Difference between revisions of "Part:BBa K2030001:Design"

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For assembly of this biobrick, the vector pSB1C3 (BBa_J04450) was cut with XbaI and PstI and purified from gel. The PCR product of pPCK1 was cut with XbaI and PstI and spin column purified. The two pieces was ligated and chemically transformed into <i>E. coli</i> DH5&alpha; and plated on LB + chloramphenicol. False positive colonies still contain the RFP from BBa_J04450 and are red. White colonies were restreaked on LB + chloramphenicol and their plasmids extracted using miniprep. The plasmids were verified by digestion with XbaI and PstI, resulting in two bands: 2044 (vector) and 797 (pPCK1). The biobrick was then sent for sequencing for further verification.
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For assembly of this biobrick, the vector pSB1C3 (BBa_J04450) was cut with XbaI and PstI and the 2044 bp band purified from gel. The PCR product of pPCK1 was cut with XbaI and PstI and spin column purified. The two pieces was ligated and chemically transformed into <i>E. coli</i> DH5&alpha; and plated on LB + chloramphenicol. False positive colonies still contain the RFP from BBa_J04450 and are red. White colonies were restreaked on LB + chloramphenicol and their plasmids extracted using miniprep. The plasmids were verified by digestion with XbaI and PstI, resulting in two bands: 2044 (vector) and 797 (pPCK1). The biobrick was then sent for sequencing for further verification.
  
 
===Source===
 
===Source===

Revision as of 10:00, 17 August 2016


pPCK1 S. cerevisiae promoter


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 221
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 364
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The complete sequence of Saccharomyces cerevisiae S288c chromosome XI (Genbank accession number BK006944) was used to design primers for amplification of this promoter.


FW: gccgcttctagagTCGTTCGTTGTACGTACATTTAC


RV: ttcttcctgcagcggccgctactagtaGTTGTTATTTTATTATGGAATAATTAGTTGC


The primers were designed to anneal at 63 °C (although PCR worked better at 61 °C), using Phusion High-Fidelity DNA Polymerase.


The uppercase nucleotides hybridizes with the template and the lowercase nucleotides contains the overhang. The overhang in the FW primer contains the last 13 bp of the prefix, which includes 6 protective bases before the XbaI site to ensure efficient cutting. The overhang in the RV primer contains the suffix with additional 6 protective bases to ensure efficient cutting with PstI.


For assembly of this biobrick, the vector pSB1C3 (BBa_J04450) was cut with XbaI and PstI and the 2044 bp band purified from gel. The PCR product of pPCK1 was cut with XbaI and PstI and spin column purified. The two pieces was ligated and chemically transformed into E. coli DH5α and plated on LB + chloramphenicol. False positive colonies still contain the RFP from BBa_J04450 and are red. White colonies were restreaked on LB + chloramphenicol and their plasmids extracted using miniprep. The plasmids were verified by digestion with XbaI and PstI, resulting in two bands: 2044 (vector) and 797 (pPCK1). The biobrick was then sent for sequencing for further verification.

Source

Genomic DNA from Saccharomyces cerevisiae CEN.PK113-5D.

References