Team:Caltech/Week 9

From 2011.igem.org

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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.<br/>
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.<br/>
-
BPA sample was too diluted for GCMS; must concentrate first.
+
BPA sample was too diluted for GCMS; must concentrate first.<br/>
 +
DDT assembly failed.
==August 9==
==August 9==
Evaporate-centrifuge BPA sample to concentrate for GCMS<br/>
Evaporate-centrifuge BPA sample to concentrate for GCMS<br/>
Create glycerol stocks of experimental ''E. coli'' strain MG-1655 for biofilm experiments<br/>
Create glycerol stocks of experimental ''E. coli'' strain MG-1655 for biofilm experiments<br/>
Did 16s sequencing experiments with a Master Mix. <br/>
Did 16s sequencing experiments with a Master Mix. <br/>
 +
Gibson assembly of pNT004 with PCRd insert<br/>
CPCR of more pNT002 colonies with VF2 and VR primers.<br/>
CPCR of more pNT002 colonies with VF2 and VR primers.<br/>
Retransform I732005 and I732019 with top ten cells. Plated on kan plates and amp plates since plasmid has resistance to both.<br/>
Retransform I732005 and I732019 with top ten cells. Plated on kan plates and amp plates since plasmid has resistance to both.<br/>
 +
Re-assembly of DDT gene using PIPE cloning and Gibson.  <br/>
===Results===
===Results===
I732019 and I732005 plates had no colonies.<br/>
I732019 and I732005 plates had no colonies.<br/>
Sequencing shows pNT003 and pNT002 colonies were self-ligated. But then what was the band on the cpcr gel?<br/>
Sequencing shows pNT003 and pNT002 colonies were self-ligated. But then what was the band on the cpcr gel?<br/>
 +
DDT assembly failed.<br/>
 +
16s gel had primer lengths, gene did not amplify.<br/>
 +
==August 10==
 +
Minimal media transfers<br/>
 +
Started enrichment cultures of water samples from Baxter and BBB ponds.<br/>
 +
Redid Gibson of pNT002, pNT003, pNT004 with pcrd inserts<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.
 +
Begin time-dependent biofilm optimization experiment with crystal violet stain.
 +
===Results===
 +
I732019 and I732005 plates had no colonies<br/>
 +
pNT004 Gibson plates had no colonies<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/>
 +
Transformation of I732005, I732017, I732019 in new XL-10 cells<br/>
 +
PCR of pSB4A5, pSB3K3, pNT002 insert, pNT003 insert. Tried PCA to assemble inserts more specifically.<br/>
 +
Continue time-dependent biofilm optimization experiment with crystal violet stain.
 +
===Results===
 +
[[File:DDT_assembly_cpcr.jpg|thumb|left|CPCR of DDT gene]]
 +
<table border="1">
 +
<tr>
 +
<th>Plate</th>
 +
<th>number of colonies</th>
 +
</tr>
 +
<tr>
 +
<td>pNT002 + top ten</td>
 +
<td>3</td>
 +
</tr>
 +
<tr>
 +
<td>pNT002 - top ten</td>
 +
<td>1</td>
 +
</tr>
 +
<tr>
 +
<td>pNT003+ top ten</td>
 +
<td>1</td>
 +
</tr>
 +
<tr>
 +
<td>pNT003 - top ten</td>
 +
<td>0</td>
 +
</tr>
 +
<tr>
 +
<td>pNT004 + top ten</td>
 +
<td>1</td>
 +
</tr>
 +
<tr>
 +
<td>pNT004 - top ten</td>
 +
<td>1</td>
 +
</tr>
 +
<tr>
 +
<td>I372017</td>
 +
<td>0</td>
 +
</tr>
 +
<tr>
 +
<td>K323089</td>
 +
<td>0</td>
 +
</tr>
 +
</table>
 +
 +
<table border="1">
 +
<tr>
 +
<th>Name</th>
 +
<th>concentration (ng/ul)</th>
 +
</tr>
 +
<tr>
 +
<td>pSB4A5</td>
 +
<td>57.1</td>
 +
</tr>
 +
<tr>
 +
<td>pSB3k3 1</td>
 +
<td>60.4</td>
 +
</tr>
 +
<tr>
 +
<td>pSB3k3 2</td>
 +
<td>31.1</td>
 +
</tr>
 +
<tr>
 +
<td>pNT002 insert</td>
 +
<td>136.9</td>
 +
</tr>
 +
<tr>
 +
<td>pNT003 insert</td>
 +
<td>72.0</td>
 +
</tr>
 +
<tr>
 +
<td>pNT002 insert PCA</td>
 +
<td>15.7</td>
 +
</tr>
 +
</table>
 +
==August 12==
 +
Continue time-dependent biofilm optimization experiment with crystal violet stain.<br/>
 +
PCR of 16s.
 +
===Results===
 +
Biobrick transformation plates
 +
<table border="1">
 +
<tr>
 +
<th>Plate</th>
 +
<th>Colonies</th>
 +
</tr>
 +
<tr>
 +
<td>I732005</td>
 +
<td>0</td>
 +
</tr>
 +
<tr>
 +
<td>I732017</td>
 +
<td>~200</td>
 +
</tr>
 +
<tr>
 +
<td>I732019</td>
 +
<td>65</td>
 +
</tr>
 +
</table>
 +
[[File:8-1216sphusion.jpg|thumb|16s amplification, lane 1 NEB 2-log ladder, lane 2 9-3A, lane 3 9-3B, lane 4 9-3C, lane 5 9-9A, lane 6 9-9B, lane 7 9-9C, lane 8 10-3A, lane 9 10-3B, lane 10 10-3C, lane 11 10-6A, lane 12 10-6B, lane 13 10-6C, lane 14 Control 1, lane 15 Control 2]]
 +
==August 13==
 +
===Results===
 +
<table border="1">
 +
<tr>
 +
<th>Plate</th>
 +
<th>Colonies</th>
 +
</tr>
 +
<tr>
 +
<td>pNT002 +</td>
 +
<td>~320</td>
 +
</tr>
 +
<tr>
 +
<td>pNT002 -</td>
 +
<td>~800</td>
 +
</tr>
 +
<tr>
 +
<td>pNT003+</td>
 +
<td>~500</td>
 +
</tr>
 +
<tr>
 +
<td>pNT003-</td>
 +
<td>~400</td>
 +
</tr>
 +
</table><br/>
 +
 +
Crystal violet biofilm results:
 +
<table border="1">
 +
<tr>
 +
<th rowspan="2">'''Starting OD'''</th>
 +
<th colspan="2">8/10</th>
 +
<th colspan="3">8/11</th>
 +
<th colspan="3">8/12</th>
 +
<th colspan="2">8/13</th>
 +
</tr>
 +
<tr>
 +
<td>5pm</td>
 +
<td>11pm</td>
 +
<td>11am</td>
 +
<td>5pm</td>
 +
<td>11pm</td>
 +
<td>11am</td>
 +
<td>5pm</td>
 +
<td>11pm</td>
 +
<td>11am</td>
 +
<td>5pm</td>
 +
</tr>
 +
<tr>
 +
<td>'''0.118'''</td>
 +
<td>.065</td>
 +
<td>.171</td>
 +
<td>.114</td>
 +
<td>.135</td>
 +
<td>.266</td>
 +
<td>.149</td>
 +
<td>.133</td>
 +
<td>.100</td>
 +
<td>.408</td>
 +
<td>.740</td>
 +
</tr>
 +
<tr>
 +
<td>'''0.170'''</td>
 +
<td>.065</td>
 +
<td>.132</td>
 +
<td>.082</td>
 +
<td>.190</td>
 +
<td>.159</td>
 +
<td>.439</td>
 +
<td>1.875</td>
 +
<td>.106</td>
 +
<td>.323</td>
 +
<td>.545</td>
 +
</tr>
 +
<tr>
 +
<td>'''0.068'''</td>
 +
<td>.065</td>
 +
<td>.106</td>
 +
<td>.184</td>
 +
<td>.198</td>
 +
<td>.210</td>
 +
<td>.121</td>
 +
<td>.201</td>
 +
<td>.145</td>
 +
<td>.039</td>
 +
<td>.881</td>
 +
</tr>
 +
</table><br/>
 +
<gallery>
 +
File:Biofilm_graphs.jpg|Biofilm experiment chart
 +
File:96-well.jpg|Biofilm experiment 96-well plate
 +
File:Cuvettes.jpg|Biofilm experiment cuvettes
 +
</gallery>
}}
}}

Latest revision as of 18:50, 8 September 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. Begin time-dependent biofilm optimization experiment with crystal violet stain.

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
Transformation of I732005, I732017, I732019 in new XL-10 cells
PCR of pSB4A5, pSB3K3, pNT002 insert, pNT003 insert. Tried PCA to assemble inserts more specifically.
Continue time-dependent biofilm optimization experiment with crystal violet stain.

Results

CPCR of DDT gene
Plate number of colonies
pNT002 + top ten 3
pNT002 - top ten 1
pNT003+ top ten 1
pNT003 - top ten 0
pNT004 + top ten 1
pNT004 - top ten 1
I372017 0
K323089 0
Name concentration (ng/ul)
pSB4A5 57.1
pSB3k3 1 60.4
pSB3k3 2 31.1
pNT002 insert 136.9
pNT003 insert 72.0
pNT002 insert PCA 15.7

August 12

Continue time-dependent biofilm optimization experiment with crystal violet stain.
PCR of 16s.

Results

Biobrick transformation plates

Plate Colonies
I732005 0
I732017 ~200
I732019 65
16s amplification, lane 1 NEB 2-log ladder, lane 2 9-3A, lane 3 9-3B, lane 4 9-3C, lane 5 9-9A, lane 6 9-9B, lane 7 9-9C, lane 8 10-3A, lane 9 10-3B, lane 10 10-3C, lane 11 10-6A, lane 12 10-6B, lane 13 10-6C, lane 14 Control 1, lane 15 Control 2

August 13

Results

Plate Colonies
pNT002 + ~320
pNT002 - ~800
pNT003+ ~500
pNT003- ~400

Crystal violet biofilm results:

Starting OD 8/10 8/11 8/12 8/13
5pm 11pm 11am 5pm 11pm 11am 5pm 11pm 11am 5pm
0.118 .065 .171 .114 .135 .266 .149 .133 .100 .408 .740
0.170 .065 .132 .082 .190 .159 .439 1.875 .106 .323 .545
0.068 .065 .106 .184 .198 .210 .121 .201 .145 .039 .881

Biofilm experiment chart

Biofilm experiment 96-well plate

Biofilm experiment cuvettes


Retrieved from "http://2011.igem.org/Team:Caltech/Week_9"