Difference between revisions of "User:Jerome Bonnet/Notebook/Part Collection"

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[http://partsregistry.org/cgi/partsdb/dna.cgi?part_name=BBa%20J61031  Bac plasmid:2007 plate3 8E]
[http://partsregistry.org/cgi/partsdb/dna.cgi?part_name=BBa%20J61031  Bac plasmid:2007 plate3 8E]
[Combining Parts according to sequence homology]
[[Combining Parts according to sequence homology]]

Revision as of 17:58, 18 September 2009

<!-- sibboleth --><div id="lncal1" style="border:0px;"><div style="display:none;" id="id">lncal1</div><div style="display:none;" id="dtext"></div><div style="display:none;" id="page">User:Jerome Bonnet/Notebook/Part Collection</div><div style="display:none;" id="fmt">yyyy/MM/dd</div><div style="display:none;" id="css">OWWNB</div><div style="display:none;" id="month"></div><div style="display:none;" id="year"></div><div style="display:none;" id="readonly">Y</div></div>

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Project Description/Abstract

From the genetic memory project, this a repository of the parts I will depose in the registry of standard biological parts. They will serve to test for the activity and crosstalk of the different Integrases and Excisionases .


Sequences are displayed in the Registry format, meaning that Biobrick prefix and suffix are omitted.

  • Protein coding sequences only (Freiburg fusion standard)

Note: ATG and Stop removed from protein sequence, encoded in Freiburg prefix and suffix. Freiburg standard Add AG amino acids in N-ter after the Methionine and TG before the stop. After checking on litterature and with Alfonso that should not be a problem ( functional N or C terminal fusions of Integrases have been made).


Bbw_1 Bxb1 integrase

This part encodes an integrase from the Serine Recombinase family. Bxb1 integrase catalyse integration of a given sequence by recombination between specific recombination sites attB and attP. In association with a specific subunit, called excisionase

Bbw_2 Bxb1 excisionase >>>> Received


Bbw_3 TP901-1 integrase >>>>> Received

Bbw_4 TP901-1 excisionase >>>>> Received


Bbw_5 PhiRV1 integrase

Bbw_6 PhiRV1 excisionase

  • Protein generators (Bba/freiburg)

(No promoter)

Note: RBS for integrase is B0030 (efficiency 0,6). Excisionases are controlled by RBS B0034 (efficiency 1). this should ensure expression of the excisionase over the stochiometric ratio with integrase, and force the excision-like reaction. Hope it will be enough, but I wanted also to be sure of a correct integrase expression for the first experiment...

Bbw_7 Bxb1 generator: RBS(B0030)-Bxb1 integrase-6His

Bbw_8 Bxb1 Int/Xis generator: RBS(B0030)-Bxb1 integrase-6His / RBS B0034-Bxb1 excisionase-6his

Bbw_9 TP901 generator: RBS(B0030)-TP901-1 integrase-6His

Bbw_10 TP901 Int/Xis generator: RBS(B0030)-TP901 integrase-6His / RBS B0034-TP901 excisionase-6his

Bbw_11 PhiRV1 generator: RBS(B0030)-PhiRV1 integrase-6His

Bbw_12 PhiRV1 Int/Xis generator: RBS(B0030)-PhiRV1 integrase-6His / RBS B0034-PhiRV1 excisionase-6his

  • DNA flippees (Bba standard)

Note: a random DNA sequence checked for: no ATG, no RBS like sequence, no TATAA box, no terminators no apparent strange RNA structure...and blasted to verify no relevant homology (pretty unique). Bear an inverted constitutive promoter J23119, from the constitutive promoters family, the stronger one. flanked by att sites for each recombinases, BP and LR.

Bbw_13 Bxb1-BP flippee >>>>> Received

Bbw_14 Bxb1-LR flippee >>>>> Received

Bbw_15 TP901-BP flippee >>>>> Received

Bbw_16 TP901-LR flippee >>>>> Received

Bbw_17 PhiRV1-BP flippee >>>>> Received

Bbw_18 PhiRV1-LR flippee >>>>> Received

  • Ssra degradation tags

BBa_M0050:AANDENYALAA. (Very fast)

oligos design: Freiburg,

parts to get: Bac plasmid:2007 plate3 8E

Combining Parts according to sequence homology

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