BBa_I760000BBa_I760000 Version 1 (Component)feruloyl-CoA hydratase
BBa_K1195004BBa_K1195004 Version 1 (Component)Cro from Lamda phage with shine delgarno added.
BBa_K987001BBa_K987001 Version 1 (Component)This is a composite part which has the function to invert the temperature activation by the part: BB
BBa_K944001BBa_K944001 Version 1 (Component)Transcriptional Regulator for Cyanide Inducible Promoter
BBa_M36291BBa_M36291 Version 1 (Component)Transcription terminator (apFAB391) (99% efficient)
BBa_K809721BBa_K809721 Version 1 (Component)DLD3 promoter + kozak + hoiln(lambda phage) + ADH1 terminator
BBa_M36257BBa_M36257 Version 1 (Component)Vitamin D2 Actuator
BBa_M36305BBa_M36305 Version 1 (Component)Transcription terminator pT-T7 from bacteriophage
BBa_I719003BBa_I719003 Version 1 (Component)feruloyl-CoA hydratase
van-1BBa_I750001 Version 1 (Component)feruloyl-CoA synthetase
BBa_K1320000BBa_K1320000 Version 1 (Component)Cd sensitive promoter with Ogr activator, PO promoter, and GFP
BBa_K327015BBa_K327015 Version 1 (Component)Lux activated, C1lam repressed switch
BBa_S03737BBa_S03737 Version 1 (Component)pLac-lox-RFP(reverse)-TT-lox-RBS-Tet (psB1A2)
BBa_I754000BBa_I754000 Version 1 (Component)Feruloyl CoA Hyratase for vanillin biosynthesis-ech
BBa_I741016BBa_I741016 Version 1 (Component)Reverse Total XylR Transcriptional Regulator Left Facing (I741011 reverse complement
BBa_K1968014BBa_K1968014 Version 1 (Component)Tcyc Phytobrick: cytochrome C gene transcriptional terminator from Saccharomyces cerevisiae
BBa_I730000BBa_I730000 Version 1 (Component)Feruloyl CoA hydratase for vanillin biosynthesis
BBa_I738002BBa_I738002 Version 1 (Component)feruloyl-CoA hydratase enzyme for biosynthesis of vanillin
BBa_I757001BBa_I757001 Version 1 (Component)Feruloy CoA hydratase 4 vanillin biosynthesis
BBa_S03736BBa_S03736 Version 1 (Component)pLac-lox-RBS-Tet (in pSB1A2)
BBa_I735000BBa_I735000 Version 1 (Component)ech gene coding sequence for feruoyl CoA hydratese
BBa_J58014BBa_J58014 Version 1 (Component)Promoter activated by OmpR-P with the reporter GFP
BBa_J58015BBa_J58015 Version 1 (Component)Mutated promoter activated by OmpR-P with the reporter GFP
BBa_K779116BBa_K779116 Version 1 (Component)Short RNA reporter bottom strand (with ROX fluorophore) MammoBlock
BBa_K2123115BBa_K2123115 Version 1 (Component)Universal promoter (Tac + JK26) for both growth phase with downstream mer operator + K081014
BBa_K2123114BBa_K2123114 Version 1 (Component)Stationary phase promoter in tandem (3 repetition) with downstream mer operator + RFP (K081014)
BBa_I728978BBa_I728978 Version 1 (Component)Promoter+RBS+CPX(Circularly-Permuted OmpX for Surface Display of Polypeptides)
BBa_K2123117BBa_K2123117 Version 1 (Component)Novel RFP device regulated by mercury: MerR (regulatory protein) + Stationary phase with mer operato
BBa_K2123116BBa_K2123116 Version 1 (Component)Universal promoter for both phase of growth in tandem with downstram mer operator + RFP (K081014)
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.