Difference between revisions of "Part:BBa K2042001:Design"

(Design Notes)
(Design Notes)
Line 9: Line 9:
 
This sequence was codon optimized for Pseudomonas putida and silente mutation was introduce for removing restriction site.
 
This sequence was codon optimized for Pseudomonas putida and silente mutation was introduce for removing restriction site.
 
We used this sequence as second enzyme in order to produce
 
We used this sequence as second enzyme in order to produce
PLA. In fact it will take lactyl coA as substract and polymerise it into PLA homopolymere
+
PLA. In fact it will take lactyl coA as substract and polymerise it into PLA homopolymere.
  
 
===Source===
 
===Source===

Revision as of 15:44, 4 September 2016


Pseudomonas resinovorans PHA synthase 1


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 87
    Illegal XhoI site found at 172
    Illegal XhoI site found at 1030
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1060
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 796


Design Notes

This sequence was codon optimized for Pseudomonas putida and silente mutation was introduce for removing restriction site. We used this sequence as second enzyme in order to produce PLA. In fact it will take lactyl coA as substract and polymerise it into PLA homopolymere.

Source

This sequence was synthetized by IDT


References

Biosynthesis of Polylactic Acid and Its Copolymers using Evolved Propionate CoA Transferase and PHA Synthase Taek Ho Yang,1 Tae Wan Kim,1 Hye Ok Kang,1 Sang-Hyun Lee,1 Eun Jeong Lee,1 Sung-Chul Lim,1 Sun Ok Oh,1 Ae-Jin Song,2 Si Jae Park,1 Sang Yup Lee2,3


Tailor-made type II Pseudomonas PHA synthases and their use for the biosynthesis of polylactic acid and its copolymer in recombinant Escherichia coli. Yang TH1, Jung YK, Kang HO, Kim TW, Park SJ, Lee SY.