Difference between revisions of "Team:Rheda Bielefeld/Parts"

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<th> Team </th>
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<th> Part </th>
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<th> Comments </th>
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<th> WLC Milwaukee <br> 2014 </th>
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<th> BBa_K1175007 <br> yesZ frim Bacillus Subtilis </th>
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<th> characterized in vitro assy <br> Statuts: It`s complicated </th>
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<th> Edinburgh 2008 </th>
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<th> BBa_K118023 <br> Codon optimized Caulobacter crescentus </th>
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<th> Caulobacter crescentus codon usage </th>
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<th> British Columbia 2016 </th>
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<th> BBa_K2139003 <br> Codon optimized Caulobacter crescentus </th>
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<th> sample not in stock <br> Endo-beta-1,4-glucanase E1 </th>
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<th> Stanford-Brown-Spelman 2014 </th>
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<th> BBa_K1499501 <br> Endo-1,4-&-beta-glucanase (EG1) / Neisseria sicca </th>
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<th> Not characterized, but Neisseria sicca is an S2 organism </th>
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The experiments with liquid nitrogen and trypsin as well as the primer design strategy were especially supported by the supervisors. No antibiotics were handled by team members.  
 
The experiments with liquid nitrogen and trypsin as well as the primer design strategy were especially supported by the supervisors. No antibiotics were handled by team members.  

Revision as of 09:42, 17 October 2018

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Parts

The core idea of our project was to detect pollen by a DNA-based method. Another plan was also to differ between the different types of pollen. Concerning this we focused mainly on the pollen most commonly causing allergic reactions in our area. To analyze and extract the DNA we had to break open the outer layer of the pollen. Some attemts to mechanicaly or chemicaly open pollen are described here:
(Link to “Pollen”) Pollen have a outer (exine) and inner (intine) layer, parts of which consist of pectine and cellulose (link to “Assays”). We therefore wanted to use Echarichia coli to produce enzymes which are able to dismantle these substances and hereby break open the pollen.
For this purpose we chose the following enzymes:
Out of the Bacillus subtilis the genes pelB and yesZ and out of Xanthomonas campestris the gene pelB. The genes pelB out of B.sub. and Xan. Code for pectinases or pectin lyases, yesZ being a beta-glucosidase, which could have enhanced the further dismanteling of the shell.
The BioBricks are supposed to be assembled performing a Gibson Assembly. For this we isolated the DNA of Bacillus subtilis and Xanthomonas campestris B100 and amplified the genes with specific primers. We wanted to clone the genes into psb1C3 and send them in. Using the E.coli vector pz9 availible to us in our Lab we planned to characterize the genes. All in all we were trying to perform 6 clonings (3 clonings into psb1C3 and 3 into pz9). The psb1C3 constructs can be seen on the left. The experimentdesign was created with snapgene.
We also thought about using other, already in iGEM existing, enzymes:
Team Part Comments
WLC Milwaukee
2014 		BBa_K1175007
yesZ frim Bacillus Subtilis 		characterized in vitro assy
Statuts: It`s complicated
Edinburgh 2008 BBa_K118023
Codon optimized Caulobacter crescentus 		Caulobacter crescentus codon usage
British Columbia 2016 BBa_K2139003
Codon optimized Caulobacter crescentus 		sample not in stock
Endo-beta-1,4-glucanase E1
Stanford-Brown-Spelman 2014 BBa_K1499501
Endo-1,4-&-beta-glucanase (EG1) / Neisseria sicca 		Not characterized, but Neisseria sicca is an S2 organism
The experiments with liquid nitrogen and trypsin as well as the primer design strategy were especially supported by the supervisors. No antibiotics were handled by team members.

What went wrong?

Why didn’t the colonings work? Possible reasons for our failure are that we tried to perform a PCR using the wrong primers or that we committed an error somewhere else in the procedure. Another possibility is that we had the wrong stem of Bacillus subtilis from the beginning, because only the stem 168 has the required genes.
We also tried to order the parts for our clonings from IDT, but they were not able to send them to us in time for us to still work with them.