IGEM:IMPERIAL/2007/Projects/Cell by date/Implementation: Difference between revisions
No edit summary |
|||
Line 19: | Line 19: | ||
__TOC__ | __TOC__ | ||
==Design Focus== | |||
{| style="background:#FAF5FF; border:1px solid #FFDAB9; color:#000000" | |||
|- style="background:#FFA07A" | |||
|| '''Chassis''' || Phase 1 || Phase 2 || Phase 3 | |||
|- style="background:#FFDAB9" | |||
|style="background:#FFA07A" | E.coli || X || || || | |||
|- style="background:#FFDAB9" | |||
| style="background:#FFA07A" | In-Vitro|| X || X || X || | |||
|- style="background:#FFDAB9" | |||
| style="background:#FFA07A" | In-Veso|| X || X || X || | |||
|} | |||
Things to consider: | |||
*Different types of promoters in different chassis | |||
*Different threshold | |||
*Different degradation time | |||
*Different reporters | |||
*Saving time by doing experiments in conjunction with other projects | |||
==First stage: Preparation of vectors and E.coli cultures== | ==First stage: Preparation of vectors and E.coli cultures== | ||
===Introduction=== | |||
This involves a series of cloning and transformation experiments (e.g. digestion, ligation, transformation). Agarose gel electrophoresis will then be used to test for products formed. Miniprep will be performed to extract the plasmid (containing our construct) from the cells, to be used in the other stages. | This involves a series of cloning and transformation experiments (e.g. digestion, ligation, transformation). Agarose gel electrophoresis will then be used to test for products formed. Miniprep will be performed to extract the plasmid (containing our construct) from the cells, to be used in the other stages. | ||
This is done in conjunction with In-veso group (using same gene constructs and plasmids). | This is done in conjunction with In-veso group (using same gene constructs and plasmids). | ||
===Materials & Methods=== | |||
[[IGEM:IMPERIAL/2007/Projects/Cell_by_date/Implementation/List of Required Parts|List of Required Parts]] | [[IGEM:IMPERIAL/2007/Projects/Cell_by_date/Implementation/List of Required Parts|List of Required Parts]] | ||
==Second stage: Calibration and Measurement of Fluorescence + Absorbance== | ==Second stage: Calibration and Measurement of Fluorescence + Absorbance== | ||
===Flurorescence=== | ===Introduction=== | ||
====Flurorescence==== | |||
This involved the use of the fluorometer to measure the fluorescence of a reporter gene (GFP), under the control of a range of promoters (pTet, pBad, pT7), at various temperatures (4<sup>o</sup>C, 25<sup>o</sup>C, 37<sup>o</sup>C, etc.), over 1h time intervals for 24 hours (or however it is deemed fit). | This involved the use of the fluorometer to measure the fluorescence of a reporter gene (GFP), under the control of a range of promoters (pTet, pBad, pT7), at various temperatures (4<sup>o</sup>C, 25<sup>o</sup>C, 37<sup>o</sup>C, etc.), over 1h time intervals for 24 hours (or however it is deemed fit). | ||
Calibration: | Calibration: | ||
*Different [GFP] vs. fluorescence | |||
*intracellular [GFP] vs. lysate [GFP] | |||
*Degradation [GFP] - half-life of 24 hours | |||
====Absorbance==== | |||
===Absorbance=== | |||
In addition, the culture is tested for absorbance use spectrometry to determine cell density at 600nm. | In addition, the culture is tested for absorbance use spectrometry to determine cell density at 600nm. | ||
Calibration: | Calibration: | ||
Dilution plating (or other methods of cell counting) vs. optical density (at 600nm) | *Dilution plating (or other methods of cell counting) vs. optical density (at 600nm) | ||
===Materials & Methods=== | |||
[[IGEM:IMPERIAL/2007/Projects/Cell_by_date/Implementation/List of Required Parts|List of Required Parts]] | |||
==Third stage: Calibration and Measurement of Fluorescence + Absorbance with DsRed-Express== | ==Third stage: Calibration and Measurement of Fluorescence + Absorbance with DsRed-Express== | ||
===Introduction=== | |||
Similar to second stage, but with the reporter gene as DsRed-Express. Preparation of cultures to be done in conjunction with Hrp Characterization System. | Similar to second stage, but with the reporter gene as DsRed-Express. Preparation of cultures to be done in conjunction with Hrp Characterization System. | ||
Calibration to be done with fluorescence for DsRed-Express as well (Note response time). | Calibration to be done with fluorescence for DsRed-Express as well (Note response time). | ||
===Materials & Methods=== | |||
[[IGEM:IMPERIAL/2007/Projects/Cell_by_date/Implementation/List of Required Parts|List of Required Parts]] | |||
---- | ---- | ||
Line 59: | Line 96: | ||
Revision as of 08:54, 31 July 2007
Cell by Date: Implementation
Design Focus
Chassis | Phase 1 | Phase 2 | Phase 3 | |
E.coli | X | |||
In-Vitro | X | X | X | |
In-Veso | X | X | X |
Things to consider:
- Different types of promoters in different chassis
- Different threshold
- Different degradation time
- Different reporters
- Saving time by doing experiments in conjunction with other projects
First stage: Preparation of vectors and E.coli cultures
Introduction
This involves a series of cloning and transformation experiments (e.g. digestion, ligation, transformation). Agarose gel electrophoresis will then be used to test for products formed. Miniprep will be performed to extract the plasmid (containing our construct) from the cells, to be used in the other stages.
This is done in conjunction with In-veso group (using same gene constructs and plasmids).
Materials & Methods
Second stage: Calibration and Measurement of Fluorescence + Absorbance
Introduction
Flurorescence
This involved the use of the fluorometer to measure the fluorescence of a reporter gene (GFP), under the control of a range of promoters (pTet, pBad, pT7), at various temperatures (4oC, 25oC, 37oC, etc.), over 1h time intervals for 24 hours (or however it is deemed fit).
Calibration:
- Different [GFP] vs. fluorescence
- intracellular [GFP] vs. lysate [GFP]
- Degradation [GFP] - half-life of 24 hours
Absorbance
In addition, the culture is tested for absorbance use spectrometry to determine cell density at 600nm.
Calibration:
- Dilution plating (or other methods of cell counting) vs. optical density (at 600nm)
Materials & Methods
Third stage: Calibration and Measurement of Fluorescence + Absorbance with DsRed-Express
Introduction
Similar to second stage, but with the reporter gene as DsRed-Express. Preparation of cultures to be done in conjunction with Hrp Characterization System.
Calibration to be done with fluorescence for DsRed-Express as well (Note response time).
Materials & Methods
Preliminary Preparation
Preliminery Data
Protocols Required:
1. Degradation time
- Endy:RNA Half-life
- λ-Reporters
2. Rate of expression at constant temperature
- Fluorometer Reading
- Noting down colour change (photographs)
3. Range of Reporters
- Flurometer Reading
- RFP
- DsRed
- Beta-Galactosidase_Assay_(A_better_Miller)
- β-galactoside - requires subtrates X-GAL
- Luciferase - requires substrate ATP, O2, and luciferin
4. Range of promoters
Refer to List of Required Parts.
Data Analysis
Refer to Modelling Tab.
Validation of Model
1. Validate [Reporter]max and Vmax value
- Fluorometer Reading
- Noting down colour change (photographs)
2. Validate transient response using best promoters/reporters
- Fluorometer Reading
- Noting down colour change (photographs)