Difference between revisions of "Part:BBa K1331004"

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<partinfo>BBa_K1331004 short</partinfo>
 
<partinfo>BBa_K1331004 short</partinfo>
  
This is an improvement of [https://parts.igem.org/Part:BBa_K317999 Part:BBa_K317999] designed by iGEM10_Tokyo-NoKoGen. Two mutations have been done to remove the PstI restriction sites (at 790 and 904) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.  
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This is an improvement of [https://parts.igem.org/Part:BBa_K317999 BBa_K317999] designed by iGEM10_Tokyo-NoKoGen. Two mutations have been done to remove the PstI restriction sites (at 790 and 904) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.  
  
 
===Usage and Biology===
 
===Usage and Biology===

Revision as of 04:10, 19 October 2014

Modified rhlB coding sequence from Pseudomonas aeruginosa SQ6


This is an improvement of BBa_K317999 designed by iGEM10_Tokyo-NoKoGen. Two mutations have been done to remove the PstI restriction sites (at 790 and 904) to meet BioBrick RFC[10] requirement without changing the amino acid sequence.

Usage and Biology

The sequence we provide here includes the whole coding sequence as well as a part of upstream noncoding sequence and a part of downstream noncoding sequence of rhlB.

RhlA together with rhlB encodes rhamnosyltransferase I for mono-rhamnolipids biosynthesis in Pseudomonas aeruginosa. This part encodes rhamnosyltransferase I subunit B, and the other part BBa_K1331001 encodes subunit A.

The noncoding sequence included in this part is for composition with rhlA (BBa_K1331001) and rhlR (BBa_K1331002). See our composite part rhlABRI (BBa_K1331005).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 1144
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 37
    Illegal NgoMIV site found at 758
    Illegal NgoMIV site found at 871
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 387