BBa_K259009

BBa_K259009 Version 1

Component

Source:
http://parts.igem.org/Part:BBa_K259009
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Petros Mina
Date created: 2009-10-12 11:00:00
Date modified: 2015-05-08 01:11:42

BioScaffold Linker - Removes Stop Codons & scars & replaces with a Gly-Ser linker



Types
DnaRegion

Roles
sequence_feature

DNA

Sequences BBa_K259009_sequence (Version 1)

Description

This part is part of a family of Bioscaffold - Linkers.

This part will help users interested in protein-fusion. The usage of the part will allow in frame assembly of 2(+) proteins by:

*Removing the stop codons from the upstream protein.
*Removing the scar created by the Assembly Standard 10 (RFC10) construction of 2(+) protein coding sequences.
*Maintaining the start codon of the downstream protein.
*Adding a flexible (Gly-Ser-Gly) linker between the two protein coding sequences.
*Acting as a translational buffer if ligation is incorrect.

Assembly Instructions



*Create an Assembly Standard 10 fusion as below ;

**Upstream Protein Part - Bioscaffold Linker - Downstream Protein Part**


[[Image:BCCS_Assembly_of_Scaffold.jpg|thumb|500px|center|The Product of Assembly between 2 proteins and the Bioscaffold Linker. ]]


*Use the BioScaffold Specific Enzymes

(i)Restrict with BpuEI to remove upstream scar (created between Upstream Protein - Bioscaffold) and stop codons from upstream protein part.

(ii)Ligate and you will get the intermediate product;

**Upstream Protein (w/out Stop codons) - Tyr - BioScaffold Linker - Downstream Protein**

*Restrict with CspCI to remove downstream scar.
*Ligate to get the final product;

**Upstream Protein - Tyr-Gly-Ser-Gly- Downstream Protein**

[[Image:BCCS_Bioscaffold_Reaction_Explanation_CspCI.jpg|thumb|500px|center|The Reaction and the product. ]]

=N.B.=



CspCI cuts with a 1 b.p discrepancy depending on the sequence. However this should not affect the restriction/ligation process as this has been taken into account and incorporated into the design. Even with the discrepancy involved the restriction/ligation process will still give the same product and in-frame fusion.

The other restriction variants of CspCI have also been taken into account and relevant BioScaffolds are being produced to be tested.

This version is for when CspCI cuts 13/10b.p. (top/bottom) on the 5' of the recognition sequence and 10/13bp (top/bottom) on the 3' of the recognition sequence.

Notes

The CspCI discrepancy had to be taken into account

Source

This part is completely designed de novo. This sequence does not occur naturally.

Sequence Annotation Location Component / Role(s)
BpuEI (rev. complement)
BpuEI
Tyr involved in restriction/ligation
Gly-Ser-Gly linker
Met involved in restriction/ligation
Translational Buffer
5' CspCI Recognition sequence
3' CspCI recognition sequence
Translational Buffer
3,8
21,26
41,43
44,52
53,55
56,65
66,68
74,77
69,73
feature/misc sequence_feature
feature/misc sequence_feature
sequence_feature feature/misc
sequence_feature feature/dna
feature/misc sequence_feature
feature/stop stop_codon
sequence_feature feature/misc
sequence_feature feature/misc
feature/stop stop_codon
igem#sampleStatus
It's complicated
igem#status
Planning
 
synbiohub#ownedBy
user/james
 
synbiohub#ownedBy
user/myers
 
synbiohub#topLevel
BBa_K259009/1