Team:TU-Munich/Results/KillSwitch

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Revision as of 23:10, 28 October 2013

Kill Switch

The Kill Switch mechanism is the most complex and ambitious aspect of our project on the protein level. For details on its design and function see here. We were very excited to start experimenting with the killswitch moss. However, when we opened the redlight filter foil, we found none of the allegedly transgenic moss lines had survived. There is a variety of possible reasons for this outcome that need to be discussed in order to improve our approach.

Figure 1: Live moss protonema

Figure 2: Dead Kill Switch moss protonema

Transformation of the large DNA constructs

The Kill Switch DNA constructs are very large and even exceed the Part Registry´s frame (see Figure 1). For the PEG-mediated moss transformation, we used plasmids linearized with EcoRI. Contrary to the targeted gene transfer described by Hohe et al., 2003, our constructs contain no flanking homologuos regions. Our random integration transformation worked successfully for our other contructs, whereas the large Kill Switch construct might need further inquiry for a suitable integration site. Due to its size, the construct might be less stable and require sensitive handling.

Figure 1: Registry entry of the PhyB/PIF6 version of the Kill Switch, BBa_K1159118

We weren´t yet able to express the Kill Switch in E.coli, which is most likely due to codon usage discrepancy. While Physcomitrella patens is not very dicriminating regarding codon usage, the function and expression of proteins designed for Physco is not guaranteed to work in E.coli.

Level of promoter activity

File:PBI 376 f1.gif

Figure 2: Comparative expression performance of different constitutive mammalian and plant promoters in Physcomitrella patens, [Gitzinger et al., 2009]

Photosensitivity

Figure 3: Working with the photosensitive protoplasts

References

[Gitzinger et al., 2009] Functional cross-kingdom conservation of mammalian and moss (Physcomitrella patens) transcription, translation and secretion machineries, Plant Biotechnol J. 2009 Feb;7(2):210

[Hohe et al., 2003] An improved and highly standardised transformation procedure allows efficient production of single and multiple targeted gene-knockouts in a moss, Physcomitrella patens, Curr Genet (2004) 44: 339–347

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 ==Transformation of the large DNA constructs==
-The Kill Switch DNA constructs are very large and even exceed the Part Registry´s frame (Fig. 1). For the PEG-mediated moss [https://2013.igem.org/Team:TU-Munich/Notebook/Methods#Transformation transformation], we used plasmids linearized with EcoRI. Contrary to the targeted gene transfer described by [http://www.plant-biotech.net/paper/CurrGenet_2003_hohe.pdf Hohe et al., 2003], our constructs contain no flanking homologuos regions. Our random integration transformation worked successfully for our other contructs, whereas the large Kill Switch construct might need further inquiry for a suitable integration site. Due to its size, the construct might be less stable and require sensitive handling.
+The Kill Switch DNA constructs are very large and even exceed the Part Registry´s frame (see Figure 1). For the PEG-mediated moss [https://2013.igem.org/Team:TU-Munich/Notebook/Methods#Transformation transformation], we used plasmids linearized with EcoRI. Contrary to the targeted gene transfer described by [http://www.plant-biotech.net/paper/CurrGenet_2003_hohe.pdf Hohe et al., 2003], our constructs contain no flanking homologuos regions. Our random integration transformation worked successfully for our other contructs, whereas the large Kill Switch construct might need further inquiry for a suitable integration site. Due to its size, the construct might be less stable and require sensitive handling.
 [[File:TUM13_PartsRegistryKillSwitch.png|thumb|center|750px| '''Figure 1''': [http://parts.igem.org/wiki/index.php?title=Part:BBa_K1159118 Registry entry] of the PhyB/PIF6 version of the Kill Switch, BBa_K1159118]]