Team:Paris/Transduction testing

From 2009.igem.org

(Difference between revisions)
(→Transduction)
(→Fusion)
 
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|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
|bgcolor="#F8F8F8"|'''Sequencing :'''
|bgcolor="#F8F8F8"|'''Sequencing :'''
-
 
unecessary  
unecessary  
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Fos : previously done
Fos : previously done
-
|bgcolor="#E0E3FE"|'''PCR :'''
+
|bgcolor="#E0E3FE"|-
-
|bgcolor="#CBD1FD"|'''PCR :'''
+
|bgcolor="#CBD1FD"|-
-
|bgcolor="#BCCDFD"|'''PCR :'''
+
|bgcolor="#BCCDFD"|-
 +
 
-
Fos : design and order.
 
|- style="background: #d8d8d8; text-align: center;"
|- style="background: #d8d8d8; text-align: center;"
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ok
ok
-
|bgcolor="#E0E3FE"|'''Verification on gel :'''
+
|bgcolor="#E0E3FE"|
-
-
-
|bgcolor="#CBD1FD"|'''Verification on gel :'''
+
|bgcolor="#CBD1FD"|
-
-
-
|bgcolor="#BCCDFD"|'''Verification on gel :'''
+
|bgcolor="#BCCDFD"|-
-
 
+
-
ok
+
|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
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ok
ok
-
|bgcolor="#E0E3FE"|'''Purification on gel :'''
+
|bgcolor="#E0E3FE"|
-
-
-
|bgcolor="#CBD1FD"|'''Purification on gel :'''
+
|bgcolor="#CBD1FD"|
-
-
-
|bgcolor="#BCCDFD"|'''Purification on gel :'''
+
|bgcolor="#BCCDFD"|
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|bgcolor="#E0E3FE"|'''Digestion:'''  
|bgcolor="#E0E3FE"|'''Digestion:'''  
-
|bgcolor="#CBD1FD"|'''Digestion:'''
+
none
-
|bgcolor="#BCCDFD"|'''Digestion:'''
+
|bgcolor="#CBD1FD"|-
 +
|bgcolor="#BCCDFD"|-
-
Fos E/X and E/P
 
-
PSB1A3 E/P
 
|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
-
|bgcolor="#F8F8F8"|'''Verification digestion:'''
+
|bgcolor="#F8F8F8"|'''Digestion checking:'''
ok
ok
-
|bgcolor="#E0E3FE"|'''Verification digestion:'''
+
|bgcolor="#E0E3FE"|'''Digestion checking:'''
-
-
+
none
-
 
+
-
|bgcolor="#CBD1FD"|'''Verification digestion:'''
+
 +
|bgcolor="#CBD1FD"|
 +
-
 +
|bgcolor="#BCCDFD"|
-
-
-
|bgcolor="#BCCDFD"|'''Verification digestion:'''
 
-
 
-
ok
 
-
 
|- style="background: #d8d8d8; text-align: center;"
|- style="background: #d8d8d8; text-align: center;"
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|bgcolor="#E0E3FE"|'''Ligation:'''  
|bgcolor="#E0E3FE"|'''Ligation:'''  
-
|bgcolor="#CBD1FD"|'''Ligation:'''
+
none
-
|bgcolor="#BCCDFD"|'''Ligation:'''
+
|bgcolor="#CBD1FD"|-
 +
|bgcolor="#BCCDFD"|'-
 +
 
-
Fos E/P :: PSB1A3 E/P
 
|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
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ok
ok
-
|bgcolor="#E0E3FE"|'''Colony PCR :'''
+
|bgcolor="#E0E3FE"|'''Colony PCR:'''
 +
none
-
-
+
|bgcolor="#CBD1FD"|-
-
 
+
-
|bgcolor="#CBD1FD"|'''Colony PCR :'''
+
-
-
-
|bgcolor="#BCCDFD"|'''Colony PCR :'''
+
|bgcolor="#BCCDFD"|-
-
 
+
-
-
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|bgcolor="#E0E3FE"|'''Miniprep:'''
|bgcolor="#E0E3FE"|'''Miniprep:'''
-
-
+
none
-
|bgcolor="#CBD1FD"|'''Miniprep:'''
+
|bgcolor="#CBD1FD"|-
-
 
+
|bgcolor="#BCCDFD"|-
-
-
+
-
 
+
-
|bgcolor="#BCCDFD"|'''Miniprep:'''
+
-
 
+
-
ok
+
|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
|bgcolor="#F8F8F8"|'''Sequencing :'''
|bgcolor="#F8F8F8"|'''Sequencing :'''
-
-
+
-ok
|bgcolor="#E0E3FE"|'''Sequencing :'''
|bgcolor="#E0E3FE"|'''Sequencing :'''
-
-
+
-none
-
|bgcolor="#CBD1FD"|'''Sequencing :'''
+
|bgcolor="#CBD1FD"|'-
-
 
+
|bgcolor="#BCCDFD"|-
-
-
+
-
|bgcolor="#BCCDFD"|'''Sequencing :'''
+
-
 
+
-
-
+
|- style="background: #d8d8d8; text-align: center;"   
|- style="background: #d8d8d8; text-align: center;"   
|bgcolor="#F8F8F8"| '''Stock glycerol:'''
|bgcolor="#F8F8F8"| '''Stock glycerol:'''
 +
none
unecessary
unecessary
|bgcolor="#E0E3FE"|'''Stock glycerol'''
|bgcolor="#E0E3FE"|'''Stock glycerol'''
-
-
+
none
-
|bgcolor="#CBD1FD"|'''Stock glycerol'''
+
|bgcolor="#CBD1FD"|-
-
 
+
|bgcolor="#BCCDFD"|-
-
-
+
-
|bgcolor="#BCCDFD"|'''Stock glycerol'''
+
-
-
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|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
|bgcolor="#F8F8F8"|'''Sequencing :'''
|bgcolor="#F8F8F8"|'''Sequencing :'''
-
 
+
ok
-
-
+
|bgcolor="#E0E3FE"|
|bgcolor="#E0E3FE"|
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|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
|bgcolor="#F8F8F8"|'''Sequencing :'''
|bgcolor="#F8F8F8"|'''Sequencing :'''
-
 
+
ok
-
-
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|bgcolor="#E0E3FE"|
|bgcolor="#E0E3FE"|
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pBAD  E/S
pBAD  E/S
-
|bgcolor="#E0E3FE"|''Digestion:'''  
+
|bgcolor="#E0E3FE"|'''Digestion:'''  
none
none
|bgcolor="#CBD1FD"|-
|bgcolor="#CBD1FD"|-
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|- style="background: #bebebe; text-align: center;"   
|- style="background: #bebebe; text-align: center;"   
-
|bgcolor="#F8F8F8"|
+
|bgcolor="#F8F8F8"|'''Sequencing'''
-
-
+
none
-
|bgcolor="#E0E3FE"|
+
|bgcolor="#E0E3FE"|'''Sequencing'''
-
-
+
none
|bgcolor="#CBD1FD"|
|bgcolor="#CBD1FD"|

Latest revision as of 03:38, 22 October 2009

iGEM > Paris > WetLab > Reception


Contents

WetLab - Reception

In this section we have two kinds of experiments :


  1. Fusion : the construction required for the fusion of the vesicles that contain the message with the receiver.
  2. Transduction : the construction of the system that will be able de decypher the message.


The first part deals with G3P , OmpAL , Jun, Fos , and AIDA protein. the second with the transduction system of the fec operon (FecA, FecR, FecI).

Fusion

Fusion : the construction required for the fusion of the vesicles that contain the message.

G3P , OmpAL , Jun, Fos , and AIDA protein.



The green color means the experiment was a success


plasmid =




Experiments ran :


Column 1 Column 2 Column 3 Column 4
PCR :

AidA and Linker : Design, synthesize and order in two parts due to the seize.

- - -


Verification on gel :

ok

- - -
Purification on gel :

ok

- - -


Digestion:

AidA CTerm Kpn1/HindIII

AidA NTerm Kpn1/HindIII

Digestion:

AidA complete E/P

PSB1A3 E/P

We did it to obtain a biobrick first

Digestion:

none

-


Digestion checking:

ok

Digestion checking:

ok


Digestion checking:

none


-


Ligation:

AidA CTerm (Kpn1/HindIII):: aidA NTerm (Kpn1/HindIII)


Ligation:

AidA complete E/P :: PSB1A3 E/P

Ligation:

none

-
Colony pCR :

ok

Colony PCR:

ok

Colony PCR :

none

-
Miniprep:

done

Miniprep:

done

Miniprep:

none

-
Sequencing :

unecessary

Sequencing :

none

Sequencing :

none


-
Stock glycerol:

-

Stock glycerol

S75

Stock glycerol

none

-




The green color means the experiment was a success


plasmid =




Experiments ran :


Column 1 Column 2 Column 3 Column 4
PCR :

Jun *: design and order to be a a mutant incapable to form homodimere.

pLac : previously done

SSOmpA : previously done

Fos : previously done

- - -


Verification on gel :

ok

-

-

-
Purification on gel :

ok

-

-



Digestion:

pLac E/X

ssOmpA E/S

Jun E/X and E/P

PSB1A3 E/P

Digestion:

none

- -


Digestion checking:

ok

Digestion checking:

none

-

-

Ligation:

pLac on PSB2K3 E/X :: ssOmpA E/S

Jun E/P :: PSB1A3 E/P

Ligation:

none

- '-


Colony PCR:

ok

Colony PCR:

none

-

-

-

-

Miniprep:

ok

Miniprep:

none

- -
Sequencing :

-ok

Sequencing :

-none

'- -
Stock glycerol:

none

unecessary

Stock glycerol

none

- -

-



G3P

Even though it has not been realized, we planned to do these experiments to verify that G3P is expressed into the bacterial surface and induces the membranal fusion.


  • Surface expression of G3P

Surface expression of G3P could be seen with antibodies.
Culture of bacteria expressing OmpA-linker-G3P construction on a membrane. Adding antibodies anti-G3P. Revelation should shows whether G3P is expressed at the surface of bacteria.


  • Floculation test

"Fusion" could be approached by a flocculation test.
Two separate bacterial population growth on media. A population (F-) expressing the OmpA-linker_G3P construction and a population (F +) which express sexual pilus (by expression of the episome F).
Then we growth bacteria without agitation and we look (compared to culture controls) the speed of sedimentation. Faster sedimentation is due to an interaction between bacterial populations showing an increase of contact time. At vesicle level, it induce membrane fusion.


Transduction

Transduction : the construction of the system that will be able de decypher the message.


The transduction system of the fec operon (FecA, FecR, FecI).



The green color means the experiment was a success


plasmid =




Experiments ran :


Column 1 Column 2 Column 3 Column 4
PCR :

pFec matrix: K12 DNA

Oligo: TM

FecI matrix: K12 DNA

Oligo: TM

FecR 1-85 matrix: K12 DNA

Oligo: TM

mRFP matrix: PSB1A3 (previous IGEM plate)

Oligo: TM


- - -
Verification on gel :

ok

- - -
Purification on gel :

ok

- - -


Digestion:

Ter E/X

mRFP E/S

- - -
Digestion checking:

ok

- - -


Ligation:

mRFP E/S Ter E/X in Ter vector

- - -
Colony PCR:

ok

- - -
Miniprep:

ok

- - -
Sequencing :

ok

-

-

-

Stock glycerol:

-

- - -




The green color means the experiment was a success


plasmid =




Experiments ran :


Column 1 Column 2 Column 3 Column 4
PCR :

pFec matrix: K12 DNA

Oligo: TM

FecI matrix: K12 DNA

Oligo: TM

FecR 1-85 matrix: K12 DNA

Oligo: TM

mRFP matrix: PSB1A3 (previous IGEM plate)

Oligo: TM


- - -
Verification on gel :

ok

-

-

-

Purification on gel :

ok

-

-

-


Digestion:

Ter E/X

mRFP E/S

- - -
Verification digestion:

ok

-

-

-


Ligation:

mRFP E/S Ter E/X in Ter vector

- - -
Colony PCR:

ok

-

-

-

-

-

Miniprep:

ok

-

-

-

Sequencing :

ok

-

-

-

Stock glycerol:

-

-

-

-




The green color means the experiment was a success


plasmid =




Experiments ran :


Column 1 Column 2 Column 3 Column 4
PCR :

FecA matrix: K12

pBAD:

OmpAs: pINR2

'- - -
Verification on gel :

ok

-

-

-

-

Purification on gel :

ok

-

-

-

-

-

-


Digestion:

pBAD E/S

Digestion:

none

- -
Digestion checking

ok

Digestion checking

none

-

-


Ligation:

none

Ligation:

none

- -
Colony PCR :

none

Colony PCR :

none

-

-

Miniprep

none

Miniprep

none

-

-

Sequencing

none

Sequencing

none

-

-

Stock glycerol:

none

Stock glycerol:

none

-

-


Retrieved from "http://2009.igem.org/Team:Paris/Transduction_testing"