Difference between revisions of "Part:BBa K3739019"
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===Biology=== | ===Biology=== | ||
LamB is an anchor protein from Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. GFP is green fluorescent protein from jellyfish ''Aequorea Victoria'', which has been widely used as reporter for decades. GFP is fused at C terminal with LamB so that GFP may be displayed on the surface of VnDX. | LamB is an anchor protein from Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. GFP is green fluorescent protein from jellyfish ''Aequorea Victoria'', which has been widely used as reporter for decades. GFP is fused at C terminal with LamB so that GFP may be displayed on the surface of VnDX. | ||
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| + | ===Usage=== | ||
| + | Here, we use BBa_3739019 to construct the expression system, which may achieve surface display on VnDX. | ||
===Characterization=== | ===Characterization=== | ||
====1. Identification==== | ====1. Identification==== | ||
The surface display system for ''Vibrio natriegens'' has never been reported before, so the performance of the surface display system of LamB needs to be verified preferentially. Surface display system bricks (BBa_K3739024, Fig. 1A) were assembled into plasmids, respectively, transformed into ''Vibrio natriegens'' through electroporation. After being verified by agarose gel electrophoresis, the plasmids have been transformed into ''Vibrio natriegens'' successfully (Fig. 1B). | The surface display system for ''Vibrio natriegens'' has never been reported before, so the performance of the surface display system of LamB needs to be verified preferentially. Surface display system bricks (BBa_K3739024, Fig. 1A) were assembled into plasmids, respectively, transformed into ''Vibrio natriegens'' through electroporation. After being verified by agarose gel electrophoresis, the plasmids have been transformed into ''Vibrio natriegens'' successfully (Fig. 1B). | ||
| − | + | https://static.igem.org/mediawiki/parts/d/d3/T--XMU-China--K3739048.png | |
| − | ::'''Fig. 1.''' Gene circuit and agarose gel electrophoresis. (A) Gene circuit of LamB-GFP (BBa_K3739019). (B)Target bands of ''LamB-GFP'' (black arrow, 2300 bp). | + | ::'''Fig. 1.''' Gene circuit and agarose gel electrophoresis. (A) Gene circuit of ''LamB-GFP'' (BBa_K3739019). (B)Target bands of ''LamB-GFP'' (black arrow, 2300 bp). |
Latest revision as of 19:43, 21 October 2021
LamB-GFP
This is an anchored proteins onto membranes through LamB and use GFP to comformation. We use BBa_K3739048 and GFP to verify LamB' s function which can anchor proteins onto membranes.
Biology
LamB is an anchor protein from Vibrio Species, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. GFP is green fluorescent protein from jellyfish Aequorea Victoria, which has been widely used as reporter for decades. GFP is fused at C terminal with LamB so that GFP may be displayed on the surface of VnDX.
Usage
Here, we use BBa_3739019 to construct the expression system, which may achieve surface display on VnDX.
Characterization
1. Identification
The surface display system for Vibrio natriegens has never been reported before, so the performance of the surface display system of LamB needs to be verified preferentially. Surface display system bricks (BBa_K3739024, Fig. 1A) were assembled into plasmids, respectively, transformed into Vibrio natriegens through electroporation. After being verified by agarose gel electrophoresis, the plasmids have been transformed into Vibrio natriegens successfully (Fig. 1B).
- Fig. 1. Gene circuit and agarose gel electrophoresis. (A) Gene circuit of LamB-GFP (BBa_K3739019). (B)Target bands of LamB-GFP (black arrow, 2300 bp).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 528
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 676
Illegal SapI.rc site found at 1246