Difference between revisions of "Part:BBa K1331001"
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This part encodes rhamnosyltransferase I subunit A.RhlA together with rhlB encodes Rhamnosyltransferase I for mono-rahmnolipids biosynthesis in ''Pseudomonas aeruginosa''. | This part encodes rhamnosyltransferase I subunit A.RhlA together with rhlB encodes Rhamnosyltransferase I for mono-rahmnolipids biosynthesis in ''Pseudomonas aeruginosa''. | ||
It includes the whole coding sequence and a part of downstream noncoding gene of RhlA. | It includes the whole coding sequence and a part of downstream noncoding gene of RhlA. | ||
− | The coding sequence is similar with[[Part:BBa_K317998]][https://parts.igem.org/Part:BBa_K317998] designed by iGEM10_Tokyo-NoKoGen, but a mutation has been done to remove the PstI restriction site(at 720) to meet BioBrick RFC[10] requirement without changing the amino acid sequence. | + | The coding sequence is similar with [[Part:BBa_K317998]][https://parts.igem.org/Part:BBa_K317998] designed by iGEM10_Tokyo-NoKoGen, but a mutation has been done to remove the PstI restriction site(at 720) to meet BioBrick RFC[10] requirement without changing the amino acid sequence. |
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Revision as of 11:09, 17 October 2014
Modified rhlA coding sequence from Pseudomonas aeruginosa SQ6
This part encodes rhamnosyltransferase I subunit A.RhlA together with rhlB encodes Rhamnosyltransferase I for mono-rahmnolipids biosynthesis in Pseudomonas aeruginosa. It includes the whole coding sequence and a part of downstream noncoding gene of RhlA. The coding sequence is similar with Part:BBa_K317998[1] designed by iGEM10_Tokyo-NoKoGen, but a mutation has been done to remove the PstI restriction site(at 720) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 69
Illegal BamHI site found at 629
Illegal XhoI site found at 805 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 294
Illegal BsaI.rc site found at 478