Difference between revisions of "Part:BBa K2255017"

Latest revision as of 02:59, 2 November 2017

p3_X.fastidiosa (Rfc25)

This part is sequence coding for the D1 and D2 of the protein 3 of XfasM23, a filamentous phage that target Xylella fastidiosa. Those domains are required for phage adsorption and entry.

This part was design with Freiburg (Rfc25) extension. Thus, it contain the restriction site NgoMIV and AgeI that are compatible and allow the missing of a start and stop codon, which ease the assemble of multiple protein domain.

This part is related to our collection part of filamentous phages attachment protein. To see all the part from this collection, you can check out the first part of this collection : BBa_K2255008

Usage and Biology

This biobrick will be use to engineer phage-like particles targetting X. fastidiosa. Check out our [http://2017.igem.org/Team:Aix-Marseille/M13_Design design page] to know more about their design.

Sequence and Features

Assembly Compatibility:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
COMPATIBLE WITH RFC[25]
1000
COMPATIBLE WITH RFC[1000]

@@ Line 3: / Line 3: @@
 <partinfo>BBa_K2255017 short</partinfo>
-This part is sequence coding for the D1 and D2 of the protein 3 of XfasM23, a filamentous phage that target Xylella fastidiosa. Those domains are required for phage adsorption and entry.
+This part is sequence coding for the D1 and D2 of the protein 3 of XfasM23, a filamentous phage that target ''Xylella fastidiosa''. Those domains are required for phage adsorption and entry.
 This part was design with Freiburg ([https://parts.igem.org/Assembly_standard_25 Rfc25]) extension. Thus, it contain the restriction site NgoMIV and AgeI that are compatible and allow the missing of a start and stop codon, which ease the assemble of multiple protein domain.