Test pLsrA/cI

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Test pLsrA/cI promoter

The pLsrA/cI promoter is constitutively off and is repressed by the lsrR protein. The addition of AI-2 should de-repress the lsrR operon causing it to glow. The addition of the cI protein should repress the promoter, causing it to not glow.


1)Control group

plsrA/cI→GFP glows

K091106+E0240


2) Test LsrR repression:

pBAD→RBS+LsrR+t+t+plsrA/cI→GFP does not glow

I13453+B0034+K091001+B0015+K091106+E0240

add AI-2

pBAD→RBS+LsrR+t+t+plsrA/cI→GFP glows

I13453+B0034+K091001+B0015+K091106+E0240

3) Test cI repression:

pBAD→RBS+cI+TT+plsrA/cI→GFP does not glow

I13453+B0034+C0051+B0015+K091106+E0240

4) Test LsrR and cI repression:

pBAD→RBS+lsrR+cI+TT+plsrA/cI→GFP does not glows

I13453+B0034+K091001+C0051+B0015+K091106+E0240

add AI-2

pBAD→RBS+lsrR+cI+TT+plsrA/cI→GFP does not glows

I13453+B0034+K091001+C0051+B0015+K091106+E0240

LsrR cI AI-2 + GFP AI-2 - GFP
0 0 1 1
1 0 1 0
0 1 0 0
1 1 0 0


Ligation plan for three test sequences

1)

K091106 ligated with E0240

need to ligate some promoter (digest with E/S) with an RBS (digest E/X) and ligate lsrR(digest with E/S) with a double terminator (digest with E/X)


2)

K091106 ligated with E0240

need to ligate some promoter (digest with E/S) with an RBS (digest E/X) and ligate lsrR(digest with E/S) with a double terminator (digest with E/X)

then ligate the promoter+RBS to the 5' end of the lsrR+TT parts together

then ligate that part 5' to the plsrA/cI+GFP


3)

ligate cI to the double terminator

the ligate the promoter+RBS from the first test sequence to the 5' end of the cI+TT

ligate this to the 5' end of the plsrA/cI+GFP


4)

ligate the cI+TT from the second test sequence to the 3' end of the lsrR coding region

then ligate the promoter+RBS from the first test sequence to the 5' end of that

next ligate the plsrA/cI to the 3' end of that entire sequence


the 2) and 4) test sequences will also need to be tested by adding AI-2

the 2) test sequence should glow and the 4) should not.