Difference between revisions of "Part:BBa K3182003"

Revision as of 09:01, 14 September 2019

PlyF307-SQ8C

Acinetobacter phage endolysin, designed to target Acinetobacter baumannii. The coding domain contains one muramidase stie and one antimicrobial peptide part. The muramidase domain . This part was designed to be assembled with BBa_K3182010.

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_K3182003 short</partinfo>
-Acinetobacter phage endolysin, designed to target Acinetobacter baumannii. This part was designed to be assembled with BBa_K3182010.
+Acinetobacter phage endolysin, designed to target Acinetobacter baumannii. The coding domain contains one muramidase stie and one antimicrobial peptide part. The muramidase domain . This part was designed to be assembled with BBa_K3182010.
-[[File:T--Linkoping_Sweden--MechofAction.png|650px|thumb|center|<b>Figure 1.</b> General mechanism of action when the antimicrobial agent is fused to BBa_K3182010 which contains the linker, thrombin site and cellulose binding domain. The cellulose binding domain enables the attachment of antimicrobial agents (such as antimicrobial peptide or enzyme) to the cellulose. This also inactivates the agents when they are expressed in its bacterial host. Later, when the bandage comes in contact with thrombin in the blood, the antimicrobial agents will be activated upon cleavage of its thrombin site.]]
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