Team:NYMU-Taipei/Project/Inhibition/Sensor

From 2013.igem.org

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=Sensing ''Nosema ceranae''=
=='''Introduction'''==
=='''Introduction'''==
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*After ''Nosema ceranae'' enter midgut of bee, we have to make ''E. coli'' sense this pathogen. ''E. coli'' with ROS-sensing promoters will response to Reactive Oxygen Species (ROS), which is produced by infected midgut cells. The following circuit behind ROS-sensing promoters will be turned on and fight against ''N.cerenae''.
+
After ''Nosema ceranae'' enters the midgut of bees, we have to make ''E. coli'' sense this pathogen. ''E. coli'' with ROS-sensing promoters will respond to Reactive Oxygen Species (ROS) produced by infected midgut cells. The following circuit behind ROS-sensing promoters will be turned on and fight against ''N. cerenae''.
-
*As for circuit design, we add a new part with a constitutive promoter [http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102] and a transcription factor(OxyR or SoxR) which can activate ROS-sensing promoters, making the quantity of inactivated transcription factors more in  ''E. coli'', in order to enhance the strength of promoters.
+
 
-
*We improve the function of a BioBrick Part: AhpC([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001])designed by [https://2010.igem.org/Team:KIT-Kyoto/Parts 2010 KIT-Tokyo team].
+
For the circuit design, we added a new composition part: [http://parts.igem.org/Part:BBa_K1104250 device:BBa_K1104250] consisting of a constitutive promoter [http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102] and a transcription factor: OxyR ([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]), which can activate ROS-sensing promoters, increasing the quantity of inactivated transcription factors in order to enhance the response of promoters. Additionally, RBS ([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034]) and double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]. Actually, the addition of [http://parts.igem.org/Part:BBa_K1104250 device:BBa_K1104250] remarkably enhanced the strength of promoter AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204]) in our experiment results.
 +
 
 +
We improved the function of a BioBrick Part: ahpC promoter ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) originally designed by [https://2010.igem.org/Team:KIT-Kyoto/Parts 2010 KIT-Tokyo team].
=='''Background''' ==
=='''Background''' ==
===''Nosema Ceranae'' Induces Oxidative Stress in the Midgut.===
===''Nosema Ceranae'' Induces Oxidative Stress in the Midgut.===
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ROS(Reactive Oxygen Species)are efficient antimicrobial molecules. Genes involved in oxidation-reduction were significantly overrepresented in the gene set upregulated upon spore infection. In response to the infection, the increase of oxidoreduction in the midgut epithelia of bees infected by ''N. ceranae'' would therefore indicate an enhanced generation of ROS. It is suggested that ROS production is a general immune response in bees' midgut to microorganism infection. There are promoters in the genome of ''E. coli'' that can be regulated by ROS. After ''Nosema ceranae'' enter midgut of bee, the regulator of promoters will be activated by ROS, trigger the following circuit fighting against ''Nosema ceranae''.
+
ROS (Reactive Oxygen Species) are efficient antimicrobial molecules. Genes involved in oxidation-reduction were significantly overrepresented in the gene set upregulated upon spore infection. In response to the infection, the increase of oxidoreduction in the midgut epithelia of bees infected by ''N. ceranae'' would therefore indicate an enhanced generation of ROS. It is suggested that ROS production is a general immune response in bees' midgut to microorganism infection. There are promoters in the genome of ''E. coli'' that can be regulated by ROS. After ''Nosema ceranae'' enter midgut of bee, the regulator of promoters will be activated by ROS, trigger the following circuit fighting against ''Nosema ceranae''.
===Literature Study of ROS-induced Promoters===
===Literature Study of ROS-induced Promoters===
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[[File: NYMU_phemH.png|frame|center|''' Figure. 1'''<br>Schematic drawing of the HemH in ''E. coli'' K12 (taken from [http://BioCyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU141 The BioCyc collection of Pathway/Genome Databases (PGDBs)]]][[File: NYMU_ptrxC.png|frame|center|''' Figure. 2'''<br>Schematic drawing of the CaiF regulon in ''E. coli'' K12 (taken from [http://BioCyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU141 The BioCyc collection of Pathway/Genome Databases (PGDBs)]]
+
Once ''N.cerenae'' infects the midgut of bees, midgut cells of bees will secrete Reactive Oxygen Species (ROS). ROS have been shown to be toxic but also function as signalling molecules which can transcriptionally activate transcription factors: OxyR ([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]). We focus on ROS-induced promoters regulated by OxyR.
 +
[[File: NYMU_OxyRactive.png|frame|1000px|center|'''OxyR Activation'''<br>OxyR regulates the H<sub>2</sub>O<sub>2</sub> response of <br />''E. coli''. H<sub>2</sub>O<sub>2</sub> oxidizes OxyR Cys199 to an R-SOH that reacts with Cys208 in an intramolecular disulphide bond.]]
 +
Activated transcription factor, OxyR, then binds to TFBS of promoters (sensor), as the pictures shown below:
 +
{|
 +
|[[File: NYMU_hemh.png|thumb|400px|center|'''[http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-12951&orgids=ECOLI HemHp]([http://parts.igem.org/Part:BBa_K1104202 K1104202])''']]
 +
|[[File: NYMU_trxc.png|thumb|490px|center|'''[http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-3104&detail-level=1 TrxCp]([http://parts.igem.org/Part:BBa_K1104201 K1104201])''']]
 +
|}
-
Once ''N.cerenae'' infect the midgut of bee, midgut cells of bee will secret Reactive oxygen species (ROS). ROS have been shown to be toxic but also function as signalling molecules which can transcriptionally activate transcription factors: OxyR and SoxR. We focus on ROS-induced promoters regulated by either OxyR or SoxR.
+
We did a study about promoters that can sense OxyR. Several promoters on the part registry can be induced by ROS: OxyR-activated promoters such as [http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001](ahpC)and [http://parts.igem.org/Part:BBa_K362005 Part:BBa_K362005](sufA)were designed and used as favorite parts by [https://2010.igem.org/Team:KIT-Kyoto/Parts 2010 KIT-Tokyo team]. They can be controlled by OxyR.
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[[File: NYMU_OxyRactive.png|frame|1000px|center|'''OxyR Activation'''<br>The OxyR transcription factor regulates the H<sub>2</sub>O<sub>2</sub> response of ''E. coli''. H<sub>2</sub>O<sub>2</sub> oxidizes OxyR Cys199 to an R-SOH that reacts with Cys208 in an intramolecular disulphide bond.]]
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[[File: NYMU_SoxRactive.png|frame|1000px|center|'''SoxR Activation'''<br>Oxidation of the SoxR [2Fe–2S] cluster by O2- causes a change in SoxR conformation, which alters the SoxR-bound operator DNA structure and results in gene activation.]]
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Activated transcription factors, such as OxyR and SoxR, then bind to TFBS of promoters(sensor), as figures show below.
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[[File: NYMU_hemh.png|thumb|400px|center|'''[http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-12951&orgids=ECOLI HemH]([http://parts.igem.org/Part:BBa_K1104202 K1104202])'''<br>]]
+
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[[File: NYMU_trxc.png|thumb|400px|center|'''[http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-3104&detail-level=1 TrxC]([http://parts.igem.org/Part:BBa_K1104201 K1104201])'''<br>]]
+
-
We did a study about promoters that can sense OxyR, or SoxR. Several promoters on part registry can be induced by ROS: OxyR-activated promoters such as [http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001](AhpC promoter)and [http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362005](SufA promoter)were designed and used as favorite parts by 2010 KIT-Tokyo team. They can be controlled by OxyR. SoxR-activated part like [http://parts.igem.org/Part:BBa_K554000 Part:BBa_K554000](SoxS promoter)was designed and used as favorite parts by [https://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Parts 2011 UNICAMP-EMSE Brazil team], which can be controlled by SoxR.
+
We also got the promoter sequences taken from [http://ecocyc.org/ Ecocyc] and tested promoters: [http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-12951&orgids=ECOLI HemHp] and [http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-3104&detail-level=1 TrxCp]. Both of them have dual binding site only interact with OxyR, cooperate with sigma factor 70, and have no E X S P cutting site. We have designed and sent them to PartRegistry as new parts: [http://parts.igem.org/Part:BBa_K1104202 Part:BBa_K1104202]、[http://parts.igem.org/Part:BBa_K1104201 Part:BBa_K1104201].
-
 
+
-
We also got the sequence and tested promoters: [http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-12951&orgids=ECOLI hemH] (Figure. 1)and [http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-3104&detail-level=1 trxC] (Figure. 2) )
+
-
on [http://www.ecocyc.org/ EcoCyc: Encyclopedia of Escherichia coli K-12 Genes and Metabolism]. Both of them have dual binding site only interact with OxyR, cooperate with sigma factor 70, and have no EXSP cutting site. We have designedand sent them to partregistry as new parts: [http://parts.igem.org/Part:BBa_K1104202 Part:BBa_K1104202]、[http://parts.igem.org/Part:BBa_K1104201 Part:BBa_K1104201].
+
=='''Method'''==
=='''Method'''==
==='''How Can ''Bee. coli'' Sense ''Nosema?'' '''===
==='''How Can ''Bee. coli'' Sense ''Nosema?'' '''===
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After ''Nosema ceranae'' infected midgut cells of bees, and , ''Bee. coli'' should sense the pathogen first before the following circuit(fighting against ''Nosema ceranae'')is triggered.
+
After ''Nosema ceranae'' infected midgut cells of bees, and ''Bee. coli'' should sense the pathogen first before the following circuit(fighting against ''Nosema ceranae'')is triggered.
After ''Nosema ceranae'' infected midgut cells of bees, ROS(Reactive Oxygen Species) will be produced by midgut cells of bee and released to the cavity. As we can see, there are many kinds of promoters (and their transcription factors) responding to ROS naturally exist in ''E. coli MG1655'' genome. We choose proper and strength enough ones from them, basing on reporting assays we made about promoetr testing. Besides, in order to enhance the strength, we designed an upstream device to enlarge the expression of the activators, so the sensitivity of ''Bee. coli'' to ROS will be sharper, and the probability of downstream circuit(fighting against ''Nosema ceranae'') being turned on.
After ''Nosema ceranae'' infected midgut cells of bees, ROS(Reactive Oxygen Species) will be produced by midgut cells of bee and released to the cavity. As we can see, there are many kinds of promoters (and their transcription factors) responding to ROS naturally exist in ''E. coli MG1655'' genome. We choose proper and strength enough ones from them, basing on reporting assays we made about promoetr testing. Besides, in order to enhance the strength, we designed an upstream device to enlarge the expression of the activators, so the sensitivity of ''Bee. coli'' to ROS will be sharper, and the probability of downstream circuit(fighting against ''Nosema ceranae'') being turned on.
==='''Circuit Design'''===
==='''Circuit Design'''===
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There are two kinds of circuit: OxyR-included circuit and SoxR-included circuit, depending on the categories of promoters controled by different transcription factor.
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In order to enhance the strength and sensitivity of ROS-sensing promoters, we made ''E. coli'' continuously produce inactivated OxyR, so that ROS can affect promoters more easily.
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In order to enhance the strength and sensitivity of ROS-sensing promoters, we make E. coli continuously produce inactivated OxyR or SoxR, so that ROS can affect promoters more easily.
+
====OxyR-included circuit====
====OxyR-included circuit====
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[[Image:NYMU_O12.png|frame|Device1+Device2]]This is one kind of the two circuits--OxyR-included circuit. Device1 is composed of a sensor (OxyR-induced promoter, including TrxC, HemH, SufA, AhpC(mutated), AhpC2D1, AhpC2, AhpCD1, AhpC1, DsbG) plus reporter ([http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]). Device2 in order to enhance the effect of ROS on ''E. coli'' is added ahead: a constitutive promoter([http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]), RBS([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034]), activator OxyR([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]),and double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015].
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[[Image:NYMU_O12.png|frame|center|'''OxyR-included circuit(Device1+Device2)''']]
 +
 
 +
In OxyR-included circuit, Device2 is composed of sensor (OxyR-induced promoter, including TrxCp, HemHp, sufA, AhpCp1000, AhpCp2D1, AhpCp2, AhpCpD1, AhpCp1, DsbGp) plus reporter ([http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]).  
 +
 
 +
Device1 in order to enhance the effect of ROS on ''E. coli'' is added ahead: a constitutive promoter([http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]), RBS([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034]), activator OxyR([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]),and double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015].
 +
 
 +
Putting Device1 [http://parts.igem.org/Part:BBa_K1104250 device:BBa_K1104250] upstream to promoter AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204]) remarkably enhanced the strength of promoter AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204]) as our experiment results shows.
 +
 
 +
{|
 +
|[[Image:NYMU_O1.png|frame|center|'''Device1 ([http://parts.igem.org/Part:BBa_K1104250 Part:BBa_K1104250])'''<br>a constitutive promoter([http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102])+ RBS([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034])+ activator OxyR([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200])+ double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]]]
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|[[Image:NYMU_O2.png|frame|center|'''Device2'''<br>a sensor (OxyR-induced promoter, including TrxCp, HemHp, sufA, AhpCp1000, AhpCp2D1, AhpCp2, AhpCpD1, AhpCp1, DsbGp) + reporter ([http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840])]]
 +
|}
 +
 
=====Parts=====
=====Parts=====
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[[File: NYMU_ J23102.png |thumb|center|400px|'''[http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]'''<br>]]
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{|
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[[File: NYMU_B0034.png |thumb|center|400px|'''RBS''' <br>([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034])]]
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|[[File: NYMU_ J23102.png |thumb|center|400px|'''[http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]''']]
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[[File: NYMU_OxyRcod.png |thumb|center|400px|'''OxyR coding'''([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]) <br>]]
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|[[File: NYMU_B0034.png |thumb|center|400px|'''RBS'''<br>([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034])]]
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[[File: NYMU_ B0015.png |thumb|center|400px|'''[http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]'''<br>]]
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|[[File: NYMU_OxyRcod.png |thumb|center|400px|'''OxyR coding'''<br>([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200])]]
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[[File:NYMU_E0840.png|thumb|center|400px|'''[http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]'''<br>]]
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|}
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{|
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|[[File: NYMU_ B0015.png |thumb|center|400px|'''[http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]''']]
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|[[File:NYMU_E0840.png|thumb|center|400px|'''[http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]''']]
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|}
=====OxyR-activated promoters=====
=====OxyR-activated promoters=====
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[[File:NYMU_ TrxC.png|thumb|center|400px|''' 1.TrxC '''<br>([http://parts.igem.org/Part:BBa_K1104201 Part:BBa_K1104201])]]
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We searched for promoters that can be induced with ROS. Most of them activated by OxyR.
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[[File:NYMU_ HemH.png|thumb|center|400px|''' 2.HemH '''<br>([http://parts.igem.org/Part:BBa_K1104202 Part:BBa_K1104202])]]
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*Promoters on Ecocyc
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[[File:NYMU_ SufA.png|thumb|center|400px|''' 3.SufA '''<br>([http://parts.igem.org/Part:BBa_K362005 Part:BBa_K362005])]]
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{|
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[[File:NYMU_Amutate1000.png|thumb|center|400px|''' 4.AhpC(mutated)'''[http://parts.igem.org/Part:BBa_K1104203 Part:BBa_K1104203]<br>]]
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|[[File:NYMU_ TrxC.png|thumb|center|400px|''' TrxCp '''<br>([http://parts.igem.org/Part:BBa_K1104201 Part:BBa_K1104201])]]
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[[File:NYMU_AhpC2D1.png|thumb|center|400px|''' 5.AhpC2D1'''<br>([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204])]]
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|[[File:NYMU_ HemH.png|thumb|center|400px|''' HemHp '''<br>([http://parts.igem.org/Part:BBa_K1104202 Part:BBa_K1104202])]]
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[[File:NYMU_AhpC2.png|thumb|center|400px|''' 6.AhpC2'''<br>([http://parts.igem.org/Part:BBa_K1104205 Part:BBa_K1104205])]]
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|}
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[[File:NYMU_AhpCD1.png|thumb|center|400px|''' 7.AhpCD1'''<br>([http://parts.igem.org/Part:BBa_K1104206 Part:BBa_K1104206])]]
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*Promoters on PartRegistry
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[[File:NYMU_AhpC1.png|thumb|center|400px|''' 8.AhpC1'''<br>([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])]]
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[[File:NYMU_ SufA.png|thumb|center|400px|''' sufA '''<br>([http://parts.igem.org/Part:BBa_K362005 Part:BBa_K362005])]]
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[[File:NYMU_DsbG.png|thumb|center|400px|''' 9.DsbG'''<br>([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])]]
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*Improved-Promoters from [http://parts.igem.org/Part:BBa_K362001 ahpC(Part:BBa_K362001)]
-
 
+
{|
-
====SoxR-included circuit====
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|[[File:NYMU_Amutate1000.png|frame|center|''' AhpCp1000'''[http://parts.igem.org/Part:BBa_K1104203 Part:BBa_K1104203]]]
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[[Image:NYMUSoxS.png|frame|Device1+Device2]]This is the other kind of the two circuits--SoxR-included circuit. The deference is activator: in this circuit OxyR is replaced with SoxR. The construct is initially built by [https://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Parts 2011 UNICAMP-EMSE Brazil team]. We made some replacement to the original circuit: the constitutive promoter, double terminator, and a reporter[http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840] downstream the promoter. It is also composed of 2 devices:One is a sensor SoxS([http://parts.igem.org/Part:BBa_K554003 Part:BBa_K554003]) plus reporter ([http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]). The other device is a constitutive promoter([http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]), RBS([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034]), activator SoxR([http://parts.igem.org/Part:BBa_K554003 Part:BBa_K554003]),and double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015].
+
|}
-
[[File:NYMU_ J23102.png|thumb|400px|center|'''[http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]'''<br>]]
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{|
-
[[File:NYMU_K554003.png|thumb|400px|center|'''SoxR'''<br>([http://parts.igem.org/Part:BBa_K554003 Part:BBa_K554003])]]
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|[[File:NYMU_AhpC2D1.png|thumb|center|400px|''' AhpCp2D1'''<br>([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204])]]
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[[File:NYMU_B0015.png|thumb|400px|center|'''[http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015''']<br>]]
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|[[File:NYMU_AhpCD1.png|thumb|center|400px|''' AhpCpD1'''<br>([http://parts.igem.org/Part:BBa_K1104206 Part:BBa_K1104206])]]
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[[File:NYMU_ SoxS.png|thumb|400px|center|'''SoxS '''<br>([http://parts.igem.org/Part:BBa_K554000 Part:BBa_K554000])]]
+
|}
-
[[File:NYMU_E0840.png|thumb|400px|center|'''[http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]'''<br>]]
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{|
 +
|[[File:NYMU_AhpC1.png|thumb|center|400px|''' AhpCp1'''<br>([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])]]
 +
|[[File:NYMU_AhpC2.png|thumb|center|400px|''' AhpCp2'''<br>([http://parts.igem.org/Part:BBa_K1104205 Part:BBa_K1104205])]]
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|[[File:NYMU_DsbG.png|thumb|center|400px|''' DsbGp'''<br>([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])]]
 +
|}
===Disscussion===
===Disscussion===
-
We test only Device2, as well as Device1+Device2. And the results of OxyR-induced promoters testing on PartRegistry are linked below:<br>
+
We tested Device2 of each OxyR-induced promoters, as well as Device1+Device2 of AhpCp2D1. And the results of OxyR-induced promoters testing on PartRegistry are linked as follows:<br>
-
#TrxC ([http://parts.igem.org/Part:BBa_K1104201:Experience Part:BBa_K1104201:Experience])
+
*TrxCp ([http://parts.igem.org/Part:BBa_K1104201:Experience Part:BBa_K1104201:Experience])
-
#HemH ([http://parts.igem.org/Part:BBa_K1104202:Experience Part:BBa_K1104202:Experience])
+
*HemHp ([http://parts.igem.org/Part:BBa_K1104202:Experience Part:BBa_K1104202:Experience])
-
#SufA ([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
+
*sufAp ([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
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#AhpC(mutated)([http://parts.igem.org/Part:BBa_K1104203:Experience Part:BBa_K1104203:Experience])
+
*AhpCp1000 ([http://parts.igem.org/Part:BBa_K1104203:Experience Part:BBa_K1104203:Experience])
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#AhpC2D1([http://parts.igem.org/Part:BBa_K1104204:Experience Part:BBa_K1104204:Experience])
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*AhpCp2D1 ([http://parts.igem.org/Part:BBa_K1104204:Experience Part:BBa_K1104204:Experience])
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#AhpC2([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
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*AhpCp2 ([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
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#AhpCD1([http://parts.igem.org/Part:BBa_K1104206:Experience Part:BBa_K1104206:Experience])
+
*AhpCpD1 ([http://parts.igem.org/Part:BBa_K1104206:Experience Part:BBa_K1104206:Experience])
-
#AhpC1([http://parts.igem.org/Part:BBa_K1104207:Experience Part:BBa_K1104207:Experience])
+
*AhpCp1 ([http://parts.igem.org/Part:BBa_K1104207:Experience Part:BBa_K1104207:Experience])
-
#DsbG([http://parts.igem.org/Part:BBa_K1104208:Experience Part:BBa_K1104208:Experience])
+
*DsbGp ([http://parts.igem.org/Part:BBa_K1104208:Experience Part:BBa_K1104208:Experience])
-
<br>The same as SoxR-induced promoter testing, we test Device2 and Device1+Device2. The construct is initially built by [https://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Parts 2011 UNICAMP-EMSE Brazil team]. We tested the Device with hydrogen peroxide instead of Paraquat(both of them are ROS). Besides, we made some replacement to the original circuit. The edited results of SoxR-induced promoters testing on PartRegistry: SoxS([http://parts.igem.org/Part:BBa_K554000:Experience Part:BBa_K554000:Experience]).
+
 
 +
[[File:NYMU pp.png|frame|center]]Above shows the strengths of the basal level of various promoters that respond to reactive oxygen species with respect to BBa_J23101.
 +
 
 +
[[Image:NYMU_2d1.png|frame|center|In the presence of Device 1, AhpCp2D1 shows 7 to 9 folds of strength (Error bars represent the 95% confidence interval)]]
==='''Part Improvement'''===
==='''Part Improvement'''===
-
[[File: NYMUAHPCP.jpg|frame|center|''' Figure. 3'''<br>]]
+
[[File:NYMU_originalA.png|frame|center|'''ahpC([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001])'''<br>There is a Pst1 site in the red rectangle.]]
-
We improve the function of a BioBrick Part: AhpC promoter([http://parts.igem.org/Part:BBa_K362001 K362001])designed by [https://2010.igem.org/Team:KIT-Kyoto/Parts 2010 KIT-Tokyo team] into four versions.On PartRegistry, the complex part(Figure. 3) according to [http://ecocyc.org/ECOLI/new-image?object=EG11384 Ecocyc]composition contains hybrid promoters, shared TFBS (Transcription Factor Binding Site), and reverse promoter DsbG.
+
We improved the function of a BioBrick Part: ahpC promoter ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) designed by [https://2010.igem.org/Team:KIT-Kyoto/Parts 2010 KIT-Tokyo team] into four versions. On the PartRegistry, the complex part according to [http://ecocyc.org/ECOLI/new-image?object=EG11384 Ecocyc] composition contains part of DsbG coding, hybrid promoters, shared TFBS (Transcription Factor Binding Site), and reverse promoter DsbGp. The intergenic region between DsbGp and AhpCp1 carries two binding sites for OxyR.
-
The intergenic region between dsbG and ahpC carries two binding sites for OxyR, a dsbG-proximal site, located 54 bp upstream of the dsbG start codon, and an ahpC-proximal site, located 290 bp upstream of the dsbG start codon.
+
-
[[File:NYMU_originalA.png|thumb|400px|center|'''AhpC promoter([http://parts.igem.org/Part:BBa_K362001 K362001])''']]
+
-
[[File:NYMU_Amutate1000.png|thumb|400px|center|'''AhpC(mutated)[http://parts.igem.org/Part:BBa_K1104203 K1104203]'''<br>We succesfully mutated the Pst1 site (ctgcag->ctacag) of K362001.]][[File:NYMU_AhpC2D1.png|thumb|400px|center|'''AhpC2D1([http://parts.igem.org/Part:BBa_K1104204 K1104204])'''<br>We delete the dsbG coding and following sequence next to dsbG reverse primer, making the functional sequence shorter, so that PCR can be more easy and efficient.]][[File:NYMU_AhpCD1.png|thumb|400px|center|'''AhpCD1([http://parts.igem.org/Part:BBa_K1104206 K1104206])'''<br>OxyR binding to the ahpC-proximal site leads to the induction of both dsbG and ahpC transcripts, while OxyR binding to the dsbG-proximal site leads to the induction of a second ahpC transcript. This transcript of ahpC and the transcript of dsbG overlap by over 100 nucleotides.]]
+
-
Because AhpC promoter([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) on PartRegistry is a hybrid promoter containing AhpC1, AhpC2, and DsbG promoter in its 1000bp, we create the new part and test it apart.
+
-
[[File:NYMU_AhpC1.png|thumb|200px|center|'''AhpC1'''<br>[http://parts.igem.org/Part:BBa_K1104207 K1104207]]][[File:NYMU_AhpC.png|frame|center|''' Figure. 4''']]
+
-
[[File:NYMU_AhpC2.png|thumb|200px|center|'''AhpC2'''<br>[http://parts.igem.org/Part:BBa_K1104205 K1104205]]][[File:NYMUAHPCP2.gif|frame|center|''' Figure. 5''']][[File:NYMU_DsbG.png|thumb|center|400px|'''DsbG'''<br>([http://parts.igem.org/Part:BBa_K1104207 K1104207])]][[File: NYMU_ dsbG.png|frame|center|''' Figure. 6'''<br>]]
+
-
===Disscussion===
+
[[File:NYMU_Amutate1000.png|thumb|600px|center|'''AhpCp1000[http://parts.igem.org/Part:BBa_K1104203 Part:BBa_K1104203]'''<br>We succesfully mutated the Pst1 site (ctgcag->ctacag) of K362001.]]
-
As the results shows, we successfully improved AhpC promoter([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]). And the results and disscussion on PartRegistry are linked below:<br>
+
{|
-
#AhpC(mutated)([http://parts.igem.org/Part:BBa_K1104203:Experience Part:BBa_K1104203:Experience])
+
|[[File:NYMU_AhpC2D1.png|thumb|400px|center|'''AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204])'''<br>We strimmed DsbG coding out of the original sequence, making the functional sequence shorter and more efficient.]]
-
#AhpC2D1([http://parts.igem.org/Part:BBa_K1104204:Experience Part:BBa_K1104204:Experience])
+
|[[File:NYMU_AhpCD1.png|thumb|400px|center|'''AhpCpD1([http://parts.igem.org/Part:BBa_K1104206 Part:BBa_K1104206])'''<br>We designed a dual-side hybrid promoter, including AhpCp1 and DsbGp(reverse), and two binding sites for OxyR. OxyR binding to TFBS leads to bidirectional transcription.]]
-
#AhpC2([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
+
|}
-
#AhpCD1([http://parts.igem.org/Part:BBa_K1104206:Experience Part:BBa_K1104206:Experience])
+
 
-
#AhpC1([http://parts.igem.org/Part:BBa_K1104207:Experience Part:BBa_K1104207:Experience])
+
Because ahpC ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) is a hybrid promoter containing AhpCp1, AhpCp2, and DsbGp promoters in its 1000bp, we created the new part and test it apart.
-
#DsbG([http://parts.igem.org/Part:BBa_K1104208:Experience Part:BBa_K1104208:Experience])
+
{|
 +
|[[File:NYMU_AhpC1.png|thumb|200px|center|'''AhpCp1'''<br>[http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207]]]
 +
|[[File:NYMU_AhpC2.png|thumb|200px|center|'''AhpCp2'''<br>[http://parts.igem.org/Part:BBa_K1104205 Part:BBa_K1104205]]]
 +
|[[File:NYMU_DsbG.png|thumb|center|400px|'''DsbGp'''<br>([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])]]
 +
|}
 +
 
 +
===Discussion===
 +
As the results show, we successfully improved ahpC promoter ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]). And the results and disscussion on the PartRegistry are linked as follows:<br>
 +
*AhpCp1000([http://parts.igem.org/Part:BBa_K1104203:Experience Part:BBa_K1104203:Experience])
 +
*AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204:Experience Part:BBa_K1104204:Experience])
 +
*AhpCp2([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
 +
*AhpCpD1([http://parts.igem.org/Part:BBa_K1104206:Experience Part:BBa_K1104206:Experience])
 +
*AhpCp1([http://parts.igem.org/Part:BBa_K1104207:Experience Part:BBa_K1104207:Experience])
 +
*DsbGp([http://parts.igem.org/Part:BBa_K1104208:Experience Part:BBa_K1104208:Experience])
 +
 
 +
[[File: NYMU_AA.png|frame|center]]Above shows promoter testing of ahpC promoter [http://parts.igem.org/Part:BBa_K362001 Part:K362001]) and its improvements, which suggests that AhpCpd1 and AhpCp1 show so weak promoter strength that we only focus on the change of promoter strength of the three promoters as following:
 +
[[File: NYMU_AAAA.png|frame|center]]
-
=='''Reference'''==
+
=='''References'''==
-
#Dussaubat, Claudia, Brunet, Jean-Luc, Higes, Mariano, Colbourne, John K., Lopez, Jacqueline, Choi, Jeong-Hyeon, Martín-Hernández, Raquel, ... Alaux, Cédric. (n.d.). Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera. Public Library of Science.
+
*Dussaubat, Claudia, Brunet, Jean-Luc, Higes, Mariano, Colbourne, John K., Lopez, Jacqueline, Choi, Jeong-Hyeon, Martín-Hernández, Raquel, ... Alaux, Cédric. (n.d.). Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera. Public Library of Science.
-
#D'Autréaux, B., & Toledano, M. B. (January 01, 2007). ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis. Nature Reviews. Molecular Cell Biology, 8, 10, 813-24.2[http://www.nature.com/nrm/journal/v8/n10/fig_tab/nrm2256_F1.html]
+
*D'Autréaux, B., & Toledano, M. B. (January 01, 2007). ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis. Nature Reviews. Molecular Cell Biology, 8, 10, 813-24.2[http://www.nature.com/nrm/journal/v8/n10/fig_tab/nrm2256_F1.html]
-
#Ryu, S. E. (June 01, 2012). Structural mechanism of disulphide bond-mediated redox switches. Journal of Biochemistry, 151, 6, 579-588.[http://jb.oxfordjournals.org/content/early/2012/05/02/jb.mvs046.full.pdf]
+
*Ryu, S. E. (June 01, 2012). Structural mechanism of disulphide bond-mediated redox switches. Journal of Biochemistry, 151, 6, 579-588.[http://jb.oxfordjournals.org/content/early/2012/05/02/jb.mvs046.full.pdf]
 +
*[http://ecocyc.org/ Ecocyc].

Latest revision as of 05:27, 28 October 2013

National Yang Ming University


Contents

Sensing Nosema ceranae

Introduction

After Nosema ceranae enters the midgut of bees, we have to make E. coli sense this pathogen. E. coli with ROS-sensing promoters will respond to Reactive Oxygen Species (ROS) produced by infected midgut cells. The following circuit behind ROS-sensing promoters will be turned on and fight against N. cerenae.

For the circuit design, we added a new composition part: [http://parts.igem.org/Part:BBa_K1104250 device:BBa_K1104250] consisting of a constitutive promoter [http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102] and a transcription factor: OxyR ([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]), which can activate ROS-sensing promoters, increasing the quantity of inactivated transcription factors in order to enhance the response of promoters. Additionally, RBS ([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034]) and double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]. Actually, the addition of [http://parts.igem.org/Part:BBa_K1104250 device:BBa_K1104250] remarkably enhanced the strength of promoter AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204]) in our experiment results.

We improved the function of a BioBrick Part: ahpC promoter ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) originally designed by 2010 KIT-Tokyo team.

Background

Nosema Ceranae Induces Oxidative Stress in the Midgut.

ROS (Reactive Oxygen Species) are efficient antimicrobial molecules. Genes involved in oxidation-reduction were significantly overrepresented in the gene set upregulated upon spore infection. In response to the infection, the increase of oxidoreduction in the midgut epithelia of bees infected by N. ceranae would therefore indicate an enhanced generation of ROS. It is suggested that ROS production is a general immune response in bees' midgut to microorganism infection. There are promoters in the genome of E. coli that can be regulated by ROS. After Nosema ceranae enter midgut of bee, the regulator of promoters will be activated by ROS, trigger the following circuit fighting against Nosema ceranae.

Literature Study of ROS-induced Promoters

Once N.cerenae infects the midgut of bees, midgut cells of bees will secrete Reactive Oxygen Species (ROS). ROS have been shown to be toxic but also function as signalling molecules which can transcriptionally activate transcription factors: OxyR ([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]). We focus on ROS-induced promoters regulated by OxyR.

OxyR Activation
OxyR regulates the H2O2 response of
E. coli. H2O2 oxidizes OxyR Cys199 to an R-SOH that reacts with Cys208 in an intramolecular disulphide bond.

Activated transcription factor, OxyR, then binds to TFBS of promoters (sensor), as the pictures shown below:

[http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-12951&orgids=ECOLI HemHp]([http://parts.igem.org/Part:BBa_K1104202 K1104202])
[http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-3104&detail-level=1 TrxCp]([http://parts.igem.org/Part:BBa_K1104201 K1104201])

We did a study about promoters that can sense OxyR. Several promoters on the part registry can be induced by ROS: OxyR-activated promoters such as [http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001](ahpC)and [http://parts.igem.org/Part:BBa_K362005 Part:BBa_K362005](sufA)were designed and used as favorite parts by 2010 KIT-Tokyo team. They can be controlled by OxyR.

We also got the promoter sequences taken from [http://ecocyc.org/ Ecocyc] and tested promoters: [http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-12951&orgids=ECOLI HemHp] and [http://biocyc.org/ECOLI/NEW-IMAGE?type=OPERON&object=TU0-3104&detail-level=1 TrxCp]. Both of them have dual binding site only interact with OxyR, cooperate with sigma factor 70, and have no E X S P cutting site. We have designed and sent them to PartRegistry as new parts: [http://parts.igem.org/Part:BBa_K1104202 Part:BBa_K1104202]、[http://parts.igem.org/Part:BBa_K1104201 Part:BBa_K1104201].

Method

How Can Bee. coli Sense Nosema?

After Nosema ceranae infected midgut cells of bees, and Bee. coli should sense the pathogen first before the following circuit(fighting against Nosema ceranae)is triggered. After Nosema ceranae infected midgut cells of bees, ROS(Reactive Oxygen Species) will be produced by midgut cells of bee and released to the cavity. As we can see, there are many kinds of promoters (and their transcription factors) responding to ROS naturally exist in E. coli MG1655 genome. We choose proper and strength enough ones from them, basing on reporting assays we made about promoetr testing. Besides, in order to enhance the strength, we designed an upstream device to enlarge the expression of the activators, so the sensitivity of Bee. coli to ROS will be sharper, and the probability of downstream circuit(fighting against Nosema ceranae) being turned on.

Circuit Design

In order to enhance the strength and sensitivity of ROS-sensing promoters, we made E. coli continuously produce inactivated OxyR, so that ROS can affect promoters more easily.

OxyR-included circuit

OxyR-included circuit(Device1+Device2)

In OxyR-included circuit, Device2 is composed of sensor (OxyR-induced promoter, including TrxCp, HemHp, sufA, AhpCp1000, AhpCp2D1, AhpCp2, AhpCpD1, AhpCp1, DsbGp) plus reporter ([http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]).

Device1 in order to enhance the effect of ROS on E. coli is added ahead: a constitutive promoter([http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]), RBS([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034]), activator OxyR([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200]),and double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015].

Putting Device1 [http://parts.igem.org/Part:BBa_K1104250 device:BBa_K1104250] upstream to promoter AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204]) remarkably enhanced the strength of promoter AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204]) as our experiment results shows.

Device1 ([http://parts.igem.org/Part:BBa_K1104250 Part:BBa_K1104250])
a constitutive promoter([http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102])+ RBS([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034])+ activator OxyR([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200])+ double terminator [http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]
Device2
a sensor (OxyR-induced promoter, including TrxCp, HemHp, sufA, AhpCp1000, AhpCp2D1, AhpCp2, AhpCpD1, AhpCp1, DsbGp) + reporter ([http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840])
Parts
[http://parts.igem.org/Part:BBa_J23102 Part:BBa_J23102]
RBS
([http://parts.igem.org/Part:BBa_B0034 Part:BBa_B0034])
OxyR coding
([http://parts.igem.org/Part:BBa_K1104200 Part:BBa_K1104200])
[http://parts.igem.org/Part:BBa_B0015 Part:BBa_B0015]
[http://parts.igem.org/Part:BBa_E0840 Part:BBa_E0840]
OxyR-activated promoters

We searched for promoters that can be induced with ROS. Most of them activated by OxyR.

  • Promoters on Ecocyc
TrxCp
([http://parts.igem.org/Part:BBa_K1104201 Part:BBa_K1104201])
HemHp
([http://parts.igem.org/Part:BBa_K1104202 Part:BBa_K1104202])
  • Promoters on PartRegistry
sufA
([http://parts.igem.org/Part:BBa_K362005 Part:BBa_K362005])
  • Improved-Promoters from [http://parts.igem.org/Part:BBa_K362001 ahpC(Part:BBa_K362001)]
AhpCp1000[http://parts.igem.org/Part:BBa_K1104203 Part:BBa_K1104203]
AhpCp2D1
([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204])
AhpCpD1
([http://parts.igem.org/Part:BBa_K1104206 Part:BBa_K1104206])
AhpCp1
([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])
AhpCp2
([http://parts.igem.org/Part:BBa_K1104205 Part:BBa_K1104205])
DsbGp
([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])

Disscussion

We tested Device2 of each OxyR-induced promoters, as well as Device1+Device2 of AhpCp2D1. And the results of OxyR-induced promoters testing on PartRegistry are linked as follows:

  • TrxCp ([http://parts.igem.org/Part:BBa_K1104201:Experience Part:BBa_K1104201:Experience])
  • HemHp ([http://parts.igem.org/Part:BBa_K1104202:Experience Part:BBa_K1104202:Experience])
  • sufAp ([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
  • AhpCp1000 ([http://parts.igem.org/Part:BBa_K1104203:Experience Part:BBa_K1104203:Experience])
  • AhpCp2D1 ([http://parts.igem.org/Part:BBa_K1104204:Experience Part:BBa_K1104204:Experience])
  • AhpCp2 ([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
  • AhpCpD1 ([http://parts.igem.org/Part:BBa_K1104206:Experience Part:BBa_K1104206:Experience])
  • AhpCp1 ([http://parts.igem.org/Part:BBa_K1104207:Experience Part:BBa_K1104207:Experience])
  • DsbGp ([http://parts.igem.org/Part:BBa_K1104208:Experience Part:BBa_K1104208:Experience])
NYMU pp.png
Above shows the strengths of the basal level of various promoters that respond to reactive oxygen species with respect to BBa_J23101.
In the presence of Device 1, AhpCp2D1 shows 7 to 9 folds of strength (Error bars represent the 95% confidence interval)

Part Improvement

ahpC([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001])
There is a Pst1 site in the red rectangle.

We improved the function of a BioBrick Part: ahpC promoter ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) designed by 2010 KIT-Tokyo team into four versions. On the PartRegistry, the complex part according to [http://ecocyc.org/ECOLI/new-image?object=EG11384 Ecocyc] composition contains part of DsbG coding, hybrid promoters, shared TFBS (Transcription Factor Binding Site), and reverse promoter DsbGp. The intergenic region between DsbGp and AhpCp1 carries two binding sites for OxyR.

AhpCp1000[http://parts.igem.org/Part:BBa_K1104203 Part:BBa_K1104203]
We succesfully mutated the Pst1 site (ctgcag->ctacag) of K362001.
AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204 Part:BBa_K1104204])
We strimmed DsbG coding out of the original sequence, making the functional sequence shorter and more efficient.
AhpCpD1([http://parts.igem.org/Part:BBa_K1104206 Part:BBa_K1104206])
We designed a dual-side hybrid promoter, including AhpCp1 and DsbGp(reverse), and two binding sites for OxyR. OxyR binding to TFBS leads to bidirectional transcription.

Because ahpC ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]) is a hybrid promoter containing AhpCp1, AhpCp2, and DsbGp promoters in its 1000bp, we created the new part and test it apart.

AhpCp1
[http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207]
AhpCp2
[http://parts.igem.org/Part:BBa_K1104205 Part:BBa_K1104205]
DsbGp
([http://parts.igem.org/Part:BBa_K1104207 Part:BBa_K1104207])

Discussion

As the results show, we successfully improved ahpC promoter ([http://parts.igem.org/Part:BBa_K362001 Part:BBa_K362001]). And the results and disscussion on the PartRegistry are linked as follows:

  • AhpCp1000([http://parts.igem.org/Part:BBa_K1104203:Experience Part:BBa_K1104203:Experience])
  • AhpCp2D1([http://parts.igem.org/Part:BBa_K1104204:Experience Part:BBa_K1104204:Experience])
  • AhpCp2([http://parts.igem.org/Part:BBa_K1104205:Experience Part:BBa_K1104205:Experience])
  • AhpCpD1([http://parts.igem.org/Part:BBa_K1104206:Experience Part:BBa_K1104206:Experience])
  • AhpCp1([http://parts.igem.org/Part:BBa_K1104207:Experience Part:BBa_K1104207:Experience])
  • DsbGp([http://parts.igem.org/Part:BBa_K1104208:Experience Part:BBa_K1104208:Experience])
NYMU AA.png
Above shows promoter testing of ahpC promoter [http://parts.igem.org/Part:BBa_K362001 Part:K362001]) and its improvements, which suggests that AhpCpd1 and AhpCp1 show so weak promoter strength that we only focus on the change of promoter strength of the three promoters as following:
NYMU AAAA.png

References

  • Dussaubat, Claudia, Brunet, Jean-Luc, Higes, Mariano, Colbourne, John K., Lopez, Jacqueline, Choi, Jeong-Hyeon, Martín-Hernández, Raquel, ... Alaux, Cédric. (n.d.). Gut Pathology and Responses to the Microsporidium Nosema ceranae in the Honey Bee Apis mellifera. Public Library of Science.
  • D'Autréaux, B., & Toledano, M. B. (January 01, 2007). ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis. Nature Reviews. Molecular Cell Biology, 8, 10, 813-24.2[http://www.nature.com/nrm/journal/v8/n10/fig_tab/nrm2256_F1.html]
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