Difference between revisions of "Part:BBa I13522:Experience"
m (→‎Method)
 
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__NOTOC__
 
__NOTOC__
−
<br> For parts BBa_I13521 and BBa_I13522, their excitation and emission maxima were determined. BBa_B0034 was used as a negative control. These data were used later in following characterization experiments as set parameters. The host was E. coli Top Ten in all experiments.
 
−
<br> Meanwhile, the graph below shows the emission scan for GFP in part BBa_I13522. Since it was the best option in terms of fluorescence yield, 395 nm was set as the excitation wavelength. As it can be seen from the graph, maximum emission wavelength is 515 nm.
 
−
<html> <div align="center" style="margin:15px 0px 0px 0px"><img style="border: 0px solid ; width: 608px; height: 316px;" alt="w7" src="https://static.igem.org/mediawiki/2010/6/66/C2.GIF"></a></div> </html>
 
  
−
The characterization was performed by METU-TURKEY IGEM 2010 Team.
+
=Characterisations of BBa_I13522=
 +
 
 +
== iGEM Team Aberdeen 2014 ==
 +
 
 +
BBa_I13522 on pSB1C3 constitutively expresses GFP in XL1Blue ''E.coli''.
 +
 
 +
 
 +
=== Aims ===
 +
BBa_I13522 was used as a positive control for comparison to [[Part:BBa_T9002]] GFP expression in response to AHL induction.
 +
 
 +
=== Method ===
 +
BBa_I13522 pSB1C3 plasmids were rescued from Spring 2014 Distribution Plate 3-6I, and transformed into competent XL1Blue ''E. coli.'' After selection on Chloramphenicol LB agar, monoclonal liquid cultures were prepared in chloramphenicol LB liquid.
 +
Cells were immobilised on a Poly-Lysine membrane in a 96well plate. GFP measured using a FluoSTAR OPTIMA fluorescence plate reader.
 +
 
 +
# 50μl 0.01% Poly-Lysine was added to each well, of a 96 well glass-bottom Plate (Whatman). Incubated at room temperature for 2 hours.
 +
# Excess Poly-Lysine removed and washed three times with sterile water. Allowed to dry at room temperature.
 +
# ''E. coli'' cultures grown overnight in a 37C shaking water bath, single culture wells diluted as required to achieve an Optical Density-600nm(OD600) of 0.02.
 +
# Unbound cells removed by lightly shaking over waste and washed three times with Phosphate-Buffered Saline (PBS). 50μl fresh LB medium was added to each well.
 +
# A FluoSTAR OPTIMA Fluoresence Plate Reader was used to measure Green (Excitation 485nm/Emission 520nm) Fluoresence every 5 minutes for 420 minutes, this incubates the samples at 37C and shakes (1mm double-orbital) for 30 seconds before each read. 
 +
 
 +
=== Results ===
 +
 
 +
BBa_I13522 transformed ''E. coli'' exhibited higher Green fluorescence than untransformed ''E. coli'', this increased over time, with absolute green fluorescence plateauing at 300minutes.
 +
 
 +
[[File:I13522(2).png|600px]]
 +
 
 +
''Figure 1 – BBa_I13522 constitutively expresses GFP. Mean green fluorescence (Excitation 485nm/Emission 520nm) of BBa_I13522 transformed E.Coli (circles) and untransformed E. coli (triangles), immobilised on Poly-Lysine. 50μl Chloramphenicol liquid LB, reading every 5 minutes, incubated at 37C and shaking, in 96well plate. ''
 +
 
 +
 
 +
=== Conclusion ===
 +
The plasmid BBa_I13522 on pSB1C3 constitutively expresses GFP when transformed into XL1Blue ''E. coli''.
 +
 
 +
 
 +
 
 +
 
 +
== KIT-Kyoto iGEM Team 2013 ==
 +
 
 +
2013 KIT-Kyoto iGEM team assessed influence of fluorescence proteins on
 +
 
 +
the growth of E.coli.
 +
We used BBa_I13521, BBa_I13522 and BBa_I13600 in order to measure the
 +
 
 +
growth.
 +
 
 +
[[File:Kairyo2.png|500px]]
 +
 
 +
We measured the turbidities of the transformants at hourly intervals
 +
 
 +
and made the growth curves.
 +
We transferred the transformant prepared to 200 mL flasks.
 +
We measured the turbidities every 1 hour.
 +
The measurements were carried out for 12 hours.
 +
 
 +
Liquid LB 50mL
 +
 
 +
Sample 20µL
 +
 
 +
Ampicillin 75µL
 +
 
 +
37°C, 125rpm
 +
 
 +
Control:HST08
 +
 
 +
As the result, it was found that eCFP and mRFP have the effect of
 +
 
 +
growth promotion relative to GFP.
 +
 
 +
 
 +
== Haynes Lab 2012 ==
 +
 
 +
 
 +
I used BBa_I13522 to demonstrate the expression of GFP in E. coli for a
 +
 
 +
biomedical engineering course at Arizona State University.
 +
* Cells: NEB10B
 +
* Medium: LB Lennox agar, 100 ug/mL ampicillin
 +
* The read area contains bacteria expressing RFP from BBa_J04450
 +
 
 +
[[Image:KAH010812.jpg|200px]]
 +
 
 +
 
 +
 
 +
== iGEM team Wageningen UR 2012 ==
 +
 
 +
This brick was used to create GFP with a coiled coil at the N-terminus
 +
 
 +
to use it as reporter for the E- and K-coil
 +
 
 +
[http://2012.igem.org/Team:Wageningen_UR/Coil_system Plug and Apply
 +
 
 +
sytem]
 +
 
 +
see [https://parts.igem.org/wiki/index.php?title=Part:BBa_K883704
 +
 
 +
BBa_K883704]; [https://parts.igem.org/wiki/index.php?
 +
 
 +
title=Part:BBa_K883705 BBa_K883705]
 +
 
 +
 
 +
== Imperial College London 2011 iGEM team ==
  
 
<html>
 
<html>
 
<p><b>Thermostability Assay</b></p>
 
<p><b>Thermostability Assay</b></p>
−
<p>For this BioBrick, the denaturation temperature was determined by heating the protein at a range of temperatures, and then measuring the fluorescence. This is a useful characterisation as it allows the selection of an appropriate reporter gene for the required temperature.</p>
+
<p>For this BioBrick, the denaturation temperature was determined by  
−
<p> Stock solutions of GFP were prepared by extracting the protein from cell lysate, and then 50μl aliquots of the solution were heated in a PCR thermocycler along a temperature gradient.</p>
+
 
−
<p>After two hours, 30μl was removed from each aliquot and diluted with 170μl of 20mM Tris buffer to give 200μl samples. The samples were then measured by fluorescence on a 96-well plate. The corresponding curve was plotted on the graph below.</p>
+
heating the protein at a range of temperatures, and then measuring the  
 +
 
 +
fluorescence. This is a useful characterisation as it allows the  
 +
 
 +
selection of an appropriate reporter gene for the required  
 +
 
 +
temperature.</p>
 +
<p> Stock solutions of GFP were prepared by extracting the protein from  
 +
 
 +
cell lysate, and then 50 µl aliquots of the solution were heated in a  
 +
 
 +
PCR thermocycler along a temperature gradient.</p>
 +
<p>After two hours, 30 µl was removed from each aliquot and diluted  
 +
 
 +
with 170 µl of 20 mM Tris buffer to give 200 µl samples. The  
 +
 
 +
fluorescence of the samples was then measured on a 96-well plate. The  
 +
 
 +
corresponding curve was plotted on the graph below.</p>
 
<div class="imgbox" style="width:720px;margin: 0 auto;">
 
<div class="imgbox" style="width:720px;margin: 0 auto;">
−
<img class="border" src="https://static.igem.org/mediawiki/2011/f/f8/ICL_Heat_Denaturation_Curve_of_Fluorescent_Proteins.png" width=700px />
+
<img class="border"  
−
<p><i>Fig. 4: Results of the heat denaturation experiment. The temperature at which half of the protein is denatured measured by looking at its fluorescence (PTm50) mRFP1: 92.3°C; GFPmut3b: 59.1°C; Dendra2: 83.7°C; sfGFP: 75.3°C.</i></p>
+
 
 +
src="https://static.igem.org/mediawiki/2011/thumb/7/75/Curve.png/800px-
 +
 
 +
Curve.png" width=700px />
 +
<p><i> Results of the heat denaturation experiment. The temperature at  
 +
 
 +
which half of the protein is denatured is measured by observing its  
 +
 
 +
fluorescence (PTm50) mRFP1: 82.2°C; GFPmut3b: 61.6°C; Dendra2: 89.1°C;  
 +
 
 +
sfGFP: 75.0°C.</i></p>
 
</div>
 
</div>
  
−
The sigmoidal curves that were calculated gave us the following function in order to find K which we also call PTm50 (temperature at which half of the protein is denatured measured by looking at its fluorescence):
+
<br>The sigmoidal curves that were calculated gave us the following  
 +
 
 +
function which also created the coefficient K which happens to relate
 +
 
 +
to PTm50 (temperature at which half of the protein is denatured  
 +
 
 +
measured by looking at its fluorescence):</br>
 
<br>
 
<br>
−
<img src= "https://static.igem.org/mediawiki/2011/0/0d/ICL_Equation_to_find_PTm50.png" width="600px"/>  
+
<img src=  
 +
 
 +
"https://static.igem.org/mediawiki/2011/0/0d/ICL_Equation_to_find_PTm50.png"  
 +
 
 +
width="600px"/>  
 
</html>
 
</html>
  
−
This characterisation was performed by the Imperial College London 2011 Team.
 
  
−
===Applications of BBa_I13522===
+
== METU-TURKEY IGEM 2010 Team ==
 +
 
 +
<br> For parts BBa_I13521 and BBa_I13522, their excitation and emission
 +
 
 +
maxima were determined. BBa_B0034 was used as a negative control. These
 +
 
 +
data were used later in following characterisation experiments as set
 +
 
 +
parameters. The host was <i>E. coli</i> Top Ten in all experiments.
 +
<br> Meanwhile, the graph below shows the emission scan for GFP in part
 +
 
 +
BBa_I13522. Since it was the best option in terms of fluorescence
 +
 
 +
yield, 395 nm was set as the excitation wavelength. As it can be seen
 +
 
 +
from the graph, maximum emission wavelength is 515 nm.
 +
<html> <div align="center" style="margin:15px 0px 0px 0px"><img
 +
 
 +
style="border: 0px solid ; width: 608px; height: 316px;" alt="w7"
 +
 
 +
src="https://static.igem.org/mediawiki/2010/6/66/C2.GIF"></a></div> </html>
 +
 
 +
 
 +
 
 +
 
 +
 
 +
 
 +
 
 +
==Reviews of I13522==
  
−
===User Reviews===
 
 
<!-- DON'T DELETE --><partinfo>BBa_I13522 StartReviews</partinfo>
 
<!-- DON'T DELETE --><partinfo>BBa_I13522 StartReviews</partinfo>
 
<!-- Template for a user review
 
<!-- Template for a user review
Line 43: Line 203:
 
<I>Antiquity</I>
 
<I>Antiquity</I>
 
|width='60%' valign='top'|
 
|width='60%' valign='top'|
−
This review comes from the old result system and indicates that this part did not work in some test.
+
This review comes from the old result system and indicates that this  
 +
 
 +
part did not work in some test.
 
|}
 
|}
 +
 +
 +
{|width='80%' style='border:1px solid gray'
 +
|-
 +
|width='10%'|
 +
<partinfo>BBa_I13522 AddReview 5</partinfo>
 +
<I>[[User:Kahaynes|Karmella]]</I>
 +
|width='60%' valign='top'|
 +
We obtained this part from the Spring 2011 distribution plate. It
 +
 +
expresses wonderfully in NEB10B cells from New England Biolabs. It does
 +
 +
not express well in the fast-growing strain DH5-alpha Turbo, which
 +
 +
we've found doesn't express transgenes very well in general.
 +
|}
 +
 +
{|width='80%' style='border:1px solid gray'
 +
|-
 +
|width='10%'|
 +
<partinfo>BBa_I13522 AddReview 5</partinfo>
 +
<I>iGEM Team Wageningen UR 2014</I>
 +
|width='60%' valign='top'|
 +
We obtained this part from the Spring 2014 distribution plate. It
 +
 +
doesn't express in ''E. coli'' DH5-alpha or NEB 5-alpha strains. We
 +
 +
sequenced this part and we concluded that this parts sequence is
 +
 +
inconsistent, missing 25 bp of the promoter sequence. Therefore, we
 +
 +
made a twin of this part, <partinfo>BBa_K1493504</partinfo>. We did
 +
 +
this by assembly of pTet (BBa_R0040) and GFP (BBa_I13504) using
 +
 +
standard BioBrick assembly. Sequencing with the forward primer VF2
 +
 +
(5'-tgccacctgacgtctaagaa-3') confirmed the right sequence.
 +
|}
 +
 
<!-- DON'T DELETE --><partinfo>BBa_I13522 EndReviews</partinfo>
 
<!-- DON'T DELETE --><partinfo>BBa_I13522 EndReviews</partinfo>

Latest revision as of 21:07, 26 October 2014


Characterisations of BBa_I13522

iGEM Team Aberdeen 2014

BBa_I13522 on pSB1C3 constitutively expresses GFP in XL1Blue E.coli.


Aims

BBa_I13522 was used as a positive control for comparison to Part:BBa_T9002 GFP expression in response to AHL induction.

Method

BBa_I13522 pSB1C3 plasmids were rescued from Spring 2014 Distribution Plate 3-6I, and transformed into competent XL1Blue E. coli. After selection on Chloramphenicol LB agar, monoclonal liquid cultures were prepared in chloramphenicol LB liquid. Cells were immobilised on a Poly-Lysine membrane in a 96well plate. GFP measured using a FluoSTAR OPTIMA fluorescence plate reader.

  1. 50μl 0.01% Poly-Lysine was added to each well, of a 96 well glass-bottom Plate (Whatman). Incubated at room temperature for 2 hours.
  2. Excess Poly-Lysine removed and washed three times with sterile water. Allowed to dry at room temperature.
  3. E. coli cultures grown overnight in a 37C shaking water bath, single culture wells diluted as required to achieve an Optical Density-600nm(OD600) of 0.02.
  4. Unbound cells removed by lightly shaking over waste and washed three times with Phosphate-Buffered Saline (PBS). 50μl fresh LB medium was added to each well.
  5. A FluoSTAR OPTIMA Fluoresence Plate Reader was used to measure Green (Excitation 485nm/Emission 520nm) Fluoresence every 5 minutes for 420 minutes, this incubates the samples at 37C and shakes (1mm double-orbital) for 30 seconds before each read. 

Results

BBa_I13522 transformed E. coli exhibited higher Green fluorescence than untransformed E. coli, this increased over time, with absolute green fluorescence plateauing at 300minutes.

I13522(2).png

Figure 1 – BBa_I13522 constitutively expresses GFP. Mean green fluorescence (Excitation 485nm/Emission 520nm) of BBa_I13522 transformed E.Coli (circles) and untransformed E. coli (triangles), immobilised on Poly-Lysine. 50μl Chloramphenicol liquid LB, reading every 5 minutes, incubated at 37C and shaking, in 96well plate.


Conclusion

The plasmid BBa_I13522 on pSB1C3 constitutively expresses GFP when transformed into XL1Blue E. coli.



KIT-Kyoto iGEM Team 2013

2013 KIT-Kyoto iGEM team assessed influence of fluorescence proteins on

the growth of E.coli. We used BBa_I13521, BBa_I13522 and BBa_I13600 in order to measure the

growth.

Kairyo2.png

We measured the turbidities of the transformants at hourly intervals

and made the growth curves. We transferred the transformant prepared to 200 mL flasks. We measured the turbidities every 1 hour. The measurements were carried out for 12 hours.

Liquid LB 50mL

Sample 20µL

Ampicillin 75µL

37°C, 125rpm

Control:HST08

As the result, it was found that eCFP and mRFP have the effect of

growth promotion relative to GFP.


Haynes Lab 2012

I used BBa_I13522 to demonstrate the expression of GFP in E. coli for a

biomedical engineering course at Arizona State University.

  • Cells: NEB10B
  • Medium: LB Lennox agar, 100 ug/mL ampicillin
  • The read area contains bacteria expressing RFP from BBa_J04450

KAH010812.jpg


iGEM team Wageningen UR 2012

This brick was used to create GFP with a coiled coil at the N-terminus

to use it as reporter for the E- and K-coil

[http://2012.igem.org/Team:Wageningen_UR/Coil_system Plug and Apply

sytem]

see [https://parts.igem.org/wiki/index.php?title=Part:BBa_K883704

BBa_K883704]; [https://parts.igem.org/wiki/index.php?

title=Part:BBa_K883705 BBa_K883705]


Imperial College London 2011 iGEM team

Thermostability Assay

For this BioBrick, the denaturation temperature was determined by heating the protein at a range of temperatures, and then measuring the fluorescence. This is a useful characterisation as it allows the selection of an appropriate reporter gene for the required temperature.

Stock solutions of GFP were prepared by extracting the protein from cell lysate, and then 50 µl aliquots of the solution were heated in a PCR thermocycler along a temperature gradient.

After two hours, 30 µl was removed from each aliquot and diluted with 170 µl of 20 mM Tris buffer to give 200 µl samples. The fluorescence of the samples was then measured on a 96-well plate. The corresponding curve was plotted on the graph below.

Results of the heat denaturation experiment. The temperature at which half of the protein is denatured is measured by observing its fluorescence (PTm50) mRFP1: 82.2°C; GFPmut3b: 61.6°C; Dendra2: 89.1°C; sfGFP: 75.0°C.


The sigmoidal curves that were calculated gave us the following function which also created the coefficient K which happens to relate to PTm50 (temperature at which half of the protein is denatured measured by looking at its fluorescence):


METU-TURKEY IGEM 2010 Team


For parts BBa_I13521 and BBa_I13522, their excitation and emission

maxima were determined. BBa_B0034 was used as a negative control. These

data were used later in following characterisation experiments as set

parameters. The host was E. coli Top Ten in all experiments.
Meanwhile, the graph below shows the emission scan for GFP in part

BBa_I13522. Since it was the best option in terms of fluorescence

yield, 395 nm was set as the excitation wavelength. As it can be seen

from the graph, maximum emission wavelength is 515 nm.

w7




Reviews of I13522

UNIQd4bbb4a50fe6a66b-partinfo-00000002-QINU

Antiquity

This review comes from the old result system and indicates that this

part did not work in some test.


•••••

Karmella

We obtained this part from the Spring 2011 distribution plate. It

expresses wonderfully in NEB10B cells from New England Biolabs. It does

not express well in the fast-growing strain DH5-alpha Turbo, which

we've found doesn't express transgenes very well in general.

•••••

iGEM Team Wageningen UR 2014

We obtained this part from the Spring 2014 distribution plate. It

doesn't express in E. coli DH5-alpha or NEB 5-alpha strains. We

sequenced this part and we concluded that this parts sequence is

inconsistent, missing 25 bp of the promoter sequence. Therefore, we

made a twin of this part, BBa_K1493504. We did

this by assembly of pTet (BBa_R0040) and GFP (BBa_I13504) using

standard BioBrick assembly. Sequencing with the forward primer VF2

(5'-tgccacctgacgtctaagaa-3') confirmed the right sequence.

UNIQd4bbb4a50fe6a66b-partinfo-00000007-QINU