Difference between revisions of "Part:BBa K4325022"
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<h3>Characterization</h3>
 
<h3>Characterization</h3>
 
<h4>1.Batch screening of pDawn(cI-LVA)-X174E-LVA-T1 in response to blue light lysis in <i>E. coli</i>.</h4>
 
<h4>1.Batch screening of pDawn(cI-LVA)-X174E-LVA-T1 in response to blue light lysis in <i>E. coli</i>.</h4>
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<p>We transformed pDawn(cI-LVA)-X174E-LVA-T1 into TOP10 and performed agarose gel electrophoresis, as shown in Figure 1,pDawn(cI-LVA)-X174E-LVA-T1 has been successfully transformed into TOP10.</p>
+
<p>We transformed pDawn(cI-LVA)-X174E-LVA-T1 into TOP10 and performed agarose gel electrophoresis, as shown in Figure 1, pDawn(cI-LVA)-X174E-LVA-T1 has been successfully transformed into TOP10.</p>
  
 
[[File:K18 1.png|400px|thumb|center|Figure 1: pDawn(cI-LVA)-RBS070-LKD-LVA-T1 and <b>(2) pDawn(cI-LVA)-X174E-LVA-T1</b> has been successfully identified in <i>E. coli</i> TOP10]]
 
[[File:K18 1.png|400px|thumb|center|Figure 1: pDawn(cI-LVA)-RBS070-LKD-LVA-T1 and <b>(2) pDawn(cI-LVA)-X174E-LVA-T1</b> has been successfully identified in <i>E. coli</i> TOP10]]

Revision as of 16:10, 11 October 2022

pDawn-X174E-LVA-T1

Description

The composite part is a generator consisting of pDawn (cI-LVA) (BBa_K1075044) and X174E-LVA (BBa_K4325007).

Usage

We inserted the pDawn (cI-LVA)(BBa_K1075044) blue light response system and the lysis gene X174E-LVA(BBa_K4325007) into the pSEVA331 expression vector, which was inserted into E.coli TOP10 and screened out the bacterial colony which grew in the dark but did not grow under the blue light to verify the responsiveness of pDawn (cI-LVA) to blue light.

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(cI-LVA)-X174E-LVA-T1 in response to blue light lysis in E. coli.

We transformed pDawn(cI-LVA)-X174E-LVA-T1 into TOP10 and performed agarose gel electrophoresis, as shown in Figure 1, pDawn(cI-LVA)-X174E-LVA-T1 has been successfully transformed into TOP10.

Figure 1: pDawn(cI-LVA)-RBS070-LKD-LVA-T1 and (2) pDawn(cI-LVA)-X174E-LVA-T1 has been successfully identified in E. coli TOP10

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.