Difference between revisions of "Team:Sorbonne U Paris/Parts"

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<h2 class="title-h2">pSAD</h2>
 
<h2 class="title-h2">pSAD</h2>
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<p>pSAD is constitutive promoter pSAD from Chlamydomonas reinhardtii. It is a high constitutive expression promoter that encodes for a ferrodoxin-binding protein of photosystem I. This pSAD promoter was submitted in 2014 by the Concordia team (BBa_K1547005). To be compatible with the PhytoBrick standard (RFC1000), an illegal BpiI restriction site was removed (A289T). We cloned P pSAD by PCR amplification in A2-A3 fusion site to use it for our retrotransposon design. Acceptor plasmid is the MoClo Universal pL0 acceptor plasmid pAGM9121. We sequenced again the sequence to be sure there is no unwanted mutations. <br><br>
 
<p>pSAD is constitutive promoter pSAD from Chlamydomonas reinhardtii. It is a high constitutive expression promoter that encodes for a ferrodoxin-binding protein of photosystem I. This pSAD promoter was submitted in 2014 by the Concordia team (BBa_K1547005). To be compatible with the PhytoBrick standard (RFC1000), an illegal BpiI restriction site was removed (A289T). We cloned P pSAD by PCR amplification in A2-A3 fusion site to use it for our retrotransposon design. Acceptor plasmid is the MoClo Universal pL0 acceptor plasmid pAGM9121. We sequenced again the sequence to be sure there is no unwanted mutations. <br><br>
 
Our part is compatible with the PhytoBrick MoClo standard. This PhytoBrick was intented to be use as constitutive promoter for the transcription unit of paromomycine in the CARGO of our synthetic retrotransposons for directed evolution on the Chlamydomoas. It is part of our reporter system to characterize the activity and transposition rate.</p>
 
Our part is compatible with the PhytoBrick MoClo standard. This PhytoBrick was intented to be use as constitutive promoter for the transcription unit of paromomycine in the CARGO of our synthetic retrotransposons for directed evolution on the Chlamydomoas. It is part of our reporter system to characterize the activity and transposition rate.</p>

Revision as of 19:00, 12 October 2018

Parts

New parts submitted to the registry



Parts name Type Part number
RBCS2i1 Protein domain BBa_K2703000
pSAD Regulatory BBa_K2703002
3'LTR_Cr Regulatory BBa_K2703003
5'LTR Regulatory BBa_K2703004
paromycin resistance gene Coding BBa_K2703008


pSAD


pSAD is constitutive promoter pSAD from Chlamydomonas reinhardtii. It is a high constitutive expression promoter that encodes for a ferrodoxin-binding protein of photosystem I. This pSAD promoter was submitted in 2014 by the Concordia team (BBa_K1547005). To be compatible with the PhytoBrick standard (RFC1000), an illegal BpiI restriction site was removed (A289T). We cloned P pSAD by PCR amplification in A2-A3 fusion site to use it for our retrotransposon design. Acceptor plasmid is the MoClo Universal pL0 acceptor plasmid pAGM9121. We sequenced again the sequence to be sure there is no unwanted mutations.

Our part is compatible with the PhytoBrick MoClo standard. This PhytoBrick was intented to be use as constitutive promoter for the transcription unit of paromomycine in the CARGO of our synthetic retrotransposons for directed evolution on the Chlamydomoas. It is part of our reporter system to characterize the activity and transposition rate.

Parts used in our project but not submitted to the registry



s
Parts name Type Part number
otsA Coding Bba_K2703001
pL0-pSAD_A2-B1 Regulatory Bba_K2703005
otsB Coding Bba_K2703006
Bba_K2703006 Regulatory Bba_K2703007
5' UTR pSAD Regulatory Bba_K2703009
Gag Pol Coding Bba_K2703010
pAGM9121 backbone Bba_K2703011