Parts

New parts submitted to the registry

Name	Function	Type	Part	State
<partinfo>BBa_K2278001</partinfo>	QS molecule generator	basic		working
<partinfo>BBa_K2278002</partinfo>	QS molecule generator	basic		not released
<partinfo>BBa_K2278011</partinfo>	Diacetyl generator	basic		issues
<partinfo>BBa_K2278021</partinfo>	D-NY15 AMP generator	basic		Working
<partinfo>BBa_K2278022</partinfo>	Leucrocin I AMP generator	basic		unsuccessful
<partinfo>BBa_K2278023</partinfo>	coT2 AMP generator	basic		unsuccessful

Existing Parts we have contributed to characterized

<partinfo>BBa_J04450</partinfo>: RFP coding device

BBa_J04450 was tested in the Vibrio harveyi background. BBa_J04450 biobrick was cloned in a broad host range plasmid (pBBR1MCS-4) and conjugated into Vibrio harveyi to demonstrate the production of RFP in this chassis.

To learn more: <partinfo>BBa_J04450</partinfo> and see our results results

<partinfo>BBa_K431009</partinfo>: glyceraldehyde 3-phosphate dehydrogenase promoter (pGAP)

The pGAP promoter was used as a constitutive promoter. The promoter was characterized by RT-qPCR using d-ny15 as reporter gene.

To learn more: <partinfo>BBa_K1800001</partinfo>, see our results

<partinfo>BBa_K1800001</partinfo>: alpha factor secretion signal

The α-factor sequence contains a kozak region and a signal sequence to secrete the produced peptides. The functionality of the signal factor was investigated by demonstrating that AMP are present in the supernatant through a toxicity assay.

To learn more: <partinfo>BBa_K180001</partinfo> and see our results

Parts used in our project but not submitted to the registry

Vh1: First part of Vibrio harveyi gene circuit

This part contains the first half of Vibrio harveyi quorum CqsS receptor which is able to detect CAI-1 family molecule. The receptor is driven by a constitutive promoter. This part has been designed due to IDT gBlocks synthesis requirements. The ordered gBlocks size should not exceed 3kb (the total length of the Vibrio harveyi circuit is 6929 bp). The XhoI restriction site naturally present in the gene was used reassemble the cqsS* sequence. Therefore, it was impossible to use pSB1C3 vector because of the presence of a XhoI restriction on the vector. This part was then subcloned in pBR322.

To learn more: see our design, and our results

Vh 2 : Second part of Vibrio harveyi gene circuit.

This part contains the second half of Vibrio harveyi quorum CqsS* receptor which is able to detect CAI-1 family molecule. It also contains the tetR repressor under the control of pQRR4 promoter. This part has been designed due to IDT gBlocks synthesis requirements. The ordered gBlocks size should not exceed 3kb (the total length of the Vibrio harveyi circuit is 6929 bp). The ApaI (not present on pSB1C3 vector) and XhoI restriction (naturally present in the cqsS* gene) were used to reassemble the synthetic circuit.

To learn more: see our design, and our results.

Vh 1+2: Vibrio harveyi invertor system

This part includes the complete cqsS* gene driven by a constitutive promoter and the tetracyclin repressor under the control of pQRR4 promoter which activation depends on CqsS* detection of quorum sensing inducers. Vh1+2 is the assembly of Vh2 in Vh1. This part was cloned in pBR322.

To learn more: see our design, and our results.

Vibrio harveyi complete gene circuit:

This part includes the complete cqsS gene driven by a constitutive promoter and the tetracycline repressor (TetR) under the control of pQRR4 promoter which activation depends on CqsS* recognition of quorum sensing inducers. The als gene, implied in the diacetyl production pathway, is under the control of pTet which can be repressed by TetR This part is the assemblage of Vh1, Vh2 and BBa_K2278011. It allows to produce diacetyl is produced upon detection of Vibrios CAI-1 quorum sensing molecule. The als gene is flanked with two restriction enzyme sites to clone a reporter gene such as rfp. The assembly of this part was not released due to technical and time issues.

To learn more: see our design, and our results

Pichia pastoris D-NY15 AMP generator:

This system allowed us to constitutively express BBa_K2278021 with a yeast promoter. This system was used to produce AMP at the highest concentration The pAOXI promoter ensures genome recombination in Pichia pastoris genome. The α-factor sequence contains a RBS and a signal sequence to secrete the produced peptides The restriction enzyme sites allow to extract individually each components of the plasmid. This construction was cloned in pPICZalpha yeast vector.

To learn more: see our<partinfo>BBa_K2278021</partinfo>,and our results

Pichia pastoris Leucrocin I AMP generator

This system allowed us to constitutively express the BBa_K2278022 with a yeast promoter. This system was used to produce AMP at the highest concentration The pAOXI promoter makes genome recombination easier in Pichia pastoris genome. The α-factor sequence contains a RBS and a signal sequence to secrete the produced peptides. The restriction enzyme sites allow to extract individually each components of the plasmid. This construction was cloned in pPICZalpha yeast vector.

To learn more: <partinfo>BBa_K2278022</partinfo>and see our results

Pichia pastoris cOT2 AMP generator:

This system allowed us to constitutively express BBa_K2278023 with a yeast promoter. This system was used to produce AMP at the highest concentration The pAOXI promoter makes genome recombination easier in Pichia pastoris genome. The α-factor sequence contains a RBS and a signal sequence to secrete the produced peptides. The restriction enzyme sites allow to extract individually each components of the plasmid. This construction was cloned in pPICZalpha yeast vector.

To learn more: <partinfo>BBa_K2278023</partinfo> and see our results.

Pichia pastoris Pichia pastoris complete module : Pichia pastoris complete module :

This system allowed us to constitutively express Odr10 receptor to detect diacetyl at any time. Odr10 pathway leads to the activation of pFUS promoter in case of diacetyl detection, hence the AMP are produced. The α-factor signal and coT2 gene are flanked with two restriction enzyme sites to clone a reporter gene such as RFP. This construction was cloned in pPICZalpha yeast vector.

To learn more: <partinfo>BBa_K2278023</partinfo>,results

Pichia pastoris Pichia pastoris complete Respond/Effector Module :

This system allowed us to constitutively express BBa_K2278023 with a yeast promoter. This system was used to produce AMP at the highest concentration The pGAP promoter makes genome recombination easier in Pichia pastoris genome. The α-factor sequence contains a RBS and a signal sequence to secrete the produced peptides The restriction enzyme sites allow to extract individually each components of the plasmid. This construction was cloned in pPICZalpha yeast vector.

To learn more: <partinfo>BBa_K2278023</partinfo>,design ----------------------------------------------------------

Parts used in our project but not submitted to the registry