Difference between revisions of "Part:BBa K079048"
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<partinfo>BBa_K079048 short</partinfo> | <partinfo>BBa_K079048 short</partinfo> | ||
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+ | Parts K079045 through K079048 are libraries intended to introduce standardization and modularity for operator sequences. | ||
+ | Each of the 4 collections has a different repressor specificity (Lac, Tet, Lambda and LexA) and consist of 3 different members with distinct binding affinities. | ||
+ | Since operators flanked by Biobrick ends are unpractical and costly to obtain both by dna sinthesys and phosphorylated oligos we designed a "Standard Collection Vector". | ||
+ | [[Image:Layout.jpg | Left |320x240 ]] | ||
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+ | This layout allows to get multiple small sequences with a single Synthesis process and specifically enable the extraction of one or a combination of operators using exclusively Biobrick prefix and suffix restriction enzymes. | ||
+ | Digestion and religation of the Collection Vector with '''Xba''' and '''Pst''' yields a single '''Operators 1''' and '''Operator 3''' vectors respectively (Es: [https://parts.igem.org/wiki/index.php?title=Part:BBa_K079019 Lac2] and [https://parts.igem.org/wiki/index.php?title=Part:BBa_K079017 Lac Symmetric]) avoiding the troubles and optimization related to the run and purification of very small bands on agarose gel. | ||
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+ | A similar approach using '''EcoRI''' give rise to a multiple Operator Vector comprising '''Operator 1 and Operator 2''' sequences, usable per se as a composite regulatory site or further restrictable with '''PstI''' to extract the single''' Operator 2''' (Es: [https://parts.igem.org/wiki/index.php?title=Part:BBa_K079018 Lac1]) | ||
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+ | The Libraries have been syntetized by Geneart in their standard pGA18 and pMA synthesis vector, they both have ColE1 high copy number origin and Ampicillin resistance.<br> | ||
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+ | [[Image:LacPlasmid.jpg |left|500 px ]] | ||
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+ | <br> | ||
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+ | [[Image:Tet.jpg |right|500 px ]] | ||
+ | <br> | ||
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+ | [[Image:CI.jpg |left|500px ]] | ||
+ | <br> | ||
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+ | [[Image:Lex.jpg |right|500px ]] | ||
+ | <br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> | ||
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+ | <br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> | ||
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+ | <br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> | ||
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+ | Right now we're ultimating the design and testing of an equally simple protocol to transfer operator sequences in Biobrick Standard Assembly Vectors using standard cloning reagents and avoiding as much as possible experimentally fragile or optimization dependent steps | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 09:34, 28 October 2008
LexA operator library
Parts K079045 through K079048 are libraries intended to introduce standardization and modularity for operator sequences.
Each of the 4 collections has a different repressor specificity (Lac, Tet, Lambda and LexA) and consist of 3 different members with distinct binding affinities.
Since operators flanked by Biobrick ends are unpractical and costly to obtain both by dna sinthesys and phosphorylated oligos we designed a "Standard Collection Vector".
This layout allows to get multiple small sequences with a single Synthesis process and specifically enable the extraction of one or a combination of operators using exclusively Biobrick prefix and suffix restriction enzymes. Digestion and religation of the Collection Vector with Xba and Pst yields a single Operators 1 and Operator 3 vectors respectively (Es: Lac2 and Lac Symmetric) avoiding the troubles and optimization related to the run and purification of very small bands on agarose gel.
A similar approach using EcoRI give rise to a multiple Operator Vector comprising Operator 1 and Operator 2 sequences, usable per se as a composite regulatory site or further restrictable with PstI to extract the single Operator 2 (Es: Lac1)
The Libraries have been syntetized by Geneart in their standard pGA18 and pMA synthesis vector, they both have ColE1 high copy number origin and Ampicillin resistance.
Right now we're ultimating the design and testing of an equally simple protocol to transfer operator sequences in Biobrick Standard Assembly Vectors using standard cloning reagents and avoiding as much as possible experimentally fragile or optimization dependent steps
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]