ETH2006 iptg

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== chemical sensing device ==
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→[[ETH Zurich 2006#System modeling|back to main page]]
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The chemical sensing device's PoPs output activity should be a monotonic function of the concentration of a certain substance in the cell's environment.
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== Chemical sensing device ==
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=== implementation alternatives ===
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The chemical sensing device's PoPS output activity should be a monotonic function of the concentration of a certain substance in the cell's environment.
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=== Implementation alternatives ===
# Lactate  lacI represses, IPTG induces ([http://partsregistry.org/Part:BBa_R0011 BBa_R0011] or [http://partsregistry.org/Part:BBa_R0010 BBa_R0010] )  
# Lactate  lacI represses, IPTG induces ([http://partsregistry.org/Part:BBa_R0011 BBa_R0011] or [http://partsregistry.org/Part:BBa_R0010 BBa_R0010] )  
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# simple sugar Arabinose ([http://partsregistry.org/Part:BBa_R0080 BBa_R0080])
# simple sugar Arabinose ([http://partsregistry.org/Part:BBa_R0080 BBa_R0080])
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I see the main difficulty in the spatial separation as the cells are growing in the petri dishes. since the inducers are water-soluble we would have to fix the chemicals onto the petri dish.
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I see the main difficulty in the spatial separation as the cells are growing in the petri dishes. Since the inducers are water-soluble we would have to fix the chemicals onto the petri dish.
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=== Current implementation ===
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Since most parts were already existing in the registry, we decided to use the LacI system with IPTG as chemical to be sensed.
[[Image:ETH_IPTG_sensing_parts.png|center|600px|complete system based on alternative 1]]
[[Image:ETH_IPTG_sensing_parts.png|center|600px|complete system based on alternative 1]]
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=== assembly procedure ===
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=== Modeling ===
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where we got it and link to theyer documentation
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[[ETH_Sim_Mod_IPTG|simulation results]]
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=== Assembly procedure ===
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''Where we got it and link to their documentation''
Progress:
Progress:
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;2006/10/04: Transformed cells, plated them
;2006/10/04: Transformed cells, plated them
;2006/10/05: Found plates empty after 18h on the table, put into incubator at 37°C
;2006/10/05: Found plates empty after 18h on the table, put into incubator at 37°C
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;2006/10/06: picked cultures onto fresh plates
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;2006/10/06: found lot of colonies, picked single ones and restreaked onto fresh plates
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=== test procedure ===
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=== test results ===
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=== parts ===
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=== Test procedure ===
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;2006/10/07: streaked transformed bacteria on 4 different plates:
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*plus IPTG, plus X-Gal
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*plus IPTG, no X-Gal
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*no IPTG, plus X-Gal
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*no IPTG, no X-Gal
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all plates contained the appropriate antibiotic (Chloramphenicol)
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=== Test results ===
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;2006/10/08: results:
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*plus IPTG, plus X-Gal: blue
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*plus IPTG, no X-Gal: white
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*no IPTG, plus X-Gal: light blue (system is leaky)
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*no IPTG, no X-Gal: white
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→[[ETH Zurich 2006#system modeling|back to main page]]
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[[Image:chem_test.jpg|600px|center]]

Latest revision as of 12:41, 1 November 2006

back to main page

Contents

Chemical sensing device

The chemical sensing device's PoPS output activity should be a monotonic function of the concentration of a certain substance in the cell's environment.

Implementation alternatives

  1. Lactate lacI represses, IPTG induces (BBa_R0011 or BBa_R0010 )
  2. Tetracycline, TetR inhibitor, Tet inducer by inhibiting TetR (or aTc, it's analog) (BBa_R0040)
  3. combination thereof (BBa_I13614 / BBa_13617 / BBa_I13623 / BBa_I13624 / BBa_I13627 / BBa_I13637 / BBa_I13653)
  4. simple sugar Arabinose (BBa_R0080)

I see the main difficulty in the spatial separation as the cells are growing in the petri dishes. Since the inducers are water-soluble we would have to fix the chemicals onto the petri dish.

Current implementation

Since most parts were already existing in the registry, we decided to use the LacI system with IPTG as chemical to be sensed.

complete system based on alternative 1

Modeling

simulation results

Assembly procedure

Where we got it and link to their documentation

Progress:

2006/10/03
Made LB-Agar plates with antibiotics
2006/10/04
Transformed cells, plated them
2006/10/05
Found plates empty after 18h on the table, put into incubator at 37°C
2006/10/06
found lot of colonies, picked single ones and restreaked onto fresh plates

Test procedure

2006/10/07
streaked transformed bacteria on 4 different plates:
  • plus IPTG, plus X-Gal
  • plus IPTG, no X-Gal
  • no IPTG, plus X-Gal
  • no IPTG, no X-Gal

all plates contained the appropriate antibiotic (Chloramphenicol)

Test results

2006/10/08
results:
  • plus IPTG, plus X-Gal: blue
  • plus IPTG, no X-Gal: white
  • no IPTG, plus X-Gal: light blue (system is leaky)
  • no IPTG, no X-Gal: white
Chem test.jpg
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