Team:Buenos Aires/Results/BBsTesting

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We can infer from this data that though they have not died, they may have enter into a '''...Alan state'''. In this way cells can survive for a period of time in media defficient in amino acid (at least, during the time course of our experiment), but grow slower. Probably it would requires more time than 3 days to observe significative cell dying.
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We can infer from this data that though they have not died, they may have enter into a '''...Alan state'''. In this way cells can survive for a period of time in media defficient in amino acid (at least, during the time course of our experiment), but grow slower. Probably this would require more time than 3 days to observe significative cell dying.

Revision as of 02:32, 27 October 2012

Contents

After the Jamboree!

When we returned from the Latin America Jamboree we focused all our efforts on completing the neccesary transformations to test our devices and our project as a whole.

We devided this task in three sections


Week 1&2 : Yeast expression vectors & Transformations

In order to construct the yeast expression plasmids we choosed 3 vectors, 2 with a tryptophan marker and 1 with an histidine marker:

  1. pCM182/5, which are centromeric plasmids with TRP1 marker, and with a doxycycline repressible promoter [Gari et al 1996].
  2. pEG202, with a 2 ori, HIS3 marker and a constitutive promoter (PADH1).


BsAs2012-plasmid-PEG202.jpg BsAs2012-plasmid-BPCM185.gif

The cloning we did was:

BBa_K792009 (PoliHa) BBa_K792010 (TRPZipper2) BBa_K792011 (PoliHb) BBa_K792012 (PoliWb)
pCM182 (TRPa) X X
pCM185 (TRPb) X X
pEG202 (HIS) X X


Protocol

  1. Digestion of plasmids and TRP/HIS export device:
    1. pCM182; pCM 185; BBa_K792010 y BBa_K792012 were digested with BamHI and Pst1 restriction enzymes.
    2. pEG202; BBa_K792009 y BBa_K792011 were digested with BamHI and Not1.
  2. Purification of digested vectors (pCM185; pCM182; pEG202)
  3. Ligation of vectors and devices according the anterior table (T4 ligase protocol, overnight)
  4. Transformation of E. Coli DH5a with the ligation products. Bacterias were plated on LB-agar with Ampicillin, and incubated over night at 37 °C.
  5. Colonies were used for liquid cultures (LB + Ampicillin) and minipreps were made.
  6. Constructions (vector + insert) were checked by digestion with restriction enzymes, and 1%-agarose gel (1kb and 100bp as markers).


Once obtained the desired constructions, we transformed yeast strains:

  1. TCY3081: W303, bar1-, ura3::PAct1-YFP
  2. TCY3128: W303, bar1-, leu2:: Pprm1-CFP 405


We got the following transformed strains:

BsAs2012-icono-Cepa1.jpg Name YFP_TRPa_TRPZipper2
Strain TCY3081 (YFP)
Plasmid pCM182 (TRPa) + BBa_K792010 (TRPZipper2)
BsAs2012-icono-Cepa2.jpg Name YFP_TRPa_PoliWb
Strain TCY3081 (YFP)
Plasmid pCM182 (TRPa) + BBa_K792012 (PoliWb)
BsAs2012-icono-Cepa3.jpg Name YFP_TRPb_TRPZipper2
Strain TCY3081 (YFP)
Plasmid pCM185 (TRPb) + BBa_K792010 (TRPZipper2)
BsAs2012-icono-Cepa4.jpg Name YFP_TRPb_PoliWb
Strain TCY3081 (YFP)
Plasmid pCM185 (TRPb) + BBa_K792012 (PoliWb)
BsAs2012-icono-Cepa6.jpg Name CFP_HIS_PoliHa
Strain TCY3128 (CFP)
Plasmid pEG202 (HIS) + BBa_K792009 (PoliHa)
BsAs2012-icono-Cepa5.jpg Name CFP_HIS_PoliHb
Strain TCY3128 (CFP)
Plasmid pEG202 (HIS) + BBa_K792011 (PoliHb)

Week 3: Synthetic Ecology Characterization

Our task is to characterize our system including the devices functioning. We want specifically to:

  1. Quantify the export of Trp as proof that the devices work
  2. Determine experimentally some of the parameters that we used in the model
  3. Characterize the growth of the transformed strains in coculture

In order to characterize the devices that we used to transform our strains we came up with the series of assays that we describe below.

Devices characterization

Secretion Rate of Trp as a function of culture growth

The first step was to actually check if the construct works: do the transformed yeast strains - with the tryptophan devices- actually secrete tryptophan into the medium?

To test this we used the following strains:

BsAs2012-icono-Cepa3.jpg BsAs2012-icono-Cepa4.jpg BsAs2012-icono-YFP-185.jpg
YFP_TRPb_TRPZipper2 YFP_TRPb_PolyWb YFP_TRPb
BsAs2012-icono-YFP.jpg
YFP
BsAs2012-icono-Cepa1.jpg BsAs2012-icono-Cepa2.jpg BsAs2012-icono-YFP-182.jpg
YFP_TRPa_TRPZipper2 YFP_TRPa_PolyWb YFP_TRPa


Protocol
  • We started 5ml cultures with 3 replica until they reached exponential phase, overnight, using a -T medium.
  • Starting OD for the assay 0.1 (exponential phase).
  • We measured OD every hour until they reached an OD: 0.8 (5 hs approximately).
  • We measured the Trp signal for each culture medium using the spectrofluorometer.

NOTE: The fluorescence meausurements taken for the Tryptophan in the medium, take into account both the aminoacid secreted by the device and the one diffused.

Therefore the secretion rates calculated will be higher than the actual ones. We used an empty plasmid as control to study tryptophan diffusion.

We used a simple model to measure the secretation rate for all the strains. Since the cultures are in exponential phase, we take

BsAs2012-eqTrp1.jpg

After a few calculations, we find that

BsAs2012-eqTrp2.jpg

Results

Next we show the average OD for each strains used, needed to calculate the export rates of Trytophan.

150

150

Figure X. check

150

Figure X. check

Tryptophan secretion at increasing histidine concentrations

We asked ourselves which was the dependance of tryptophan secretion on the amount of histidine in medium. We carried on this test in order to determine whether the secretion of tryptophan depends on the concentration of another aminoacid in the media, such as histidine and what would be the necessary amount of histidine in medium for the start of our system.

In this experiment we used strains:


BsAs2012-icono-Cepa3.jpg BsAs2012-icono-Cepa4.jpg BsAs2012-icono-YFP-185.jpg
YFP_TRPb_TRPZipper2 YFP_TRPb_PolyWb YFP_TRPb (control)




Protocol
  1. Starters of each strain used were grown over night in -T media, at 30 °C in shaker.
  2. After 12 hs, cells were pelleted and washed with -HT media.
  3. Cultures with increasing concentrations of histidine (0X, 1X, 1/4X and 1/16X) were set at an initial OD: 0.1, for each strain with 2 replica.
  4. We left the cultures in shaker at 30ºC for 5 hours. After that time, we measured the final OD reached by cultures with the use of a spectrophotometer and the amount of tryptophan present in medium with a spectrofluorometer.
Results

BsAs2012TrpvHis.jpg

BsAs2012Trpratio.jpg

BsAs2012ratioTrpvHisbypromotor.jpg

Strain characterization

Experimental determination of strains death rate

We set out to determine how long can auxotroph cells[link] survive in media that lacks both Trytophan and Histidine. These values are the death parameters for CFP and YFP strains used in our model[link]. These were taken as equal in the mathematical analysis for simplicity but now we would like to test whether this approximation is accurate.

Given that our system most likely will present a lag phase until a certain amount of both AmioAcids is accumulated in the media, will the cells be viable until this occurs? This is a neccesary check of our system's feasability.

Protocol

For this experiment we used

BsAs2012-icono-YFP.jpg BsAs2012-icono-CFP.jpg
YFP Strain CFP Strain
  • We set cultures of the two auxotroph strains without being transformed (YFP and CFP) in medium –HT at an initial OD of 0.01.
  • Each day we plated the same amount of µl of the culture and counted the number of colonies obtain in each plate. We set 3 replica of each strain.
Result
Strain Replica Monday Tuesday Wednesday
CFP 1 260 320 285
CFP 2 267 314 76
CFP 3 413 362 278
YFP 1 230 316 688
YFP 2 291 194 524
YFP 3 449 344 725

Table: Number of colonies counted per plate.

We expect to see a decrease in the number of colonies - because of cell death. We found that this was not the case, in the experiment's time lapse. However we observed that the size of the colonies was smaller everyday as can be seen in the following pictures.

FOTOS DE LAS PLACAS AQUIIII!


We can infer from this data that though they have not died, they may have enter into a ...Alan state. In this way cells can survive for a period of time in media defficient in amino acid (at least, during the time course of our experiment), but grow slower. Probably this would require more time than 3 days to observe significative cell dying.


100px 100px
FigureX.

Growth dependence on the Trp and His concentration

An important thing in order to characterize the system is the dependence of the growth rate on the culture with the concentration of the crossfeeding aminoacids, tryptophane (Trp) and histidine (His).

This would allow us to estimate one of the parameters used in our model (the EC50, which is the amount of aminoacid at which the culture reaches half of the maximum growth).


Protocol

1. For this experiment we would use strains YFP and CFP (non-transformed, without devices). We started cultures of 5 ml of initial OD: 0.025 for:

Strain YFP at the following media [Trp] = 1x; 0.5x; 0.25x; 0.125x; 0.0625x, 0.03125x
Strain CFP at the following media [His] = 1x; 0.5x; 0.25x; 0.125x; 0.0625x, 0.03125x
Strain YFP at Synthetic Complete media
Strain CFP at Synthetic Complete media

2. Cultures would be left overnight (12 hs) at 30°C with agitation and we measured OD reached with the use of spectrophotometer.

Results

To be done with our strains soon.

Coculture of transformed strains

We did the first experiment to test whether our system works and how two transformed strains grow together.

We designed an assay to do so; following the growth of these strains:

BsAs2012-icono-CFP-202.jpg BsAs2012-icono-YFP-185.jpg
CFP_His YFP_TRPb


Transformed cells coculture and controls.
Treatment Strain A Strain B
1 YFP_TRPb_TRPZipper2 CFP_HIS_PolyHa
2 YFP_TRPb_TRPZipper2 CFP_HIS
3 YFP_TRPb_TRPZipper2
4 YFP_TRPb CFP_HIS_PolyHa
5 CFP_HIS_PolyHa
6 YFP_TRPb CFP_HIS
7 CFP_HIS
8 YFP_TRPb

Protocol

  1. Starters of strains were grown over night at 30°C, according the scheme showed in the table
  2. The next day cultures were sonicated briefly in low power, and OD was measured in order to check they were in exponential phase.
  3. Cells were centrifugated and then washed with medium –HT.
  4. We set the culture of strains at OD: 0.02 in 5 ml of medium –HT with 3 replica, according to Table 1.
  5. At 0, 1, 2, 3, 4, 5, 6, 7, 8 and 22 hours we took samples of 20 µl.
  6. Samples were placed in a 384 wells plate, with 20 µl of cyclohexamide 2x (final concentration 1x) in each of the wells.
  7. We used epifluorescence microscope in order to determinate the strain proportion of each coculture. The density of the culture was calculated based on the cell density at in each wells.
Strain Media
YFP_TRPb_TRPZipper2 -T
YFP_TRPb -T
CFP_HIS_PolyHa -H
CFP_HIS -H
Bsas2012-Wells.png
384 wells plate to be used for epifluorescence microscope.


Results