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Team:LMU-Munich/Bacillus Introduction
From 2012.igem.org
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'''1) Transformation of ''B. subtilis''''' | '''1) Transformation of ''B. subtilis''''' | ||
| - | <br>''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. 2. | + | <br>As ''B. subtilis'' and ''E. coli'' are model organisms they have an established genetics. The advantage of ''B. subtilis'' is that it is naturally competent. So it is not complicated to conduct genetical manipulations. It 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. 2. |
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For these reasons, in some cases ''B. subtilis'' can be the chassis of choice. Unfortunately, very few iGEM teams have worked with this model organism, and there is at this time no established BioBrick system to use ''B. subtilis'' as a chassis.</p> | For these reasons, in some cases ''B. subtilis'' can be the chassis of choice. Unfortunately, very few iGEM teams have worked with this model organism, and there is at this time no established BioBrick system to use ''B. subtilis'' as a chassis.</p> | ||
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| - | '''2) | + | '''2) Differentiation''' |
| - | + | ''B. subtilis'' is able to differentiate into cells with different morphology and function (Fig. 3), the most severe form being the endospore which is produced under stress conditions. These spores are resistant towards environmental influences. But if they sense favour conditions they can germinate again. In our project, we will exploit the production of endospores. Because they are extremely stable they are good vehicles for our fusion proteins with certain functions. | |
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| - | <font color="#000000"; size="2"><p align="justify">Fig. 3: The vegetative cycle is very similiar to the one of ''E. coli.'' But if there is a stress | + | <font color="#000000"; size="2"><p align="justify">Fig. 3: The vegetative cycle is very similiar to the one of ''E. coli.'' But if there is a stress like for example starvation, the cells enter sporulation, where they first undergo a polar cell division, followed by the formation of the endospore. If the enviromental conditions are suitable again, the spore will then germinate and reenter the vegetative cycle.</p></font> |
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Revision as of 22:40, 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 ]
Bacillus subtilis - a new chassis for iGEM
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. To introduce B. subtilis, we want to highlight some important aspects of this organism, which are listed in the table below.
| Organism | B. subtilis | E. coli |
|---|---|---|
| Type | gram-positive rod | gram-negative rod |
| Motility | + | + |
| Transformation | natural competence | artificial competence |
| Vectors | integrative & replicative | replicative |
| Sporulation | + | - |
| Differentiation | + | - |
| Safety | [http://www.fda.gov/Food/FoodIngredientsPackaging/GenerallyRecognizedasSafeGRAS/default.htm GRAS] | [http://www.fda.gov/Food/FoodIngredientsPackaging/GenerallyRecognizedasSafeGRAS/default.htm GRAS] |
In general, bacteria can be divided into two groups that differ in essential characteristics: gram-positive and gram-negative. Escherichia coli is a model organism for the gram-negative bacteria. A model organism for the gram-positive microorganisms is B. subtilis, which we work with. The natural habitat of B. subtilis is soil, so it is forced to adapt to environmental changes. Hence B. subtilis is very complex. There are many differentiations and survival strategies that B. subtilis can engages (Fig. 1): Due to its natural competence it can uptake DNA and integrate it into its genome. To be flexibel to the environment and move towards nutrients or avoid toxics it is motile with the aid of its peritrich flagella. There is even cannibalism as one differentation form. If the conditions get to bad for living cells, B. subtilis can form spores. These are very stable vehicles where bacteria are resistant towards e.g. desiccation, heat and pressure. If these spores sense better conditions they are able to germinate again.
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There are two major differences between B. subtilis and E. coli that are of interest to us:
1) Transformation of B. subtilis
As B. subtilis and E. coli are model organisms they have an established genetics. The advantage of B. subtilis is that it is naturally competent. So it is not complicated to conduct genetical manipulations. It 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. 2.
For these reasons, in some cases B. subtilis can be the chassis of choice. Unfortunately, very few iGEM teams have worked with this model organism, and there is at this time no established BioBrick system to use B. subtilis as a chassis.
</p>
2) Differentiation
B. subtilis is able to differentiate into cells with different morphology and function (Fig. 3), the most severe form being the endospore which is produced under stress conditions. These spores are resistant towards environmental influences. But if they sense favour conditions they can germinate again. In our project, we will exploit the production of endospores. Because they are extremely stable they are good vehicles for our fusion proteins with certain functions.
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