Team:LMU-Munich/Bacillus Introduction

From 2012.igem.org

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There are two major differences between ''B. subtilis'' and ''E. coli'' that are of interest to us:
There are two major differences between ''B. subtilis'' and ''E. coli'' that are of interest to us:
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'''1) Transformation of ''B. subtilis'''''  
'''1) Transformation of ''B. subtilis'''''  
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<br><p align="justify">As ''B. subtilis'' and ''E. coli'' are model organisms, they have established genetics. The advantage of ''B. subtilis'' is that it is naturally competent. So it is very easy to conduct genetic manipulations. It can replicate plasmids as ''E. coli'' does, but there is a much more elegant way of bringing in exogenous DNA fragments. When flanked by regions homologous to the ''B. subtilis'' genome, it will be integrated at high efficiency via homologous recombination at this locus and subsequently be replicated with the chromosome (Fig. 2). This leads to stable, single-copy genomic alterations. Thereby avoiding, copy-number artifacts occuring with replicative plasmids. This different way of genetic manipulations requires the use of integrative vectors as provided by our [https://2012.igem.org/Team:LMU-Munich/Bacillus_BioBricks BacillusBioBrickBox]. For this reason, ''B. subtilis'' is an ideal genetic platform for Synthetic Bioloy. But so far, very few iGEM teams have worked with this model organism due to the lack of suitable BioBrick-compatible genetic tools.</p>
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<p align="justify">As ''B. subtilis'' and ''E. coli'' are model organisms, they have established genetics. The advantage of ''B. subtilis'' is that it is naturally competent. So it is very easy to conduct genetic manipulations. It can replicate plasmids as ''E. coli'' does, but there is a much more elegant way of bringing in exogenous DNA fragments. When flanked by regions homologous to the ''B. subtilis'' genome, it will be integrated at high efficiency via homologous recombination at this locus and subsequently be replicated with the chromosome (Fig. 2). This leads to stable, single-copy genomic alterations. Thereby avoiding, copy-number artifacts occuring with replicative plasmids. This different way of genetic manipulations requires the use of integrative vectors as provided by our [https://2012.igem.org/Team:LMU-Munich/Bacillus_BioBricks BacillusBioBrickBox]. For this reason, ''B. subtilis'' is an ideal genetic platform for Synthetic Bioloy. But so far, very few iGEM teams have worked with this model organism due to the lack of suitable BioBrick-compatible genetic tools.</p>
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'''2) Differentiation'''
'''2) Differentiation'''
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<br><p align="justify">''B. subtilis'' is able to differentiate into cells with different morphologies and functions (Fig. 1 and Fig. 3). The most characteristic form is the endospore, which is produced under nutrient starvation. In our project, we will exploit the production of endospores. Because they are extremely stable, they are perfect vehicles for the display of functional fusion proteins on their surface as illustrated by our [https://2012.igem.org/Team:LMU-Munich/Spore_Coat_Proteins '''Sporo'''bead] module.
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<p align="justify">''B. subtilis'' is able to differentiate into cells with different morphologies and functions (Fig. 1 and Fig. 3). The most characteristic form is the endospore, which is produced under nutrient starvation. In our project, we will exploit the production of endospores. Because they are extremely stable, they are perfect vehicles for the display of functional fusion proteins on their surface as illustrated by our [https://2012.igem.org/Team:LMU-Munich/Spore_Coat_Proteins '''Sporo'''bead] module.
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Revision as of 01:33, 27 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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