BBa_K640000BBa_K640000 Version 1 (Component)Codon optimized Luciferase for use in microalgae
BBa_K535006BBa_K535006 Version 1 (Component)PFOR -> D. africanus Pyruvate-Ferredoxin OxidoReductase
CFP optBBa_K566003 Version 1 (Component)CFP optimized for E. coli
Mnt optBBa_K566008 Version 1 (Component)Mnt repressor optimized for E. coli
PenI invBBa_K566010 Version 1 (Component)PenI repressor optimized for E. coli (inverted sequence)
BBa_K566007BBa_K566007 Version 1 (Component)PenI repressor optimized for E. coli
cI434 optBBa_K566011 Version 1 (Component)cI434 repressor from phage 434 optimized for E. coli cI (+LVA)
cI optBBa_K566012 Version 1 (Component)cI repressor from Lambda phage optimized for E. coli cI (+LVA)
RFP optBBa_K566013 Version 1 (Component)RFP optimized for E. coli (+LVA)
BBa_K615003BBa_K615003 Version 1 (Component)E. coli strain for TolC one-hybrid selection system
BBa_K640004BBa_K640004 Version 1 (Component)Device for conjugation of plasmids from E. coli to pseudomonas
BBa_K640005BBa_K640005 Version 1 (Component)Device for conjugating plasmids from E. coli to pseudomonas
Cph8 geneBBa_K566026 Version 1 (Component)Cph8 gene for red-photoreceptor (constitutive expression)
BBa_K615004BBa_K615004 Version 1 (Component)Zif268 binding site-His3-URA3 construct for one-hybrid selection
BBa_K823050BBa_K823050 Version 1 (Component)luc luciferase, codon optimized for Bacillus subtilis+ RBS+Term
BBa_J100092BBa_J100092 Version 1 (Component)Constitutive promoter for M1-162
BBa_J100098BBa_J100098 Version 1 (Component)Promoter for the argF gene
BBa_K748007BBa_K748007 Version 1 (Component)Biofilm formation device. yddV gene with the IPTG inducible promoter.
BBa_J72186BBa_J72186 Version 1 (Component)TrimR, pir expression cassette for genomic integration
BBa_J72209BBa_J72209 Version 1 (Component)kanamycin + ampicillin resistant p15A vector for 2ab assembly
BBa_K812000BBa_K812000 Version 1 (Component)Biobricked pCS2+ plasmid for frogs and chicken
BBa_K812001BBa_K812001 Version 1 (Component)Biobricked pSC2+ plasmid with pElastase promoter for frog use
BBa_K812012BBa_K812012 Version 1 (Component)OsTirI Ubiquitinase E3 for AID tagged protein degradation in the presence of auxin
BBa_K812013BBa_K812013 Version 1 (Component)GFP-AID OsTirI polysistronic system for auxin detection in tadpole
BBa_K812014BBa_K812014 Version 1 (Component)Auxin production device for expression in tadpole
LipABBa_K836000 Version 1 (Component)lipA from B. cepacia (codon usage optimized for E. coli)
DGATBBa_K836001 Version 1 (Component)O-acyltransferase WSD from Acinetobacter sp. (codon usage optimized for R. opacus)
DGATBBa_K836002 Version 1 (Component)O-acyltransferase WSD from Acinetobacter sp. (codon usage optimized for R. opacus) as used
lipABBa_K836003 Version 1 (Component)lipA from B. cepacia (codon usage optimized for E. coli)
gpSBBa_K836004 Version 1 (Component)Lysis inhibitor from Enterobacteria phage lambda (codon usage optimized for R. opacus)
BBa_K836005BBa_K836005 Version 1 (Component)Lysozyme from Rhodococcus phage RER2 (codon usage optimized for R, opacus)
gpSBBa_K836006 Version 1 (Component)Lysis protein S from Enterobacteria phage lambda (codon usage optimized for R. opacus)
nitRBBa_K836007 Version 1 (Component)Nitrilase regulator from R. rhodochrous (codon usage optimized for R. opacus)
SEGASEGA_collection Version 1 (Collection)In the Standardized Genome Architecture (SEGA), genomic integration of DNA fragments is enabled by λ-Red recombineering and so-called landing pads that are a common concept in synthetic biology and typically contain features that i) enable insertion of additional genetic elements and ii) provide well-characterized functional parts such as promoters and genes, and iii) provides insulation against genome context-dependent effects. The SEGA landing pads allow for reusable homology regions and time-efficient construction of parallel genetic designs with a minimal number of reagents and handling steps. SEGA bricks, typically synthetic DNA or PCR fragments, are integrated on the genome simply by combining the two reagents (i.e. competent cells and DNA), followed by incubation steps, and successful recombinants are identified by visual inspection on agar plates. The design of the SEGA standard was heavily influenced by the Standard European Vector Architecture (SEVA). SEGA landing pads typically hosts two major genetic “control elements” that influence gene expression on the transcriptional (C1), and translational (C2) level. Furthermore, landing pads contain gadgets such as selection and counterselection markers.
SBOLDesigner CAD ToolSBOLDesigner Version 3.1 (Agent)SBOLDesigner is a simple, biologist-friendly CAD software tool for creating and manipulating the sequences of genetic constructs using the Synthetic Biology Open Language (SBOL) 2 data model. Throughout the design process, SBOL Visual symbols, a system of schematic glyphs, provide standardized visualizations of individual parts. SBOLDesigner completes a workflow for users of genetic design automation tools. It combines a simple user interface with the power of the SBOL standard and serves as a launchpad for more detailed designs involving simulations and experiments. Some new features in SBOLDesigner are the ability to add variant collections to combinatorial derivations, enumerating those collections, and the ability to view sequence features hierarchically. There are also some small changes to the way that preferences work in regards to saving a design with incomplete sequences.
Intein_assisted_Bisection_MappingIntein_assisted_Bisection_Mapping_collection Version 1 (Collection)Split inteins are powerful tools for seamless ligation of synthetic split proteins. Yet, their use remains limited because the already intricate split site identification problem is often complicated by the requirement of extein junction sequences. To address this, we augmented a mini-Mu transposon-based screening approach and devised the intein-assisted bisection mapping (IBM) method. IBM robustly revealed clusters of split sites on five proteins, converting them into AND or NAND logic gates. We further showed that the use of inteins expands functional sequence space for splitting a protein. We also demonstrated the utility of our approach over rational inference of split sites from secondary structure alignment of homologous proteins. Furthermore, the intein inserted at an identified site could be engineered by the transposon again to become partially chemically inducible, and to some extent enabled post-translational tuning on host protein function. Our work offers a generalizable and systematic route towards creating split protein-intein fusions and conditional inteins for protein activity control.
Cello E. Coli PartsEco1C1G1T1_collection Version 1 (Collection)These are the Cello parts for E. Coli circuits
rTT+pRBBa_K093003 Version 1 (Component)Convergent Promoter System: Forward Module: rTT+lambda pR
Q04510+RFPBBa_K131018 Version 1 (Component)Intermediate for the Response circuit
BBa_K101016BBa_K101016 Version 1 (Component)Dually repressed promoter with sites for TetR and P22MNT binding
BBa_K125810BBa_K125810 Version 1 (Component)slr2016 signal sequence + GFP fusion for secretion of GFP
OriTRBBa_J01003 Version 1 (Component)OriT-R (Origin of transfer for the R-plasmid nic region)
pBSEP1BBa_K090401 Version 1 (Component)Gram-positive Shuttle Vector for Episomal Expression
BBa_K090403BBa_K090403 Version 1 (Component)Gram-positive Shuttle Vector for Chromosomal Integration
BBa_C0361BBa_C0361 Version 1 (Component)luxI (+LVA) - Codon-optimised for E.coli
BBa_C0378BBa_C0378 Version 1 (Component)lasI (+LVA) - Codon-optimised for E.coli
BBa_C0362BBa_C0362 Version 1 (Component)luxR - codon-optimised for E.coli
BBa_J24817BBa_J24817 Version 1 (Component)dLaRAP firefly luciferase reporter device for promoters
BBa_J24818BBa_J24818 Version 1 (Component)dLaRAP firefly luciferase reporter device for promoters
BBa_J24819BBa_J24819 Version 1 (Component)dLaRAP firefly luciferase reporter device for promoters with J23101