Difference between revisions of "Part:BBa K3002123"

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This composite part contains the PAR-promoter (<a href="https://parts.igem.org/Part:BBa_K3002027">BBa_K3002027</a>) in combination with the RPL23-Terminator (<a href="https://parts.igem.org/Part:BBa_K3002006">BBa_K3002006</a>), the SP20-His-tag (<a href="https://parts.igem.org/Part:BBa_K3002018">BBa_K3002018</a>), the secretion signal cCA (<a href="https://parts.igem.org/Part:BBa_K3002007">BBa_K3002007</a>) and the coding sequence of the MHETase (<a href="https://parts.igem.org/Part:BBa_K3002037">BBa_K3002037</a>) plus the MoClo connectors for positions B1-B2 (<a href="https://parts.igem.org/Part:BBa_K3002302">BBa_K3002302</a>), B2-B3 (<a href="https://parts.igem.org/Part:BBa_K3002303">BBa_K3002303</a>), B4-B5 (<a href="https://parts.igem.org/Part:BBa_K3002304">BBa_K3002304</a>) and B5-B6 (<a href="https://parts.igem.org/Part:BBa_K3002305">BBa_K3002305</a>).  
 
This composite part contains the PAR-promoter (<a href="https://parts.igem.org/Part:BBa_K3002027">BBa_K3002027</a>) in combination with the RPL23-Terminator (<a href="https://parts.igem.org/Part:BBa_K3002006">BBa_K3002006</a>), the SP20-His-tag (<a href="https://parts.igem.org/Part:BBa_K3002018">BBa_K3002018</a>), the secretion signal cCA (<a href="https://parts.igem.org/Part:BBa_K3002007">BBa_K3002007</a>) and the coding sequence of the MHETase (<a href="https://parts.igem.org/Part:BBa_K3002037">BBa_K3002037</a>) plus the MoClo connectors for positions B1-B2 (<a href="https://parts.igem.org/Part:BBa_K3002302">BBa_K3002302</a>), B2-B3 (<a href="https://parts.igem.org/Part:BBa_K3002303">BBa_K3002303</a>), B4-B5 (<a href="https://parts.igem.org/Part:BBa_K3002304">BBa_K3002304</a>) and B5-B6 (<a href="https://parts.igem.org/Part:BBa_K3002305">BBa_K3002305</a>).  
 
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Since the combination of SP20 HA tag with the MHETase and secretion signal cCA leads to glycosylation of the MHETase and enhances the secretion of the enzyme significantly we also designed a construct harboring a His-tag instead of a HA-tag. His-tag is designed to allow purification of MUT-PETase via Ni-NTA column and to differentiate between HA-tagged MHETase and His-tagged MUT-PETase.
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<h1> The Chlamy Yummy Project Collection </h1>
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We are proud to present our MoClo part collection for C. reinhardtii - the <a href="https://2019.igem.org/Team:TU_Kaiserslautern/Part_Overview"> Chlamy Yummy project collection</a>.
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These 67 parts are all parts used during our project and were specifically designed and codon optimized for Chlamydomonas.  Among them are basic parts (L0) of a novel mutant of the PETase (<a href="https://parts.igem.org/Part:BBa_K3002014">BBa_K3002014</a>), the wildtype PETase and MHETase as well as a variety of functional composite parts (L1+2). Containing different tags as well as selection markers, this collection serves as a perfect base for plastic degradation projects with Chlamydomonas. These parts were tested and optimized thoroughly and we can guarantee that they work 100%. Because this is a MoClo collection, the parts are highly standardized for worldwide application. The combination with other part collections works fast and easy. While in MoClo, nomenclature is a bit different from the iGEM BioBricks, it is quickly explained:
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Level 0 parts are equivalent to basic parts, e.g. Promoters, coding sequences, etc.
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Level 1 parts are combinations of basic parts and usually form functional transcription units.
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Level 2 parts are combinations of Level 1 parts, in case you want to transfer multiple transcription units at once. For example, you can pair your gene of interest with a selection marker.
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The great thing about the Kaiser Collection and MoClo is that the ligation works in a one pot, one step reaction, as the Type IIs restriction enzymes cut out their own recognition sites. This way, multiple constructs can be combined linearly in a fixed order to create complex structures. This is ensured by the standardized overlaps that assign the parts one of 10 positions in the final constructs.
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After trying MoClo once, you won’t go back to traditional ligation. It is incredibly easy and reliable.
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Visit our <a href="https://2019.igem.org/Team:TU_Kaiserslautern/Part_Overview">parts site</a> to get an overview over all parts.
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<!-- Add more about the biology of this part here
 
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Revision as of 16:43, 13 December 2019


Level 1 MHETase + cCA + sp20-His

This composite part contains the PAR-promoter (BBa_K3002027) in combination with the RPL23-Terminator (BBa_K3002006), the SP20-His-tag (BBa_K3002018), the secretion signal cCA (BBa_K3002007) and the coding sequence of the MHETase (BBa_K3002037) plus the MoClo connectors for positions B1-B2 (BBa_K3002302), B2-B3 (BBa_K3002303), B4-B5 (BBa_K3002304) and B5-B6 (BBa_K3002305).

Since the combination of SP20 HA tag with the MHETase and secretion signal cCA leads to glycosylation of the MHETase and enhances the secretion of the enzyme significantly we also designed a construct harboring a His-tag instead of a HA-tag. His-tag is designed to allow purification of MUT-PETase via Ni-NTA column and to differentiate between HA-tagged MHETase and His-tagged MUT-PETase.

The Chlamy Yummy Project Collection

We are proud to present our MoClo part collection for C. reinhardtii - the Chlamy Yummy project collection.

These 67 parts are all parts used during our project and were specifically designed and codon optimized for Chlamydomonas. Among them are basic parts (L0) of a novel mutant of the PETase (BBa_K3002014), the wildtype PETase and MHETase as well as a variety of functional composite parts (L1+2). Containing different tags as well as selection markers, this collection serves as a perfect base for plastic degradation projects with Chlamydomonas. These parts were tested and optimized thoroughly and we can guarantee that they work 100%. Because this is a MoClo collection, the parts are highly standardized for worldwide application. The combination with other part collections works fast and easy. While in MoClo, nomenclature is a bit different from the iGEM BioBricks, it is quickly explained:

Level 0 parts are equivalent to basic parts, e.g. Promoters, coding sequences, etc.

Level 1 parts are combinations of basic parts and usually form functional transcription units.

Level 2 parts are combinations of Level 1 parts, in case you want to transfer multiple transcription units at once. For example, you can pair your gene of interest with a selection marker.

The great thing about the Kaiser Collection and MoClo is that the ligation works in a one pot, one step reaction, as the Type IIs restriction enzymes cut out their own recognition sites. This way, multiple constructs can be combined linearly in a fixed order to create complex structures. This is ensured by the standardized overlaps that assign the parts one of 10 positions in the final constructs. After trying MoClo once, you won’t go back to traditional ligation. It is incredibly easy and reliable. Visit our parts site to get an overview over all parts.



Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1327
    Illegal PstI site found at 1651
    Illegal PstI site found at 1994
    Illegal PstI site found at 2804
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 249
    Illegal PstI site found at 1327
    Illegal PstI site found at 1651
    Illegal PstI site found at 1994
    Illegal PstI site found at 2804
    Illegal NotI site found at 1662
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2572
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1327
    Illegal PstI site found at 1651
    Illegal PstI site found at 1994
    Illegal PstI site found at 2804
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1327
    Illegal PstI site found at 1651
    Illegal PstI site found at 1994
    Illegal PstI site found at 2804
    Illegal NgoMIV site found at 1260
    Illegal NgoMIV site found at 1721
    Illegal NgoMIV site found at 1751
    Illegal NgoMIV site found at 2066
    Illegal NgoMIV site found at 2084
    Illegal NgoMIV site found at 2120
    Illegal NgoMIV site found at 2763
  • 1000
    COMPATIBLE WITH RFC[1000]