IGEM:IMPERIAL/2007/Projects/Biofilm Detector/Implementation: Difference between revisions

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*Measure of life-span of system
*Measure of life-span of system


 
==Experiments with E. coli as a model of biofilm==
===Experiment I===
===Experiment I===
'''Detector system:'''Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
'''Detector system:'''Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
Line 281: Line 281:
*Test detector system with AHL secreting E coli, as a model of the biofilm
*Test detector system with AHL secreting E coli, as a model of the biofilm


==Experiments with biofilm==
===Experiment J===
===Experiment J===
'''Detector system:'''Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
'''Detector system:'''Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
<br>'''Signaling system:''' Biofilm produced in lab
<br>'''Signaling system:''' Biofilm produced in lab
*Test detector system on biofilm produced in lab
*Test detector system on biofilm produced in lab

Revision as of 08:06, 2 August 2007

Biofilm Detection: Implementation


Biobricks

  • Construct, clone and growth over 5(??) day period
  • General protocols for cloning and making the constructs: General Protocols

Experiments in E. coli

Our initial aim is to test our simple systems in the E. coli chassis. E.coli is a well defined chassis in which most system function. This first phase of experimentation is to ensure that our system works.

Test for AHL Sensitivity

Detector system: Chassis: E. coli, DNA: pLux without hrp system, Reporter: GFP
Signaling system: AHL induced
The sensitivity of the system is to be determined through this experiment. To do this, we induce E. coli cells transfected with the construct with known concentrations of HSL. We then record the increase in GFP, such that we can calculate the rate of GFP production relative to concentration of AHL in solution.
Aims:

  • To determine the rate of change of protein production relative to concentration of AHL
  • To determine the response time relative to concentration of AHL
  • To determine the steady state response of protein relative to concentration of AHL
Variables and Controls
  • Independent variable: [AHL]
    • Range: 0 - 200nM
    • Steps/Intervals: 10nM
  • Dependent variable: Increase in GFP fluorescence over time
    • Response: Over period of 2 hours
    • Sampling intervals:
      1. 5min over first 40min
      2. 10min thereafter
  • Repetitions of experiment(n): 5
  • Predicted length of experiment: 2 days
  • Status: Scheduled for 9th August
Equipment

Day 1:

  • 1 eppindorf of competant cell
  • 10 µl of DNA
  • 0.5 ml LB medium
  • 1 ampicillin plate

Day 2:

  • 40 ml LB medium
  • 270 µl ampicillin stock (4 mg/ml)

Day ?:

  • 21x 25 ml LB medium in reaction tubes
Protocol

Day 1:

  1. Transform plasmid into cells using electroporation
  2. Grow in 0.5 ml LB for 1 hour
  3. Plate on ampicillin plate and leave overnight at 37°C with shaking

Day 2:

  1. Make 8 of 5 ml LB medium with 62.5 µl ampicillin in a centrifuge tubes
  2. Pick 8 colonies and innoculate in tubes
  3. Leave overnight at 37°C with shaking

Day 3:

  1. Make 5 of 550 ml LB medium with 690 µl ampicillin in sterile conical flask
  2. Innoculate in 5 cultures into the the conical flasks
  3. Leave overnight at 37°C with shaking

Day 4:

  1. Operate a water bath at 30°C
  2. Aliquot the 550 ml cultures into 25 ml reaction tubes[?]
  3. Add 53.3075 ng AHL each time to increase [AHL] in steps of 10nM
  4. Begin the timer when AHL is added
  5. At 5 minute intervals for the first 40 minutes, and 10 minute intervals thereafter:
    1. Sample a 1 ml of the reaction mixture
    2. Immediately chill in ice (to slow the rate of reaction)
    3. Centrifuge at maximum speed for 30 seconds to pellet the cells
    4. Remove the supernatant and resuspend the pellet in 1ml distilled water
    5. Put in a spectrometer and excite it at 501nm and detect at 511nm
      [Note: Use solution at 0 minutes as a blank, assume no fluorescence is present prior to activation]

Test for temperature Sensitivity

Detector system: Chassis: E. coli, DNA: pLux without hrp system, Reporter: GFP
Signaling system: AHL induced
The sensitivity of the system to temperature is to be determined through this experiment. To do this, we induce E. coli cells transfected with the construct with a known concentration of HSL. We then record the increase in GFP in response to different temperatures.
Aims:

  • To determine the rate of change of protein production relative to temperature
  • To determine the response time relative to different temperatures
  • To determine the steady state response of protein relative to different temperatures
Variables and Controls
  • Independent variable: Temperature
    • Range: 20 - 40°C
    • Steps/Intervals: 5°C
  • Dependent variable: Change in GFP Fluorescence over time
    • Response: Over period of 2 hours
    • Sampling intervals:
    1. 5min over first 40min
    2. 10min thereafter
  • Repetitions of experiment(n): 5
  • Predicted length of experiment: 1 day ~ 5 hours
  • Status: scheduled for ?? August
Equipment

Day 1:

Day 2:

Day ?:

Protocol

Day 1:

Day 2:

Day 3:

Day 4:


  • Measure of GFP response to varying temperature conditions:
    1. Renew the bacteria with an 25ml of LB with ampicillin (?)
    2. Add ??? ng AHL to the reaction mixture
    3. Keep reaction mixtures at different temperatures from 20°C to 40°C
    4. Take 1ml samples and record fluorescence as above

Test for temperature dependence of the lifespan

Detector system: Chassis: E. coli, DNA: pLux without hrp system, Reporter: GFP
Signaling system: AHL induced
The sensitivity of the system to temperature is to be determined through this experiment. To do this, we induce E. coli cells transfected with the construct with a known concentration of HSL. Different cell cultures are kept at different constant temperatures and their response measured
Aims:

  • To determine the rate of change of protein production relative to temperature
  • To determine the degradation of the system relative to different temperatures
Variables and Controls
  • Independent variable: Temperature
    • Range: 20 - 40°C
    • Steps/Intervals: 5°C
  • Dependent variable: Rate of Fluorescence
    • Sampling intervals:
    1. Monitor once daily
  • Repetitions of experiment(n): 3
  • Predicted length of experiment: 1 - 5 days

(Important Requirement: Experiment should be started on a Monday)

  • Status: scheduled for ?? August
Equipment

Day 1:

Day 2:

Day ?:

Protocol

Day 1:

Day 2:

Day 3:

Day 4:

  • Measure of life-span of system
    1. Grow the bacteria in 15ml of LB with ampicillin
    2. Keep reaction mixtures at different temperatures from 20°C to 40°C
    3. Add ??? ng AHL to the reaction mixture
    4. Take 1ml samples and record fluorescence as above

Experiment B

Detector system: Chassis: E coli, DNA: pLux without hrp system, Reporter: B-D-Galactosidase
Signaling system: AHL induced

  • Measure of B-D-Galactosidase response to varying AHL concentrations:
    1. Same as exp A
  • Measure of B-D-Galactosidase response to varying temperature conditions:
    1. Same as exp A
  • Measure of life-span of system
    1. Same as exp A

Experiment C

Detector system: Chassis: E coli, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
Signaling system: AHL induced

  • Measure of B-D-Galactosidase response to varying AHL concentrations:
    1. Same as exp A
  • Measure of B-D-Galactosidase response to varying temperature conditions:
    1. Same as exp A
  • Measure of life-span of system
    1. Same as exp A

Experiments in Vitro

Experiment D

Detector system:Chassis: In-vitro, DNA: pLux without hrp system, Reporter: GFP
Signaling system: AHL induced

  • Measure of GFP response to varying AHL concentrations:
  • Measure of GFP response to varying temperature conditions:
  • Measure of life-span of system

Experiment E

Detector system:Chassis: In-vitro, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
Signaling system: AHL induced

  • Measure of B-D-Galactosidase response to varying AHL concentrations:
  • Measure of B-D-Galactosidase response to varying temperature conditions:
  • Measure of life-span of system

Experiments in veso

Experiment F

Detector system:Chassis: In-veso, DNA: pLux without hrp system, Reporter: GFP
Signaling system: AHL induced

  • Measure of GFP response to varying AHL concentrations:
  • Measure of GFP response to varying temperature conditions:
  • Measure of life-span of system

Experiment G

Detector system:Chassis: In-veso, DNA: pLux without hrp system, Reporter: B-D-Galactosidase
Signaling system: AHL induced

  • Measure of B-D-Galactosidase response to varying AHL concentrations:
  • Measure of B-D-Galactosidase response to varying temperature conditions:
  • Measure of life-span of system

Experiment H

Detector system:Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
Signaling system: AHL induced

  • Measure of B-D-Galactosidase response to varying AHL concentrations:
  • Measure of B-D-Galactosidase response to varying temperature conditions:
  • Measure of life-span of system

Experiments with E. coli as a model of biofilm

Experiment I

Detector system:Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
Signaling system: AHL secreting Bacteria

  • Test detector system with AHL secreting E coli, as a model of the biofilm

Experiments with biofilm

Experiment J

Detector system:Chassis: In-veso, DNA: pLux with hrp system, Reporter: B-D-Galactosidase
Signaling system: Biofilm produced in lab

  • Test detector system on biofilm produced in lab