Difference between revisions of "Part:BBa K108001:Design"

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===References===
 
===References===
  
−
1. Simultaneous expression of glutaryl-7-aminocephalosporanic acid acylase gene and lysis genes of phage lambda in a recombinant E. coli. Journal of Molecular Catalysis B: Enzymatic. 2006, 43:118–123.
+
1. Construction and Selection of the Novel Recombinant Escherichia coli Strain for Poly(beta-Hydroxybutyrate) Production. Journal of Bioscienve and Bioengineering. 2000, 89(4):307-311.
  
 
2. NCBI
 
2. NCBI

Revision as of 06:52, 25 October 2008

SRRz


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

PCR using primers with biobrick prefix and surfix, and then cloned into pSB1AC3.

Source

SRRz was cloned from Enterobacteria phage lambda genome (reference 1 and 2).

References

1. Construction and Selection of the Novel Recombinant Escherichia coli Strain for Poly(beta-Hydroxybutyrate) Production. Journal of Bioscienve and Bioengineering. 2000, 89(4):307-311.

2. NCBI