Difference between revisions of "Part:BBa K3002112:Experience"
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+ | <p>The MHETase is expressed in the cytosol of C.reinhardtii. This part is essential for the degradation of MHET into its final degradation products TPA and EG. | ||
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+ | <p></p><div class="figure"> | ||
+ | <img src="https://2019.igem.org/wiki/images/1/1b/T--TU_Kaiserslautern--resultsFigure4.svg"/> | ||
+ | <p class="caption"><span class="phat">Expression of the enzymes MUT-PETase and MHETase in <i>Chlamydomonas</i> <i>reinhardtii</i>. | ||
+ | </span><span class="accent">(a)</span> Level 2 MoClo construct harboring the aadA selection marker and the coding sequences for MUT-PETase, and MHETase (see Figure 1 for part description). <span class="accent">(b)</span> The UVM4 strain was transformed with the construct shown in <span class="accent">(a)</span>. 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. | ||
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Latest revision as of 01:59, 22 October 2019
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The MHETase is expressed in the cytosol of C.reinhardtii. This part is essential for the degradation of MHET into its final degradation products TPA and EG.
UNIQ1e6555de31622864-partinfo-00000001-QINU UNIQ1e6555de31622864-partinfo-00000002-QINU