Difference between revisions of "Part:BBa M50436:Experience"

 
(2 intermediate revisions by 2 users not shown)
Line 5: Line 5:
  
 
===Applications of BBa_M50436===
 
===Applications of BBa_M50436===
This protein can be used to speed up enterobactin synthesis slightly.
+
This protein can be used to speed up enterobactin synthesis slightly in ''E. coli''. It works in tandem with entC (BBa_M50435), facilitating the transformation of chorismate to isochorismate.
  
 
===User Reviews===
 
===User Reviews===
Line 20: Line 20:
 
<!-- DON'T DELETE --><partinfo>BBa_M50436 EndReviews</partinfo>
 
<!-- DON'T DELETE --><partinfo>BBa_M50436 EndReviews</partinfo>
  
We used this sequence as a part of a 2,3-DHB Biosynthesis construct (Part:BBa_M50437). We ordered the plasmid from DNA2.0 and transformed it into ''E. coli'', then plated the ''E. coli'' on LB + kanamycin. We saw colonies successfully grow up. We also ran a Western Blot for this protein and a saw a band of the expected size, indicating this protein was successfully synthesized.
+
We used this sequence as a part of a 2,3-DHB Biosynthesis construct (Part:BBa_M50437). We ordered the plasmid from DNA2.0 and transformed it into ''E. coli'', then plated the ''E. coli'' on LB + kanamycin. We saw colonies successfully grow up. We also ran a Western Blot for this protein and a saw a band of the expected size, indicating this protein was successfully synthesized. See https://parts.igem.org/Part:BBa_M50437:Experience for a detailed assessment.

Latest revision as of 01:01, 12 June 2018


This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_M50436

This protein can be used to speed up enterobactin synthesis slightly in E. coli. It works in tandem with entC (BBa_M50435), facilitating the transformation of chorismate to isochorismate.

User Reviews

UNIQ94c22debb55681a9-partinfo-00000000-QINU UNIQ94c22debb55681a9-partinfo-00000001-QINU

We used this sequence as a part of a 2,3-DHB Biosynthesis construct (Part:BBa_M50437). We ordered the plasmid from DNA2.0 and transformed it into E. coli, then plated the E. coli on LB + kanamycin. We saw colonies successfully grow up. We also ran a Western Blot for this protein and a saw a band of the expected size, indicating this protein was successfully synthesized. See https://parts.igem.org/Part:BBa_M50437:Experience for a detailed assessment.