Difference between revisions of "Part:BBa K424018"

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<partinfo>BBa_K424018 short</partinfo>
 
<partinfo>BBa_K424018 short</partinfo>
  
Pseudomonas aeruginosa species of bacteria produce the rhamnosyltransferase 1 complex (RhlAB) that is the key enzyme responsible for transferring the rhamnose moiety to the b-hydroxyalkanoic acid moiety to biosynthesize rhamnolipid.
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Pseudomonas aeruginosa species of bacteria produce the rhamnosyltransferase gene complex (RhlAB) that is the key enzyme responsible for transferring the rhamnose moiety to the b-hydroxyalkanoic acid moiety to biosynthesize rhamnolipid.
How to used it??
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How to used it?
 
We developed this standarized part to be inserted into E. coli for rhamnolipid production through the key enzyme rhamnosyltranferase. For this we provide to E. coli the proper sustrate to rhamnosiltransferase biosinthesize rhamnolipids in vitro.
 
We developed this standarized part to be inserted into E. coli for rhamnolipid production through the key enzyme rhamnosyltranferase. For this we provide to E. coli the proper sustrate to rhamnosiltransferase biosinthesize rhamnolipids in vitro.
  

Revision as of 20:01, 15 October 2010

Rhamnosiltransferase BioBrick (Rh1AB_BB)

Pseudomonas aeruginosa species of bacteria produce the rhamnosyltransferase gene complex (RhlAB) that is the key enzyme responsible for transferring the rhamnose moiety to the b-hydroxyalkanoic acid moiety to biosynthesize rhamnolipid. How to used it? We developed this standarized part to be inserted into E. coli for rhamnolipid production through the key enzyme rhamnosyltranferase. For this we provide to E. coli the proper sustrate to rhamnosiltransferase biosinthesize rhamnolipids in vitro.

Sequence and Features


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