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Team:Toulouse/Result/parts/Submitted parts
From 2014.igem.org
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| - | <div class="technology"><a href="http://parts.igem.org/Part:BBa_K1364021">BBa_K1364021</a>: Integrative plasmid for <i>Bacillus subtilis</i></div> | + | <div class="technology"><a href="http://parts.igem.org/Part:BBa_K1364021">BBa_K1364021</a>: Integrative plasmid for <i>Bacillus subtilis</i> (pSBbs4E)</div> |
<div class="thelanguage"> | <div class="thelanguage"> | ||
| - | <p class="texte"> | + | <p class="texte">This part is an empty backbone vector for the usage in Bacillus subtilis. It integrates in the thrC locus and can be selected with Erythromycin cassette. It has a Ampicillin resistance for cloning in E.coli. |
</p> | </p> | ||
<p class="title4">Design</p> | <p class="title4">Design</p> | ||
| - | <p class="texte"> | + | <p class="texte">We digested pKL190 plasmid and PCR products of BBa_J04450 with BamHI and EcoRI. We proceded to ligation.</p> |
<p class="title4">Type</p> | <p class="title4">Type</p> | ||
| - | <p class="texte"> | + | <p class="texte">Backbone</p> |
<p class="title4">Tests</p> | <p class="title4">Tests</p> | ||
| - | <p class="texte">This part was | + | <p class="texte">This part was tested by transforming <i>B. subtilis</i>. Clones obtained were Auxotrophic of Threonine and resistant to Erythromycin.</p> |
<p class="title4">References</p> | <p class="title4">References</p> | ||
| - | <p class="texte"> | + | <p class="texte"> |
| - | + | R. Bernard, K.A. Marquis, and D.Z. Rudner. <b>Nucleoid occlusion prevents cell division during replication fork arrest in Bacillus subtilis</b>Mol Microbiol. Nov 2010; 78(4): 866–882.</p> | |
<p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 13); return false">Collapse</a></p> | <p style="text-align:right;font-size:1.3em;"><a href="#" class="collapseLink" onClick="ddaccordion.collapseone('technology', 13); return false">Collapse</a></p> | ||
</div> | </div> | ||
Revision as of 21:58, 16 October 2014
Parts
What did we send to the Registry?
Results > Parts
Submitted parts
We have deposed 16 new BioBrick parts to the Registry.
All of them were cloned into the standard plasmid pSB1C3, tested and sequenced.
I. Chemotaxis
This part is designed to enable a N-acetylglucosamine based chemotaxis in Bacillus subtilis.
Design
The encoded protein is a chimera of two proteins:
- the methyl accepting Chemotaxis protein (McpA from Bacillus subtilis which is required for taxis towards glucose.
- the N-acetylglucosamine regulated methyl-accepting chemotaxis protein from Vibrio cholerae (VCD).
The chimeric protein contains the intracellular domains of McpA from Bacillus subtilis to enable the transduction of the signal:
these domains correspond to the amino acids 1-37 and 282-610.
The extracellular domain of VCD is inserted between the intracellular regions of McpA
to sense N-acetylglucosamine and corresponds to the amino acids 31-310.
Type
Translation unit
Tests
This part is not tested yet.
References
Uniprot:
- McpA
- N-acetylglucosamine regulated methyl-accepting chemotaxis protein
This part is designed to enable a N-acetylglucosamine based chemotaxis in Bacillus subtilis.
Design
This expression cassette is designed for the expression of an antifungal peptide, D4E1 and for its secretion in Bacillus subtilis. It is composed of the strong, constitutive promotor of B. subtilis Pveg (K823003), strong RBS for B. subtilis (K780002), the open reading frame of D4E1 and a double terminator (B0015)
Type
Generator
Tests
This part was not tested yet.
References
Uniprot:
- McpA
- N-acetylglucosamine regulated methyl-accepting chemotaxis protein
II. Binding
This part is designed to enable the binding of Bacillus subtilis to the fungi wall made of chitin.
Design
This part is composed of a Cell Wall Binding (CWB) sequence
and a Chitin Binding Domain (CBD) linked with a 6 amino acids linker.
The CWB domain has been extracted from LytC (BBa_K316030) of the iGEM 2010 Imperial College team.
The CBD is composed of the Domain 4 of the GbpA protein of Vibrio cholerae,
a protein reported to mediate bacterial attachment to chitin.
It has been shown that the Domain 4 was essential to bind chitin.
Type
Generator
Tests
This part was tested with chitin beads. (See Binding module)
References
- Wong E, Vaaje-Kolstad G, Ghosh A, Hurtado-Guerrero R, Konarev PV, et al. (2012)
- The Vibrio cholerae Colonization Factor GbpA Possesses a Modular Structure that Governs Binding to Different Host Surfaces. PLoS Pathog 8(1): e1002373. doi:10.1371/journal.ppat.1002373
III. Fungicides
GAFP-1
The Gastrodia anti-fungal protein(GAFP-1), also known as gastrodianin, is a mannose and chitin binding lectin originating from the Asiatic orchid Gastrodia elata, a traditional Chinese medicinal herb cultured for thousands of years. GAFP-1 is composed of 15 amino acids LDSLSFSYNNFEEDD and is able to inhibit the growth of multiples species of plant pathogenic fungi.
Design
This part is composed of a Strong RBS (K780002) and the open reading frame of the Gastrodia anti-fungal protein 1 (GAFP-1) optimized for its expression and its secretion in Bacillus subtilis. The codon optimization was made thanks to the DNA 2.0 software program.
Type
Translational unit
Tests
This part was tested on the fungi Trichoderma reesei (See Fungicides module)
References
- Wong E, Vaaje-Kolstad G, Ghosh A, Hurtado-Guerrero R, Konarev PV, et al. (2012)
- The Vibrio cholerae Colonization Factor GbpA Possesses a Modular Structure that Governs Binding to Different Host Surfaces. PLoS Pathog 8(1): e1002373. doi:10.1371/journal.ppat.1002373
The Gastrodia anti-fungal protein(GAFP-1), also known as gastrodianin, is a mannose and chitin binding lectin originating from the Asiatic orchid Gastrodia elata, a traditional Chinese medicinal herb cultured for thousands of years. GAFP-1 is composed of 15 amino acids LDSLSFSYNNFEEDD and is able to inhibit the growth of multiples species of plant pathogenic fungi.
Design
This part is composed of a Strong RBS (K780002), the open reading frame of the Gastrodia anti-fungal protein 1 (GAFP-1) and a double terminator B0015. optimized for its expression and its secretion in Bacillus subtilis. The codon optimization was made thanks to the DNA 2.0 software program.
Type
Composite part
Tests
This part was tested on the fungi Trichoderma reesei (See Fungicides module)
References
- Wong E, Vaaje-Kolstad G, Ghosh A, Hurtado-Guerrero R, Konarev PV, et al. (2012)
- The Vibrio cholerae Colonization Factor GbpA Possesses a Modular Structure that Governs Binding to Different Host Surfaces. PLoS Pathog 8(1): e1002373. doi:10.1371/journal.ppat.1002373
This expression cassette is designed for the expression and secretion of the Gastrodia anti-fungal protein(GAFP-1), also known as gastrodianin. GAFP-1 is a mannose and chitin binding lectin originating from the Asiatic orchid Gastrodia elata, a traditional Chinese medicinal herb cultured for thousands of years. GAFP-1 is composed of 15 amino acids LDSLSFSYNNFEEDD and is able to inhibit the growth of multiples species of plant pathogenic fungi.
Design
This part is composed of the strong, constitutive promoter of Bacillus subtilis Pveg (K823003), strong RBS (K780002), the open reading frame of the Gastrodia anti-fungal protein 1 (GAFP-1) and a double terminator (B0015). optimized for its expression and its secretion in Bacillus subtilis. The codon optimization was made thanks to the DNA 2.0 software program.
Type
Generator
Tests
This part was tested on the fungi Trichoderma reesei (See Fungicides module)
References
- Wong E, Vaaje-Kolstad G, Ghosh A, Hurtado-Guerrero R, Konarev PV, et al. (2012)
- The Vibrio cholerae Colonization Factor GbpA Possesses a Modular Structure that Governs Binding to Different Host Surfaces. PLoS Pathog 8(1): e1002373. doi:10.1371/journal.ppat.1002373
D4E1
D4E1 is a linear synthetic peptide of 17 amino acids which has shown to have antifungal activities by complexing with a sterol present in conodial wall of a varety of fungi.
Design
This part is composed of a Strong RBS (K780002), the open reading frame of D4E1 and a Double terminator (B0015) optimized for its expression and its secretion in Bacillus subtilis. This part was optimized for the expression and its secretion in Bacillus subtilis thanks to the DNA 2.0 software program.
Type
Translational unit
Tests
This part was tested on the fungi Trichoderma reesei (See Fungicides module)
References
- De Lucca AJ, Bland JM, Grimm C, Jacks TJ, Cary JW, Jaynes JM, Cleveland TE, Walsh TJ. Fungicidal properties, sterol binding, and proteolytic resistance of the synthetic peptide D4E1.
- Can J Microbiol. 1998 Jun;44(6):514-20.
D4E1 is a linear synthetic peptide of 17 amino acids which has shown to have antifungal activities by complexing with a sterol present in conodial wall of a varety of fungi.
Design
This part is composed of the strong, constitutive promotor of B. subtilis Pveg (K823003), a strong RBS (K780002), the open reading frame of D4E1 and a double terminator (B0015). This part was optimized for the expression and its secretion in Bacillus subtilis thanks to the DNA 2.0 software program.
Type
Translational unit
Tests
This part was tested on the fungi Trichoderma reesei (See Fungicides module)
References
- De Lucca AJ, Bland JM, Grimm C, Jacks TJ, Cary JW, Jaynes JM, Cleveland TE, Walsh TJ. Fungicidal properties, sterol binding, and proteolytic resistance of the synthetic peptide D4E1.
- Can J Microbiol. 1998 Jun;44(6):514-20.
EcAMP-1
EcAMP-1 is an antimicrobial peptide of 37 amino acids
originated from the specie Echinochloa crus-galli,
a type of wild grass.
This peptide has a particular structure : it is helical because of two disulfide bonds.
EcAMP-1 has shown to have antifungal activities. Its mode of action may be the prevention of hyphae elongation.
This part was added to the Registry by the iGEM Utah State team in 2013.
Design
This part is composed of the constitutive promoter Pveg and
strong RBS for B. subtilis
(K733013) and
the open reading frame of EcAMP-1.
The EcAMP-1 part was codon optimized for E. coli by the iGEM Utah State team
and thanks to the Life Technologies GeneArt software program.
Type
Generator
Tests
This part is not tested yet.
References
Svetlana B. Nolde, Alexander A. Vassilevski, Eugene A. Rogozhin, Nikolay A. Barinov, Tamara A. Balashova, Olga V. Samsonova, Yuri V. Baranov, Alexey S. Arseniev and Eugene V. Grishin. Disulfide-stabilized Helical Hairpin Structure and Activity of a Novel Antifungal Peptide EcAMP1 from Seeds of Barnyard Grass (Echinochloa crus-galli). The journal of Biological Chemistry. 2011, Vol. 286, 25145–25153
EcAMP-1 is an antimicrobial peptide of 37 amino acids
originated from the specie Echinochloa crus-galli,
a type of wild grass.
This peptide has a particular structure : it is helical because of two disulfide bonds.
EcAMP-1 has shown to have antifungal activities. Its mode of action may be the prevention of hyphae elongation.
This part was added to the Registry by the iGEM Utah State team in 2013.
Design
This part is composed of the constitutive promoter Pveg and
strong RBS for B. subtilis
(K733013),
the open reading frame of EcAMP-1 and
a double terminator (B0015).
The EcAMP-1 part was codon optimized for E. coli by the iGEM Utah State team
and thanks to the Life Technologies GeneArt software program.
Type
Generator
Tests
This part is not tested yet.
References
Svetlana B. Nolde, Alexander A. Vassilevski, Eugene A. Rogozhin, Nikolay A. Barinov, Tamara A. Balashova, Olga V. Samsonova, Yuri V. Baranov, Alexey S. Arseniev and Eugene V. Grishin. Disulfide-stabilized Helical Hairpin Structure and Activity of a Novel Antifungal Peptide EcAMP1 from Seeds of Barnyard Grass (Echinochloa crus-galli). The journal of Biological Chemistry. 2011, Vol. 286, 25145–25153
EcAMP-1 is an antimicrobial peptide of 37 amino acids
originated from the specie Echinochloa crus-galli,
a type of wild grass.
This peptide has a particular structure : it is helical because of two disulfide bonds.
EcAMP-1 has shown to have antifungal activities. Its mode of action may be the prevention of hyphae elongation.
This part was added to the Registry by the iGEM Utah State team in 2013.
We observed the presence of the stop codon in the suffix. When we have digested this Biobrick, it disappeared. So we added this codon in upstream of the suffix and now, we can reuse this Biobrick.
Design
This part is composed of the constitutive promoter Pveg and
strong RBS for B. subtilis
(K733013),
the revised open reading frame of EcAMP-1 (with a stop codon) and
a double terminator (B0015).
The EcAMP-1 part was codon optimized for E. coli by the iGEM Utah State team
and thanks to the Life Technologies GeneArt software program.
Type
Composite
Tests
This part was not tested yet
References
Svetlana B. Nolde, Alexander A. Vassilevski, Eugene A. Rogozhin, Nikolay A. Barinov, Tamara A. Balashova, Olga V. Samsonova, Yuri V. Baranov, Alexey S. Arseniev and Eugene V. Grishin. Disulfide-stabilized Helical Hairpin Structure and Activity of a Novel Antifungal Peptide EcAMP1 from Seeds of Barnyard Grass (Echinochloa crus-galli). The journal of Biological Chemistry. 2011, Vol. 286, 25145–25153
Fungicide operons
Design
This part is designed for the co-expression of two different peptides with anti-fungal activities : D4E1 and GAFP-1. It is composed of the strong, constitutive promotor of B. subtilis Pveg (K823003) and the translation unit with GAFP-1 and D4E1 (BBa_K1364012).
Type
Generator
Tests
This part was tested on the fungi Trichoderma reesei (See Fungicides module)
References
See BBa_K1364002 and BBa_K1364003.Basic tools
This part is designed to enable the expression of a Red Fluorescent Protein in Bacillus subtilis under the control of a constitutive promotor Pveg. This construction has been checked by sequencing and has shown to work also in E. coli
Design
This part is composed of a constitutive promotor Pveg (K823003), spoVG RBS (K143021), the coding sequence of the RFP (E1010) and a double terminator (B0015)
Type
Reporter
Tests
This part was tested in both E.coli and B. subtilis. The sequences was verified by sequencing.
This part is designed to enable the expression of a Red Fluorescent Protein in Bacillus subtilis under the control of a constitutive promotor PlepA. This construction has been checked by sequencing and has shown to work also in E. coli
Design
This part is composed of a constitutive promotor PlepA (K823002), spoVG RBS (K143021), the coding sequence of the RFP (E1010) and a double terminator (B0015)
Type
Reporter
Tests
This part was tested in both E.coli and B. subtilis. The sequences was verified by sequencing.
PlepA is a constitutive promotor in Bacillus subtilis (BBa_K823002) coupled with a RBS spoVG (BBa_K143021). To get the highest level of translation from this Promoter-RBS combination it must be connected to a coding region preceded by a coding region prefix. A standard prefix will increase the distance between the RBS and the start codon, reducing translational efficiency. This construction is also working with E. coli and has been verified by sequencing.
Type
Composite
Tests
This part was checked by sequencing
This part is an empty backbone vector for the usage in Bacillus subtilis. It integrates in the thrC locus and can be selected with Erythromycin cassette. It has a Ampicillin resistance for cloning in E.coli.
Design
We digested pKL190 plasmid and PCR products of BBa_J04450 with BamHI and EcoRI. We proceded to ligation.
Type
Backbone
Tests
This part was tested by transforming B. subtilis. Clones obtained were Auxotrophic of Threonine and resistant to Erythromycin.
References
R. Bernard, K.A. Marquis, and D.Z. Rudner. Nucleoid occlusion prevents cell division during replication fork arrest in Bacillus subtilisMol Microbiol. Nov 2010; 78(4): 866–882.
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