  8. Spin cells down at 6K rpm for 2 minutes
  9. Remove all but ~100uL supernatant media
  10. Resuspend cells gently in remaining media
  11. Plate cells on LB + ab plates
  12. Incubate plates overnight at 37C




DNA Work


Plasmid Prep from cultures (using QIAprep Spin Miniprep Kit)

  1. Pick and individual colony from a plate and inoculate 2ml LB + ab media
  2. Incubate culture overnight at 37C
  3. Transfer culture to 2 ml microfuge tube
  4. Spin cells down at 13K rpm for 2 min at RT and remove supernatant
  5. Resuspend cells in 250 ul Buffer P1 (stored at 4 C)
  6. Add 250 ul Buffer P2 and mix thoroughly by inverting-- the solution should turn blue
  7. Add 350 ul Buffer N3 and mix immediately and thoroughly by inverting-- the solution should turn colorless
  8. Centrifuge sample at 13K rpm for 10 minutes
  9. Transfer supernatant to a fresh QIAprep spin column, leaving cell debris pellet behind
  10. Centrifugre supernatant into column at 13K rpm for 1 minute
  11. Remove the flowthrough
  12. Wash column with 0.5 ml Buffer PB; apply to column and spin through at 13K rpm for 1 minute
  13. Remove the flowthrough
  14. Wash column with 0.75 ml Buffer PE; apply to column and spin through at 13K rpm for 1 minute
  15. Remove the flowthrough
  16. Spin out residual liquid at 13K rpm for 1 minute
  17. Place column in a fresh 1.5 ml microfuge tube
  18. Elute DNA; apply 40 ul Buffer EB to column, incubate at room temperature for 2 minutes and spin out of column at 13K rpm for one minute


DNA quantification

  1. Diluite DNA as appropriate in water (1<= DF <=1/100) to a total volume of 50 ul
  2. Similarly dilute blank DNA buffer solution with water to a total volume of 50 ul
  3. Read absobance of blank and DNA sample at lambda = 260 and 280
  4. Calculate [DNA]; [DNA](ng/ul) = DF*A260*50
  5. Determine sample purity; pure DNA A260/A280 = 1.8


Retrieved from "http://2009.igem.org/Team:Minnesota/Project"