Difference between revisions of "Team:Aix-Marseille/Composite Part"

(→‎BBa_K1941009 : FliC Desulfovibrio vulgaris producer)
 
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====Lysine decarboxylase DesA :====
 
====Lysine decarboxylase DesA :====
  
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Lysine descarboxylase DesA from ''Streptomyces coelicolor'' is an enzyme from the lyase family that converts lysine into cadaverin. The enzyme releases the carbonyl group of the lysin amino acid. Cadaverine (1,5-diaminopentane) is a primary diamine which alkaline environment. Acidic pH and an anaerobic environment both induce the synthesis of Lysine decarboxylase.
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This DNA sequence codes a [http://metacyc.org/gene?orgid=META&id=SCO2782 Lysine decarboxylase] (''Streptomyces coelicolor'') which is an enzyme from the lyase family that converts lysine into cadaverine. The enzyme releases the carbonyl group of the lysin amino acid. Cadaverine (or 1,5-diaminopentane) is a primary diamine which renders the medium alkaline. The lysine decarboxylase is an enzyme whose synthesis is promoted by anaerobiosis and an acidic pH.  
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In bacteriology, this enzyme is sought through the middle of Moeller lysine or medium lysine Taylor.  
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This enzyme is also the first step in the production of desferrioxame B which is a siderophore.
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We succeed to produce DesA under an Arabinose indcution.
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[[File:T--Aix-Marseille--result9.png|center|350px]]
  
 
We registered the original sequence of this subpart in the iGEM registry of standard parts ([http://parts.igem.org/Part:BBa_K1951000 BBa_K1951000]). We optimized our sequence for ''E. coli'' and ordered the synthesis by addition of an inducible promoter.
 
We registered the original sequence of this subpart in the iGEM registry of standard parts ([http://parts.igem.org/Part:BBa_K1951000 BBa_K1951000]). We optimized our sequence for ''E. coli'' and ordered the synthesis by addition of an inducible promoter.
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As you can see in [http://parts.igem.org/Part:BBa_K1951004 the registry] all our expectations on this BioBrick were validated and it worked fine.
 
As you can see in [http://parts.igem.org/Part:BBa_K1951004 the registry] all our expectations on this BioBrick were validated and it worked fine.
  
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===[http://parts.igem.org/Part:BBa_K1951011 BBa_K1951011] : Desferrioxamine B producer pathway <i> Streptomyces coelicolor </i> producer===
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===[http://parts.igem.org/Part:BBa_K1951011 BBa_K1951011] : Desferrioxamine B pathway producer in <i> Streptomyces coelicolor </i> ===
  
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[[File:T--Aix-Marseille--desABCD.jpeg|600px|center|thumb|Desferrioxamine B pathway]]
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<div class="emph">
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The purpose of this biobrick is to produce desferrioxamine B siderophore by a controled manner, for controlled potential toxicity. This is also to reconstruct the full pathway of this siderophore production.  
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The purpose of this biobrick is to produce desferrioxamine B siderophore by a controled manner, for controlled potential toxicity.
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This biobrick was made from 6 parts:
 
This biobrick was made from 6 parts:
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* [http://parts.igem.org/Part:BBa_K1951002 BBa_K1951002]
 
* [http://parts.igem.org/Part:BBa_K1951002 BBa_K1951002]
 
* [http://parts.igem.org/Part:BBa_K1951003 BBa_K1951003]
 
* [http://parts.igem.org/Part:BBa_K1951003 BBa_K1951003]
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 +
</div>
  
  
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==== A precious metal binder ====  
 
==== A precious metal binder ====  
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Previous work showed that siderophores are able to catch other metals by default. Especifically, many articles showed a high affinity of Desferrioxamine B ( produce by ''Streptomyces coelicolor'') for tetravalent metal ions like platinum. These results encouraged us to make a biobrick coding the sequence corresponding to the 4 enzymes involved on the metabolic pathway of Desferrioxamine B. <i>E. coli</i> was used to produce this biobrick. Produce a gram positive bacteria pathway in a gram negative bacteria is restrictive <ref> Wandersman & Delepaire https://www.ncbi.nlm.nih.gov/pubmed/15487950  </ref> , considering the risk of toxicity for the conductress bacteria. To counter this potential issue, we regulate trasnscription using the control of an inductible promotor (pBAD/araC).
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Previous work showed that siderophores are able to catch other metals by default. Especifically, many articles showed a high affinity of Desferrioxamine B (produce by ''Streptomyces coelicolor'') for tetravalent metal ions like platinum. These results encouraged us to make a biobrick coding the sequence corresponding to the 4 enzymes involved on the metabolic pathway of Desferrioxamine B. <i>E. coli</i> was used to produce this biobrick. Produce a gram positive bacteria pathway in a gram negative bacteria is restrictive <ref> Wandersman & Delepaire https://www.ncbi.nlm.nih.gov/pubmed/15487950  </ref> , considering the risk of toxicity for themselves. To counter this potential issue, we regulate transcription using the control of an inductible promotor (pBAD/araC).
  
 
====A medical treatment====
 
====A medical treatment====
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==== Pathway demonstration ====
 
==== Pathway demonstration ====
  
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[[File:T--Aix-Marseille--result4.jpeg|500px|right|thumb|Test of our biobrick proteins production using a SDS page and comassie. - : no induction ; + : induction with 0.02% arabinose at Abs(600nm)=0.4]]
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[[File:T--Aix-Marseille--result7.jpeg|500px|right|thumb|Test of our biobrick proteins production using a SDS PAGE and coomassie blue staining. - : no induction ; + : induction with 0.02% arabinose at Abs(600nm)=0.4]]
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We investigated if the DesA, DesB, DesC and DesD proteins were well produced by our biobrick using SDS PAGE.  
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We investigated if the DesA, DesB, DesC and DesD proteins were well produced by our biobrick [http://parts.igem.org/Part:BBa_K1951011 BBa_K1951011] using SDS PAGE.  
  
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To do this we performed SDS PAGE and stained with comassie blue using cells containing this biobrick in plasmid backbone [https://2016.igem.org/Team:Aix-Marseille/Experiments/Protocols Find here the protocol] From an over night starter, cells were diluted and grown from Abs(600nm)=0.2 to Abs(600nm)=1.  
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To do this we performed SDS PAGE [https://2016.igem.org/Team:Aix-Marseille/Experiments/Protocols#Protocol_.2312_:_SDS_page_and_coomassie_blue (protocol)] and stained with coomassie blue using cells containing this biobrick. From an over night starter, cells were diluted and grown from Abs(600nm)=0.2 to Abs(600nm)=1.  
 
Then 1UOD of cells (1.67ml at 0.6OD) was collected and centrifuged at 5000g for 5min.  
 
Then 1UOD of cells (1.67ml at 0.6OD) was collected and centrifuged at 5000g for 5min.  
 
After removal of the supernatant, the cell pellet was resuspended in 50µL SDS-PAGE sample buffer.  
 
After removal of the supernatant, the cell pellet was resuspended in 50µL SDS-PAGE sample buffer.  
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We heated the mix at 95°C during 15min
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We heated the mix at 95°C during 15min.
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[https://2016.igem.org/Team:Aix-Marseille/Experiments/Protocols Find here the protocol]
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The sample was loaded onto a polyacrylamide gel and migrated during 50min at 180V.  
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The mixture was loaded onto a polyacrylamide gel and migrated during 50min at 180V.  
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Staining was done using coomassie blue.
 
Staining was done using coomassie blue.
  
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We compared the production of proteins in different backgrounds :  
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We compared the production of proteins in different background :  
  
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- <i>E. coli</i>  Tg1 strain without any plasmide (negative temoin)
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- <i>E. coli</i>  TG1 strain with pSB1C3 containing the RFP coding sequence (negative control)
  
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- <i>E. coli</i>  Tg1 strain with pSB1C3 containing the RFP coding sequence (negative temoin)
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- <i>E. coli</i>  TG1 strain with <i>des</i> operon ([http://parts.igem.org/Part:BBa_K1951011 BBa_K1951011]) before and after induction. (You can observe the production of the 4 proteins on the figure on the right; left : before induction, right : after induction)
  
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- <i>E. coli</i>  Tg1 strain complemented with our biobrick Bba_K1951011 before and after induction. (you can observe the production of the 4 proteins on the figure below on the left; right : before induction, left : after induction)
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Results showed the production of the 4 proteins DesA, DesB, DesC and DesD, all involved in the desferrioxamine B biosynthesis pathway. We can notice that a leak of the promoter pBAD, indeed we note the production of Des proteins without arabinose induction.
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Results showed the production of the 4 proteins DesA, DesB, DesC and DesD, all involved in the desferrioxamine B biosynthesis pathway.
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==Biosorption parts ==
 
==Biosorption parts ==
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[[File:T--Aix-Marseille--fliC.png|400px|right]]
 
[[File:T--Aix-Marseille--fliC.png|400px|right]]
 
This part is a composite part composed of 2 Biobricks :
 
This part is a composite part composed of 2 Biobricks :
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* [http://parts.igem.org/Part:BBa_K1951005 BBa_K1951005] : <div class="emph">Flagellin C
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* [http://parts.igem.org/Part:BBa_K1951005 BBa_K1951005] : Flagellin C
 
* [http://parts.igem.org/Part:BBa_K880005 BBa_K880005] : Strong promoter, strong RBS combination
 
* [http://parts.igem.org/Part:BBa_K880005 BBa_K880005] : Strong promoter, strong RBS combination
  
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Flagellin C (FliC) protein from ''Escherichia coli'' strain is the main protein constitutive of the flagelar filament and is involved to promote bacterial swimming. This sequence is conserved in many bacterial strains. It has been demonstrated that flagellin has the ability to adsorb precious metal such as platinum or gold.
 
Flagellin C (FliC) protein from ''Escherichia coli'' strain is the main protein constitutive of the flagelar filament and is involved to promote bacterial swimming. This sequence is conserved in many bacterial strains. It has been demonstrated that flagellin has the ability to adsorb precious metal such as platinum or gold.
 
We made a FliC mutant by transduction using phage P1 in a ''E. Coli'' W3110 strain. Then we have complemented the ''fliC'' mutant W3110 with [http://parts.igem.org/Part:BBa_K1951008 BBa_K1951008] and performed a swimming test for every background. The result has shown that swimming was recovered into the complemented ''fliC'' mutant W3110
 
We made a FliC mutant by transduction using phage P1 in a ''E. Coli'' W3110 strain. Then we have complemented the ''fliC'' mutant W3110 with [http://parts.igem.org/Part:BBa_K1951008 BBa_K1951008] and performed a swimming test for every background. The result has shown that swimming was recovered into the complemented ''fliC'' mutant W3110
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====Flagellin C swimming test====
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We constructed a fliC deletion mutant that is unable to swim, from the wild-type strain W3110. The ability to swim was restored to this mutant by our biobrick, as can be seen in the illustration here. This demonstrated that the protein can be correctly inserted into flagella and functions.
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[[File:T--Aix-Marseille--result3.jpeg|500px|center]]
  
 
====Part Assembly:====
 
====Part Assembly:====
 
The subparts were assembled using standard BioBrick Assembly.
 
The subparts were assembled using standard BioBrick Assembly.
  
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===[http://parts.igem.org/Part:BBa_K1941009 BBa_K1941009] : FliC <i> ''Desulfovibrio vulgaris'' </i> producer===
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===[http://parts.igem.org/Part:BBa_K1951009 BBa_K1941009] : FliC <i> ''Desulfovibrio vulgaris'' </i> producer===
  
 
====General====
 
====General====
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Flagellin C (FliC) protein from <i>Desulfovibrio vulgaris</i> strain is the main protein constitutive of the flagellum filament and is involved to promote bacterial swimming. This sequence is conserved in many bacterial strains as the capacity of swimming given by the flagellum confers a great selective advantage.
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Flagellin (FliC) protein from <i>Desulfovibrio vulgaris</i> strain is the main protein constitutive of the flagellum filament and is involved in bacterial swimming. This protein is conserved in many bacterial strains as the capacity of swimming given by the flagellum confers a great selective advantage.
  
 
[[File:T--Aix-Marseille--biosorption.jpeg|350px|right|]]
 
[[File:T--Aix-Marseille--biosorption.jpeg|350px|right|]]
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* There exists a specific innate immune receptor that recognizes flagellin, Toll-like receptor 5 (TLR5). <ref> Kathrani A. & al, 2012 http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0030117) </ref>
 
* There exists a specific innate immune receptor that recognizes flagellin, Toll-like receptor 5 (TLR5). <ref> Kathrani A. & al, 2012 http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0030117) </ref>
  
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===[http://parts.igem.org/Part:BBa_K19410010 BBa_K1941010] : CsgA <i> ''Escherichia coli'' </i> producer===
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===[http://parts.igem.org/Part:BBa_K1941010 BBa_K1941010] : CsgA <i> ''Escherichia coli'' </i> producer===
  
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CsgA is the major structural subunit of the curli fimbriae. Curli are coiled surface structures that assemble preferentially at growth temperatures below 37 degrees Celsius. Curli are the major proteinaceous component of a complex extracellular matrix produced by many ''Enterobacteriaceae''. Curli were first discovered in the late 1980s on ''Escherichia coli'' strains that caused bovine mastitis, and have since been implicated in many physiological and pathogenic processes of ''E. coli'' and ''Salmonella'' spp. Curli fibers are involved in adhesion to surfaces, cell aggregation, and biofilm formation. Curli also mediate host cell adhesion and invasion, and they are potent inducers of the host inflammatory response. The biobrick contains a strong promotor.
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CsgA is the major structural subunit of the curli fimbriae. Curli fibers are involved in adhesion to surfaces, cell aggregation, and biofilm formation<ref name="Curli">[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838481/ Michelle M. Barnhart and Matthew R. Chapman 2010, Annual Review of Microbiology]</ref>. Curli also mediate host cell adhesion and invasion, and they are potent inducers of the host inflammatory response. The biobrick contains a strong promotor.
  
 
<references/>
 
<references/>
  
 
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Latest revision as of 01:56, 20 October 2016