Difference between revisions of "Part:BBa K3814067"
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<partinfo>BBa_K3814067 short</partinfo> | <partinfo>BBa_K3814067 short</partinfo> | ||
− | fliK Landing Pad (34%) | + | This is the fliK Landing Pad (34%), an integral part of the USYD 2021 team's project. We aim to produce naturally transformable (NT) E. coli by inserting the NT genes of another species into it. We have chosen 23 genes from Acinetobacter baylyi and have planned to insert them into the fliK gene in the E. coli. We have devised a novel recombineering strategy that allows for homologous recombination to insert large amounts of DNA sequentially into the chromosome, and this 'landing pad' is the beginning of this process. It provides all the foundations for the 23 A. baylyi genes to be inserted into the chromosome and be expressed. |
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===Usage and Biology=== | ===Usage and Biology=== | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K3814067 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3814067 SequenceAndFeatures</partinfo> | ||
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===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K3814067 parameters</partinfo> | <partinfo>BBa_K3814067 parameters</partinfo> | ||
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Latest revision as of 15:49, 21 October 2021
fliK Landing Pad (34%)
This is the fliK Landing Pad (34%), an integral part of the USYD 2021 team's project. We aim to produce naturally transformable (NT) E. coli by inserting the NT genes of another species into it. We have chosen 23 genes from Acinetobacter baylyi and have planned to insert them into the fliK gene in the E. coli. We have devised a novel recombineering strategy that allows for homologous recombination to insert large amounts of DNA sequentially into the chromosome, and this 'landing pad' is the beginning of this process. It provides all the foundations for the 23 A. baylyi genes to be inserted into the chromosome and be expressed.
Usage and Biology
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1087
Illegal NheI site found at 1110
Illegal NheI site found at 2383 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2529
Illegal XhoI site found at 1219 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 2555
Illegal NgoMIV site found at 2923
Illegal NgoMIV site found at 3083
Illegal AgeI site found at 1513 - 1000COMPATIBLE WITH RFC[1000]