Team:Bielefeld-Germany/Labjournal/week18

From 2012.igem.org

(Difference between revisions)
(Monday August 27th)
(Week 18 (08/27 - 09/02/12))
 
(123 intermediate revisions not shown)
Line 1: Line 1:
{{Team:Bielefeld/Head}}
{{Team:Bielefeld/Head}}
-
<div style="text-align:justify;">
 
-
==Week 18 (08/27 - 09/02/12)==
 
-
===Monday August 27th===
+
<html>
-
<!--
+
<style type="text/css">
-
* '''Team ''A. thaliana'' laccase:''' Today we finally had a less stressful day, so that we had the time to fulfill our ''A. thaliana'' laccase mission. Since the RNA isolation was not as easy as expected and the PCRs weren´t successful so far, we washed our cDNA and gave this project a last try. Today´s PCR was with actin to check the quality of our cDNA (remember last time there weren´t even any actin bands).
+
-
The set up was
+
-
-->
+
-
* '''Team Cultivation & Purification:'''
+
-
** We exchanged the buffer of the purificated ''E.coli'' laccase from 14th of august, which showed a promising band in the SDS-Page.
+
-
** We cultivated ''E.coli'' KRX with plasmids containing laccases from ''E.coli'', ''B.pumilus'', ''T.thermophilus'', ''B.halodurans'' and ''X.campestris'' with positive (Ligase A) and negative control (without plasmid).-->Settings: 1L flask without baffles, autoinduction medium, final volume: 250 mL, 60 µg/mL chloramphenicol, 37°C, 120 rpm for 12 h
+
-
** Cells were disrupted via sonication and laccase was purified by using the HisTrap column
+
-
** A new preculture was made for the next cultivation
+
-
===Tuesday August 28th===
+
ul {list-style-image:none;}
-
** '''Team Cultivation & Purification:'''
+
#bodyContent{
-
*** The band appearing in the SDS-Page of the cultivation of the 14th of august was analysed via Maldi-Tof and we a positive result: we got our laccase!
+
    background-color: white;
-
*** We made a SDS-Page from yesterday's cultivation and got the same band for ''E.coli'' cultivation, so we reproduced our result:) It seems, that the higher temperature had the essential influence on the production.
+
}
-
*** Started a new cultivation of ''E.coli'' KRX with plasmids containing laccases from ''E.coli'', ''B.pumilus'', '#T.thermophilus'', ''B.halodurans'' and ''X.campestris'' with positive (Ligase A) and negative control (''E.coli'' KRX without plasmid). -->Settings: 300 mL flasks without baffles, autoinduction medium with 0,35 mM CuCl2 added, final volume: 60 mL, 37 °C, 120 rpm, 12 hours
+
-
*** Made cell disruption via sonification and purificated the protein via HisTrap column. This time the column was better cleaned by using the twofold volume of 500 mM imidazol.
+
-
*** New precultes were prepared for the next cultivation
+
-
• Vorkultur ansetzen E.coli 15 mL, K529710 mit Ligase A, LB,37°C, Schikanen
+
-
===Wednesday August 29th===
+
</style>
-
* '''Team Cellulose Binding Domain:'''
+
 
-
Isolation of CBDcex+GFP VI and CBDcex X+XII
+
<!-- navigator -->
-
Restriktion of them with NotI showed right bands (about 400 bp for CBDcex and 1200 bp for CBDcex+GFP)
+
<div id="nav" class="tabs">
-
* '''Team Site Directed Mutagenesis:'''
+
<div class="scroller">
-
New Primers for X.campestris arrived.
+
<ul style="list-style-type:none">
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/Starting"><strong>Prologue</strong></a></li>
 +
                <li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week1"><strong>Week 1</strong></a></li>
 +
                <li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week2"><strong>Week 2</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week3"><strong>Week 3</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week4"><strong>Week 4</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week5"><strong>Week 5</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week6"><strong>Week 6</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week7"><strong>Week 7</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week8"><strong>Week 8</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week9"><strong>Week 9</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week10"><strong>Week 10</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week11"><strong>Week 11</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week12"><strong>Week 12</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week13"><strong>Week 13</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week14"><strong>Week 14</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week15"><strong>Week 15</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week16"><strong>Week 16</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week17"><strong>Week 17</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week18"><strong>Week 18</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week19"><strong>Week 19</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week20"><strong>Week 20</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week21"><strong>Week 21</strong></a></li>
 +
<li><a href="https://2012.igem.org/Team:Bielefeld-Germany/Labjournal/week22"><strong>Week 22</strong></a></li>
 +
 
 +
</ul>
 +
 
 +
</div>
 +
</div>
 +
</html>
 +
 
 +
<div style="text-align:justify;">
 +
==Week 18 (08/27 - 09/02/12)==
-
===Thursday August 30th===
 
-
===Friday August 31th===
 
-
===Saturday September 1st===
 
-
===Sunday September 2nd===
 
-
* '''Team Activity Tests:''' This week we had Team Modeling over and they told us about their concerns. To continue modeling they wanted to have a look at the activity of our laccase from ''T. versicolor'' but with different ABTS concentrations. Especially the were interested in the first time points after adding ABTS. This should give them enough information to calculate the enzyme activity. We didn't want to wait, so we started immediately with our standard activity test. Our tested ABTS concentrations were: 0.5µl, 1µl, 2µl, 4µl and 8µl. We got nice activity curves but also noticed, that the activity saturated quickly and therefore the initial activity of our laccase can not be measured accurately. Of course Team Modeling got our data just in time, but we also want to start new activity tests with half of the amount of laccase. So we are still trying to keep our lovely Team Modeling satisfied.
 
{{Team:Bielefeld/Sponsoren}}
{{Team:Bielefeld/Sponsoren}}

Latest revision as of 21:29, 25 September 2012


Week 18 (08/27 - 09/02/12)

55px Logo merck.jpg BioCircle.JPG Bielefeld2012 Evonik.jpg Bielefeld2012 Baxter.png Logo knauer.jpg Logo iit.jpg Bielefeld2012 BIEKUBA.jpg Logo biometra.jpg Logo bio-nrw.png Bielefeld2012 Logo ERASynbio.jpg