Difference between revisions of "Part:BBa K4765120"

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===Usage and Biology===
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| <html><img style="width:640px" src="https://static.igem.wiki/teams/4765/wiki/zsl/ribozyme-test-sequence.png" alt="contributed by Fudan iGEM 2023"></html>
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| '''Figure1 Linker sequences between the first CDS (stayGold) and the second CDS (mScarlet)'''
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PmeI linker was borrowed from Liu<ref>Liu, Y., Wu, Z., Wu, D., Gao, N., & Lin, J. (2022). Reconstitution of Multi-Protein Complexes through Ribozyme-Assisted Polycistronic Co-Expression. ACS Synthetic Biology, 12(1), 136–143. https://doi.org/10.1021/acssynbio.2c00416</ref> to facilitate cloning, and no specific secondary RNA structure. Stem-loop 1 was used to stabilize the first RNA after ribozyme cleavage, and we test it function in [https://parts.igem.org/Part:BBa_K4765129 BBa_K4765129]. After the ribozyme Twister<ref>Chen, Y., Cheng, Y., & Lin, J. (2022). A scalable system for the fast production of RNA with homogeneous terminal ends. RNA biology, 19(1), 1077–1084. https://doi.org/10.1080/15476286.2022.2123640</ref>, stem-loop 2 function together with RBS to facilitate translation. T7_RBS [https://parts.igem.org/Part:BBa_K4162006 BBa_K4162006] is shown, and a stronger RBS [https://parts.igem.org/Part:BBa_B0030 BBa_B0030] or a weaker RBS [https://parts.igem.org/Part:BBa_J61100 BBa_J61100] if needed
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Revision as of 04:15, 8 October 2023


ribozyme test: T7 leaky expression

contributed by Fudan iGEM 2023

Introduction

This composite part is utilized to assess the cleavage efficiency of Twister P1， stem-loop’s ability of preventing mRNA degradation and the strength of different ribosome binding site (RBS). It is regulated by T7 promoter ,lac operator and T7 terminator. From its upstream to understream includes StayGold, stem-loop, Twister P1 and mScarlet.

A ribozyme is proved to have cleavage ability when green and red fluorescence are emitted at the same time. We can assess the cleavage efficiency of ribozyme based on the ratio of red-green fluorescence intensity when the stem-loop is unchanged.

We can also assess stem-loop’s ability of preventing mRNA degradation based on the ratio of red-green fluorescence intensity when the ribozyme is unchanged.

Furthermore, the orginal T7_RBS can be replaced by other RBSs. We can test the strength of one RBS based on ratio of red-green fluorescence intensity.

Usage and Biology

This composite part is an easy and effective tool to select the fit ribozyme, stem-loop and RBS.

Characterization

Sequencing map

contributed by Fudan iGEM 2023
Figure1 Linker sequences between the first CDS (stayGold) and the second CDS (mScarlet)

PmeI linker was borrowed from Liu[1] to facilitate cloning, and no specific secondary RNA structure. Stem-loop 1 was used to stabilize the first RNA after ribozyme cleavage, and we test it function in BBa_K4765129. After the ribozyme Twister[2], stem-loop 2 function together with RBS to facilitate translation. T7_RBS BBa_K4162006 is shown, and a stronger RBS BBa_B0030 or a weaker RBS BBa_J61100 if needed

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NotI site found at 1409
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 700
    Illegal BsaI.rc site found at 720


  1. ↑ Liu, Y., Wu, Z., Wu, D., Gao, N., & Lin, J. (2022). Reconstitution of Multi-Protein Complexes through Ribozyme-Assisted Polycistronic Co-Expression. ACS Synthetic Biology, 12(1), 136–143. https://doi.org/10.1021/acssynbio.2c00416
  2. ↑ Chen, Y., Cheng, Y., & Lin, J. (2022). A scalable system for the fast production of RNA with homogeneous terminal ends. RNA biology, 19(1), 1077–1084. https://doi.org/10.1080/15476286.2022.2123640