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Team:LMU-Munich/Data/Knockout
From 2012.igem.org
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<p align="justify">We induced our germination-mutant strains to sporulate in Difco sporulation media. We quantified the cells and spores per milliliter of each culture using a Neubauer cell counting chamber. Then we plated known dilutions of culture, and measured the germination rate of mutant spores in a germination assay (see [https://2012.igem.org/Team:LMU-Munich/Lab_Notebook/Protocols Protocols]). The germination assays were carried out several times, and yielded similar results each time. For these results, see "Mutant Germination Rates" graph.</p> | <p align="justify">We induced our germination-mutant strains to sporulate in Difco sporulation media. We quantified the cells and spores per milliliter of each culture using a Neubauer cell counting chamber. Then we plated known dilutions of culture, and measured the germination rate of mutant spores in a germination assay (see [https://2012.igem.org/Team:LMU-Munich/Lab_Notebook/Protocols Protocols]). The germination assays were carried out several times, and yielded similar results each time. For these results, see "Mutant Germination Rates" graph.</p> | ||
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| - | <p align="justify">The plate growth demonstrates the inability of our mutant spores to germinate. We can say that | + | <br> |
| - | The plates below demonstrate the procedure of the germination assay. Plates here include those containing heated and unheated cultures, and show both germinable spores (B42) and spores unable to germinate (B47). | + | <p align="justify">The plate growth demonstrates the inability of our mutant spores to germinate. We can say that fewer than 1 out of 3x10^7 spores of strains B40, B41, B43, B46, and B47 germinated. |
| + | The plates below demonstrate the procedure of plating for the germination assay. Plates here include those containing heated and unheated cultures, and show both germinable spores (B42) and spores unable to germinate (B47). These plating experiments allowed us to quantify the number of ingerminable spores in each culture. | ||
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The purpose of plating both heated and unheated cultures was to demonstrate the viability of the unheated cells in each culture. This makes evident that the lack of colonies on heated plates is not due to the inability of the strain to grow, but from the inability of spores to germinate into vegetative cells capable of growing.</p> | The purpose of plating both heated and unheated cultures was to demonstrate the viability of the unheated cells in each culture. This makes evident that the lack of colonies on heated plates is not due to the inability of the strain to grow, but from the inability of spores to germinate into vegetative cells capable of growing.</p> | ||
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Revision as of 09:16, 26 September 2012
The LMU-Munich team is exuberantly happy about the great success at the World Championship Jamboree in Boston. Our project Beadzillus finished 4th and won the prize for the "Best Wiki" (with Slovenia) and "Best New Application Project".
[ more news ]
Knockouts of germination genes
We induced our germination-mutant strains to sporulate in Difco sporulation media. We quantified the cells and spores per milliliter of each culture using a Neubauer cell counting chamber. Then we plated known dilutions of culture, and measured the germination rate of mutant spores in a germination assay (see Protocols). The germination assays were carried out several times, and yielded similar results each time. For these results, see "Mutant Germination Rates" graph.
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The plate growth demonstrates the inability of our mutant spores to germinate. We can say that fewer than 1 out of 3x10^7 spores of strains B40, B41, B43, B46, and B47 germinated.
The plates below demonstrate the procedure of plating for the germination assay. Plates here include those containing heated and unheated cultures, and show both germinable spores (B42) and spores unable to germinate (B47). These plating experiments allowed us to quantify the number of ingerminable spores in each culture.
The purpose of plating both heated and unheated cultures was to demonstrate the viability of the unheated cells in each culture. This makes evident that the lack of colonies on heated plates is not due to the inability of the strain to grow, but from the inability of spores to germinate into vegetative cells capable of growing.
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