Regulatory

Part:BBa_K3927004

Designed by: Chew Chin Wei   Group: iGEM21_NUS_Singapore   (2021-10-13)
Revision as of 10:37, 18 October 2021 by CWChew (Talk | contribs) (Design)


C120-CYC-TetR (S. cerevisiae)

This composite part encodes for part BBa_K3927001 C120-CYCp promoter controlling Part BBa_C0040, expressing TetR in the presence of blue light, followed by Part BBa_K1486025 ADH terminator. Dependent on EL222 expressed in situ., recommended that S. cerevisiae chassis has part BBa_K3570021 NLS-vp16-EL222 in order for this part to work.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]

Description

Usage

Design

Designs were remade for a third iteration of the blue light repression circuit (figure 1). Because directly using EL222 to hinder the promoter did not work, an inverter circuit was constructed such that repression of the promoter was reliant on EL222 driven expression. To achieve this, a TetO site was inserted into the identified repression site 25 base pairs downstream of the TATA box in the PGK1 promoter, and a secondary cassette containing the part BBa_C0040 coding for a tetR protein under the control of the initial C120-CYC promoter was conjugated to it. It was hypothesized that under blue light exposure, C120-CYC would activate the production of TetR, which would then repress the PGK1 promoter.

Figure 1:pTetrepress construct schematic.

Characterization

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Categories
Parameters
None