Difference between revisions of "Part:BBa K424018:Design"
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===References===
 
===References===
  
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Qinhong Wang, Xiangdong Fang, Baojun Bai, Xiaolin Liang, Patrick J. Shuler, William A. Goddard III, Yongchun Tang. 2007. [[Engineering Bacteria for Production of Rhamnolipid as an Agent for Enhanced Oil Recovery]]. Biotechnology and Bioengineering Volume 98, Issue 4, pages 842–853.
+
Qinhong Wang, Xiangdong Fang, Baojun Bai, Xiaolin Liang, Patrick J. Shuler, William A. Goddard III, Yongchun Tang. 2007. '''Engineering Bacteria for Production of Rhamnolipid as an Agent for Enhanced Oil Recovery'''. Biotechnology and Bioengineering Volume 98, Issue 4, pages 842–853.
  
−
Ochsner UA, Fiechter A, Reiser J. 1994. Isolation, characterization, and expression in Escherichia coli of the Pseudomonas aeruginosa rhlAB genes encoding a rhamnosyltransferase involved in rhamnolipid biosurfactant synthesis. J Biol Chem 269:19787–19795.
+
Ochsner UA, Fiechter A, Reiser J. 1994. '''Isolation, characterization, and expression in Escherichia coli of the Pseudomonas aeruginosa rhlAB genes encoding a rhamnosyltransferase involved in rhamnolipid biosurfactant synthesis'''. J Biol Chem 269:19787–19795.
  
−
Maier RM, Soberon-Chavez G. 2000. Pseudomonas aeruginosa rhamnolipids: biosynthesis and potential applications. Appl Microbiol Biotechnol 54(5):625–633.
+
Maier RM, Soberon-Chavez G. 2000. '''Pseudomonas aeruginosa rhamnolipids: biosynthesis and potential applications'''. Appl Microbiol Biotechnol 54(5):625–633.

Revision as of 20:58, 27 October 2010

Rhamnosiltransferase BioBrick (Rh1AB_BB)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 169
    Illegal BamHI site found at 729
    Illegal XhoI site found at 905
    Illegal XhoI site found at 2191
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 1084
    Illegal NgoMIV site found at 1805
    Illegal NgoMIV site found at 1918
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 394
    Illegal BsaI site found at 1434
    Illegal BsaI.rc site found at 578


Design Notes

The RhlAB gene complex have shown illegal restriction sites by the restriccition enzymes of the assembly standard protocol 10. We face this problem by applying the mutagenesis protocol that consist in doing silent mutation that change the nucleotides of our rhlAB gene that is cutted by the Pstl restriction enzyme. Then we will get an standardized coding sequence of the rhlAB gene compatible with the Assembly Standard 10.

Source

Pseudomonas aeruginosa from INDICASAT lab. and the genomic sequence of RhlAB was reviwed in genBank (ID 878955 and 878954) http://www.ncbi.nlm.nih.gov/nuccore/L28170.1

References

Qinhong Wang, Xiangdong Fang, Baojun Bai, Xiaolin Liang, Patrick J. Shuler, William A. Goddard III, Yongchun Tang. 2007. Engineering Bacteria for Production of Rhamnolipid as an Agent for Enhanced Oil Recovery. Biotechnology and Bioengineering Volume 98, Issue 4, pages 842–853.

Ochsner UA, Fiechter A, Reiser J. 1994. Isolation, characterization, and expression in Escherichia coli of the Pseudomonas aeruginosa rhlAB genes encoding a rhamnosyltransferase involved in rhamnolipid biosurfactant synthesis. J Biol Chem 269:19787–19795.

Maier RM, Soberon-Chavez G. 2000. Pseudomonas aeruginosa rhamnolipids: biosynthesis and potential applications. Appl Microbiol Biotechnol 54(5):625–633.