Team:Uppsala-SwedenWeek16

From 2010.igem.org

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</TR>
</TABLE>
</TABLE>
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J1C3, J2C3 and J3C1 was picked to build the K4,K5,K6 based on the gelpictures from 27/8/2010. Therefore we do not proceed with the ligated J-construct from the 16/9 due we have good enough samples from August month
 +
 +
Concentration measurement and swithch the backbone from pSB1C3 to psB1A3
 +
 +
<TABLE WIDTH=591 BORDER=1 BORDERCOLOR="#000000" CELLPADDING=7 CELLSPACING=0>
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<TR VALIGN=TOP>
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<TD WIDTH=69>
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<P LANG="sv-SE" CLASS="western"><BR>
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</P>
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</TD>
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<TD WIDTH=70>
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<P CLASS="western" STYLE="margin-bottom: 0in"><SPAN LANG="sv-SE">DNA-conc.</SPAN></P>
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<P LANG="sv-SE" CLASS="western"><BR>
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</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western" STYLE="margin-bottom: 0in">DNA-vol
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</P>
 +
<P CLASS="western"><SPAN LANG="sv-SE">Digestion</SPAN></P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western" STYLE="margin-bottom: 0in">Restr.Enzym</P>
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<P LANG="sv-SE" CLASS="western">E &amp; P</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western" STYLE="margin-bottom: 0in">FD
 +
Buffer</P>
 +
<P LANG="sv-SE" CLASS="western">10x</P>
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</TD>
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<TD WIDTH=70>
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<P CLASS="western"><SPAN LANG="sv-SE">H</SPAN><SUB><SPAN LANG="sv-SE">2</SPAN></SUB><SPAN LANG="sv-SE">0</SPAN></P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">Total</P>
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</TD>
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</TR>
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<TR VALIGN=TOP>
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<TD WIDTH=69>
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<P CLASS="western"><SPAN LANG="sv-SE">J1</SPAN><SPAN LANG="sv-SE">C3</SPAN></P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">97.2</P>
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</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">10.3</P>
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</TD>
 +
<TD WIDTH=70>
 +
<P CLASS="western"><SPAN LANG="sv-SE">0.5 &amp; 0.5</SPAN></P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">2</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">6.7</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">20</P>
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</TD>
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</TR>
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<TR VALIGN=TOP>
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<TD WIDTH=69>
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<P LANG="sv-SE" CLASS="western">J2C3</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">73.6</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">13.6</P>
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</TD>
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<TD WIDTH=70>
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<P CLASS="western"><SPAN LANG="sv-SE">0.5 &amp; 0.5</SPAN></P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">2</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">3.4</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">20</P>
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</TD>
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</TR>
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<TR VALIGN=TOP>
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<TD WIDTH=69>
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<P LANG="sv-SE" CLASS="western">J3C1</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">71.2</P>
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</TD>
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<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">14.0</P>
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</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">0.5 &amp; 0.5</P>
 +
</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">2</P>
 +
</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">3</P>
 +
</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">20</P>
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</TD>
 +
</TR>
 +
<TR VALIGN=TOP>
 +
<TD WIDTH=69>
 +
<P CLASS="western"><SPAN LANG="sv-SE">c</SPAN><SPAN LANG="sv-SE">cdbA3</SPAN></P>
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</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">180.0</P>
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</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">5</P>
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</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">0.5 &amp; 0.5</P>
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</TD>
 +
<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">2</P>
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</TD>
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<TD WIDTH=70>
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<P LANG="sv-SE" CLASS="western">12</P>
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</TD>
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<TD WIDTH=70>
 +
<P LANG="sv-SE" CLASS="western">20</P>
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</TD>
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</TR>
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</TABLE>
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 +
Ligation and transformation according the protocol
 +
 +
Phusion colony-PCR for K1, K2, K3, G1, G2 with Phusion Polymerase
 +
 +
[[Image:Image:Labnotes html m6b5aec6d.jpg|300px|thumb|left|K1 K2 K3 G1 G2]]
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 +
[[Image:Labnotes html 42a7cca1.jpg|300px|thumb|K1 K2 K3 G1 G2]]
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 +
[[Image:Labnotes html m75fca8ff.jpg|300px|thumb|K1 K2 K3 G1 G2]]
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 +
We had unsatisfied results with our colonies fluorescence measurement and we suspected that the LacI protein didn’t suppress the fluorescent protein enough. One possible explanation would that BB_P0412 contains BB_C0012 which is the coding region for the LacI protein were degraded too effectively by the LVA degradation tail. As a consequence the R0010, a LacI promoter suppressing the three plasmids flourescent expression, didn’t bind enough LacI and therefore you could detect some flourescence.
 +
 +
Since J-construct contains the BB_R0010 as well, the K4, K5 and K6 construction were postponed.
 +
 +
Therefore we switch the BB_C0012 to another LacI-coding sequence that excluded the degradation tail., called LacIB115 which is in psB1AK3. With the restriction enzymes ApaI and PstI , both restriction sites surround the LacI coding region for psB1AK3 and I-construct. Afterdigestion of both plamids, you run the gel and cut out the band with LacI (without the degradation tail and the I-construction backbone and assembly those two parts.

Revision as of 19:47, 26 October 2010

Week-16

Start to apply high fidelity PCR due the construct are getting larger and the regular Taq polymerase may not perform as well as the Phusion Polymerase at this length. Based on the company´s manual, we calculated the


Temperatur

Time

Cycle

Initial denaturation

98

30 s

1

Denaturation

98

10

30

Annealing

55.3

10s

30

Extension

72

1 min 45 s

30

Final extension

72

5 min

1


4

forever



The purpose of this was to get more reliable band when doing a PCR and running the gel.

Mastermix

Volume (µL)

H20

10.8

5X phusion HF Buffer

4

dNTPs

2

VF2

1

VR

1

DNA-template

1

Phusion Polymerase

0.2


J1C3, J2C3 and J3C1 was picked to build the K4,K5,K6 based on the gelpictures from 27/8/2010. Therefore we do not proceed with the ligated J-construct from the 16/9 due we have good enough samples from August month

Concentration measurement and swithch the backbone from pSB1C3 to psB1A3


DNA-conc.

DNA-vol

Digestion

Restr.Enzym

E & P

FD Buffer

10x

H20

Total

J1C3

97.2

10.3

0.5 & 0.5

2

6.7

20

J2C3

73.6

13.6

0.5 & 0.5

2

3.4

20

J3C1

71.2

14.0

0.5 & 0.5

2

3

20

ccdbA3

180.0

5

0.5 & 0.5

2

12

20

Ligation and transformation according the protocol

Phusion colony-PCR for K1, K2, K3, G1, G2 with Phusion Polymerase

File:Image:Labnotes html m6b5aec6d.jpg
K1 K2 K3 G1 G2
K1 K2 K3 G1 G2
K1 K2 K3 G1 G2

We had unsatisfied results with our colonies fluorescence measurement and we suspected that the LacI protein didn’t suppress the fluorescent protein enough. One possible explanation would that BB_P0412 contains BB_C0012 which is the coding region for the LacI protein were degraded too effectively by the LVA degradation tail. As a consequence the R0010, a LacI promoter suppressing the three plasmids flourescent expression, didn’t bind enough LacI and therefore you could detect some flourescence.

Since J-construct contains the BB_R0010 as well, the K4, K5 and K6 construction were postponed.

Therefore we switch the BB_C0012 to another LacI-coding sequence that excluded the degradation tail., called LacIB115 which is in psB1AK3. With the restriction enzymes ApaI and PstI , both restriction sites surround the LacI coding region for psB1AK3 and I-construct. Afterdigestion of both plamids, you run the gel and cut out the band with LacI (without the degradation tail and the I-construction backbone and assembly those two parts.

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