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Team:KULeuven/Lab/Blue Light Receptor
From 2009.igem.org
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*Strain: from lab | *Strain: from lab | ||
*Primers: self made and ordered | *Primers: self made and ordered | ||
| - | ** | + | **For PCR |
***Forward: CATCAT GAATTCGCGGCCGCTTCTAGAG TTT GAC AGG TTC GTC GTC | ***Forward: CATCAT GAATTCGCGGCCGCTTCTAGAG TTT GAC AGG TTC GTC GTC | ||
***Reverse: CTGCAGCGGCCGCTACTAGTA CCT CTG TTA AAA ATG TTA ATC AAT GTT AAG | ***Reverse: CTGCAGCGGCCGCTACTAGTA CCT CTG TTA AAA ATG TTA ATC AAT GTT AAG | ||
| - | ** | + | **For ‘cleaning’ |
| - | *** | + | ***Under construction |
| - | * | + | *The GFP ({{kulpart|BBa_E0240}})came from the freezer (-80) at the lab |
==Steps== | ==Steps== | ||
Revision as of 10:59, 10 August 2009
Contents |
Planning
Goal
Purifying the promoter region of the blue light receptor from E. Coli. This region needs to be ‘cleaned’ and possible restriction sites need to be mutated out. Afterwards a biobrick can be made.
Required
- E.Coli strain ( MC4100)
- Primers (1) for PCR: already ordered (nummers: 2171 (FP) - 2172 (RP))
- Primers (2) for ‘cleaning’ region (under construction)
- GFP with RBS and Terminator sequence
Where from
- Strain: from lab
- Primers: self made and ordered
- For PCR
- Forward: CATCAT GAATTCGCGGCCGCTTCTAGAG TTT GAC AGG TTC GTC GTC
- Reverse: CTGCAGCGGCCGCTACTAGTA CCT CTG TTA AAA ATG TTA ATC AAT GTT AAG
- For ‘cleaning’
- Under construction
- For PCR
- The GFP ()came from the freezer (-80) at the lab
Steps
- PCR reaction to purify suspected promoter region.Probably has a promoter, RBS and SpeI restriction site.
- partial digestion with SpeI. After, run agarose gel to identify the correctly cut sequence and then perform a gel extraction. cut with EcoRI.
- cut GFP with EcoRI and XbaI.Couple PCR fragment to GFP. measure reactivity of the promoter.
- cut vector with SpeI and use klenow to create blunt ends. then ligate together. use initial primers to recreate restriction sites and to select correctly ligated sequences. link to GFP to check the activity of the sequence.
- “cleaning” region to strictly promoter. Cutting in different pieces and measuring the GFP activity:
a. Same reverse primer, shortening through forward primer. b. Once there is no activity anymore with forward primer, keep it constant and shorten reverse inkorten c. Once promoter found: updating those primers with a pre en suffix to make a biobrick out of the promoter
important
following conditions need to be kept in account:
- for growth of the bacteria: 37°C
- for expression of the genes regulated by ycgF/E system: 16°C
- at 16°C: expression will start after 50h and a very slow reversion to the ground state of ycgF
- working with a colony in the dark and one in light so that the effects of cold temperature on the gene expression pattern can be calculated out.
- blue light does NOT induce stress and cell death in E. Coli
- to monitor growth of the cells, measurement at OD 578 can be used
