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 | + | 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 | + | 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:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE 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 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1084
Illegal NgoMIV site found at 1805
Illegal NgoMIV site found at 1918 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 394
Illegal BsaI site found at 1434
Illegal BsaI.rc site found at 578