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

(→‎BBa_K1951011 : Desferrioxamine B producer pathway Streptomyces coelicolor producer)
(→‎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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The purpose of this biobrick is to produce desferrioxamine B siderophore by a controled manner, for controlled potential toxicity.
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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.  
  
 
This biobrick was made from 6 parts:
 
This biobrick was made from 6 parts:
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* [http://parts.igem.org/Part:BBa_K1951003 BBa_K1951003]
 
* [http://parts.igem.org/Part:BBa_K1951003 BBa_K1951003]
  
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== What about siderophores? ==
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</div>
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[[File:T--Aix-Marseille--siderophore.jpeg|300px|right|thumb|Modele of the siderophore cycle in <i> E. coli </i>]]
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===General===
 
 
Siderophores are small, high-affinity iron chelating compounds secreted by microorganisms such as bacteria, fungi and grasses. Siderophores are amongst the strongest soluble Fe3+ binding agents known.
 
Siderophores are small, high-affinity iron chelating compounds secreted by microorganisms such as bacteria, fungi and grasses. Siderophores are amongst the strongest soluble Fe3+ binding agents known.
  
 
==== 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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* Desferrioxamine B may modulate expression and release of inflammatory mediators by specific cell types.
 
* Desferrioxamine B may modulate expression and release of inflammatory mediators by specific cell types.
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==== Pathway demonstration ====
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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 [http://parts.igem.org/Part:BBa_K1951011 BBa_K1951011] using SDS PAGE.
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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.
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Then 1UOD of cells (1.67ml at 0.6OD) was collected and centrifuged at 5000g for 5min.
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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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The sample was loaded onto a polyacrylamide gel and migrated during 50min at 180V.
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Staining was done using coomassie blue.
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We compared the production of proteins in different background :
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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 <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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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.
  
 
==Biosorption parts ==
 
==Biosorption parts ==
  
 
=== [http://parts.igem.org/Part:BBa_K1951008 BBa_K1951008] : FliC ''E. coli'' producer===
 
=== [http://parts.igem.org/Part:BBa_K1951008 BBa_K1951008] : FliC ''E. coli'' producer===
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<div class="emph">
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We also improved an existing BioBrick, Glasgow 2014 team's BioBrick ([http://parts.igem.org/Part:BBa_K1463604 BBa K1463604]), making our brick ([http://parts.igem.org/Part:BBa_K1951008 BBa K1951008]). This BioBrick is an improvement of the orignial BioBrick in three ways:
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* The codon usage has been optimized to ensure a strong expression in E.coli,
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* The RBS has no mutation so the flagellin is well expressed,
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* Our swimming test show that the swimming phenotype of the BioBick is improved thanks to our changes.
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All the functional tests and experiments, show this part is functional, are listed [https://2016.igem.org/Team:Aix-Marseille/Composite_Part#BBa_K1951008_:_FliC_E._coli_producer here].
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</div>
  
 
====Part Composition:====
 
====Part Composition:====
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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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====Part Assembly:====
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====Flagellin C swimming test====
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The subparts were assembled using standard BioBrick Assembly.
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====Biobrick amelioration====
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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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This biobrick has been improved from a previous one designed by Glasgow 2014 team. Please find the link of this biobrick below :
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http://parts.igem.org/Part:BBa_K1463601
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[[File:T--Aix-Marseille--result3.jpeg|500px|center]]
  
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Instead of [http://parts.igem.org/Part:BBa_J23106 BBa_J23106] and [http://parts.igem.org/Part:BBa_J23116 BBa_J23116], we used strong promoter, strong RBS combination for high expression levels of the flagellin. By the combination of  [http://parts.igem.org/Part:BBa_Bba_K880005 BBa_Bba_K880005] and  [http://parts.igem.org/Part:BBa_K1951005 BBa_K1951005], we made a high flagellin expression vector able to recover swimming.
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====Part Assembly:====
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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.
  
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[[File:T--Aix-Marseille--biosorption.jpeg|200px|right|thumb|Representative electron micrographs of nanoparticles produced by ''D.
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[[File:T--Aix-Marseille--biosorption.jpeg|350px|right|]]
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alaskensis'' G20.  Pd is found on the surface of the cell <ref> https://www.ncbi.nlm.nih.gov/pubmed/25686718 </ref> ]]
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====Metal Biosorption Capacity====  
 
====Metal Biosorption Capacity====  
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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