Latest revision as of 22:03, 20 October 2015

Project Results

Transformation Efficiency Kit, RFP construct (iGEM)

Before using our competent E. coli TOP10 cells in the important experiments, we used the Transformation Efficiency Kit to test the efficiency of our competent cells!

The kit includes five vials of each different DNA concentration: 50 pg/μl, 20 pg/μl, 10 pg/μl, 5 pg/μl, 0.5 pg/μl of purified DNA from BBa_J04450 (RFP construct) in plasmid backbone pSB1C3.

The first test transformation (50 μl of competent cells, 20 μl plated) showed very poor results:

First test transformation of own competent E.coli TOP10 with the iGEM Transformation Efficiency Kit containing RFP

DNA concentration	0.5 pg/μl	5 pg/μl	10 pg/μl	20 pg/μl	50 pg/μl
# of colonies	0	0	2	0	13
efficiency (cfu)	0	0	3.8x 10⁶	0	3.4x 10⁶

Results	efficiency
average	1.4x 10⁶
weighted	3.5x 10⁶

The second test transformation (200 μl of competent cells, 100 μl plated) showed still poor results but we decided to continue working with our cells:

Second test transformation of own competent E.coli TOP10 with the iGEM Transformation Efficiency Kit containing RFP

DNA concentration	0.5 pg/μl	5 pg/μl	10 pg/μl	20 pg/μl	50 pg/μl
# of colonies	1	13	1	35	28
efficiency (cfu)	8.0x 10⁶	1.0x 10⁷	4.0x 10⁵	7.0x 10⁶	2.3x 10⁶

Results	efficiency
average	5.6x 10⁶
weighted	3.7x 10⁶

RFP

RFP

RFP (RFP DsRed) was amplified from pHT315_rfp by PCR (Fig.1). Colonies on a plate were given to us by the Applied and Genomic Microbiology department. Primers contained restriction sites for KpnI and SacI in order to make them compatible for insertion into the multiple cloning site of the pBAD/His A vector. The PCR products were examined in a 0,8% agarose gel by electrophoresis.

Fig.1) A gel of the RFP DsRed PCR product showed the bands to be at the correct height.

After purification of the PCR product it was ligated into pJET1.2 by subcloning (blunt end ligation). This vector serves to clone the fluorescent protein without triggering its activity, which may interact with the expression vector or the chosen E.coli strain.

Ligation into pJET1.2 was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit, restricted with KpnI and SacI and examined in a gel (Fig.2).

Fig.2) Once restriction controls showed the correct bands, both pJET_RFP_3 and pJET_RFP_7 were sent for sequencing by the G2L laboratory.

Sequencing of both samples was correct and proved that RFP_3 and RFP_7 were properly inserted into the pJET vector. We decided to keep on working with pJET_RFP_3. The plasmid was transformed with E.coli TOP10 and E.coli BL21. Cryocultures were frozen for a strain collection.

The next step was a big restriction of the whole plasmid extract with the correspondent pair of restriction enzymes. That allowed us to isolate the RFP inserts carrying the desired restriction sites (KpnI and SacI). The fragments were purified with the PEQLAB peqGOLD Gel Extraction Kit before T4 ligation. The RFP_3 insert was ligated into pBAD/His A by the T4 ligation system (sticky end ligation) according to the protocol in the methods collection and transformed into E.coli TOP10. This vector serves to express the fluorescent protein by triggering its activity.

After over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit and restricted with KpnI and SacI.

To build a component for our Flexosome, we decided to fuse pBAD_RFP with the ACEL (Acetivibrio cellulolyticus) dockerin. Both components, restricted with KpnI and SacI and purified with the PEQLAB peqGOLD Gel Extraction Kit were ligated by the T4 ligation system. After transformation into E.coli TOP10 and over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit, restricted with EcoRI and examined in a gel (Fig.3).

Fig.3) Once restriction control showed the correct band height, pBAD_RFP_ACEL was sent for sequencing by the G2L laboratory.

RESULTS

Sanger sequencing showed correct sequences for the Flexosome bit pBAD_RFP_ACEL.

MICROSCOPY

To check the activity of RFP, an induction series with 0,2%, 2% and 5% L-Arabinose in the cell culture medium was prepared. Fluorescence microscopy was performed with the RFP DsRed filter (excitation at 536 nm, emission at 582 nm). Unfortunately no fluorescence could be detected throughout the whole project with different constructs. Neither in the pJET_RFP_3, nor in the pBAD constructs (pBAD_RFP_3 and pBAD_RFP_ACEL) induced with 0,2%, 2% and 5% L-Arabinose in the medium. Since the DNA sequences have been confirmed to be correct by Sanger sequencing it might be a problem of expression.

FUTURE PLANS

In future we want to exchange our vector system (pET100 instead of pBAD) to ensure that pBAD is not somehow interfering with our chosen E. coli strain.

Esterase and Phosphatase

Phosphatase and Esterase

Esterase was amplified from pET101_E064 and phosphatase from pTOPOXL_PLP07 by PCR for each enzyme (Fig.1). Both plasmids were given to us by the Applied and Genomic Microbiology department. Primers contained restriction sites KpnI and SacI for esterase and XhoI and PstI for the phosphatase in order to make them compatible for insertion into the multiple cloning site of the pBAD vector. The genes for these two enzymes had been found in screenings of metagenomic libraries.

After purification of the PCR products, they were ligated into pJET by blunt end ligation. This vector serves to clone the enzymes without triggering their activity, which may interact with the vector or the E.coli. In the case of phosphatase, the PCR products needed to be purified by gel extraction, to eliminate left over template plasmids, which could interfere with the transformation.

Ligation into pJET was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted with a Quiaprep spin Miniprep kit and restricted with either KpnI and SacI or XhoI and PstI, depending on the Enzyme (Fig.2&3).

Restriction control esterase pJET iGEM Gottingen2015.jpeg

Control restriction pJET phosphatase iGEM Goettingen2015.jpeg

Once restrictions showed the correct bands, both pJET containing esterase and phosphatase were sent for sequencing by the G2L laboratory.

The sequencing was successful and proved that both enzymes were properly inserted into the vector. The next step was a big restriction of the whole plasmid extract with the correspondent pair of restriction enzymes. That allowed us to isolate the enzyme inserts carrying the desired restriction sites. The fragments were purified with the peqGOLD Gel extraction kit.

The esterase was then ligated into the pBAD vector containing the CCEL (Clostridium cellulolyticum) dockering. Competent E. coli Top10 cells were transformed and the pBAD_Est_CCEL construct was isolated from the positive clones with a Quiaprep spin Miniprep kit.

A restriction control with SacI for the esterase constructs was run in a 0,8% agarose gel (Fig. 4). Samples #2, #3 and #9 correspond to the linear plasmid containing the insert. Phosphatase construct was control restricted with EcoRI (Fig. 5), in this case 13 of 14 samples showed successful insertion of the enzyme fragment into the vector.

Control restriction pBAD Est CCEL iGEM Goettingen2015.jpeg

Pho CTHE control restriction iGEM Gottingen2015.jpg

Future plans

The next steps include changing to a better expression vector in order to test and measure the activity of the enzymes, especially to ensure that the fusion with the dockerins is not interfering with the function of the enzymes. Finally the aim is to combine the purified enzyme-dockerin proteins with the synthetic scaffold and prove the self assemby of the Flexosome tool.

Cellulase

The cellulase gene was amplified using PCR. The primers which were used contained the restriction sites for ligation into the pBAD vector. The cellulase PCR products were then checked on 0.8 % agarose gel.

Figure 1: Cellulase PCR product was run on a 0.8 % agarose gel. The desired cellulase sequence is at 2496 bp.

The cellulase PCR products were then purified by using the QIAquick® PCR Purification Kit (QIAGEN). After the PCR products were purified, the concentration of DNA was measured by Nanodrop 2000c Spectrophotometer.

Restriction control of pBAD_CCEL and cellulase PCR product

The purified cellulase PCR product and the pBAD_CCEL vector were restricted by following a double digest protocol with SacI and PvuII enzymes. After restriction control products were purified by using the QIAquick® PCR Purification Kit (QIAGEN) the concentration of DNA was measured by Nanodrop 2000c Spectrophotometer.

Ligation of Cellulase into pBAD- CCEL

The cellulase gene was then ligated into the pBAD vector containing the CCEL (Clostridium

cellulolyticum ) dockerin.

For ligation of the cellulase PCR product into the restricted pBAD_CCEL vector, the Thermo Fisher T4 Ligase Sticky End Ligation protocol was followed.

Transformation of pBAD_CellulaseCCEL into chemically competent Top10 E. coli cells

pBAD_CellulaseCCEL was transformed into competent Top10 E. coli cells by using the heat shock transformation method.

Figure 2: Transformation of pBAD_CellulaseCCEL into competent Top 10 E. coli cells. The image shows plates with successful transformants.

Colonies from transformation plates were inoculated into LB medium containing ampicillin (100 µg/ml).

Plasmid Extraction: peqGold Plasmid Miniprep Kit

Plasmid extraction was done for colonies inoculated in LB medium by using peqGold Plasmid Miniprep kit and plasmid concentration was measured by using Nanodrop 2000c Spectrophotometer.

Restriction control was done with the enzymes SacI and PvuII from Thermo fisher scientific. Restricted plasmids were checked on a 0.8 % agarose gel.

Figure 3: Restriction control of the pBAD_CellulaseCCEL construct from TOP10 E. coli positive clones by with SacI and PvuII. Colony 1 has the desired insert.

The correct insert was confirmed through sequencing.

BioBricks

Dockerin Biobricks

The dockerins ACEL (Acetivibrio cellulolyticus), BCEL (Bacteroides cellulosolvens), CCEL (Clostridium cellulolyticum) and CTHE (Clostridium thermocellum) were amplified from pBAD_ACEL, pBAD_BCEL, pBAD_CCEL and pBAD_CTHE with primers to add the desired EcoRI and PstI restriction sites by PCR. Primers contained restriction sites for EcoRI and PstI in order to make them compatible for insertion into the iGEM shipping vector pSB1C3.

After purification, the PCR products were restricted with EcoRI and PstI, as well as pSB1C3. Afterwards the restricted dockerins were ligated into pSB1C3 by T4 ligation (sticky end ligation) and transformed into E. coli TOP10.

Ligation into pSB1C3 was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit and test restricted with EcoRI (pSB1C3_CCEL and pSB1C3_ACEL) and EcoRI and PstI (pSB1C3_BCEL) (Fig.1). We lost CTHE due to failing transformations at this point.

Once restriction controls showed the correct bands, pSB1C3_CCEL, pSB1C3_ACEL and pSB1C3_BCEL were sent for sequencing.

Colour BioBricks

We also wanted to improve already existing BioBricks by fusing our dockerins to the colours eforRed (BBa_K592012) and amilCP (BBa_K592009) that were submitted from the University of Uppsala (Sweden) in 2011.

So we chose to fuse eforRed to BCEL and amilCP to CCEL. Since the plasmids of the two colour proteins were not distributed with the current plate of the iGEM Distribution Kit, we ordered those parts including the right restriction sites as gBlocks from IDT.

As a first step eforRed and amilCP were restricted with KpnI and SacI to make them compatible with our dockerins in pBAD.

After purification restricted colours were ligated into pBAD_BCEL and pBAD_CCEL by T4 ligation (sticky end ligation) and transformed into E. coli TOP10.

Ligation into pBAD was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit and test restricted with KpnI (Fig.2).

TeamGoettingen2015 Rest control pBAD eforRed BCEL and amilCP CCEL Goettingen2015.jpeg

Once restriction controls showed the correct bands, pBAD_amilCP_CCEL #1 and pBAD_eforRed_BCEL were sent for sequencing. Sequencing showed that both plasmids were correct.

To make our constructs compatible with the iGEM shipping vector pSB1C3 the desired EcoRI and PstI restrictions sites were added by PCR.

After purification, the PCR products were restricted with EcoRI and PstI, the same with pSB1C3, and afterwards ligated into pSB1C3 by T4 ligation (sticky end ligation) and transformed into E. coli TOP10.

After over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit and test restricted with EcoRI (Fig.3). Due to the reason that our dockerin CCEL contains an internal PstI restriction site we continued working only with the eforRed_BCEL construct.

TeamGoettingen2015 Rest control pSB1C3 eforRed BCEL Goettingen2015.jpeg

Once restriction controls showed the correct band, pSB1C3_eforRed_BCEL was sent for sequencing. Sequencing showed that the plasmids were correct.

RESULTS

Sequencing showed that the dockerins ACEL and CCEL contain an internal PstI restriction site. Therefore all the constructs containing ACEL or CCEL showed in the end truncated dockerin sequences and could not be send in as BioBricks.

We also build a construct where the enzyme esterase was fused to our CCEL dockerin (pBAD_Est_CCEL) following the same strategy. But again, due to the reason that our dockerin CCEL contains an internal PstI restriction site we had to stop our work at this point.

Furthermore we collaborated with the current iGEM team of Aachen and tried to fuse three of their enzymes to our constructs but could not finish our work here.

ACHIEVENTS

Sequences of pSB1C3_BCEL and pSB1C3_eforRed_BCEL were correct and submitted as BioBricks to iGEM:

pSB1C3_BCEL (BBa_K1865000)

pSB1C3_eforRed_BCEL (BBa_K1865001)

Scaffoldin Purification

Scaffoldin purification

After induction according to the methods collection, the targeted ScaA scaffoldin was purified by nickel affinity chromatography using Ni-NTA-agarose columns in a Äkta prime system (Fig. 1A). Following the addition of Imidazol two peaks were obtained. The fractions of interest were visualized in a SDS-PAGE gel (Fig. 1B). The gel showed that only the second fraction presents the expected size of 111kDa. However some other bands appeared along this fraction, therefore in order to obtain even more pure protein a Size Exclusion Chromatography (SEC) was done.

Histag purification iGEM Goettingen2015.jpeg

The SEC was done with a HiLoad Superdex 200 16/600 column (GE Healthcare) (Fig. 2A). SDS gel shows that a high concentration of the desired protein was obtained and most of the previous contaminating bands were eliminated. Nevertheless there was an unknown band of low weight present in every fraction, apparently it could be a second protein from E. coli with some affinity to the Scaffoldin than is then is co-purified with it (Fig. 2B).

Future plans include to incubate the Scafoldin with the purified enzyme-dockerin construct in order to prove that the Flexosome can assembly by itself.

Copurification

Copurification of Scaffoldin and Enzyme-Dockerin

The main peaks after gelfiltration from the scaffoldin CTHE (see results scaffoldin) and CellulaseCCEL (Fig.1) were pooled and concentrated.

B1-B3 were pooled for copurification.

They were then mixed and incubated together at 37°C for 15 min with agitation.

The solution was then used in another gelfiltration (Fig.2). The resulting peaks were run on a SDS-gel (Fig.3) and checked for cellulase activity.

Fig.2) The peak at A5-A7 may be the bound scaffoldin and dockerin, whilst the unbound proteins are expected between B3 and C9.

The first peak from the copurification showed a distinct cellulase activity. As the peak ran considerably higher than expected than either the scaffoldin or the CellulaseCCEL in the gelfitration, it can be expected that this peak contains a successfully formed complex between CellulaseCCEL and the CTHE scaffoldin.

Giant Jamboree: Poster and Presentation

Did you missed our presentation? Do you want to see our poster again? No problem, here you can find the files:

Media:IGEM-presentation_final_team_Goettingen.ppt

Media:Poster_teamGoettingen_2015.pdf

@@ Line 39: / Line 39: @@
 }
-#menu1, #menu2, #menu3{
+#menu1, #menu2, #menu3, #menu4, #menu5, #menu6, #menu7, #menu8{
      display:none;
      width:90%;
@@ Line 62: / Line 62: @@
 <p>Before using our competent <em>E. coli</em> TOP10 cells in the important experiments, we used the Transformation Efficiency Kit to test the efficiency of our competent cells!</p>
-<p>The kit includes five vials of each different DNA concentration: 50pg/&mu;l, 20pg/&mu;l, 10pg/&mu;l, 5pg/&mu;l, 0.5pg/&mu;l of purified DNA from BBa_J04450 (RFP construct) in plasmid backbone pSB1C3.</p>
+<p>The kit includes five vials of each different DNA concentration: 50 pg/&mu;l, 20 pg/&mu;l, 10 pg/&mu;l, 5 pg/&mu;l, 0.5 pg/&mu;l of purified DNA from BBa_J04450 (RFP construct) in plasmid backbone pSB1C3.</p>
 <p>&nbsp;</p>
 <p>The first test transformation (50 &mu;l of competent cells, 20 &mu;l plated) showed very poor results:</p>
@@ Line 76: / Line 76: @@
              </td>
              <td>
-                 <p align="center">0.5pg/&mu;l</p>
+                 <p align="center">0.5 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">5pg/&mu;l</p>
+                 <p align="center">5 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">10pg/&mu;l</p>
+                 <p align="center">10 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">20pg/&mu;l</p>
+                 <p align="center">20 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">50pg/&mu;l</p>
+                 <p align="center">50 pg/&mu;l</p>
              </td>
          </tr>
@@ Line 122: / Line 122: @@
              </td>
              <td>
-                 <p align="center">3.8x10<sup>6</sup></p>
+                 <p align="center">3.8x 10<sup>6</sup></p>
              </td>
              <td>
@@ Line 128: / Line 128: @@
              </td>
              <td>
-                 <p align="center">3.4x10<sup>6</sup></p>
+                 <p align="center">3.4x 10<sup>6</sup></p>
              </td>
          </tr>
@@ Line 149: / Line 149: @@
              </td>
              <td valign="bottom" nowrap="nowrap" width="68">
-                 <p align="right">1.4x10<sup>6</sup></p>
+                 <p align="right">1.4x 10<sup>6</sup></p>
              </td>
          </tr>
@@ Line 157: / Line 157: @@
              </td>
              <td valign="bottom" nowrap="nowrap" width="68">
-                 <p align="right">3.5x10<sup>6</sup></p>
+                 <p align="right">3.5x 10<sup>6</sup></p>
              </td>
          </tr>
@@ Line 177: / Line 177: @@
              </td>
              <td>
-                 <p align="center">0.5pg/&mu;l</p>
+                 <p align="center">0.5 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">5pg/&mu;l</p>
+                 <p align="center">5 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">10pg/&mu;l</p>
+                 <p align="center">10 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">20pg/&mu;l</p>
+                 <p align="center">20 pg/&mu;l</p>
              </td>
              <td>
-                 <p align="center">50pg/&mu;l</p>
+                 <p align="center">50 pg/&mu;l</p>
              </td>
          </tr>
@@ Line 217: / Line 217: @@
              </td>
              <td>
-                 <p align="center">8.0x10<sup>6</sup></p>
+                 <p align="center">8.0x 10<sup>6</sup></p>
              </td>
              <td>
-                 <p align="center">1.0x10<sup>7</sup></p>
+                 <p align="center">1.0x 10<sup>7</sup></p>
              </td>
              <td>
-                 <p align="center">4.0x10<sup>5</sup></p>
+                 <p align="center">4.0x 10<sup>5</sup></p>
              </td>
              <td>
-                 <p align="center">7.0x10<sup>6</sup></p>
+                 <p align="center">7.0x 10<sup>6</sup></p>
              </td>
              <td>
-                 <p align="center">2.3x10<sup>6</sup></p>
+                 <p align="center">2.3x 10<sup>6</sup></p>
              </td>
          </tr>
@@ Line 250: / Line 250: @@
              </td>
              <td valign="bottom" nowrap="nowrap" width="68">
-                 <p align="right">5.6x10<sup>6</sup></p>
+                 <p align="right">5.6x 10<sup>6</sup></p>
              </td>
          </tr>
@@ Line 258: / Line 258: @@
              </td>
              <td valign="bottom" nowrap="nowrap" width="68">
-                 <p align="right">3.7x10<sup>6</sup></p>
+                 <p align="right">3.7x 10<sup>6</sup></p>
              </td>
          </tr>
@@ Line 299: / Line 299: @@
 <p>&nbsp;</p>
 <p><strong>MICROSCOPY</strong></p>
-<p><span lang="EN-US">To check the activity of RFP, an induction series with 0,2%, 2% and 5% L-Arabinose in the cell culture medium was prepared. Fluorescence microscopy was performed with the RFP DsRed filter (excitation at 536 nm, emission at 582 nm). Unfortunately no fluorescence could be detected throughout the whole project with different constructs. Neither in the pJET_RFP_3, nor in the pBAD constructs (pBAD_RFP_3 and pBAD_RFP_ACEL) induced with 0,2%, 2% and 5% L-Arabinose in the medium. Nevertheless every time the DNA sequences were correct (Sanger sequencing). It might be a problem of expression.
+<p><span lang="EN-US">To check the activity of RFP, an induction series with 0,2%, 2% and 5% L-Arabinose in the cell culture medium was prepared. Fluorescence microscopy was performed with the RFP DsRed filter (excitation at 536 nm, emission at 582 nm). Unfortunately no fluorescence could be detected throughout the whole project with different constructs. Neither in the pJET_RFP_3, nor in the pBAD constructs (pBAD_RFP_3 and pBAD_RFP_ACEL) induced with 0,2%, 2% and 5% L-Arabinose in the medium. Since the DNA sequences have been confirmed to be correct by Sanger sequencing it might be a problem of expression.
 <p>&nbsp;</p>
 <p><strong>FUTURE PLANS</strong></p>In future we want to exchange our vector system (pET100 instead of pBAD) to ensure that pBAD is not somehow interfering with our chosen <em>E. coli</em> strain.</span></p>
@@ Line 312: / Line 312: @@
 <p>
      Esterase was amplified from pET101_E064 and phosphatase from pTOPOXL_PLP07 by PCR for each enzyme (Fig.1). Both plasmids were given to us by the Applied
-     and Genomic Microbiology department. Primers contained restriction sites KpnI and SacI for esterase and XhoI and PstI for the phospahtase in order to make
+     and Genomic Microbiology department. Primers contained restriction sites <em>Kpn</em>I and <em>Sac</em>I for esterase and <em>Xho</em>I and <em>Pst</em>I for the phosphatase in order to make
-     them compatible for insertion into the multiple cloning site of the pBAD vector .The genes for these two enzymes had been found in screenings of
+     them compatible for insertion into the multiple cloning site of the pBAD vector. The genes for these two enzymes had been found in screenings of
      metagenomic libraries.
 </p>
@@ Line 326: / Line 326: @@
 <p>
      Ligation into pJET was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted
-     with a Quiaprep spin Miniprep kit and restricted with either KpnI and SacI or XhoI and PstI, depending on the Enzyme (Fig.2&amp;3).
+     with a Quiaprep spin Miniprep kit and restricted with either <em>Kpn</em>I and <em>Sac</em>I or <em>Xho</em>I and <em>Pst</em>I, depending on the Enzyme (Fig.2&amp;3).
 </p>
 </html>
@@ Line 347: / Line 347: @@
 </p>
 <p>
-     A restriction control with SacI was run in a 0,8% agarose gel (Fig. 4). Samples #2, #3 and #9 correspond<strong> </strong>to the linear plasmid containing
+     A restriction control with <em>Sac</em>I for the esterase constructs was run in a 0,8% agarose gel (Fig. 4). Samples #2, #3 and #9 correspond<strong> </strong>to the linear plasmid containing the insert.  Phosphatase construct was control restricted with <em>EcoR</em>I (Fig. 5), in this case 13 of 14 samples showed successful insertion of the enzyme fragment into the vector.
-    the insert.
 </p>
 </html>
-[[File:Control_restriction_pBAD_Est_CCEL_iGEM_Goettingen2015|500px|thumb|center|]]
+[[File:Control restriction pBAD Est CCEL iGEM Goettingen2015.jpeg|600px|thumb|center|]]
 <html>
+</html>
+[[File:Pho_CTHE_control_restriction_iGEM_Gottingen2015.jpg |600px|thumb|center|]]
+<html>
 <p>
-     The phosphatase fragment was fused to the pBAD and the correspondent dockerin by Fusion PCR.
+     <strong>Future plans</strong>
 </p>
+<p>
+    The next steps include changing to a better expression vector in order to test and measure the activity of the enzymes, especially to ensure that the fusion with the dockerins is not interfering with the function of the enzymes. Finally the aim is to combine the purified enzyme-dockerin proteins with the synthetic scaffold and prove the self assemby of the Flexosome tool.
+</p>
+</div>
+<a href="" onClick=" $('#menu5').slideToggle(300, function callback() {  }); return false;"><h1>Cellulase</h1></a>
+<div id="menu5"><p>
+</p>
+<p>
+    The cellulase gene was amplified using PCR. The primers which were used contained the restriction sites for ligation into the pBAD vector. The cellulase
+    PCR products were then checked on 0.8 % agarose gel.
+</p>
+</html>
+[[File:TeamGoettingen_CellulasePCR.jpg|300px|center|thumb|Figure 1: Cellulase PCR product was run on a 0.8 % agarose gel. The desired cellulase sequence is at 2496 bp.]]
+<html>
+<p>
+    The cellulase PCR products were then purified by using the <strong>QIAquick® PCR Purification Kit (QIAGEN). </strong>After the PCR products were purified,
+    the concentration of DNA was measured by Nanodrop 2000c Spectrophotometer.<strong></strong>
+</p>
+<p>
+    <strong>Restriction control of pBAD_CCEL and cellulase PCR product</strong>
+</p>
+<p>
+    The purified cellulase PCR product and the pBAD_CCEL vector were restricted by following a double digest protocol with SacI and PvuII enzymes. After
+    restriction control products were purified by using the <strong>QIAquick® PCR Purification Kit (QIAGEN) </strong>the concentration of DNA was measured by
+    Nanodrop 2000c Spectrophotometer.<strong></strong>
+</p>
+<p>
+    <strong>Ligation of Cellulase into pBAD- CCEL</strong>
+</p>
+<p>
+    The cellulase gene was then ligated into the pBAD vector containing the CCEL (<em>Clostridium</em>
+</p>
+<p>
+    <em>cellulolyticum</em>
+    ) dockerin.
+</p>
+<p>
+    For ligation of the cellulase PCR product into the restricted pBAD_CCEL vector, the Thermo Fisher T4 Ligase Sticky End Ligation protocol was followed.
+</p>
+<p>
+    <strong>Transformation of pBAD_CellulaseCCEL into chemically competent Top10 <em>E. coli </em>cells</strong>
+</p>
+<p>
+    pBAD_CellulaseCCEL was transformed into competent Top10 <em>E. coli </em>cells by using the heat shock transformation method.
+</p>
+</html>
+[[File:TeamGoettingen_pBAD_CellulaseCCEL_Trafo.jpg|300px|center|thumb|Figure 2: Transformation of pBAD_CellulaseCCEL into competent Top 10 E. coli cells. The image shows plates with successful transformants.]]
+<html>
+<p>
+    Colonies from transformation plates were inoculated into LB medium containing ampicillin (100 µg/ml).
+</p>
+<p>
+    <strong>Plasmid Extraction: peqGold Plasmid Miniprep Kit</strong>
+</p>
+<p>
+    Plasmid extraction was done for colonies inoculated in LB medium by using peqGold Plasmid Miniprep kit and plasmid concentration was measured by using
+    Nanodrop 2000c Spectrophotometer.
+</p>
+<p>
+    Restriction control was done with the enzymes SacI and PvuII from Thermo fisher scientific.<strong> </strong>Restricted plasmids were checked on a 0.8 %
+    agarose gel.
+</p>
+</html>
+[[File:TeamGoettingen_Restriction_pBAD_CellulaseCCEL.jpg|300px|center|thumb|Figure 3: Restriction control of the pBAD_CellulaseCCEL construct from TOP10 E. coli positive clones by with SacI and PvuII.  Colony 1 has the desired insert.]]
+<html>
+<p>
+    The correct insert was confirmed through sequencing.
+</p>
 </div>
+<a href="" onClick=" $('#menu4').slideToggle(300, function callback() {  }); return false;"><h1>BioBricks</h1></a>
+<div id="menu4">
-<h4> Project Achievements </h4>
+<p>
-<h5>What should this page contain?</h5>
+    <strong>Dockerin Biobricks</strong>
-<p>Here you can describe the results of your project and your future plans. </p>
+</p>
-<ul>
+<p>
-<li> Clearly and objectively describe the results of your work.</li>
+The dockerins ACEL (<em>Acetivibrio cellulolyticus</em>), BCEL (<em>Bacteroides cellulosolvens</em>), CCEL (<em>Clostridium cellulolyticum</em>) and CTHE (<em>Clostridium thermocellum</em>) were amplified from pBAD_ACEL, pBAD_BCEL, pBAD_CCEL and pBAD_CTHE with primers to add the desired <em>Eco</em>RI and    <em>Pst</em>I restriction sites by PCR. Primers contained restriction sites for <em>Eco</em>RI and <em>Pst</em>I in order to make them compatible for
-<li> Future plans for the project </li>
+    insertion into the iGEM shipping vector pSB1C3.
-<li> Considerations for replicating the experiments </li>
+</p>
-</ul>
+<p>
+    After purification, the PCR products were restricted with <em>Eco</em>RI and <em>Pst</em>I, as well as pSB1C3. Afterwards the restricted dockerins were
+    ligated into pSB1C3 by T4 ligation (sticky end ligation) and transformed into <em>E. coli</em> TOP10.
+</p>
+<p>
+    Ligation into pSB1C3 was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted
+    with the QIAGEN QIAprep Spin Miniprep Kit and test restricted with <em>Eco</em>RI (pSB1C3_CCEL and pSB1C3_ACEL) and <em>Eco</em>RI and <em>Pst</em>I
+    (pSB1C3_BCEL) (Fig.1). We lost CTHE due to failing transformations at this point.
+</p>
-<p>You can also include a list of bullet points (and links) of the successes and failures you have had over your summer. It is a quick reference page for the judges to see what you achieved during your summer.</p>
+</html>
+[[File:Rest_control_pSB1C3_ACEL_CCEL_BCEL.jpeg|600px|thumb|center|]]
+<html>
-<ul>
+<p>
-<li>A list of linked bullet points of the successful results during your project</li>
+    Once restriction controls showed the correct bands, pSB1C3_CCEL, pSB1C3_ACEL and pSB1C3_BCEL were sent for sequencing.
-<li>A list of linked bullet points of the unsuccessful results during your project. This is about being scientifically honest. If you worked on an area for a long time with no success, tell us so we know where you put your effort.</li>
+</p>
-</ul>
+<p>&nbsp;</p>
+<p>
+    <strong>Colour BioBricks</strong>
+</p>
+<p>
+    We also wanted to improve already existing BioBricks by fusing our dockerins to the colours eforRed (<a href="http://parts.igem.org/Part:BBa_K592012"style="color: #000066">BBa_K592012</a>) and amilCP (<a href="http://parts.igem.org/Part:BBa_K592009"style="color: #000066">BBa_K592009</a>) that were
+    submitted from the University of Uppsala (Sweden) in 2011.
+</p>
+<p>
+    So we chose to fuse eforRed to BCEL and amilCP to CCEL. Since the plasmids of the two colour proteins were not distributed with the current plate of the
+    iGEM Distribution Kit, we ordered those parts including the right restriction sites as gBlocks from IDT.
+</p>
+<p>
+    As a first step eforRed and amilCP were restricted with <em>Kpn</em>I and <em>Sac</em>I to make them compatible with our dockerins in pBAD.
+</p>
+<p>
+    After purification restricted colours were ligated into pBAD_BCEL and pBAD_CCEL by T4 ligation (sticky end ligation) and transformed into <em>E. coli</em>
+    TOP10.
+</p>
+<p>
+    Ligation into pBAD was followed according to the protocol in the methods collection. After over-night incubation colonies were picked, plasmids extracted
+    with the QIAGEN QIAprep Spin Miniprep Kit and test restricted with <em>Kpn</em>I (Fig.2).
+</p>
+</html>
+[[File:TeamGoettingen2015_Rest_control_pBAD_eforRed_BCEL_and_amilCP_CCEL_Goettingen2015.jpeg|600px|thumb|center|]]
+<html>
-<h4>Inspiration</h4>
+<p>
-<p>See how other teams presented their results.</p>
+    Once restriction controls showed the correct bands, pBAD_amilCP_CCEL #1 and pBAD_eforRed_BCEL were sent for sequencing. Sequencing showed that both
-<ul>
+    plasmids were correct.
-<li><a href="https://2014.igem.org/Team:TU_Darmstadt/Results/Pathway">2014 TU Darmstadt </a></li>
+</p>
-<li><a href="https://2014.igem.org/Team:Imperial/Results">2014 Imperial </a></li>
+<p>
-<li><a href="https://2014.igem.org/Team:Paris_Bettencourt/Results">2014 Paris Bettencourt </a></li>
+    To make our constructs compatible with the iGEM shipping vector pSB1C3 the desired <em>Eco</em>RI and <em>Pst</em>I restrictions sites were added by PCR.
-</ul>
+</p>
+<p>
+    After purification, the PCR products were restricted with <em>Eco</em>RI and <em>Pst</em>I, the same with pSB1C3, and afterwards ligated into pSB1C3 by T4
+    ligation (sticky end ligation) and transformed into <em>E. coli</em> TOP10.
+</p>
+<p>
+    After over-night incubation colonies were picked, plasmids extracted with the QIAGEN QIAprep Spin Miniprep Kit and test restricted with <em>Eco</em>RI
+    (Fig.3). Due to the reason that our dockerin CCEL contains an internal <em>Pst</em>I restriction site we continued working only with the eforRed_BCEL
+    construct.
+</p>
+</html>
+[[File:TeamGoettingen2015_Rest_control_pSB1C3_eforRed_BCEL_Goettingen2015.jpeg|600px|thumb|center|]]
+<html>
+<p>
+    Once restriction controls showed the correct band, pSB1C3_eforRed_BCEL was sent for sequencing. Sequencing showed that the plasmids were correct.
+</p>
+<p>
+    <strong>RESULTS</strong>
+</p>
+<p>
+    Sequencing showed that the dockerins ACEL and CCEL contain an internal <em>Pst</em>I restriction site. Therefore all the constructs containing ACEL or CCEL
+    showed in the end truncated dockerin sequences and could not be send in as BioBricks.
+</p>
+<p>
+    We also build a construct where the enzyme esterase was fused to our CCEL dockerin (pBAD_Est_CCEL) following the same strategy. But again, due to the
+    reason that our dockerin CCEL contains an internal <em>Pst</em>I restriction site we had to stop our work at this point.
+</p>
+<p>
+    Furthermore we <a href="https://2015.igem.org/Team:Goettingen/Collaborations"style="color: #000066">collaborated</a> with the current iGEM team of Aachen and tried to fuse three of their enzymes to our constructs but could not finish our work here.
+</p>
+<p>
+    <strong>ACHIEVENTS<a name="_GoBack"></a></strong>
+</p>
+<p>
+    <strong>Sequences of pSB1C3_BCEL and pSB1C3_eforRed_BCEL were correct and submitted as BioBricks to iGEM:</strong>
+</p>
+<p>
+    pSB1C3_BCEL (<a href="http://parts.igem.org/Part:BBa_K1865000"style="color: #000066">BBa_K1865000</a>)
+</p>
+<p>
+    pSB1C3_eforRed_BCEL (<a href="http://parts.igem.org/Part:BBa_K1865001"style="color: #000066">BBa_K1865001</a>)
+</p>
+</div>
+<a href="" onClick=" $('#menu6').slideToggle(300, function callback() {  }); return false;"><h1>Scaffoldin Purification</h1></a>
+<div id="menu6">
+<p>
+    <strong>Scaffoldin purification</strong>
+</p>
+<p>
+    After induction according to the methods collection, the targeted ScaA scaffoldin was purified by nickel affinity chromatography using Ni-NTA-agarose columns in a Äkta prime system (Fig. 1A). Following the addition of Imidazol two peaks were obtained. The fractions of interest were visualized in a SDS-PAGE gel (Fig. 1B). The gel showed that only the second fraction presents the expected size of 111kDa. However some other bands appeared along this fraction, therefore in order to obtain even more pure protein a Size Exclusion Chromatography (SEC) was done.
+</p>
+</html>
+[[File:Histag_purification_iGEM_Goettingen2015.jpeg|600px|thumb|center|]]
+<html>
+<p>
+    The SEC was done with a HiLoad Superdex 200 16/600 column (GE Healthcare) (Fig. 2A). SDS gel shows that a high concentration of the desired protein was
+    obtained and most of the previous contaminating bands were eliminated. Nevertheless there was an unknown band of low weight present in every fraction,
+    apparently it could be a second protein from E. coli with some affinity to the Scaffoldin than is then is co-purified with it (Fig. 2B).
+</p>
+</html>
+[[File:SEC_iGEM_Gottingen2015.jpeg|600px|thumb|center|]]
+<html>
+<p>
+  Future plans include to incubate the Scafoldin with the purified enzyme-dockerin construct in order to prove that the Flexosome can assembly by itself.
+</p>
+</div>
+<a href="" onClick=" $('#menu7').slideToggle(300, function callback() {  }); return false;"><h1>Copurification</h1></a>
+<div id="menu7">
+<p>
+    Copurification of Scaffoldin and Enzyme-Dockerin
+</p>
+<p>
+    The main peaks after gelfiltration from the scaffoldin CTHE (see results scaffoldin) and CellulaseCCEL (Fig.1) were pooled and concentrated.
+</p>
+</html>
+[[File:TeamGoettingen_GeFi_CellulaseCCEL.jpg|650px|centre|thumb|B1-B3 were pooled for copurification.]]
+<html>
+<p>
+    They were then mixed and incubated together at 37°C for 15 min with agitation.
+</p>
+<p>
+    The solution was then used in another gelfiltration (Fig.2). The resulting peaks were run on a SDS-gel (Fig.3) and checked for cellulase activity.
+</p>
+</html>
+[[File:TeamGoettingen_Copurification_CTHE_CellulaseCCEL.jpg|650px|centre|thumb|Fig.2) The peak at A5-A7 may be the bound scaffoldin and dockerin, whilst the unbound  proteins are expected between B3 and C9.]]
+<html>
+<p>
+    The first peak from the copurification showed a distinct cellulase activity. As the peak ran considerably higher than expected than either the scaffoldin
+    or the CellulaseCCEL in the gelfitration, it can be expected that this peak contains a successfully formed complex between CellulaseCCEL and the CTHE
+    scaffoldin.
+</p>
+</div>
+<a href="" onClick=" $('#menu8').slideToggle(300, function callback() {  }); return false;"><h1>Giant Jamboree: Poster and Presentation</h1></a>
+<div id="menu8">
+<p>
+Did you missed our presentation? Do you want to see our poster again?
+No problem, here you can find the files:
+</p>
+<p>
+</html>
+[[Media:IGEM-presentation_final_team_Goettingen.ppt]]
+<html>
+</p>
+<p>
+</html>
+[[Media:Poster_teamGoettingen_2015.pdf]]
+<html>
+</p>
 </div>
 </html>

Difference between revisions of "Team:Goettingen/Results"