Team:LMU-Munich/Bacillus Introduction

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==''Bacillus subtilis'' - a new chassis for iGEM==
==''Bacillus subtilis'' - a new chassis for iGEM==
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We chose to work with ''Bacillus subtilis'' to set new horizons and offer tools for this model organism to the ''Escherichia coli''-dominated world of iGEM. In addition, ''B. subtilis'' produces spores which we use for our '''Sporo'''beads. To introduce ''B. subtilis'' to the iGEM world, we want to present some important aspects of this organism, as they differ from the commonly used ''Escherichia coli''.
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<p align="justify">We chose to work with ''Bacillus subtilis'' to set new horizons and offer tools for this model organism to the ''Escherichia coli''-dominated world of iGEM. In addition, ''B. subtilis'' produces spores which we use for our '''Sporo'''beads. To introduce ''B. subtilis'' to the iGEM world, we want to present some important aspects of this organism, as they differ from the commonly used ''Escherichia coli''.</p>
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In contrast to ''E. coli'', the model organism ''B. subtilis'' is a gram-postivite rod. It is a facultatively aerobic soil bacterium which can move with its peritrichous flagella. Under ideal conditions, it has a doubling time of 45 minutes. ''B. subtilis'' is, in contrast to ''E. coli'', naturally competent, which means that e.g. under nutrient limitation, 10% of cells in a populaton get competent and take up DNA. Also unique for ''B. subtilis'' is that the vegetative cells can differentiate under nutrient limitations into spores, which we use in our project '''Bead'''zillus. Concerning working with ''B. subtilis'', it is important to know that there are integrative vectors which can integrate into the genome of the organism, in contrast to ''E. coli'', for which there are only replicative vectors. Also both organisms have [http://en.wikipedia.org/wiki/Generally_recognized_as_safe GRAS] state.
 
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Visit our [[Team:LMU-Munich/Lab_Notebook/Protocols|Protocols page]] for details how to work with ''B. subtilis''
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<p align="justify">In contrast to ''E. coli'', the model organism ''B. subtilis'' is a gram-postivite rod. It is a facultatively aerobic soil bacterium which can move with its peritrichous flagella. Under ideal conditions, it has a doubling time of 45 minutes. ''B. subtilis'' is, in contrast to ''E. coli'', naturally competent, which means that e.g. under nutrient limitation, 10% of cells in a populaton get competent and take up DNA. Also unique for ''B. subtilis'' is that the vegetative cells can differentiate under nutrient limitations into spores, which we use in our project '''Bead'''zillus. Concerning working with ''B. subtilis'', it is important to know that there are integrative vectors which can integrate into the genome of the organism, in contrast to ''E. coli'', for which there are only replicative vectors. Also both organisms have [http://en.wikipedia.org/wiki/Generally_recognized_as_safe GRAS] state.
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<br>Visit our [[Team:LMU-Munich/Lab_Notebook/Protocols|Protocols page]] for details how to work with ''B. subtilis''
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'''2)''' ''B. subtilis'' can replicate exogenous DNA via an origin of replication on a plasmid as ''E. coli'' does, but there is a much more elegant way of bringing in exogenous DNA stretches. When flanked by homologous regions to the bacterial genome, it will integrate at high efficiency via homologous recombination at this locus and furthermore be replicated with the genome. This has the advantage that if comparing different variables, not only the enviroment is always the same, but also the copy number is from cell to cell and from strain to strain the same, which is not always the case for replicative plasmids. This integrative way of bringing in exogenous DNA was exploited by us when producing the BioBrick compatible ''Bacillus'' vectors. The comparision between these two ways of bringing in exogenous DNA is depicted in Fig. 3.
'''2)''' ''B. subtilis'' can replicate exogenous DNA via an origin of replication on a plasmid as ''E. coli'' does, but there is a much more elegant way of bringing in exogenous DNA stretches. When flanked by homologous regions to the bacterial genome, it will integrate at high efficiency via homologous recombination at this locus and furthermore be replicated with the genome. This has the advantage that if comparing different variables, not only the enviroment is always the same, but also the copy number is from cell to cell and from strain to strain the same, which is not always the case for replicative plasmids. This integrative way of bringing in exogenous DNA was exploited by us when producing the BioBrick compatible ''Bacillus'' vectors. The comparision between these two ways of bringing in exogenous DNA is depicted in Fig. 3.
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Revision as of 19:10, 26 September 2012

iGEM Ludwig-Maximilians-Universität München Beadzillus

Bacillus in urban culture.jpg

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".

IGEM HQ LMU prize.jpg

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