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Besides the hCas9 operon the tracer RNA and the spacer array are also required to get a successful CRISPR response. In this project we constructed biobrick compatible tracer RNA and several pre-programmed spacers arrays. We ordered these parts as synthetic DNA already containing the biobrick prefix and suffix.</p> | Besides the hCas9 operon the tracer RNA and the spacer array are also required to get a successful CRISPR response. In this project we constructed biobrick compatible tracer RNA and several pre-programmed spacers arrays. We ordered these parts as synthetic DNA already containing the biobrick prefix and suffix.</p> | ||
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− | The PCR fragments that were amplified from the Heler plasmid were designed in such a way that they already contained the overhangs for the Gibson assembly. The first | + | The first gblock was used to remove the XbaI site and introduce the iGEM prefix and suffix. This part was first placed in the pSB1A3 vector to form the backbone for the Gibson assembly. After the restriction ligation it was transformed into <i>E. coli dh5α</i> and colonies were picked to grow overnight. The overnight cultures were miniprepped to isolate the plasmids from the cells. The plasmid had to be linearized using PCR before it could be put together with the other fragments. </li> |
− | < | + | <li> |
− | The | + | The PCR fragments that were amplified from the Heler plasmid were designed in such a way that they already contained the overhangs for the Gibson assembly. The first DNA fragment was used to remove the EcorI site, the other DNA fragment was used to remove the ......</li> |
− | < | + | <li>The second gblock was used to introduce the I473F mutation. </li> |
− | + | <p>To combine all the fragments that we created we used a Gibson assembly. We transformed the product into <i>E. coli dh5α</i>. We isolated the plasmid and performed several PCR reactions with different primers to confirm that it contained the desired product. After the gels seemed to be correct we sent the plasmid for sequencing and further verification. Unfortunately, it turned out that the gblock containing the I473F mutation that we used for the assembly was not synthesized correctly. It did not contain the correct sequence, however it still had the expected size which is why we did not catch it earlier when we checked it on gel. Due to time constraints of the parts submission deadline, we were not able to order the gblock again and repeat the construction of the biobrick compatible hCas9.</p> | |
− | + | ||
− | To combine all the fragments that we | + | <p>So we were not able to construct a biobrick compatible hCas9 in time for the parts submission deadline. However, it would still be interesting for our project to see if hCas9 would work when expressed in <i>L. lactis</i> or <i>E. coli</i>. To do this we isolated the hCas9 operon including the repeats from S. pyogenes plasmid pRH180. For comparison we also isolated the regular Cas9 operon from the pWJ40 plasmid. The vectors that we used are pBAD, an arabinose inducable E. coli expression vector, and pNZ8048, a nisin inducable L. lactis expression vector. We used overhang PCR to get the correct overhangs for the insert and the linearized vectors for the Gibson assembly. |
− | < | + | |
− | So we were not able to construct a biobrick compatible hCas9 in time for the parts submission deadline. However, it would still be interesting for our project to see if hCas9 would work when expressed in L. lactis or E. coli. To do this we isolated the hCas9 operon including the repeats from S. pyogenes plasmid pRH180. For comparison we also isolated the regular Cas9 operon from the pWJ40 plasmid. The vectors that we used are pBAD, an arabinose inducable E. coli expression vector, and pNZ8048, a nisin inducable L. lactis expression vector. We used overhang PCR to get the correct overhangs for the insert and the linearized vectors for the Gibson assembly. | + | |
Revision as of 15:52, 29 October 2017
DESIGN
Design
Introduction
Bacteria with
hCas9
- The first gblock was used to remove the XbaI site and introduce the iGEM prefix and suffix. This part was first placed in the pSB1A3 vector to form the backbone for the Gibson assembly. After the restriction ligation it was transformed into E. coli dh5α and colonies were picked to grow overnight. The overnight cultures were miniprepped to isolate the plasmids from the cells. The plasmid had to be linearized using PCR before it could be put together with the other fragments.
- The PCR fragments that were amplified from the Heler plasmid were designed in such a way that they already contained the overhangs for the Gibson assembly. The first DNA fragment was used to remove the EcorI site, the other DNA fragment was used to remove the ......
- The second gblock was used to introduce the I473F mutation.
Biobrick construction
As a basis for the biobrick compatible hCas9 operon we used the Cas9 CRISPR operon from Streptococcus pyogenes. To make this into a biobrick compatible hCas9 operon we had to introduce the I473F mutation(Heler et al.), remove the prohibited restriction sites it contains and attach the biobrick prefix and suffix.To achieve this we used a combination of synthetic DNA(gBlocks) and DNA fragments that were PCR amplified from pWJ40(containing the Cas9 operon). All fragments were finally put together using Gibson Assembly. All cloning steps were performed in E. coli DH5α. Figure 1 gives an overview of all the cloning steps that were used. Besides the hCas9 operon the tracer RNA and the spacer array are also required to get a successful CRISPR response. In this project we constructed biobrick compatible tracer RNA and several pre-programmed spacers arrays. We ordered these parts as synthetic DNA already containing the biobrick prefix and suffix.
To combine all the fragments that we created we used a Gibson assembly. We transformed the product into E. coli dh5α. We isolated the plasmid and performed several PCR reactions with different primers to confirm that it contained the desired product. After the gels seemed to be correct we sent the plasmid for sequencing and further verification. Unfortunately, it turned out that the gblock containing the I473F mutation that we used for the assembly was not synthesized correctly. It did not contain the correct sequence, however it still had the expected size which is why we did not catch it earlier when we checked it on gel. Due to time constraints of the parts submission deadline, we were not able to order the gblock again and repeat the construction of the biobrick compatible hCas9.
So we were not able to construct a biobrick compatible hCas9 in time for the parts submission deadline. However, it would still be interesting for our project to see if hCas9 would work when expressed in L. lactis or E. coli. To do this we isolated the hCas9 operon including the repeats from S. pyogenes plasmid pRH180. For comparison we also isolated the regular Cas9 operon from the pWJ40 plasmid. The vectors that we used are pBAD, an arabinose inducable E. coli expression vector, and pNZ8048, a nisin inducable L. lactis expression vector. We used overhang PCR to get the correct overhangs for the insert and the linearized vectors for the Gibson assembly.
Validation construction
As mentioned earlier we were not able to construct the biobrick compatible hCas9 operon. So the experiment that will be described next was not executed. To validate that hCas9 is capable of acquiring spacers in both L. lactis and E.coli, we wanted to perform an on plate acquisition assay.(protocol) In this assay we would have measured the rate at which spacers would be acquired. For this assay we first would have inserted the hCas9 operon into an inducible expression vector. We were planning to use an arabinose inducible pBad vector for E. coli and a nisin inducible pNZ8048 vector for L. lactis. For comparison we would also have included the regular Cas9 operon. The cells would then be exposed to phages and the surviving colonies isolated. Using PCR we could than have measured the increase in size of the spacer array. The amount of surviving colonies and the sizes of the spacer array’s would have given an indication about the efficiency/activity of the hCas9 operon in L. lactis.CRISPR array
Biobrick construction
dCas9
- Kuipers OP, de Ruyter PG, Kleerebezem M, de Vos WM. Journal of Biotechnology. 1998;64:15–21
- van de Guchte, M., van der Vossen, J.M.B.M., Kok, J. and Venema, G. (1989) Appl. Environ. Microbiol. 55, 224-228
- Explanation of the engineering principles your team used in your design
- Discussion of the design iterations your team went through
- Experimental plan to test your designs
Biobrick construction
We started out by trying to transform the dCas9 from the biobrick dCas9-Ω submission (part BBa_K1723000) into competent Escherichia coli DH5alpha cells, since the part is already in biobrick format and only requires removal of the Ω-subunit (link to primer design). However, we were not able to recover successful transformants. Therefore we decided to pursue another strategy utilizing the addgene plasmid pJWV102-PL-dCas9 (link to benchling), which was supplied to us by our supervisor Chenxi.To start off we PCR amplified the dCas9 out of the plasmid using primers .. & … In this PCR reaction a XbaI as well as a PstI site restriction site were incorporated in front of and behind dCas9, enabling dCas9 integration into an iGEM Vector (link) via restriction ligation. Next we removed the EcoRI site, since this was still present in the Addgene plasmid and interfering with Biobrick compatibility. In order to accomplish this, two sets of quick-change primers were designed (image of sequence dCas9 plasmid part containing EcoRI site and all four primers).
To change the PAM, four mutations were required (see table). Since all mutations are positioned at the end of the gene, a gBlock was designed containing the end of dCas9 with all four mutations. To exchange the gblock with the original end of dCas9 the BamHI restriction site was used. The end of the gblock contained the biobrick suffix. To insure that only mutated dCas9 would be transformed, the correct fragment was subjected to a gel-extraction after restriction of the pSB1C3: dCas9 plasmid.
From this sub-project both the biobrick-compatible dCas9 (part page") and dCas9-VRER (part page) were submitted to the iGEM HQ. We ordered two fragments of synthetic DNA(gBlocks) to introduce the I473F mutation and make the hCas9 operon biobrick compatible. To make the ......