Difference between revisions of "Part:BBa K1951001"
(→Experiment summary) |
|||
Line 24: | Line 24: | ||
<!-- --> | <!-- --> | ||
− | + | ===Sequence and Features=== | |
<partinfo>BBa_K1951001 SequenceAndFeatures</partinfo> | <partinfo>BBa_K1951001 SequenceAndFeatures</partinfo> | ||
Revision as of 12:51, 17 October 2016
Contents
DesA, lysine decarboxylase coding sequence
General information
Monooxygenase is an enzyme that incorporate one hydroxyl group into substrates in many metabolic pathways. In this reaction, the two atoms of dioxygen are reduced to one hydroxyl and one H2O molecule by the concomitant oxidation of NAD(P)H. It is also the second step in the production of desferrioxamine B in Streptomyces coelicolor, allowing the transformation of cadeverine into N-hydroxycadaverine.
Lysine descarboxylase (Streptomyces coelicolor) is an enzyme from the lyase family that converts lysine to cadaverine.
Design summary
All forbidden restriction sites have been removed.
Codons have been optimized for E.coli to allow a maximal transcription level.
Experiment summary
The following biobrick functionality has been tested by our team in two different composite parts we designed :
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 569
Illegal BglII site found at 794 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 221
Illegal NgoMIV site found at 469
Illegal AgeI site found at 974 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 943