Difference between revisions of "Part:BBa K4325026"

(2022 SZPT-China)
 
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<partinfo>BBa_K4325026 short</partinfo>
 
<partinfo>BBa_K4325026 short</partinfo>
 
===Description===
 
===Description===
This composite part is a generator containing pDawn (cI-LVA) (<partinfo>BBa_K1075044</partinfo>) and LKD (<partinfo>BBa_K4325004</partinfo>).
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This composite part is a generator containing pDawn(cI-LVA) (<partinfo>BBa_K1075044</partinfo>), RBS070 (<partinfo>BBa_K4325002</partinfo>), LKD (<partinfo>BBa_K4325004</partinfo>) and  T1 terminator(<partinfo>BBa_K3033016</partinfo>).
 
===Usage===
 
===Usage===
<p>The pDawn (cI-LVA) blue light response system (<partinfo>BBa_K1075044</partinfo>) and lysis gene LKD (<partinfo>BBa_K4325004</partinfo>) were inserted into the pSEVA331 expression vector, which was inserted into <i>E. coli</i> TOP10, screened out the bacterial colony which grew in the dark but did not grow under blue light. Finally, the pSEVA331-pDawn-RBS070-LKD-T1 plasmid was selected and inserted into <i> G. hansenii</i> ATCC53582 by electroporation to verify the responsiveness of pDawn (cI-LVA) under blue light.</p>
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<p>We inserted the blue light responsive system pDawn(cI-LVA) (BBa_K1075044) and lysis gene LKD (BBa_K4325004) into the pSEVA331 expression vector, which was incorporated into <i>E. coli</i> TOP10 and screened for the bacterial colonies which grew in the dark but did not grow under blue light. Finally, the plasmids containing pDawn(cI-LVA)-RBS070-LKD-T1 were selected and introduced into <i>G. hansenii</i> ATCC53582 by electroporation to verify the responsiveness of pDawn(cI-LVA) to blue light.</p>
[[File:K26 11.png|600px|thumb|center|Figure 1: <p></p>Gene circuit of pDawn (cI-LVA)-RBS070-LKD-T1.]]
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[[File:K26 11.png|600px|thumb|center|Figure 1: Gene circuit of pDawn(cI-LVA)-RBS070-LKD-T1.]]
  
 
===Sequence and Features===
 
===Sequence and Features===
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=2022 SZPT-China=
 
=2022 SZPT-China=
 
<h3>Characterization</h3>
 
<h3>Characterization</h3>
<h4>1.Batch screening of pSEVA331-pDawn(cI-LVA)-RBS070-LKD-T1 in response to blue light lysis in <i>E. coli</i> TOP10.</h4>
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<h4>1.Batch screening of pDawn-RBS070-LKD-T1 by evaluating the response to blue light.</h4>
 
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<p>As shown in Figure 2,except for the 11<sup>th</sup> and 13<sup>th </sup> bacterial colony,almost all of the bacterial colony did not grow under blue light. To further explore the lysis effect of pSEVA331-pDawn (cI-LVA) -RBS070-LKD-T1-TOP10, we measured the OD <sub>600</sub> values of pSEVA331-pDawn (cI-LVA) -RBS070-LKD-T1-TOP10 and ploting the growth curve diagram. As shown in Figure 3, the pSEVA331-pDawn (cI-LVA) -RBS070-LKD-T1-TOP10 lysis effect was well in the first eight hours, but was unstable after fifteen hours.</p>
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[[File:K26 22.png|600px|thumb|center|Figure 2: <p></p>Growth condition of pDawn (cI-LVA)-RBS070-LKD-T1-TOP10 in the dark and under the light]]
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[[File:K26 3.png|600px|thumb|center|Figure 3: <p></p> Growth curve diagramof pDawn (cI-LVA)-RBS070-LKD-T1-TOP10]]
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<h4>pSEVA331-pDawn(cI-LVA)-RBS070-LKD-T1 in response to blue photolysis in <i>G. hansenii</i> ATCC53582.</h4>
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<p>As shown in Figure 3, we successfully indicated the  pDawn (cI-LVA) -RBS070-LKD-T1 into <i>G. hansenii</i> ATCC53582 by electroporation</p>
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[[File:K26 44.png|600px|thumb|center|Figure 4: <p></p>Successfully identification withagarose gel electrophoresis <p></p>  
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<p>As shown in Figure 2, except for the 11<sup>th</sup> and 13<sup>th</sup> bacterial colonies, other bacterial colonies did not grow under blue light. To further explore the lysis effect of pDawn(cI-LVA)-RBS070-LKD-T1-TOP10, we tracked the OD<sub>600</sub> values of pDawn(cI-LVA)-RBS070-LKD-T1-TOP10 and plotted the growth curves diagram. As shown in Figure 3, the lysis effect of pDawn(cI-LVA)-RBS070-LKD-T1-TOP10 meets our expectation in the first eight hours, but it is unstable after fifteen hours.</p>
(1)pSEVA331-pDawn(cI-LVA)-RBS070-LKD-T1-<i>G. hansenii</i> ATCC53582 <p></p>
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(2)pSEVA331-pDawn (cI-LVA)-LKD-T1-<i>G. hansenii</i> ATCC53582 <p></p>
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(3)pSEVA331-pDawn(cI-LVA)- RBS070-X174E-T1-<i>G. hansenii</i> ATCC53582 <p></p>
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(4)pSEVA331-pDawn(cI-LVA)-X174E-T1-<i>G. hansenii</i> ATCC53582 ]]
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[[File:K26 2.png|600px|thumb|center|Figure 2: Growth conditions of <i>E.coli</i>TOP10-pDawn(cI-LVA)-RBS070-LKD-T1 in the dark and under the light.]]
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[[File:K26 33.png|600px|thumb|center|Figure 3: Growth curves diagram of <i>E.coli</i> TOP10-pDawn(cI-LVA)-RBS070-LKD-T1.]]
 
<h3>References</h3>
 
<h3>References</h3>
<p>[1]Robert Ohlendorf, Roee R. Vidavski, Avigdor Eldar et.al.From Dusk till Dawn: One-Plasmid Systems for Light-Regulated Gene Expression.Journal of Molecular Biology, 08 Jan 2012, 416(4):534-542.</p>
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<p>[1] Robert Ohlendorf, Roee R. Vidavski, Avigdor Eldar et.al.From Dusk till Dawn: One-Plasmid Systems for Light-Regulated Gene Expression.Journal of Molecular Biology, 08 Jan 2012, 416(4):534-542.</p>
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<p>[2] [2]Ceyssens, P.-J. et al. Genomic analysis of Pseudomonas aeruginosa phages LKD16 and LKA1: establishment of the phiKMV subgroup within the T7 supergroup. J. Bacteriol. 188, 6924-31 (2006).</p>

Latest revision as of 14:40, 12 October 2022

pDawn-RBS070-LKD-T1

Description

This composite part is a generator containing pDawn(cI-LVA) (BBa_K1075044), RBS070 (BBa_K4325002), LKD (BBa_K4325004) and T1 terminator(BBa_K3033016).

Usage

We inserted the blue light responsive system pDawn(cI-LVA) (BBa_K1075044) and lysis gene LKD (BBa_K4325004) into the pSEVA331 expression vector, which was incorporated into E. coli TOP10 and screened for the bacterial colonies which grew in the dark but did not grow under blue light. Finally, the plasmids containing pDawn(cI-LVA)-RBS070-LKD-T1 were selected and introduced into G. hansenii ATCC53582 by electroporation to verify the responsiveness of pDawn(cI-LVA) to blue light.

Figure 1: Gene circuit of pDawn(cI-LVA)-RBS070-LKD-T1.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2171
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 63
    Illegal NgoMIV site found at 195
    Illegal NgoMIV site found at 289
    Illegal NgoMIV site found at 582
    Illegal NgoMIV site found at 1076
    Illegal NgoMIV site found at 1094
    Illegal NgoMIV site found at 1184
    Illegal AgeI site found at 414
    Illegal AgeI site found at 1542
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1643
    Illegal BsaI.rc site found at 525


2022 SZPT-China

Characterization

1.Batch screening of pDawn-RBS070-LKD-T1 by evaluating the response to blue light.

As shown in Figure 2, except for the 11th and 13th bacterial colonies, other bacterial colonies did not grow under blue light. To further explore the lysis effect of pDawn(cI-LVA)-RBS070-LKD-T1-TOP10, we tracked the OD600 values of pDawn(cI-LVA)-RBS070-LKD-T1-TOP10 and plotted the growth curves diagram. As shown in Figure 3, the lysis effect of pDawn(cI-LVA)-RBS070-LKD-T1-TOP10 meets our expectation in the first eight hours, but it is unstable after fifteen hours.

Figure 2: Growth conditions of E.coliTOP10-pDawn(cI-LVA)-RBS070-LKD-T1 in the dark and under the light.
Figure 3: Growth curves diagram of E.coli TOP10-pDawn(cI-LVA)-RBS070-LKD-T1.

References

[1] Robert Ohlendorf, Roee R. Vidavski, Avigdor Eldar et.al.From Dusk till Dawn: One-Plasmid Systems for Light-Regulated Gene Expression.Journal of Molecular Biology, 08 Jan 2012, 416(4):534-542.

[2] [2]Ceyssens, P.-J. et al. Genomic analysis of Pseudomonas aeruginosa phages LKD16 and LKA1: establishment of the phiKMV subgroup within the T7 supergroup. J. Bacteriol. 188, 6924-31 (2006).