Part:BBa_C0062:Experience

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User Reviews

UNIQfbeb1fa3f1642673-partinfo-00000000-QINU

•••• ETH Zurich 2014

Characterization of the promoter's sensitivity to 3OC6-HSL depending on LuxR concentration Background information Results Figure 1 Characterization of two-order crosstalk Background information Modeling crosstalk Each experimental data set was fitted to an Hill function using the Least Absolute Residual method. The fitting of the graphs was performed using the following equation : rFluo = the relative fluorescence (absolute measured fluorescence value over OD)[a.u.] a = basal expression rate [a.u.](“leakiness”) b = maximum expression rate [a.u.]("full induction") n = Hill coefficient (“cooperativity”) Km = Half-maximal effective concentration (“sensitivity”) [AHL]= AHL concentration [nM] Parameters of HillFunction for crosstalk with LuxR (with 95% confidence bounds) 3OC6-HSL 3OC12-HSL C4-HSL Plux a = 1043 (966.8, 1139) [a.u.] n = 0.89 (0.79, 0.99) Km = 0.1892 (0.1392, 0.2391) [nM] b = 2.129e4 (2.065e4, 2.192e4) [a.u.] a = 900.5 (882, 918.9) [a.u.] n = 1.049 (0.9976, 1.1) Km = 78.32 (73.18, 83.47) [nM] b = 1.866e4 (1.834e4, 1.899e4) [a.u.] No crosstalk Plas a = 3.996 (0, 9.185) [a.u.] n = 0.5198 (0.2879, 0.7517) Km = 382.3 (0, 1206) [nM] b = 261 (155.5, 366.5) [a.u.] No crosstalk No crosstalk Prhl No crosstalk No crosstalk No crosstalk First-order crosstalk First Level crosstalk: LuxR binds to different HSL and activates the promoter Plux Second Level crosstalk: LuxR binds to 3OC6-HSL, its natural HSL, and activates different promoter Second order crosstalk: Combination of both cross-talk levels Other regulatory proteins, like LuxR, bind to different HSL and activates the promoter. Results Table 1 Crosstalk matrix for the regulator LuxR (BBa_C0062) In all the measurements conducted to create this matrix the regulator LuxR was the basis and was induced in six different variations shown.

••••• SUN(Tsinghua)

Part was sequenced and functional. LuxR was used in our Portable Pathogen Detector.

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••••• wmholtz

Using this part, I have successfully constructed and tested a quorum sensing circuit in E. coli.

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••••• Youri

This part was used and tested as a subpart in K546000, K546001, K546002, K546003, K546005 and K546546. This part functioned in all cases.

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Kevin (iGEM Braunschweig 2013)

The plasmid pSB1C3 BBa_C0062 from the 2013 distribution Kit was transformed in E. coli XL1 BlueMRF. Sequencing with standard verification primer VF2 confirmed matching sequence of backbone DNA up to the EcoRI restriction site. The rest of the sequence (not shown) does not match the registry entry. 96 145 pSB1C3 LuxR (96) GAGGCAGAATTTCAGATAAAAAAAATCCTTAGCTTTCGCTAAGGATGATT C0062 VF2 (1) GAGGCAGAATTTCAGATAAAAAAAATCCTTAGCTTTCGCTAAGGATGATT 146 195 pSB1C3 LuxR (146) TCTGGAATTCGCGGCCGCTTCTAGAGATGAAAAACATAAATGCCGACGAC C0062 VF2 (51) TCTGGAATTCGACGCAA-TGGGTGCGCTGTCTACTAAATACAACGACACC 196 245 pSB1C3 LuxR (196) ACATACAGAATAATTAATAAAATTAAAGCTTGTAGAAGCAATAATGATAT C0062 VF2 (100) CCGGAAAAAGCCTCCCGTACTTACGACGCTCACCGTGACGGTTTCGTTAT 246 pSB1C3 LuxR (246) TAATCAATGC... C0062 VF2 (150) CGCTGGCGGC... A restriction assay (Figure 1) showed that the sequenced part has no XbaI restriction site following the EcoRI site indicating another part in front of BBa_C0062 with a length of at least 1000 bp.

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UNIQfbeb1fa3f1642673-partinfo-00000007-QINU