Team:Groningen/23 August 2010

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Analasys was done by THT and SDS page.
Analasys was done by THT and SDS page.
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'''
 
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Biofilm formation experiment'''
 
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Bacillus Subtilis cultures were grown overnight in a Petridish containing 20mL of LB medium and a piece of ceramics to spurr the biofilm formation. The following cultures wehre grown:
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'''Biofilm formation experiment'''
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Bacillus Subtilis, Bacillus Subtilis ΔTasA, Bacillus Subtilis wit chaplin E1, Bacillus Subtilis with chaplin H1, Bacillus Subtilis ΔTasA with chaplin E1, Bacillus Subtilis ΔTasA with chaplin H1
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''Bacillus Subtilis'' cultures were grown overnight in a Petridish containing 20mL of LB medium and a piece of ceramics to spurr the biofilm formation. The following cultures wehre grown:
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''
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Bacillus Subtilis'', ''Bacillus Subtilis'' ΔTasA, ''Bacillus Subtilis'' wit chaplin E1, ''Bacillus Subtilis'' with chaplin H1, ''Bacillus Subtilis'' ΔTasA with chaplin E1, ''Bacillus Subtilis'' ΔTasA with chaplin H1
All cultures where inoculated with 100uL of overnight culture. All cultures where run in duplicate, one induced with 1%subtilin, and one without subtilin as a negative control.
All cultures where inoculated with 100uL of overnight culture. All cultures where run in duplicate, one induced with 1%subtilin, and one without subtilin as a negative control.
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We assumed that the ΔTasA would not form a biofilm and the normal phenotype could be restored by the expression of chaplins.  Furthermore we assumed that the normal ''Bacillus Subtilis'' biofilm would have atered properties.
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{{Team:Groningen/Footer}}
{{Team:Groningen/Footer}}

Revision as of 13:25, 23 October 2010

iGEM Groningen 2010

Hydrophobofilm
pushing coatings into a greener future


Expression experiment - David & Peter
The second expression experiment.
Analasys was done by THT and SDS page.

Biofilm formation experiment

Bacillus Subtilis cultures were grown overnight in a Petridish containing 20mL of LB medium and a piece of ceramics to spurr the biofilm formation. The following cultures wehre grown: Bacillus Subtilis, Bacillus Subtilis ΔTasA, Bacillus Subtilis wit chaplin E1, Bacillus Subtilis with chaplin H1, Bacillus Subtilis ΔTasA with chaplin E1, Bacillus Subtilis ΔTasA with chaplin H1

All cultures where inoculated with 100uL of overnight culture. All cultures where run in duplicate, one induced with 1%subtilin, and one without subtilin as a negative control.

We assumed that the ΔTasA would not form a biofilm and the normal phenotype could be restored by the expression of chaplins. Furthermore we assumed that the normal Bacillus Subtilis biofilm would have atered properties.


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