Difference between revisions of "Part:BBa K3629003"
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__NOTOC__ | __NOTOC__ | ||
| − | <partinfo> | + | <partinfo>BBa_K3629003 short</partinfo> |
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| + | TEF1 promoter from <i>Yarrowia lipolytica</i> and the first 42nts (14 codons) of the Lip2 signal peptide [https://parts.igem.org/Part:BBa_K1592000 (BBa_K1592000)]from <i>Y. lipolytica.</i> | ||
__TOC__ | __TOC__ | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
| + | The part contains wild-type TEF1 promoter (nucleotides 1227374 to 1226969) from <i> Yarrowia lipolytica</i> W29 chromosome C (GenBank Accession #CP028450.1) matching [https://parts.igem.org/Part:BBa_K211700 BBa_K2117000], and the first 42nts (14 codons) of the Lip2 signal peptide from <i>Y. lipolytica </i>[https://parts.igem.org/Part:BBa_K1592000 (BBa_K1592000)] | ||
===Design=== | ===Design=== | ||
| − | + | This promoter is composed of the wild-type TEF1 promoter [https://parts.igem.org/Part:BBa_K2117000 (BBa_K2117000)] and the first part of the Lip2 signal peptide [https://parts.igem.org/Part:BBa_K1592000 (BBa_K1592000)]. It was designed to be exchanged with the TEFin promoter [https://parts.igem.org/Part:BBa_K3629001 (BBa_K3629001)] placed in our other expression constructs with a Lip2 signal peptide in case the TEFin promoter was not working properly. | |
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| + | [https://parts.igem.org/Part:BBa_K3629012 BBa_K3529012]= <i>T. reesei</i> CBHII expression construct<br> | ||
| + | [https://parts.igem.org/Part:BBa_K3629013 BBa_K3629013]= Modified <i>P. funiculosum</i> CBHI expression construct<br> | ||
| + | [https://parts.igem.org/Part:BBa_K3629014 BBa_K3629014]= <i>N. crassa</i> CBHI expression construct <br> | ||
| + | [https://parts.igem.org/Part:BBa_K3629016 BBa_K3629016]= Modified <i>T. reesei</i> EGI expression construct <br> | ||
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| + | To do this, the above expression constructs must be in a vector and then digested with BmtI and HindIII to expose the Gibson Y and Gibson | ||
| + | X homology sequences respectively. Meanwhile, this part (BBa_K3629003) must be digested with BbsI to expose the same homology sequences. Once the digested products are placed together in the same tube with the Gibson reagents, the TEFin promoter will be swapped for the TEF1 promoter while maintaining the Lip2 signal peptide for secretion. | ||
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| + | To directly attach this part to a gene (not for exchanging promoters) Gibson 1 is used to assemble this promoter with the coding sequence (the coding sequence must have the remaining 57nts of the Lip2 signal peptide at its N-terminus)into the nourseothricin destination vector [https://parts.igem.org/Part:BBa_K3629015 (BBa_K3629015)]. The coding sequence must also have Gibson 2 at the end to ligate into the destination vector successfully (figure 1). | ||
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| + | [[Image:T--Calgary--BBa_K3629003.png|500px|thumb|center|Figure 1. Assembly of BBa_K3629003 with another GOI with the Lip2 signal peptide into the nourseothricin destination vector (BBa_K3629015)]] | ||
===Sequence and Features=== | ===Sequence and Features=== | ||
| − | <partinfo> | + | <partinfo>BBa_K3629003 SequenceAndFeatures</partinfo> |
===References=== | ===References=== | ||
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<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
===Functional Parameters=== | ===Functional Parameters=== | ||
| − | <partinfo> | + | <partinfo>BBa_K3629003 parameters</partinfo> |
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Latest revision as of 00:59, 27 October 2020
Yarrowia lipolytica TEF1 promoter with first half of Lip2 signal peptide
TEF1 promoter from Yarrowia lipolytica and the first 42nts (14 codons) of the Lip2 signal peptide (BBa_K1592000)from Y. lipolytica.
Usage and Biology
The part contains wild-type TEF1 promoter (nucleotides 1227374 to 1226969) from Yarrowia lipolytica W29 chromosome C (GenBank Accession #CP028450.1) matching BBa_K2117000, and the first 42nts (14 codons) of the Lip2 signal peptide from Y. lipolytica (BBa_K1592000)
Design
This promoter is composed of the wild-type TEF1 promoter (BBa_K2117000) and the first part of the Lip2 signal peptide (BBa_K1592000). It was designed to be exchanged with the TEFin promoter (BBa_K3629001) placed in our other expression constructs with a Lip2 signal peptide in case the TEFin promoter was not working properly.
BBa_K3529012= T. reesei CBHII expression construct
BBa_K3629013= Modified P. funiculosum CBHI expression construct
BBa_K3629014= N. crassa CBHI expression construct
BBa_K3629016= Modified T. reesei EGI expression construct
To do this, the above expression constructs must be in a vector and then digested with BmtI and HindIII to expose the Gibson Y and Gibson X homology sequences respectively. Meanwhile, this part (BBa_K3629003) must be digested with BbsI to expose the same homology sequences. Once the digested products are placed together in the same tube with the Gibson reagents, the TEFin promoter will be swapped for the TEF1 promoter while maintaining the Lip2 signal peptide for secretion.
To directly attach this part to a gene (not for exchanging promoters) Gibson 1 is used to assemble this promoter with the coding sequence (the coding sequence must have the remaining 57nts of the Lip2 signal peptide at its N-terminus)into the nourseothricin destination vector (BBa_K3629015). The coding sequence must also have Gibson 2 at the end to ligate into the destination vector successfully (figure 1).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 53
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]