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Team:NRP-UEA-Norwich/Project Parts
From 2014.igem.org
BioBrick Parts
New Parts
Bax (Bba_K1467203)
A reporter gene which, when transcribed, produces Bax protein that has a role in positively regulating cell apoptosis. The part has been made compatible with the GoldenGate MoClo Assembly Standard by removal of internal BsaI and BpiI recognition sequences.
Mannopine synthase (MAS) Promoter (Bba_K1467104)
A plant specific constitute promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites.
BS3 Promoter (Bba_K1467102)
A plant specific, TALE inducible promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The promoter becomes active in the presence of the TALE AvrBS3, driving the expression of coding regions.
PDF1.2 Promoter (Bba_K1467103)
A plant specific, Methyl Jasmonate inducible promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The promoter becomes active in the presence of methyl jasmonate (high methyl jasmonate levels indicate plant stress, often as a result of pathogen infection), driving the expression of coding regions.
AvrBS3 TALE (Bba_K1467205)
TAL (transcription activator-like) Effector that induces the BS3 promoter allowing safe testing of pathogen induced systems in the laboratory. The part has been made compatible with the GoldenGate MoClo Assembly Standard by removal of internal BsaI and BpiI recognition sequences.
Improved parts
RFP coding device - Golden Gate Module Flipper (Bba_K1467100)
A "GoldenGate Flipper" that can be used to convert Pro + 5U (promoter and 5' untranslated leader) modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. It consists of the RFP reporter (BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.
RFP coding device - Golden Gate Module Flipper (Bba_K1467200)
A "GoldenGate Flipper" that can be used to convert CDS1 modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. It consists of the RFP reporter (BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.
RFP coding device - Golden Gate Module Flipper (Bba_K1467300)
A "GoldenGate Flipper" that can be used to convert 3U + Ter (3' untranslated region and terminator) modules from the GoldenGate MoClo Assembly Standard into standard BioBricks. It consists of the RFP reporter (BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.
RFP coding device - Golden Gate Module Flipper (Bba_K1467400)
This part is a "GoldenGate Flipper" that can be used to assemble complete transcriptional units from GoldenGate MoClo Standard Parts producing a standard BioBrick. It consists of the RFP reporter (from BBa_J04450) flanked by an inverted pair of BsaI recognition sequences. GoldenGate MoClo parts can be flipped into BrioBrick parts in a one-pot, one-step, digestion-ligation GoldenGate cloning reaction.
35s Promoter (Bba_K1467101)
A plant specific constitutive promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The part was originally obtained from the Cauliflower Mosaic Virus and is intended for use as a constitutive promoter for gene expression experiments in plants. The part is an improvement on the part BBa_K414006.
AmilCP (Bba_K1467201)
A reporter chromoprotein which produces strong blue colour when expressed. A variation of the part BBa_K592009 that has been improved by removal of internal BsaI and BpiI recognition sequences- making it compatible with the GoldenGate MoClo Assembly Standard.
AmilGFP (Bba_K1467202)
A reporter chromoprotein which produces strong yellow colour when expressed. A variation of the part BBa_K592010 that has been improved by removal of internal BsaI and BpiI recognition sequences- making it compatible with the GoldenGate MoClo Assembly Standard.
GFP (Bba_K1467204)
A reporter protein that produces green fluorescence under UV light when expressed. A variation of the part BBa_E0040 that has been improved by removal of internal BsaI and BpiI recognition sequences- making it compatible with the GoldenGate MoClo Assembly Standard.
Plant specific parts
Mannopine synthase (MAS) Promoter (Bba_K1467104)
A plant specific constitute promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites.
BS3 Promoter (Bba_K1467102)
A plant specific, TALE inducible promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The promoter becomes active in the presence of the TALE AvrBS3, driving the expression of coding regions.
PDF1.2 Promoter (Bba_K1467103)
A plant specific, Methyl Jasmonate inducible promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The promoter becomes active in the presence of methyl jasmonate (high methyl jasmonate levels indicate plant stress, often as a result of pathogen infection), driving the expression of coding regions.
35s Promoter (Bba_K1467101)
A plant specific constitutive promoter that has been made GoldenGate compatible by removal of internal BSAI and Bpi1 sites. The part was originally obtained from the Cauliflower Mosaic Virus and is intended for use as a constitutive promoter for gene expression experiments in plants.
AvrBS3 TALE (Bba_K1467205)
TAL (transcription activator-like) Effector that induces the BS3 promoter allowing safe testing of pathogen induced systems in the laboratory. The part has been made compatible with the GoldenGate MoClo Assembly Standard by removal of internal BsaI and BpiI recognition sequences.
Compound parts
Our compound parts (e.g. Complete transcriptional units) had to be assembled in a plasmid backbone suitable for replication in Agrobacterium (as described on our System page), and so it was not possible to submit our compound parts to the Registry. Below is a list of the compound parts that we made and tested in plants. In collaboration with Valencia and Cambridge we are submitting an RCF for plants to allow future teams using plant chassis to do this.
| Promoter | Coding Sequence | Terminator | Infiltration Result |
|---|---|---|---|
| 35s (BBa_K1467101) | GFP (BBa_K1467204) | ocs (octopine synthase) | GFP expression under UV light |
| BS3 (BBa_K1467102) | GFP (BBa_K1467204) | ocs | No GFP expression under UV light |
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| Present a poster and talk at the iGEM Jamboree. | Poster and Presentation in final stages. | ||
| The description of each project must clearly attribute work done by the students and distinguish it from work done by others, including host labs, advisors, instructors, sponsors, professional website designers, artists, and commercial services. | Contributions from those outside of the team are stated on our Attributions page | ||
| Document at least one new standard BioBrick Part or Device used in your project/central to your project and submit this part to the iGEM Registry. |
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