Team:USP-Brazil/LaBioTec

From 2013.igem.org

(Difference between revisions)
Line 16: Line 16:
Plate media and store remaining volume <br/>
Plate media and store remaining volume <br/>
1g of SDS (1%) was added to the lysis buffer<br/>  
1g of SDS (1%) was added to the lysis buffer<br/>  
-
Brought a plaque with Pichia pastoris (GS115) recently plated. </p>
+
Brought a plaque with <i>Pichia pastoris</i> (GS115) recently plated. </p>
<p><b>27 May - 7 June</b><br/>
<p><b>27 May - 7 June</b><br/>
-
Extract the genomic DNA of Pichia pastoris<br/>
+
Extract the genomic DNA of <i>Pichia pastoris</i><br/>
Obs: In some wells, the water volume was completely evaporated.<br/>
Obs: In some wells, the water volume was completely evaporated.<br/>
-
Gradient PCR using the F_Paox1_GIB and R_Paox1_Kozak_GIB primers for Paox1 amplification and determinate optimum temperature and DNA template concentration</p>
+
Gradient PCR using the F_Paox1_GIB and R_Paox1_Kozak_GIB primers for P<sub>AOX1</sub> amplification and determinate optimum temperature and DNA template concentration</p>
<ul>
<ul>
<li>T<sub>melting</sub>: 55ºC, 58ºC, 60ºC, 62ºC and 65ºC
<li>T<sub>melting</sub>: 55ºC, 58ºC, 60ºC, 62ºC and 65ºC
<li>gDNA = 303.32 ng (10X), 30.332 ng (100X) e 3.0332 ng (1000X)
<li>gDNA = 303.32 ng (10X), 30.332 ng (100X) e 3.0332 ng (1000X)
</ul></p>
</ul></p>
-
<p>Verify on an Agarose Gel if the PCR was successful </p>
+
<p>Verify on an agarose Gel if the PCR was successful </p>
Line 32: Line 32:
To the evaporation test we fixed the styrofoam box on shaker. <br/>
To the evaporation test we fixed the styrofoam box on shaker. <br/>
The evaporation test was needed after an observation about the shaker’s coolers localization. It was found out that the hot wind generated for temperature adjustment cause an strong temperature gradient in some shaker areas.<br/>
The evaporation test was needed after an observation about the shaker’s coolers localization. It was found out that the hot wind generated for temperature adjustment cause an strong temperature gradient in some shaker areas.<br/>
-
To Growth curve measure it was used a cuvette measuring 9 points at all, with two initial ODs:</p>
+
Draw growth curve</p>
-
 
+
-
<p> *COLOCAR OS GRAFICOS QUE TAO NO BIOTEC LAB NOTEBOOK*</p>
+
-
 
+
-
<p> Figure 5: growth curve of Pichia pastoris. Gray x mark the actual data; colored circles represents the mean and the line is the fitted logistic curve as shown in Equation 1.</p>
+
<p><b>17 June - 21 June</b><br/>  
<p><b>17 June - 21 June</b><br/>  
-
Evaluate the behaviour of Pichia pastoris growth with crescent ethanol concentration on media by performing a Pichia pastoris Ethanol Survival test protocol
+
Evaluate the behaviour of <i>Pichia pastoris</i> growth with crescent ethanol concentration on media by performing a <i>Pichia pastoris</i> Ethanol Survival test protocol. </br>
-
We achieved the following results for the two initial Pichia pastoris cultures:
+
Some samples were also grown on cultures plates to qualitatively evaluate their viability.</p>
-
 
+
-
Table 1
+
-
 
+
-
(COLOCAR OS GRAFICOS QUE TAO NO DRIVE)
+
-
 
+
-
<p>Some samples were also grown on cultures plates to qualitatively evaluate their viability.</p>
+
<p><b>1 July - 7 July</b><br/>
<p><b>1 July - 7 July</b><br/>
-
Evaluate the viability of P. pastoris through lyophilization process using a monosodium glutamate and milk as cryoprotectants <br/>  
+
Evaluate the viability of <i>P. pastoris</i> through lyophilization process using a monosodium glutamate and milk as cryoprotectants <br/>  
-
First, a sample of the inoculum was took and diluted in a range from 10^⁻1 to 10^-8 with YPD liquid media using serial dilution (180 uL of media, 20 uL of inoculum).<br/>  
+
First, a sample of the inoculum was took and diluted in a range from 10<sup>-1</sup> to 10<sup>-8</sup> with YPD liquid media using serial dilution (180 uL of media, 20 uL of inoculum).<br/>  
-
All dilutions were plated in triplicate and put to grow under 30 celsius for 48 hours<br/>  
+
All dilutions were plated in triplicate and put to grow under 30 Celsius for 48 hours<br/>  
-
4 different samples of the inoculum were put in 2,0 mL eppendorfs and in small flasks, well mixed, fast frozen with liquid nitrogen, opened and put under lyophilization for 24 hours</p>
+
4 different samples of the inoculum were put in 2,0 mL tubes and in small flasks, well mixed, fast frozen with liquid nitrogen, opened and put under lyophilization for 24 hours</p>
-
Table 2
+
<p style=color:red><b>Table 1</b> </p>
-
<p>After lyophilization, the 4 different samples were suspended in 1 mL water and serially diluted  from 10¹ to 10⁸ in YPD media, plated in triplicate and put to grow for 48 hours on 30 celsius<br/>  
+
<p>After lyophilization, the 4 different samples were suspended in 1 mL water and serially diluted from 10 to 10<sup>-8</sup> in YPD media, plated in triplicate and put to grow for 48 hours on 30 Celsius<br/>  
Plates with the first inoculum and with the four different lyophilized samples were photographed and the colonies were counted.<br/>  
Plates with the first inoculum and with the four different lyophilized samples were photographed and the colonies were counted.<br/>  
Pre Lyophilization inoculum results (the number of CFU of each resuspension drops is in parenthesis)</p>
Pre Lyophilization inoculum results (the number of CFU of each resuspension drops is in parenthesis)</p>
-
Table 3
+
<p style=color:red><b>Table 2</b> </p>
<p><b>10 July - 19 July</b><br/>  
<p><b>10 July - 19 July</b><br/>  
-
1 mL of inoculum was centrifuged and resuspended in 500 uL(“X”). The same were made with 2 mL of inoculum.(“2X”)<br/>  
+
1 mL of inoculum was centrifuged and resuspended in 500 uL. The same were made with 2 mL of inoculum.<br/>  
-
3 replicates of the first resuspended inoculum (“X”) was mixed with 250 uL of milk solution and 250 uL of monosodium glutamate solution(1,2 e 3). The same was made with the second inoculum (2X), but in only one sample.<br/>  
+
3 replicates of the first resuspended inoculum were mixed with 250 uL of milk solution and 250 uL of monosodium glutamate solution (1,2 and 3). The same was made with the second inoculum, but in only one sample.<br/>  
-
(NAO TA MUITO CLARO ACIMA!)
+
All samples were lyophilized for 24 hours. A sample of 1 mL of the inoculum was plated under serial dilutions from 10<sup>-1</sup> to 10<sup>8</sup>.<br/>  
-
 
+
The lyophilized samples were resuspended  in 1 mL of water, serially diluted from 10<sup>-1</sup> to 10<sup>-6</sup> and plated.<br/>  
-
 
+
-
All samples were lyophilized for 24 hours. A sample of 1 mL of the inoculum was plated under serial dilutions from 10¹ to 10⁸.<br/>  
+
-
The lyophilized samples were resuspended  in 1 mL of water, serially diluted from 10¹ to 10⁶ and plated.<br/>  
+
The plates from the pure inoculum demonstrated growth after 24 hours and 30 Celsius, but not enough.</p>
The plates from the pure inoculum demonstrated growth after 24 hours and 30 Celsius, but not enough.</p>
-
 
<p><b>22 July - 10 August</b><br/>  
<p><b>22 July - 10 August</b><br/>  
-
Pichia were grown to the stationary phase and a new lyophilization was done. The initial OD was 0.314 for a 40 times dilution (OD of 12.56).<br/>  
+
<i>Pichia</i> were grown to the stationary phase and a new lyophilization was done. The initial OD was 0.314 for a 40 times dilution (OD of 12.56).<br/>  
The lyophilization process went wrong ):<br/>  
The lyophilization process went wrong ):<br/>  
A new inoculum has been done and let to grow until the stationary phase.<br/>  
A new inoculum has been done and let to grow until the stationary phase.<br/>  
Samples of inoculum were centrifuged and resuspended and mixed with milk solution and of monosodium glutamate solution as before<br/>  
Samples of inoculum were centrifuged and resuspended and mixed with milk solution and of monosodium glutamate solution as before<br/>  
-
All samples but one were lyophilized for 24 hours. This one sample that wasn’t lyophilized (control) was plated under serial dilutions from 10³ to 10⁸<br/>  
+
All samples but one were lyophilized for 24 hours. This one sample that was not lyophilized (control) was plated under serial dilutions from 10<sup>-3</sup> to 10<sup>-8</sup><br/>  
To evaluate the viability of resuspended lyophilized samples in ethanol solutions 5 lyophilized samples were resuspended:<br/>  
To evaluate the viability of resuspended lyophilized samples in ethanol solutions 5 lyophilized samples were resuspended:<br/>  
<ul>
<ul>
Line 88: Line 74:
<li> And one in 20% Ethanol solution,
<li> And one in 20% Ethanol solution,
</ul></p>
</ul></p>
-
<p>and serially diluted from 10¹ to 10⁸ and plated from 10³ to 10⁸. The dilutions were plated like the previous tests. One resuspension in water was plated right after the addition of water (as a control). All other resuspensions were plated 4 hours after the end of lyophilization process to check the viability of cells after a possible genetic response time of our future genetic construction.<br/>  
+
<p>and serially diluted from 10<sup>-1</sup> to 10<sup>-8</sup> and plated from 10<sup>-3</sup> to 10<sup>-8</sup>. The dilutions were plated like the previous tests. One resuspension in water was plated right after the addition of water (as a control). All other resuspensions were plated 4 hours after the end of lyophilization process to check the viability of cells after a possible genetic response time of our future genetic construction.<br/>  
The resuspensions on YPD plates do not showed satisfactory results because of bad milk solution pipetting due to high viscosity. It is better to use fresh milk for lyophilization preparation
The resuspensions on YPD plates do not showed satisfactory results because of bad milk solution pipetting due to high viscosity. It is better to use fresh milk for lyophilization preparation
Started the lyophilization process again with a new milk solution.</p>
Started the lyophilization process again with a new milk solution.</p>
Line 108: Line 94:
<li> Methanol - 50uL in final volume pf 10ml [5uL/mL] - 0,5%
<li> Methanol - 50uL in final volume pf 10ml [5uL/mL] - 0,5%
</ul></p>
</ul></p>
-
gDNA extraction was performed </p>
+
gDNA extraction was performed</p>
-
 
+
-
FAZ TABELA:
+
<p><b>10 September - 11 September</b><br/>  
<p><b>10 September - 11 September</b><br/>  
Plates with MD and colonies - colony PCR</p>  
Plates with MD and colonies - colony PCR</p>  
-
96 well plate
+
<p>96 well plate</br>
-
1 Negative control
+
<ul>
-
2 Non-transformed Pichia
+
<li>1 Negative control
-
3 Candidate
+
<li>2 Non-transformed <i>Pichia</i>
-
4 Candidate
+
<li>3 Candidate
-
5 Candidate
+
<li>4 Candidate
-
6 Candidate
+
<li>5 Candidate
-
7 Candidate
+
<li>6 Candidate
-
8 Candidate
+
<li>7 Candidate
-
9 Pichia - cultivation from MD plate
+
<li>8 Candidate
-
10 Pichia YPDgen 0,25 mg/mL
+
<li>9 <i>Pichia</i> - cultivation from MD plate
-
11 Pichia YPDgen 0,25 mg/mL
+
<li>10 <i>Pichia</i> YPDgen 0,25 mg/mL
-
12 Duplicate from 9 (Pichia - cultivation from MD plate)
+
<li>11 <i>Pichia</i> YPDgen 0,25 mg/mL
-
+
<li>12 Duplicate from 9 (<i>Pichia</i> - cultivation from MD plate)
-
+
</ul></p>
-
A 0
+
<p><ul>
-
B 0,0078125
+
<li>A 0
-
C 0,015625
+
<li>B 0,0078125
-
D 0,03125
+
<li>C 0,015625
-
E 0,0625
+
<li>D 0,03125
-
F 0,125
+
<li>E 0,0625
-
G 0,25 mg/ml geneticin
+
<li>F 0,125
-
H 1% Methanol/YPD 2uL
+
<li>G 0,25 mg/ml geneticin
 +
<li>H 1% Methanol/YPD 2uL
 +
</ul></p>
<P>Resuspend colonies in YPD
<P>Resuspend colonies in YPD
Line 144: Line 130:
PCR reaction and agarose gel<br/>  
PCR reaction and agarose gel<br/>  
PCR reactions of the colonies A2,A5,A6,A8,B1,C1,C2,D1,D2,E1,F2 and G1 were made.<br/>  
PCR reactions of the colonies A2,A5,A6,A8,B1,C1,C2,D1,D2,E1,F2 and G1 were made.<br/>  
-
The reactions aim in the confirmation of the transformation from Pichia pastoris, using primers that identify the RFP sequence. <br/>  
+
The reactions aim in the confirmation of the transformation from <i>Pichia pastoris</i>, using primers that identify the RFP sequence. <br/>  
Colony D2 was plated in YPD 0,25 mg/mL and colonies formed used for fluorescence test.<br/>   
Colony D2 was plated in YPD 0,25 mg/mL and colonies formed used for fluorescence test.<br/>   
To confirm that non transformed colonies didn´t amplified in our reaction we performed another reaction with non transformants, some other candidates from our plate and a previous positive test. <br/>  
To confirm that non transformed colonies didn´t amplified in our reaction we performed another reaction with non transformants, some other candidates from our plate and a previous positive test. <br/>  
Line 150: Line 136:
Apparently all were sensible to antibiotics, except for 9.<br/>  
Apparently all were sensible to antibiotics, except for 9.<br/>  
Cultivation was homogenized and incubated again at 30°C/200rpm.</p>  
Cultivation was homogenized and incubated again at 30°C/200rpm.</p>  
 +
<p>Cytometer<br/>  
<p>Cytometer<br/>  
<ul>
<ul>
Line 173: Line 160:
</ul></p>
</ul></p>
-
FAZ TABELA:
+
<p>M/E - Methanol/Ethanol mixture
 +
<ul>
 +
<li>200 mM/200mM
 +
<li>200 mM/100mM
 +
<li>200 mM/12,5mM
 +
<li>100 mM/200mM
 +
<li>100 mM/100mM
 +
<li>100 mM/12,5mM
 +
<li>12,5 mM/200mM
 +
<li>12,5 mM/100mM
 +
<li>12,5 mM/12,5mM
 +
</ul></p>
 +
<p>Methanol
 +
<ul>
 +
<li>400mM
 +
<li>200mM
 +
<li>100mM
 +
<li>50mM
 +
<li>25mM
 +
<li>12,5mM
 +
</ul></p>
 +
<p>Ethanol
 +
<ul>
 +
<li>400mM
 +
<li>200mM
 +
<li>100mM
 +
<li>50mM
 +
<li>25mM
 +
<li>12,5mM
 +
</ul></p>
-
M/E - Methanol/Ethanol mixture
 
-
200 mM/200mM
 
-
200 mM/100mM
 
-
200 mM/12,5mM
 
-
100 mM/200mM
 
-
100 mM/100mM
 
-
100 mM/12,5mM
 
-
12,5 mM/200mM
 
-
12,5 mM/100mM
 
-
12,5 mM/12,5mM
 
-
 
-
FAZ TABELA:
 
-
 
-
Methanol
 
-
400mM
 
-
200mM
 
-
100mM
 
-
50mM
 
-
25mM
 
-
12,5mM
 
-
 
-
Ethanol
 
-
400mM
 
-
200mM
 
-
100mM
 
-
50mM
 
-
25mM
 
-
12,5mM
 
-
 
<p>Windows restart experiment, no result for this plate.<br/>  
<p>Windows restart experiment, no result for this plate.<br/>  
-
Fluorescence Plate test was redone<br/>  
+
Fluorescence Plate test was redone</p>  
-
Table 4(?)
+
<p style=color:red><b>Table 3</b> </p>
-
Evaporation loss was intense. <br/>  
+
<p>Evaporation loss was intense. <br/>  
Video from results - http://www.youtube.com/watch?v=Hjp5icDJkog </p>
Video from results - http://www.youtube.com/watch?v=Hjp5icDJkog </p>
Line 238: Line 225:
-
Table 5(?)
+
<p style=color:red><b>Table 4</b> </p>
<p>Experiment Video - http://www.youtube.com/watch?v=2MtZSJXGtyk - Result in [LINK]Results. </p>
<p>Experiment Video - http://www.youtube.com/watch?v=2MtZSJXGtyk - Result in [LINK]Results. </p>

Revision as of 00:25, 28 September 2013

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Notebook

LaBioTec

20 May - 24 May
Preparation of Lysis buffer using LiOAc (200 mM).
YPD Media preparation and autoclaving.
Plate media and store remaining volume
1g of SDS (1%) was added to the lysis buffer
Brought a plaque with Pichia pastoris (GS115) recently plated.

27 May - 7 June
Extract the genomic DNA of Pichia pastoris
Obs: In some wells, the water volume was completely evaporated.
Gradient PCR using the F_Paox1_GIB and R_Paox1_Kozak_GIB primers for PAOX1 amplification and determinate optimum temperature and DNA template concentration

  • Tmelting: 55ºC, 58ºC, 60ºC, 62ºC and 65ºC
  • gDNA = 303.32 ng (10X), 30.332 ng (100X) e 3.0332 ng (1000X)

Verify on an agarose Gel if the PCR was successful

10 June - 14 June
To the evaporation test we fixed the styrofoam box on shaker.
The evaporation test was needed after an observation about the shaker’s coolers localization. It was found out that the hot wind generated for temperature adjustment cause an strong temperature gradient in some shaker areas.
Draw growth curve

17 June - 21 June
Evaluate the behaviour of Pichia pastoris growth with crescent ethanol concentration on media by performing a Pichia pastoris Ethanol Survival test protocol.
Some samples were also grown on cultures plates to qualitatively evaluate their viability.

1 July - 7 July
Evaluate the viability of P. pastoris through lyophilization process using a monosodium glutamate and milk as cryoprotectants
First, a sample of the inoculum was took and diluted in a range from 10-1 to 10-8 with YPD liquid media using serial dilution (180 uL of media, 20 uL of inoculum).
All dilutions were plated in triplicate and put to grow under 30 Celsius for 48 hours
4 different samples of the inoculum were put in 2,0 mL tubes and in small flasks, well mixed, fast frozen with liquid nitrogen, opened and put under lyophilization for 24 hours

Table 1

After lyophilization, the 4 different samples were suspended in 1 mL water and serially diluted from 10 to 10-8 in YPD media, plated in triplicate and put to grow for 48 hours on 30 Celsius
Plates with the first inoculum and with the four different lyophilized samples were photographed and the colonies were counted.
Pre Lyophilization inoculum results (the number of CFU of each resuspension drops is in parenthesis)

Table 2

10 July - 19 July
1 mL of inoculum was centrifuged and resuspended in 500 uL. The same were made with 2 mL of inoculum.
3 replicates of the first resuspended inoculum were mixed with 250 uL of milk solution and 250 uL of monosodium glutamate solution (1,2 and 3). The same was made with the second inoculum, but in only one sample.
All samples were lyophilized for 24 hours. A sample of 1 mL of the inoculum was plated under serial dilutions from 10-1 to 108.
The lyophilized samples were resuspended  in 1 mL of water, serially diluted from 10-1 to 10-6 and plated.
The plates from the pure inoculum demonstrated growth after 24 hours and 30 Celsius, but not enough.

22 July - 10 August
Pichia were grown to the stationary phase and a new lyophilization was done. The initial OD was 0.314 for a 40 times dilution (OD of 12.56).
The lyophilization process went wrong ):
A new inoculum has been done and let to grow until the stationary phase.
Samples of inoculum were centrifuged and resuspended and mixed with milk solution and of monosodium glutamate solution as before
All samples but one were lyophilized for 24 hours. This one sample that was not lyophilized (control) was plated under serial dilutions from 10-3 to 10-8
To evaluate the viability of resuspended lyophilized samples in ethanol solutions 5 lyophilized samples were resuspended:

  • Two of them in 1 mL of water,
  • One in 10% Ethanol solution,
  • One in 15% Ethanol solution,
  • And one in 20% Ethanol solution,

and serially diluted from 10-1 to 10-8 and plated from 10-3 to 10-8. The dilutions were plated like the previous tests. One resuspension in water was plated right after the addition of water (as a control). All other resuspensions were plated 4 hours after the end of lyophilization process to check the viability of cells after a possible genetic response time of our future genetic construction.
The resuspensions on YPD plates do not showed satisfactory results because of bad milk solution pipetting due to high viscosity. It is better to use fresh milk for lyophilization preparation Started the lyophilization process again with a new milk solution.

16 August - 20 August
Master Mix preparation
Precipitate 300uL of the digested material by ethanol
Transformation of competent cells with linearized pPIC9K-RFP with BgLII and purified by precipitation in ethanol by electroporation
Incubation on ice for 10min
Plaque in YPD/ gen 0,25mg/uL, YPD and MD

3 September
Repicking of colonies from plates Genet + YPD (3 colonies) and ND (14 colonies) in new plates of Genet + YPD.
Growth of the 7 candidates in medium with YPD + Genet + Methanol
The seven candidates mentioned above were tested in medium YPD + Genet + methanol to see with the RFP is expressed.
The suspensions made above were used to inoculate medium with geneticin and methanol. The concentrations used were:

  • Geneticin - 40uL in final volume of 10mL [4uL/mL]
  • Methanol - 50uL in final volume pf 10ml [5uL/mL] - 0,5%

gDNA extraction was performed

10 September - 11 September
Plates with MD and colonies - colony PCR

96 well plate

  • 1 Negative control
  • 2 Non-transformed Pichia
  • 3 Candidate
  • 4 Candidate
  • 5 Candidate
  • 6 Candidate
  • 7 Candidate
  • 8 Candidate
  • 9 Pichia - cultivation from MD plate
  • 10 Pichia YPDgen 0,25 mg/mL
  • 11 Pichia YPDgen 0,25 mg/mL
  • 12 Duplicate from 9 (Pichia - cultivation from MD plate)

  • A 0
  • B 0,0078125
  • C 0,015625
  • D 0,03125
  • E 0,0625
  • F 0,125
  • G 0,25 mg/ml geneticin
  • H 1% Methanol/YPD 2uL

Resuspend colonies in YPD Inoculate
Plate YPDs/amtibiotic straight in YPD
PCR reaction and agarose gel
PCR reactions of the colonies A2,A5,A6,A8,B1,C1,C2,D1,D2,E1,F2 and G1 were made.
The reactions aim in the confirmation of the transformation from Pichia pastoris, using primers that identify the RFP sequence.
Colony D2 was plated in YPD 0,25 mg/mL and colonies formed used for fluorescence test.
To confirm that non transformed colonies didn´t amplified in our reaction we performed another reaction with non transformants, some other candidates from our plate and a previous positive test.
Colonies 2,5,6,7,9 and 12 showed growth. They were tested in regard to DO, except 12 which was a duplicate from 9.
Apparently all were sensible to antibiotics, except for 9.
Cultivation was homogenized and incubated again at 30°C/200rpm.

Cytometer

  • 20uL of cells grown for 24h in YPD/1% Methanol received 280uL of phosphate buffer 100mmM pHG.
  • Volume was transferred to cytometry tubes and analysed.

Apparently there were no induced cells, only on sample 12 there was 1,5% more cells with fluorescence.
Tests

  • H2 - Control, non transformed and induced cell
  • H5,H6,H7,H9,H12 and X - candidates, transformed cells, grown in plates.

Obs: Cell X came from plate C, inducted with 0,5% methanol and 1% methanol.

18 September - 20 September
To check RFP expression a fluorescence plate test was performed

  • Readings every hour
  • Incubation: 30°C
  • Agitation: 0
  • Conditions tested: Medium FM22 - 50000 cels / well

M/E - Methanol/Ethanol mixture

  • 200 mM/200mM
  • 200 mM/100mM
  • 200 mM/12,5mM
  • 100 mM/200mM
  • 100 mM/100mM
  • 100 mM/12,5mM
  • 12,5 mM/200mM
  • 12,5 mM/100mM
  • 12,5 mM/12,5mM

Methanol

  • 400mM
  • 200mM
  • 100mM
  • 50mM
  • 25mM
  • 12,5mM

Ethanol

  • 400mM
  • 200mM
  • 100mM
  • 50mM
  • 25mM
  • 12,5mM

Windows restart experiment, no result for this plate.
Fluorescence Plate test was redone

Table 3

Evaporation loss was intense.
Video from results - http://www.youtube.com/watch?v=Hjp5icDJkog

24 September
Fluorescence Plate test

  • Reading: every half hour
  • Incubation: 30°C
  • Agitation: 1mm
  • Agitation pattern: Orbital
  • Time under agitation: 13 min ON, 17 min OFF
  • Ex: 584 nm
  • Em: 619 nm
  • Gain: 63
  • Number of reads: 10
  • Integration time: 40 ms

Conditions tested:

  • YP (Yeast extract and Peptone)
  • FM22 (Basal salt medium)
  • YP + Sortbitol 20mM
  • Initial OD (Optic density): 0,1

*Optic film added to prevent evaporation

Table 4

Experiment Video - http://www.youtube.com/watch?v=2MtZSJXGtyk - Result in [LINK]Results.

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