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| | {{:Team:LMU-Munich/Templates/Page Header|File:Bacillus in urban culture.jpg}} | | {{:Team:LMU-Munich/Templates/Page Header|File:Bacillus in urban culture.jpg}} |
| - | [[File:Bacillus_introduction_banner.jpg|620px|link=]] | + | [[File:Bacillus introduction banner.resized WORDS.JPG|620px|link=]] |
| - | [[File:Bacilluss Intro.png|100px|right]]
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| - | <p></p>
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| | + | [[File:Bacilluss_Intro.png|100px|right|link=]] |
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| | ==''Bacillus subtilis'' - a new chassis for iGEM== | | ==''Bacillus subtilis'' - a new chassis for iGEM== |
| | + | <br> |
| | + | <div class="box"> |
| | + | ====Introduction==== |
| | + | {| width="100%" style="text-align:center;"| |
| | + | |<p align="justify">Introduction to ''B. subtilis'' and background information.</p> |
| | + | |[[File:Tabelle.png|right|150px|link=Team:LMU-Munich/Data/introintro]] |
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| | + | ! colspan="2" |[[File:LMU Arrow purple.png|40px|link=Team:LMU-Munich/Data/introintro]] |
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| | + | </div> |
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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. To introduce ''B. subtilis'', we want to highlight some important aspects of this organism, which are listed in the table below.</p>
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| | + | There are two major differences between ''B. subtilis'' and ''E. coli'' that are of interest to us: |
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| - | {| class="colored" width="100%"
| + | <div class="box"> |
| - | |-
| + | ====Transformation of ''B. subtilis''==== |
| - | !Organism
| + | {| width="100%" style="text-align:center;"| |
| - | !''B. subtilis''
| + | |<p align="justify">Cloning strategy for the work of '' B. subtilis''.</p> |
| - | !''E. coli''
| + | |[[File:Integration.png|right|150px|link=Team:LMU-Munich/Data/integration]] |
| - | |-
| + | |
| - | !<font color="#EBFCE4">Type</font>
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| - | |gram-positive rod
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| - | |gram-negative rod
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| - | !Motility
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| - | |<font size=4>'''+'''
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| - | |<font size=4>'''+'''
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| - | |-
| + | |
| - | !Transformation
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| - | |natural competence
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| - | |artificial competence
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| - | |-
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| - | !Vectors
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| - | |integrative & replicative
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| - | |replicative
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| - | |-
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| - | !Sporulation
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| - | |<font size=4>'''+'''
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| - | |<font size=4>'''-''' | + | |
| - | |- | + | |
| - | !Differentiation
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| - | |<font size=4>'''+''' | + | |
| - | |<font size=4>'''-'''
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| - | |-
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| - | !Safety
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| - | |[http://www.fda.gov/Food/FoodIngredientsPackaging/GenerallyRecognizedasSafeGRAS/default.htm GRAS] | + | |
| - | |[http://www.fda.gov/Food/FoodIngredientsPackaging/GenerallyRecognizedasSafeGRAS/default.htm GRAS] | + | |
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| | + | ! colspan="2" |[[File:LMU Arrow purple.png|40px|link=Team:LMU-Munich/Data/integration]] |
| | |} | | |} |
| | + | </div> |
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| - | <br> | + | <div class="box"> |
| - | <p align="justify"> 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.</p>
| + | ====Differentiation==== |
| - | | + | {| width="100%" style="text-align:center;"| |
| - | | + | |<p align="justify">The life cycle of ''B. subtilis'' and the different cell stages.</p> |
| - | {| style="color:black;" cellpadding="3" width="70%" cellspacing="0" border="0" align="center" style="text-align:left;" | + | |[[File:Figures Bacillus Intro fig1.png|right|150px|link=Team:LMU-Munich/Data/differentiation]] |
| - | | style="width: 70%;background-color: #EBFCE4;" | | + | |
| - | {|
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| - | |[[File:LMU Bacillus life.png|center|450px]] | + | |
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| - | | style="width: 70%;background-color: #EBFCE4;" |
| + | ! colspan="2" |[[File:LMU Arrow purple.png|40px|link=Team:LMU-Munich/Data/differentiation]] |
| - | {| style="color:black;" cellpadding="0" width="95%" cellspacing="0" border="0" align="center" style="text-align:center;"
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| - | |style="width: 70%;background-color: #EBFCE4;" | | + | |
| - | <font color="#000000"; size="2">Fig. 1: Schematic representation of the distinct cell types that differentiate in the communities of ''Bacillus subtilis''.<br> ([http://www.ncbi.nlm.nih.gov/pubmed/20030732 Lopez & Kolter, 2010])</font>
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| | |} | | |} |
| - | |}
| + | </div> |
| - | |}
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| - | <p align="justify"> | + | |
| - | There are two major differences between ''B. subtilis'' and ''E. coli'' that are of interest to us:
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| | <br> | | <br> |
| | <br> | | <br> |
| - | '''1) Transformation of ''B. subtilis'''''
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| - | <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.
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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>
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| - | </p>
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| - | <br> | + | <div class="box"> |
| - | | + | ====Project Navigation==== |
| - | | + | {| width="100%" align="center" style="text-align:center;" |
| - | {| style="color:black;" cellpadding="3" width="70%" cellspacing="0" border="0" align="center" style="text-align:left;" | + | |[[File:Bacilluss_Intro.png|100px|link=Team:LMU-Munich/Bacillus_Introduction]] |
| - | | style="width: 70%;background-color: #EBFCE4;" | | + | |[[File:BacillusBioBrickBox.png|100px|link=Team:LMU-Munich/Bacillus_BioBricks]] |
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| + | |[[File:SporeCoat.png|100px|link=Team:LMU-Munich/Spore_Coat_Proteins]] |
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| + | |[[File:GerminationSTOP.png|100px|link=Team:LMU-Munich/Germination_Stop]] |
| - | |[[File:LMU-Munich-insertion-Intro1.png|500px|center]] | + | |
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| - | |[[File:LMU-Munich-integration-Arrow.png|70px|center]] | + | |[[Team:LMU-Munich/Bacillus_Introduction|<font size="2">'''''Bacillus'''''<BR>Intro</font>]] |
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| + | |[[Team:LMU-Munich/Bacillus_BioBricks|<font size="2" face="verdana">'''''Bacillus'''''<BR>'''B'''io'''B'''rick'''B'''ox</font>]] |
| - | |[[File:LMU-Munich-insertion-Intro2.png|500px|center]] | + | |[[Team:LMU-Munich/Spore_Coat_Proteins|<font size="2" face="verdana">'''Sporo'''beads</font>]] |
| - | |- | + | |[[Team:LMU-Munich/Germination_Stop|<font size="2" face="verdana">'''Germination'''<BR>STOP</font>]] |
| - | | style="width: 70%;background-color: #EBFCE4;" |
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| - | {| style="color:black;" cellpadding="0" width="95%" cellspacing="0" border="0" align="center" style="text-align:center;"
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| - | |style="width: 70%;background-color: #EBFCE4;" | | + | |
| - | <font color="#000000"; size="2"><p align="justify">Fig. 2: Exogenous DNA is shown in red while the bacterial genome is black a) The propagation of exogenous DNA if brought in as replicative plasmid. The number of plasmids per cell can vary. b) The propagation of exogenous DNA if it is able to integrate into the genome via homologous recombination</p></font> | + | |
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| | |} | | |} |
| | + | </div> |
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| - | '''2) Integration of DNA'''
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| - | ''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. We will exploit the production of endospores in our project '''Bead'''zillus. The life cycle of ''B. subtilis'' is depicted in Fig. 2.
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| - | |[[File:Figures Bacillus Intro fig1.png|500px|center]]
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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 condition like 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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| - | <div class="box">
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| - | ====Project Navigation====
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| - | {| width="100%" align="center" style="text-align:center;"
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| - | |[[File:Bacilluss_Intro.png|100px|link=Team:LMU-Munich/Bacillus_Introduction]]
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| - | |[[File:BacillusBioBrickBox.png|100px|link=Team:LMU-Munich/Bacillus_BioBricks]]
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| - | |[[File:SporeCoat.png|100px|link=Team:LMU-Munich/Spore_Coat_Proteins]]
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| - | |[[File:TerminationSTOP.png|100px|link=Team:LMU-Munich/Germination_Stop]]
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| - | |[[Team:LMU-Munich/Bacillus_Introduction|<font size="2">'''''Bacillus'''''<BR>Intro</font>]]
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| - | |[[Team:LMU-Munich/Bacillus_BioBricks|<font size="2" face="verdana">'''''Bacillus'''''<BR>'''B'''io'''B'''rick'''B'''ox</font>]]
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| - | |[[Team:LMU-Munich/Spore_Coat_Proteins|<font size="2" face="verdana">'''Sporo'''beads</font>]]
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| - | |[[Team:LMU-Munich/Germination_Stop|<font size="2" face="verdana">'''Germination'''<BR>STOP</font>]]
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| - | |}
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| - | </div>
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| | {{:Team:LMU-Munich/Templates/Page Footer}} | | {{:Team:LMU-Munich/Templates/Page Footer}} |
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