Difference between revisions of "Part:BBa K3921000"

 
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<partinfo>BBa_K3921000 short</partinfo>
 
<partinfo>BBa_K3921000 short</partinfo>
  
PcpcG2-68: a turncated promoter from PcpcG2-172
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PcpcG2-68 is a truncated promoter from PcpcG2-172 (https://parts.igem.org/Part:BBa_K2012015)
PcpcG2-68 is a truncated promoter from PcpcG2-172.   <br><br>[[File:T--XHD-Wuhan-B-China--108.png|600px|thumb|left|Figure1]]     The original ccaS/ccaR/cpcG2 cassette was amplified from the genome of Synechocystis PCC6803. The open reading frame of the output gene cpcG2 was then seamlessly replaced with lacZ [1]. The light-controlled promoter is then named PcpcG2-238 by Tabor's study, in which they found a constitutive promoter through BPROM prediction that contributes to leakiness and low dynamic range. They truncated PcpcG2-238 to create PcpcG2-172 [2]. We hypothesized that the upstream sequence of PcpcG2-172 contributes little to CcaR~P binding, therefore we decided to truncate PcpcG2-172 into PcpcG2-68 to reduce the length of PcpcG2 promoter. <br> <br>  We tested PcpcG2-172 and PcpcG2-68 under the regulation of a series of CcaRs with different RBS strength. [[File:T--XHD-Wuhan-B-China--109.png|600px|thumb|left|Figure2]]We constructed a series of circuits containing combinations of J61-RBSs and PcpcG2-68/172. A total of 14 pSC101 plasmids were co-transformed with p15A plasmid respectively into MG1655-△EnvZ strain. These strains were cultivated under red or green light for 5 hours using a 24-well plate adapted device, then tested for eGFP expression level by a plate reader.<br>[[File:T--XHD-Wuhan-B-China--110.png|600px|thumb|left|Figure3]]The result reveals that in most cases, PcpcG2-68 is slightly weaker than PcpcG2-172, while exhibiting similar fold-change pattern to PcpcG2-172. To be noticed that after changing weaker RBSs, we found two combinations both have a higher fold-change than the original version of J61100. This result conforms with our model prediction: between the expression level of J23109-J61100 and J23117-J61100 there is a peak of fold-change yet to be achieved for both 68 and 172. Please view <a href="https://2021.igem.org/Team:XHD-Wuhan-B-China/Model">https://2021.igem.org/Team:XHD-Wuhan-B-China/Model</a> for more details. <br><br><br>In conclusion, the truncated promoter PcpcG2-68 has the similar pattern under the control of green/red light as PcpcG2-172, but is shorter and more convenient to construct. For example, when constructing an array of sgRNAs, PcpcG2-68 has a big advantage over PcpcG2-172: reducing the volume of the circuit and cheaper to synthesis. <br>[[File:T--XHD-Wuhan-B-China--111.png|600px|thumb|left|Figure4]]References<br>[1]. Tabor JJ, Levskaya A, Voigt CA. Multichromatic control of gene expression in Escherichia coli. J Mol Biol. 2011 Jan 14;405(2):315-24. <br>[2]. Schmidl SR, Sheth RU, Wu A, Tabor JJ. Refactoring and optimization of light-switchable Escherichia coli two-component systems. ACS Synth Biol. 2014 Nov 21;3(11):820-31. <br>
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<br>[[File:T--XHD-Wuhan-B-China--108(1).png|900px|thumb|left|Figure1. PcpcG2-172 and PcpcG2-68]]<br>The original ccaS/ccaR/cpcG2 cassette was amplified from the genome of Synechocystis PCC6803. The open reading frame of the output gene cpcG2 was then seamlessly replaced with lacZ [1]. The light-controlled promoter is then named PcpcG2-238 by Tabor's study, in which they found a constitutive promoter through BPROM prediction that contributes to leakiness and low dynamic range. They truncated PcpcG2-238 to create PcpcG2-172 [2]. We hypothesized that the upstream sequence of PcpcG2-172 contributes little to CcaR~P binding, therefore we decided to truncate PcpcG2-172 into PcpcG2-68 to reduce the length of PcpcG2 promoter. <br> <br>  We tested PcpcG2-172 and PcpcG2-68 under the regulation of a series of CcaRs with different RBS strength.
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[[File:T--XHD-Wuhan-B-China--109(1).png|900px|thumb|left|Figure2. Circuit Construction]]<br><br>
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We constructed a series of circuits containing combinations of J61-RBSs and PcpcG2-68/172. A total of 14 pSC101 plasmids were co-transformed with p15A plasmid respectively into MG1655-△EnvZ strain. These strains were cultivated under red or green light for 5 hours using a 24-well plate adapted device, then tested for eGFP expression level by a plate reader.<br>[[File:T--XHD-Wuhan-B-China--110(1).png|900px|thumb|left|Figure3. Fluorescence ubder green/red light.]]<br><br>
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The result reveals that in most cases, PcpcG2-68 is slightly weaker than PcpcG2-172, while exhibiting similar fold-change pattern to PcpcG2-172. To be noticed that after changing weaker RBSs, we found two combinations both have a higher fold-change than the original version of J61100. This result conforms with our model prediction: between the expression level of J23109-J61100 and J23117-J61100 there is a peak of fold-change yet to be achieved for both 68 and 172. Please view https://2021.igem.org/Team:XHD-Wuhan-B-China/Model for more details. <br><br>In conclusion, the truncated promoter PcpcG2-68 has the similar pattern under the control of green/red light as PcpcG2-172, but is shorter and more convenient to construct. For example, when constructing an array of sgRNAs, PcpcG2-68 has a big advantage over PcpcG2-172: reducing the volume of the circuit and cheaper to synthesis. <br>[[File:T--XHD-Wuhan-B-China--111(1).png|900px|thumb|left|Figure4. A gRNA array. ]]<br><br>
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<p>References<br>[1]. Tabor JJ, Levskaya A, Voigt CA. Multichromatic control of gene expression in Escherichia coli. J Mol Biol. 2011 Jan 14;405(2):315-24. <br>[2]. Schmidl SR, Sheth RU, Wu A, Tabor JJ. Refactoring and optimization of light-switchable Escherichia coli two-component systems. ACS Synth Biol. 2014 Nov 21;3(11):820-31. <br></p>
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
===Usage and Biology===

Latest revision as of 15:42, 21 October 2021


PcpcG2-68: a turncated promoter from PcpcG2-172

PcpcG2-68 is a truncated promoter from PcpcG2-172 (https://parts.igem.org/Part:BBa_K2012015)


Figure1. PcpcG2-172 and PcpcG2-68

The original ccaS/ccaR/cpcG2 cassette was amplified from the genome of Synechocystis PCC6803. The open reading frame of the output gene cpcG2 was then seamlessly replaced with lacZ [1]. The light-controlled promoter is then named PcpcG2-238 by Tabor's study, in which they found a constitutive promoter through BPROM prediction that contributes to leakiness and low dynamic range. They truncated PcpcG2-238 to create PcpcG2-172 [2]. We hypothesized that the upstream sequence of PcpcG2-172 contributes little to CcaR~P binding, therefore we decided to truncate PcpcG2-172 into PcpcG2-68 to reduce the length of PcpcG2 promoter.

We tested PcpcG2-172 and PcpcG2-68 under the regulation of a series of CcaRs with different RBS strength.
Figure2. Circuit Construction


We constructed a series of circuits containing combinations of J61-RBSs and PcpcG2-68/172. A total of 14 pSC101 plasmids were co-transformed with p15A plasmid respectively into MG1655-△EnvZ strain. These strains were cultivated under red or green light for 5 hours using a 24-well plate adapted device, then tested for eGFP expression level by a plate reader.
Figure3. Fluorescence ubder green/red light.


The result reveals that in most cases, PcpcG2-68 is slightly weaker than PcpcG2-172, while exhibiting similar fold-change pattern to PcpcG2-172. To be noticed that after changing weaker RBSs, we found two combinations both have a higher fold-change than the original version of J61100. This result conforms with our model prediction: between the expression level of J23109-J61100 and J23117-J61100 there is a peak of fold-change yet to be achieved for both 68 and 172. Please view https://2021.igem.org/Team:XHD-Wuhan-B-China/Model for more details.

In conclusion, the truncated promoter PcpcG2-68 has the similar pattern under the control of green/red light as PcpcG2-172, but is shorter and more convenient to construct. For example, when constructing an array of sgRNAs, PcpcG2-68 has a big advantage over PcpcG2-172: reducing the volume of the circuit and cheaper to synthesis.
Figure4. A gRNA array.


References
[1]. Tabor JJ, Levskaya A, Voigt CA. Multichromatic control of gene expression in Escherichia coli. J Mol Biol. 2011 Jan 14;405(2):315-24.
[2]. Schmidl SR, Sheth RU, Wu A, Tabor JJ. Refactoring and optimization of light-switchable Escherichia coli two-component systems. ACS Synth Biol. 2014 Nov 21;3(11):820-31.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]