Difference between revisions of "Part:BBa K3733044"

 
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Use a constitutive promoter (BBa_J23110), RNA thermometer (BBa_K3247005), strong RBS (BBa_B0034), antitoxin MntA (BBa_K3733009), toxin HepT (BBa_K3733010),and a strong transcriptional terminator Lambda t1 transcriptional terminator (BBa_K864601). Will express the HepT toxin below 28 ℃ to commit suicide and will not commit suicide above 37 ℃ because of the expression of MntA.
 
Use a constitutive promoter (BBa_J23110), RNA thermometer (BBa_K3247005), strong RBS (BBa_B0034), antitoxin MntA (BBa_K3733009), toxin HepT (BBa_K3733010),and a strong transcriptional terminator Lambda t1 transcriptional terminator (BBa_K864601). Will express the HepT toxin below 28 ℃ to commit suicide and will not commit suicide above 37 ℃ because of the expression of MntA.
 
===Sequence and Features===
 
<partinfo>BBa_K3733044 SequenceAndFeatures</partinfo>
 
  
 
===Usage and Biology===
 
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===Functional Parameters===
 
===Functional Parameters===
 
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To verify the function of this composite part, we transferred it into <i>E.coli</i> DH5α. Meanwhile, we also transformed blank plasmid (only with ori and cmR) into DH5α as control group. We incubated engineered bacteria at 37 ℃ and 28 ℃, taking the bacteria with blank plasmid as control. As the <b>Figure 1</b> shows, medium of experimental group shaked at 28 ℃ is more limpid than ones shaked at 37 ℃; however, in the control group, the medium shaked at 28 ℃ is almost as turbid as ones shaked at 37 ℃.
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To verify the function of this composite part, we transferred it into <i>E.coli</i> DH5α. Meanwhile, we also transformed blank plasmid (only with <i>ori</i> and <i>cmR</i>) into DH5α as control group. We incubated engineered bacteria at 37 ℃ and 28 ℃, taking the bacteria with blank plasmid as control. As the <b>Figure 1</b> shows, medium of experimental group shaked at 28 ℃ is more limpid than ones shaked at 37 ℃; however, in the control group, the medium shaked at 28 ℃ is almost as turbid as ones shaked at 37 ℃.
 
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<center><img src="(这里是图片链接)" style="width:793px;height:360px"></center>
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<center><img src="https://static.igem.org/mediawiki/parts/3/34/T--HZAU-China-MntA-comp-1.png" style="width:793px;height:360px"></center>
<center><b>Figure 1. A.</b> The comparison photo of the experimental group (toxin-antitoxin system) and control group incubated at both 37 ℃ and 28 ℃ for 12 hours. <b>B.</b> The specific date of OD<sub>600</sub> of them.</center>
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<center><b>Figure 1. A.</b> The comparison photo of the experimental group (toxin-antitoxin system) and control group incubated at both 37 ℃ and 28 ℃ for 12 hours. Sch.2 means the experimental group (toxin-antitoxin system). Control means the control group. <b>B.</b> The specific OD<sub>600</sub> data of the experimental group and control group. </center>
 
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<center><img src="https://static.igem.org/mediawiki/parts/1/19/T--HZAU-China-HepT-comp-2.png" style="width:600px;height:360px"></center>
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<center><img src="https://static.igem.org/mediawiki/parts/e/e6/T--HZAU-China-MntA-comp-2.png" style="width:600px;height:360px"></center>
 
<center><b>Figure 2.</b> The quantitative growth curves in 12 hours at 28 ℃. </center>
 
<center><b>Figure 2.</b> The quantitative growth curves in 12 hours at 28 ℃. </center>
 
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<center><img src="https://static.igem.org/mediawiki/parts/d/d7/T--HZAU-China-MntA-comp-3.png" style="width:500px;height:360px"></center>
<center><b>Figure 3.</b> The comparison photo of the bacteria transferred from 28 ℃ to 37 ℃ and the bacteria cultured at 37 ℃ all along.</center>
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<center><b>Figure 3.</b> The comparison photo of the bacteria transferred from 28 ℃ to 37 ℃ and the bacteria cultured at 37 ℃ all along. </center>
 
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===Sequence and Features===
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K3733044 SequenceAndFeatures</partinfo>
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
<!-- Uncomment this to enable Functional Parameter display  

Latest revision as of 15:23, 21 October 2021


Toxin/antitoxin HepT/MntA suicide system working at low temperatures

Use a constitutive promoter (BBa_J23110), RNA thermometer (BBa_K3247005), strong RBS (BBa_B0034), antitoxin MntA (BBa_K3733009), toxin HepT (BBa_K3733010),and a strong transcriptional terminator Lambda t1 transcriptional terminator (BBa_K864601). Will express the HepT toxin below 28 ℃ to commit suicide and will not commit suicide above 37 ℃ because of the expression of MntA.

Usage and Biology

This composite part is one of temperature-based suicide schemes for the engineered bacteria functioning in mammal intestine. It was designed to lead bacteria to commit suicide as they are leaked into the environment (at low temperatures) but do not affect the growth of engineered bacteria in intestine (at high temperatures).

Functional Parameters

To verify the function of this composite part, we transferred it into E.coli DH5α. Meanwhile, we also transformed blank plasmid (only with ori and cmR) into DH5α as control group. We incubated engineered bacteria at 37 ℃ and 28 ℃, taking the bacteria with blank plasmid as control. As the Figure 1 shows, medium of experimental group shaked at 28 ℃ is more limpid than ones shaked at 37 ℃; however, in the control group, the medium shaked at 28 ℃ is almost as turbid as ones shaked at 37 ℃.

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Figure 1. A. The comparison photo of the experimental group (toxin-antitoxin system) and control group incubated at both 37 ℃ and 28 ℃ for 12 hours. Sch.2 means the experimental group (toxin-antitoxin system). Control means the control group. B. The specific OD600 data of the experimental group and control group.

We also plotted the quantitative growth curves at 28 ℃ in this suicide scheme .We got OD600 data changing over time by culturing our engineered bacteria and control bacteria in an automatic microplate reader for 12 hours. Compared with controls, the growth of our engineered bacteria was inhibited obviously(Figure 2).

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Figure 2. The quantitative growth curves in 12 hours at 28 ℃.

To further verify the temperature sensibility of this composite part, we reput bacteria cultured at 28 ℃ into an oribital shaker at 37 ℃ overnight. Compared with themselves, the medium becomes turbid observably at 37 ℃, which means this part could make engineered bacteria kill themselves at 28 ℃ and let them survive at 37 ℃, working as expected(Figure 3).

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Figure 3. The comparison photo of the bacteria transferred from 28 ℃ to 37 ℃ and the bacteria cultured at 37 ℃ all along.

Sequence and Features

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]