Regulatory

Part:BBa_K3002001:Experience

Designed by: Dorothée Klein   Group: iGEM19_TU_Kaiserslautern   (2019-10-10)
Revision as of 03:17, 22 October 2019 by MSchlosser (Talk | contribs) (→‎Applications of BBa_K3002001)


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Applications of BBa_K3002001

Cytosolic Expression

Expression of the enzymes MUT-PETase and MHETase in Chlamydomonas reinhardtii. (a) Level 2 MoClo construct harboring the aadA selection marker and the coding sequences for MUT-PETase, and MHETase (see Figure 1 for part description). (b) The UVM4 strain was transformed with the construct shown in (a). 11 spectinomycin-resistant transformants were inoculated in TAP and samples taken after 3 days. Extracted whole-cell proteins were analysed by SDS-PAGE and immunoblotting using an anti-HA antibody. MW – molecular weight. The black arrow represents the MHETase, the white arrow the MUT-PETase. The expression of both MHETase (~70 kDa) and MUT-PETase (~35 kDa) is visible in colonies 18, 22 and 27. The UVM4 recipient strain and a strain expressing the HA-tagged ribosomal chloroplastic 50S protein L5 (RPL5) served as negative and positive controls, respectively.

Both MUT-PETase and MHETase show cytosolic expression and secretion when containing the cCA secretion signal. The PSAD promoter is a reliable regulatory element for the aadA coding sequence and thus allows a selection of transformants.

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