Difference between revisions of "Team:USP-EEL-Brazil/Design"
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Revision as of 04:48, 15 October 2018
Design
The sequences of our target genes were found in the CAZy data bank, where laccases are identified as enzymes from the Auxiliary Activity Family 1 (AA1):
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• Laccase from Pleurotus ostreatus NRRL0366:3471 pb - 533 aa
• Laccase from Phoma sp. UHH 5-1-03 (DSM 2245):3073 pb - 607 aa
To analyze and remove the introns, we used the FGENESH tool from Softberry. After that, to verify if the gene sequence expressed a functional protein we used the Translate toolfrom Expazy. There we confirmed our sequences as correct. Once our laccases are from fungi and we plan to express them into a bacterial chassis, we had to remove the signal peptide. To do so, we used the SignalP 4.1 tool from DTU Bioinformatics .
Completed this process we removed any restriction sites for EcoRI, NotI, PstI and SpeI from the gene. For the synthesis, we inserted an RBS sequence and the biobrick prefix and suffix, obtaining the following gene features:
Our final biobrick construct constituted on the following parts:
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Obtained from the iGEM Registry: BBa_R0010 and found on the 2018 DNA Distribution Kit |
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| Sequence obtained from iGEM Registry BBa_B0030 and synthetised with the gene. |
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Designed and synthetised by the team |
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Designed and synthetised by the team |
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Found on the pSBIC3 backbone |
Also, our instructor Evandro Mulinari provided for us a laccase from Laccase from Thielavia terrestris NRRL 8126 of his own design.
The gene was designed in such a way that, when expressed, the protein contains peptides with cleavage sites for TEV followed by thioredoxin and 6 histidines at the N-terminus, to make the protein purification easier.
This laccase (Lac TT) was inserted into the pETTrx-1a / LIC vector, witch contains resistance to kanamycin and has the expression regulated by the Lac operon. The transformation done into E. coli Rosetta Gami 2 (DE3).