Team:DTU-Denmark-2/results/Proofofconcept/fungi

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<b>Proof of concept in fungi</b><br> <br>
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Several separate devices were conducted with Plug ‘n’ Play assembly to verify if the system will work in fungi as well as in mammalian cells. The idea was to target the fungi with a fluorescence protein to specific compartments and in general to express the fluorescence proteins. All the devices have the same promoter, terminator and marker cassette, though with different gene of interest and were all transformed in laboratory <i> Aspergillus nidulans</i> stain:<i> argB2, pyrG89, veA1</i> by random non-homologues-end-joining integration. 
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We succeed in proving that Plug ‘n’ Play assembly easily transformed and expressed in fungi as we succeed in tagging A. nidulans with two fluorescence proteins. The transformants with integration of our 4 devices change morphology compared with the wild type control strain since the DNA were randomly intergraded and have inflicted some pathways in the fungi.
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The results are displayed in the following section.
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<b>Device 22</b><br>
<b>Device 22</b><br>
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The results shows fluorescence spread evenly in the hyphae which correlate with that in device 22, the gene of interest, only consists of a green fluorescence protein GFP with no specific target.
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<b>Device 23</b><br>
<b>Device 23</b><br>
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The results shows fluorescence spread evenly in the hyphae and with spots of fluorescence. Device 23 consists of GFP with a target signal to the peroxisomes which can explain the spots compared to the results from device 22. We cannot conclude that the signal is accumulated in the peroxisomes since they are not dyed, though can it be concluded that the GFP signal is target a specific place and accumulated somewhere in the fungi compared to the results from device 22.
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<b>Device 24</b><br>
<b>Device 24</b><br>
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The results shows fluorescence spread evenly in the hyphae which correlate with that in device 23, the gene of interest, only consists of a green fluorescence protein RFP with no specific target.
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<b>Device 25</b><br>
<b>Device 25</b><br>
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The results show spots of fluorescence as in Device 23. Device 25 consists of RFP with a target signal to the nucleus which can explain the spots compared to the results from device 22 and the spores with a single nuclei contains a lot of RFP signal. We cannot conclude that the signal is accumulated in the nucleus since they are not dyed, though can it be concluded that the RFP signal is target a specific place and accumulated somewhere.
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THe control strain shows no auto-fluorescence.
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Revision as of 23:39, 15 September 2011



Proof of concept in fungi

 Several separate devices were conducted with Plug ‘n’ Play assembly to verify if the system will work in fungi as well as in mammalian cells. The idea was to target the fungi with a fluorescence protein to specific compartments and in general to express the fluorescence proteins. All the devices have the same promoter, terminator and marker cassette, though with different gene of interest and were all transformed in laboratory Aspergillus nidulans stain: argB2, pyrG89, veA1 by random non-homologues-end-joining integration.

We succeed in proving that Plug ‘n’ Play assembly easily transformed and expressed in fungi as we succeed in tagging A. nidulans with two fluorescence proteins. The transformants with integration of our 4 devices change morphology compared with the wild type control strain since the DNA were randomly intergraded and have inflicted some pathways in the fungi.

The results are displayed in the following section.

Device 22
 The results shows fluorescence spread evenly in the hyphae which correlate with that in device 22, the gene of interest, only consists of a green fluorescence protein GFP with no specific target.



Aspergillus nidulans with device 22 - DIC light. Aspergillus nidulans with device 22 - YFP light.
Aspergillus nidulans with device 22 - Front Aspergillus nidulans with device 22 - Back



Device 23
 The results shows fluorescence spread evenly in the hyphae and with spots of fluorescence. Device 23 consists of GFP with a target signal to the peroxisomes which can explain the spots compared to the results from device 22. We cannot conclude that the signal is accumulated in the peroxisomes since they are not dyed, though can it be concluded that the GFP signal is target a specific place and accumulated somewhere in the fungi compared to the results from device 22.



Aspergillus nidulans with device 23 - DIC light. Aspergillus nidulans with device 23 - YFP light.
Aspergillus nidulans with device 23 - Front Aspergillus nidulans with device 23 - Back

Device 24
 The results shows fluorescence spread evenly in the hyphae which correlate with that in device 23, the gene of interest, only consists of a green fluorescence protein RFP with no specific target.



Aspergillus nidulans with device 24 - DIC light. Aspergillus nidulans with device 24 - RFP light.
Aspergillus nidulans with device 24 - Front Aspergillus nidulans with device 24 - Back

Device 25
 The results show spots of fluorescence as in Device 23. Device 25 consists of RFP with a target signal to the nucleus which can explain the spots compared to the results from device 22 and the spores with a single nuclei contains a lot of RFP signal. We cannot conclude that the signal is accumulated in the nucleus since they are not dyed, though can it be concluded that the RFP signal is target a specific place and accumulated somewhere.



Aspergillus nidulans with device 25 - DIC light. Aspergillus nidulans with device 25 - RFP light.
Aspergillus nidulans with device 25 - Front Aspergillus nidulans with device 25 - Back

Control

THe control strain shows no auto-fluorescence.

Wild type Aspergillus nidulans - DIC light. Wild type Aspergillus nidulans - RFP light. Wild type Aspergillus nidulans - YFP light.
Wild type Aspergillus nidulans - Front Wild type Aspergillus nidulans - Back

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