Difference between revisions of "Part:BBa K3606104"

Revision as of 07:12, 25 October 2020

P1 driven mcbABCD

BBa_K3606104 is one of a series of composite parts designed to screen a suitable strength promoter for mcbABCD.

Usage and Biology:

P1, which is a constitutive promoter, will continuously drive expression of mcbABCD. McbABCD is responsible for producing MccB17.

Design:

In our design the proper expression level of mcbABCD is very important. Since its product MccB17 acts as antibiotic, its low expression will make it unable to kill the surrounding bacteria and cannot improve its competitiveness in the intestine. But considering its toxicity, its high expression will also increase the burden of survival of engineered bacteria. So we need to test a collection of promoters, and find the most suitable one for it.

Characterization:

Further Application:

To use this part, simply clone it into a low-copy plasmid vector, transfer into E.coli, incubate overnight. You can also understand the strength of P1 through my experimental results.

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
INCOMPATIBLE WITH RFC[25]
Illegal AgeI site found at 78
Illegal AgeI site found at 261
1000
COMPATIBLE WITH RFC[1000]

@@ Line 3: / Line 3: @@
 <partinfo>BBa_K3606104 short</partinfo>
-tba
+BBa_K3606104 is one of a series of composite parts designed to screen a suitable strength promoter for mcbABCD.
+<h2>Usage and Biology:</h2>
+P1, which is a constitutive promoter, will continuously drive expression of mcbABCD. McbABCD is responsible for producing MccB17.
+<h2>Design:</h2>
+In our design the proper expression level of mcbABCD is very important. Since its product MccB17 acts as antibiotic, its low expression will make it unable to kill the surrounding bacteria and cannot improve its competitiveness in the intestine. But considering its toxicity, its high expression will also increase the burden of survival of engineered bacteria.
+So we need to test a collection of promoters, and find the most suitable one for it.
+<h2> Characterization:</h2>
+<h2>Further Application:</h2>
+To use this part, simply clone it into a low-copy plasmid vector, transfer into E.coli, incubate overnight. You can also understand the strength of P1 through my experimental results.
 <!-- Add more about the biology of this part here