Team:Caltech/Week 9

From 2011.igem.org

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Line 36: Line 36:
Redid Gibson of pNT002, pNT003, pNT004 with pcrd inserts<br/>
Redid Gibson of pNT002, pNT003, pNT004 with pcrd inserts<br/>
Transformed cells with I732017 and K323089 for some source of lacZ<br/>
Transformed cells with I732017 and K323089 for some source of lacZ<br/>
 +
Re-assembly of DDT gene using PIPE cloning and Gibson, transformed into different cells.
===Results===
===Results===
I732019 and I732005 plates had no colonies<br/>
I732019 and I732005 plates had no colonies<br/>
pNT004 Gibson plates had no colonies<br/>
pNT004 Gibson plates had no colonies<br/>
CPCR of pNT002 colonies had no insert bands<br/>
CPCR of pNT002 colonies had no insert bands<br/>
 +
DDT assembly transformations showed colonies<br/>
 +
 +
==August 11==
 +
Colony PCR of DDT gene colonies<br/>
 +
 +
===Results===
 +
}}
}}

Revision as of 00:59, 12 August 2011


Caltech iGEM 2011



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August 8

Testing for biofilms grown on 96-well plate and Erlenmeyer flasks with crystal violet
PCR of 16s
Transformation of I732019, I732005, J23119 from source plate in XL-10 gold.
Re-assembly of DDT gene using alternate method
GCMS of p450-degraded BPA samples Obtain experimental strain (biofilm-forming) MG-1655 E. coli and grow overnight in SOC

Results

Bacteria-incubated well remained cystal violet stained after several rinses, indicating the presence of a biofilm, in contrast to the clear control well.

96-well plate with XL-10 biofilm grown for two days, visualized with 1% crystal violet

Glass beads with XL-10 biofilm grown for two days, visualized with 1% crystal violet

Got successful amplification of 16s in LA River sample 9-9. In both gels, the controls had no bands and all other sample lanes had no bands.
BPA sample was too diluted for GCMS; must concentrate first.
DDT assembly failed.

August 9

Evaporate-centrifuge BPA sample to concentrate for GCMS
Create glycerol stocks of experimental E. coli strain MG-1655 for biofilm experiments
Did 16s sequencing experiments with a Master Mix.
Gibson assembly of pNT004 with PCRd insert
CPCR of more pNT002 colonies with VF2 and VR primers.
Retransform I732005 and I732019 with top ten cells. Plated on kan plates and amp plates since plasmid has resistance to both.
Re-assembly of DDT gene using PIPE cloning and Gibson.

Results

I732019 and I732005 plates had no colonies.
Sequencing shows pNT003 and pNT002 colonies were self-ligated. But then what was the band on the cpcr gel?
DDT assembly failed.
16s gel had primer lengths, gene did not amplify.

August 10

Minimal media transfers
Started enrichment cultures of water samples from Baxter and BBB ponds.
Redid Gibson of pNT002, pNT003, pNT004 with pcrd inserts
Transformed cells with I732017 and K323089 for some source of lacZ
Re-assembly of DDT gene using PIPE cloning and Gibson, transformed into different cells.

Results

I732019 and I732005 plates had no colonies
pNT004 Gibson plates had no colonies
CPCR of pNT002 colonies had no insert bands
DDT assembly transformations showed colonies

August 11

Colony PCR of DDT gene colonies

Results


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