Team:ZJU-China/Part Collection
PARTS COLLECTION
Overview
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Parts for Oscillation
| Part Number | Part Type | Short Description | Long Description |
|---|---|---|---|
| BBa_K1886000 | Device | pluxR->luxS | luxS is controlled by pluxR promoter. luxS is a kind of DPD synthetase, which could produce DPD (4,5-dihydroxy 2,3-pentanedione) under the cooperation of Pfs enzyme. DPD exists widely in Gram-negative bacteria and Gram-positive bacteria as the signaling factor for quorum sensing, in order to complete the information transfer process within different kinds of bacteria. |
| BBa_K1886001 | Device | AHL single-cycled oscillation pluxL-luxR-pluxR-luxI(LAA tag)-pluxL-luxR-pluxR-aiiA(LAA tag) | This circuit is composed of the constitutive promoter -- broken Ptet and membrane protein cph8. Under dark conditions, protein cph8 could transfer its phosphoryl group to intracellular protein ompR (ompR is native protein carried by E.coli), and this process could be inhibited by 650-nm light. |
| BBa_K1886002 | Device | AHL,DPD double-cycled oscillation pluxL-luxR-pluxR-luxI(LAA tag)-pluxL-luxR-pluxR-aiiA(LAA tag)-luxpR-luxS | Two molecules of luxR binds with AHL (catalyzed by luxI), and this compound will promote the activity of pluxR. pluxR controls the expression of gene aiiA , encoding the enzyme which degrades AHLs. And all of these form an AHL single-cycled oscillation. |
Parts for Light Control
| Part Number | Part Type | Short Description | Long Description |
|---|---|---|---|
| BBa_K1886003 | Device | PcpcG2-sfGFP-ccaR | This circuit is composed of the inducible promoter cpcG2 and reporter gene and intracellular protein gene ccaR. ccaR could activate the cpcG2 promoter after being phosphorylated. cpcG2 could be activated by the phosphorylated ccaR protein, and induce the expression of reporter gene sfGFP. |
| BBa_K1886004 | Coding | ccaS | This circuit is composed of the constitutive promoter and photosensitive protein gene ccaS . ccaS protein is membrane protein. After being activated by 520-nm light, it could transfer its phosphoryl group to the intracellular protein ccaR,and this process could be inhibited by 650-nm light. |
| BBa_K1886005 | Device | Constitutive promoter-ho1-pcyA | This circuit is composed of the constitutive promoter, ho1 chromoprotein and pcya chormoprotein. They facilitate Membrane protein ccaS and cph8 to be activated by light of certain wavelength. |
| BBa_K1886006 | Device | broken Ptet-cph8 | This circuit is composed of the constitutive promoter -- broken Ptet and membrane protein cph8. Under dark conditions, protein cph8 could transfer its phosphoryl group to intracellular protein ompR (ompR is native protein carried by E.coli), and this process could be inhibited by 650-nm light. |
Parts for AND Logic Gate
| Part Number | Part Type | Short Description | Long Description |
|---|---|---|---|
| BBa_K1886007 | Device | AND GATE-input | This is the input part of AND GATE. After being induced by IPTG, plac promoter activates the expression of T7 RNA polymerase which contains two amber mutations (T7 ptag) . After being induced by L-arabinose, pBAD promoter activates the expression of a special tRNA (supD), which is used to identify amber mutation. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase. Therefore, only when the two inputs exist together, T7 RNA polymerase can be expressed, and then T7 promoter can be activated to express the downstream gene. |
| BBa_K1886008 | Device | AND GATE-output-1 | This is a report system to test the AND GATE made up of SupD tRNA coding gene and T7 polymerase with two amber mutations. T7 promoter is a very specific promoter which is transcribed only by specific T7 RNA polymerase. Following the PT7 promoter is the reporter gene GFP, Only when the two inputs are given, the GFP gene can be expressed. |
| BBa_K1886009 | Device | AND GATE-output-2 | This is a report system to test the AND GATE made up of SupD tRNA coding gene and T7 polymerase with two amber mutations. T7 promoter is a very specific promoter which is transcribed only by specific T7 RNA polymerase. Following the PT7 promoter is the reporter gene RFP, Only when the two inputs are given, the RFP gene can be expressed. |
| BBa_K1886010 | Device | AND GATE-input（AHL+green light) | The circuit to receive input signals is composed of AND GATE, quorum sensing promoter and light-controlled promoter. After being induced by AHL, pLuxR promoter activates the expression of T7 RNA polymerase (T7 ptag) which contains two amber mutations. After being induced by green light, PcpcG2 promoter activates the expression of a special tRNA (supD), which is used to identify amber mutation. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase. Therefore, when AHL and green light exist together, T7 RNA polymerase will be expressed, and then T7 promoter will be activated to express the downstream gene. |
| BBa_K1886011 | Device | AND GATE-input（AHL+red light) | The circuit to receive input signals is composed of AND GATE, quorum sensing promoter and light-controlled promoter. After being induced by AHL, pLuxR promoter activates the expression of T7 RNA polymerase (T7 ptag) which contains two amber mutations. The expression of a special tRNA (supD), which is used to identify amber mutation, is activated by Pλ promoter without the restraint of CL protein. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase, and red light could inhibit the produce of CL protein(for more information, see the part"PompC-NOT Gate"). Therefore, when AHL and red light exist together, T7 RNA polymerase will be expressed, and then T7 promoter will be activated to express the downstream gene. |
| BBa_K1886012 | Device | AND GATE-input（DPD+green light) | The circuit to receive input signals is composed of AND GATE, quorum sensing promoter and light-controlled promoter. After being induced by DPD, plsrA promoter activates the expression of T7 RNA polymerase which contains two amber mutations (T7ptag) . After being induced by green light, PcpcG2 promoter activates the expression of a special tRNA (supD), which is used to identify amber mutation. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase. Therefore, when DPD and green light exist together, T7 RNA polymerase will be expressed, and then T7 promoter will be activated to express the downstream gene. |
| BBa_K1886013 | Device | AND GATE-input（DPD+ red light) | The circuit to receive input signals is composed of AND GATE, quorum sensing promoter and light-controlled promoter. After being induced by DPD, plsrA promoter activates the expression of T7 RNA polymerase which contains two amber mutations(T7ptag) . The expression of a special tRNA (supD), which is used to identify amber mutation, is activated by Pλ promoter without the restraint of CL protein. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase, and red light could inhibit the produce of CL protein(for more information, see the part"PompC-NOT Gate"). Therefore, when DPD and green light exist together, T7 RNA polymerase will be expressed, and then T7 promoter will be activated to express the downstream gene. |
| BBa_K1886014 | Device | AND GATE-input（red light+IPTG） | The circuit to receive input signals is composed of AND GATE, plac promoter and light-controlled promoter. After being induced by IPTG, plac promoter activates the expression of T7 RNA polymerase (T7 ptag) which contains two amber mutations. The expression of a special tRNA (supD), which is used to identify amber mutation, is activated by Pλ promoter without the restraint of CL protein. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase, and red light could inhibit the produce of CL protein(for more information, see the part"PompC-NOT Gate"). Therefore, when IPTG and red light exist together, T7 RNA polymerase will be expressed, and then T7 promoter will be activated to express the downstream gene. |
| BBa_K1886015 | Device | AND GATE-input（green light+IPTG） | The circuit to receive input signals is composed of AND GATE, plac promoter and light-controlled promoter. After being induced by IPTG, plac promoter activates the expression of T7 RNA polymerase (T7 ptag) which contains two amber mutations. After being induced by green light, PcpcG2 promoter activates the expression of a special tRNA (supD), which is used to identify amber mutation. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase. Therefore, when IPTG and green light exist together, T7 RNA polymerase will be expressed, and then T7 promoter will be activated to express the downstream gene. |
| BBa_K1886016 | Device | AND GATE-input（IPTG+ara） | This is the input part of AND GATE. After being induced by L-arabinose, pbad promoter activates the expression of T7 RNA polymerase which contains two amber mutations (T7 ptag) . After being induced by IPTG, plac promoter activates the expression of a special tRNA (supD), which is used to identify amber mutation. In the wild-type E.coli, amber mutation will inhibit the translation of T7 RNA polymerase. Therefore, only when the two inputs exist together, T7 RNA polymerase can be expressed, and then T7 promoter can be activated to express the downstream gene. |
Contact Us
Room 413,Biology lab center, Zijingang Campus
Zhejiang University, YuHangTang Road NO.866
Hangzhou, China
iGEM ZJU-China 2016 Team
igem_zjuchina_2016@outlook.com
igem_zjuchina_2016@outlook.com
