Team:Edinburgh/Notebook/Blue light sensor

From 2010.igem.org

Revision as of 15:09, 22 October 2010 by Macbereska (Talk | contribs)





Blue Light Sensor


14/07/10

Received parts from Lausanne:

  • BBa_191006 (113 ng/µL) – LovTAP alone
  • BBa_191004 (166 ng/µL) – Readout
  • BBa_191003 (230 ng/µL) – whole system
  • BBa_191009 (85 ng/µL) – mutant
  • Sosnick vector containing TrpR (393 ng/µL) – vector


16/07/10

Transformations using 100 µL of cells, 900 µL broth

  • K191004 - amp
  • K191003 - kanamycin
  • K191009 – kanamycin
  • Sosnick vector with TrpR – amp

Note: Labeling on tubes is unclear – K191009 and K191004 got mixed up, so plating both tubes on both Kan and amp


22/07/10

  • Minipreps: K0998010 – 5x (1 didn’t grow, but did anyway)
  • Blue sensors (3 biobricks and Sosnick vector) – cultures set to grow overnight

25/07/10 Digest of the blue light sensor minipreps was performed with EcoRI and BamHI; samples:

  • 3- K191004; 900ul, (3)
  • 4- K191004; 100ul, (2)
  • 5-K191009; 100ul, (1)
  • 6- K191009; 100ul, (6)
  • 7- K191009; 900ul, (4)
  • 8- K191009; 100ul, (2)
  • 9- K191003; 900ul, (2)
  • 10- K191003; 900ul, (5)
  • 11- K191003; 100ul, (4)
  • 12- K191003; 100ul, (1)
  • 13- K191004; 100ul, (3)
  • 14- K191004; 900ul, (5)

Lanes- 1- marker, 2-9 sampels as in order, 10-empty, 11, 12- marker instead of the samples- need to run last two again

Gel 1.jpg Gel 2.jpg LAST TWO LANES- NSAMPLES NO 13 AND 14 FROM THE ABOVE LIST


28/07/10

Double transformants made using a novel cowboy procedure- double transformation with 4ul of each piece od DNA. Chances of succes- very very low... But at least it will be proved that it won't work! Trans. 1: BBa_K191004+ K191003- read out + LovTap Trans. 2: BBa_K191004+ K191009- read out + mutated LovTap

30/7/10 set up experiments to see if the blue light sensor will activate the response system under the daylight. Both liquid cultures and plates were set up, with red and white colonies- first supposed to turn white in the daylight and stay red in the dark (under the foil), second ones- no change of the colour. The same applies to the liquid cultures. However, the experiment failed- no proper growth was observed, and if there was a growth - it was very weak. No pigment observed, apart from the small points in the centre. Hypothesis- not stable plasmids-- cells look like they are not really resistant. Recorded growth:

K191004+9 control K191004+9 K191004+3 control K191004+3
DARK ++ , white +++ , white ++ , white +++ , white with red points
LIGHT + , white +++ , white with red point + -almost no growth ++ white


2/8/10

Run the digest of the minipreps from the white and red cultures of double transformants. No proper DNA band in the solution- repeat the procedure or not? Don't know what to do.... again. File:Gel 3.jpg Collect the thoughts and ideas and start again tomorrow!

6/8/10

double transformants were prepared again, using non-cowboy procedure. 04 cells were first MADE COMPETENT, then transformed with 03 and 09, also 1 neg control was plated. Grow white on the intitial plate, then turned red if subcultured.

7-8/08

'Subbed these to duplicate fresh plates and incubated overnight at room temperature either under a fluorescent lamp or wrapped in foil - all white in both cases (and growth not great, probably because of low temperature)'. The plates were moved to 37C with the lamp /one under the light, one in the dark. so far -no results, checking in an hour/.

Another idea- check for stability of the insert- we don't know if the plasmids are compatibile. Streaking from original plates to check if single colonies will be a mixture of white and red or just red- origin? no plasmid maps from Lausanne. by Chairman-->' If we can't find this information, I think our best course is to PCR out both inserts and combine them in a single vector, preferably pSB1C3.'


9/8/2010

to do:

  • primers for the parts to put them in a vector
  • check the lamp every hour!!

go thruough Lausanne website to find the plasmid maps get back to Mexico about the parts and etc. find out the conditions for the blue light sensor assay!

10/08/10

  • assay with dark/light liquid cultures - fluorescence measurment and OD, after 5 h in the shaker under lamp- see video and pictures
  • email to Mexico

11/08/10

  • primer designed for combining LOVTap and Readout1 into 1 cell
  • repeated assay with the smae samples, after overngiht in RT and %5h under lamp (for the light samples) and RT without shaking
  • primary cultures streaked to amp/kan/IPTG plates- part 4+9 and 4+3 -three clones each

12/08/10

  • results analysis after LOVTap experiment:check file, add graphs later.
  • email from Mexico about Blue promoter

16/08/10

  • streaked single clone for 9+4 and 3+4 (clones number 5 and 2, respectively)- for tomorrow's experiment
  • minipreped mysterious double transformants and Sacb smples
  • tried out the box on the shaker- unscrewed the things.
  • made the graphs from the second reading
  • 03 and 09 LovTap taken for sequencing.

to do: decide on the illumination length and think about controls and how many samples do you want to put. check Lausanne website t-test to check to importancy of the differences between the means.

17/07/10

  • desinged experimental set up for the LovTap blue light response experiment /see next day/
  • BAD NEWS: there is a suspicion of 1bp deletion in LovTap!!! Chairman noticed it when he was checking the parts base by base. Should have done it much much earlier probably to save the time...
  • BAD NEWS: lack of the proper thinking put in doubt all the results from previous two experiments (that is why you can't find any files of it attached)- there was no IPTG added to the samples, therefore LOVTap expression was not induced- no point to do T-test right now... :( Well, at least I will learn from it and add it next time!


18/08/10

  • tested LovTap under the blue light
  • conditions:

Liquid cultures (same as for minipreps) were grown overnight in 37C with antibiotics. The next day, bottles with 3.5 ml of broth were inoculated with the 0.5 ml of appropriate cultures (0.5. ml of broth added as a control).

  • sample designation: (# refers to the clone number form the original plate). Original plates are the ones made on INSERT THE DATE LAZY and have 2 clones on each plates (clones1-3 are K191003&4 double transformants, clones 4-6 are K191009+4 double transformants).
  1. K191003+4 (#1) + Amp + Kan + IPTG + LIGHT
  2. K191003+4 (#1) + Amp + Kan IPTG + DARK
  3. K191003+4 (#2) + Amp + Kan IPTG + LIGHT
  4. K191003+4 (#2) + Amp + Kan IPTG + DARK
  5. K191009+4 (#4) + Amp + Kan IPTG +LIGHT
  6. K191009+4 (#4) + Amp + Kan IPTG +DARK
  7. K191009+4 (#5) + Amp + Kan IPTG +LIGHT
  8. K191009+4 (#5) + Amp + Kan IPTG +DARK
  9. K191004 ONLY #2+ Amp + LIGHT
  10. K191004 ONLY #2+ Amp + DARK
  11. neg. control- broth, Amp + Kan + IPTG + LIGHT
  • samples designated DARK were wrapped in the aluminium foil straight after the inoculation; the cap was not wrapped (not see through anyway)so that samples could be easily taken without unwrapping the bottles from the foil.
  • All the samples were then taken to the shaker in the hot room and placed in prepared spots: for the dark- anywhere on an easily accessible holder, for light- in 2 rows of holders.
  • Light samples were covered with the cardboard box with blue LEDs attached on the sides, in a way to optimize light accession to the samples (ask Sarah for the details). Box was securely taped to the shaker.
  • Measurments were taken every half an hour: 200ul of the samples were placed in the numbered cuvette and then 800ul of water was added. Readings of fluroscence (green mode) were taken in standard fluorescence units (SFU, two readings each). Then optical density was measured (upstairs in the incubator room) at 360 nm wavelength. Control was used to calibrate the machine (set ref button). Also 2 readings were taken. Samples were shaken by inversion prior to taking measurment.
  • Experiment was stopped after 3 hours (6 sets of reading taken).
  • Result analysis

see the Excel file attached:

File:LovTap FAIL exp 18aug.xls

To generate the data for the graph:

  1. means were calculated from 2 readings of optical density and fluorescence
  2. (mean SFU minus background SFU) was divided by (mean OD minus background OD, if different from 0).
  3. table was made for the samples at different points of time- e.g. sample 1 after 30 min, 60 min, 90 min, 120 min etc.
  4. graph was made with series named the same as the samples

File:Untitled.JPG

    • BAD BAD VERY BAD NEWS: after 2 hours of measurments the results of the sequencing were know and revealed that THERE IS A 1BP DELETION IN LOVTAP 03 AND 09 WHICH RESULTS IN FRAMESHIFT AND LACK OF THE FUNCTIONAL PRODUCT!!!! :(:(:( despite this information, it was decided that the experiment will be finished and analysed as initially planned.

19/08/2010

  • Pcr- mutagenensis of LovTap- Mabel, adding missing bp.
  • Puryfing PCR product from the solution.


20/8/2010

  • PCR run on the gel -correct band of ~5.5. kb size, suggest that the PCR worked well. couple of other fainter bands
  • Self -ligation overnight (MABEL self ligation- 12ul of H2O, 4ul of DNA, 2 ul of Ligase buffer, 1 ul of T4 DNA ligase, 1ul of T4 polynucleotide kinase.
  • transformation and setting up the liquid cultures for the minipreps over the weekend.

23/08/2010

  • mini-prep DNA from the colonies after PCR- marker worn off in the shaker,so 3.2. and 9.1. got mixed up- probably sequencing necessary to distinguish the mutated version from non-mutated
  • digest minipreps with EcoRI, run the gel
  • run 5ul of the ligated 03 and 09 on the gel /also Richards samples/.

24/08/2010

  • repeated digest of mutated LovTap samples: 3.1, 3.?, 3.3., 3.4 9.?, 9.2 with EcoRi
  • minipreped 6 more clones of mutated LovTap 03 and 09 from the same plate, labelled- 3.6, 3.7, 3.8, 9.4, 9.5, 9.6. Run the digest with EcoRI. Note: 3.7 sample is higly diluted as 80ul of EB was used instead of 40ul. oops.
  • delivered mutated 3.? and 9.2 minipreped clones for sequencing /only 2 reactions: each sample- forward/.

04/10/10 We may have a working LovTap construct + red/white (RFP) reporter system thanks to Mexico.


Minor characterisation experiment:
-LovTap constructed with red-white RFP reporter
-If activated, the blue light sensor transformants should produce red colonies
-Blue light sensor containing-colonies from transformant plate streaked onto two plates
-One plate left in the light, the other left in the dark
-If the one in the light grows red and the one in the dark doesn't, it is a good indication that the construct is working

8/10/2010

  • repetaed LOVTap charactierzation- with TrpR mutant and WT under light/dark conidtion.
  • no clear response was seen.

22/10/2010'

  • checking temperature response of LOVTap
  • setting up samples with CMM minum medium, enriched in thymine, trace elements and glucoe.

CELLS FAIL TO GROW!

Retrieved from "http://2010.igem.org/Team:Edinburgh/Notebook/Blue_light_sensor"