Difference between revisions of "Part:BBa K3105682"
Line 3: | Line 3: | ||
<partinfo>BBa_K3105682 short</partinfo> | <partinfo>BBa_K3105682 short</partinfo> | ||
− | Manganese Peroxidase (MnP) cloned in-frame with α-factor from Saccharomyces cerevisiae. This construct is controlled by the AOX1 promotor, which is inducible by methanol. | + | Manganese Peroxidase (MnP) cloned in-frame with α-factor from <I>Saccharomyces cerevisiae</I>. This construct is controlled by the AOX1 promotor, which is inducible by methanol. |
+ | <br><br> | ||
+ | ===Characterization=== | ||
+ | <div> | ||
+ | The part was expressed in X-33 <I>P.pastoris</I> cells using the pPICZαB shuttle vector. Cultures were induced with methanol and analysed on SDS-PAGE. MnP was successfully expressed and secreted (Figure 1). | ||
+ | |||
+ | |||
+ | |||
+ | [[File:T--Uppsala Universitet--MnP-Gel-new without-legend.png|800px|thumb|left|<b>Figure 1: Expression and secretion of Manganese Peroxidase (MnP)</b> <br> | ||
+ | X-33 <I>P. pastoris</I> cells were transformed with pPICZαB_MnP, induced (i), fractionated into pellets (P) and supernatants (S), and analysed by 10 % SDS-PAGE stained with Coomassie Blue. u, uninduced <br> | ||
+ | Induction bands are visible at approximately 70 kDa for both P and S (red arrows), showing secretion of MnP.]] | ||
+ | |||
+ | <br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> | ||
+ | |||
+ | |||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 22:53, 19 October 2019
Expression construct MnP
Manganese Peroxidase (MnP) cloned in-frame with α-factor from Saccharomyces cerevisiae. This construct is controlled by the AOX1 promotor, which is inducible by methanol.
Characterization
The part was expressed in X-33 P.pastoris cells using the pPICZαB shuttle vector. Cultures were induced with methanol and analysed on SDS-PAGE. MnP was successfully expressed and secreted (Figure 1).
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1438
Illegal BglII site found at 1730
Illegal XhoI site found at 1189 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 2491
- 1000COMPATIBLE WITH RFC[1000]