Difference between revisions of "Part:BBa K4325026"
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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) and LKD | + | <p>This composite part is a generator containing pDawn (CI-LVA) (<partinfo>BBa_K1075044</partinfo>) and LKD |
===Usage=== | ===Usage=== | ||
<p>The pDawn (CI-LVA) blue light responsive system (<partinfo>BBa_K1075044</partinfo>) and lysis cassette LKD (<partinfo>BBa_K4325004</partinfo>) were linked with the pSEVA331 expression vector. Then these constructs were transformed into <i>. E. coli</i> TOP10 and screened for strain that grew well in dark but failed to grow under blue light. Finally, the pSEVA331-pDawn-RBS070-LKD-T1 plasmid were obtained and genomically inserted into <i>G. hansenii </i> ATCC53582 for further responsiveness verification of pDawn (CI-LVA) to blue light.</p> | <p>The pDawn (CI-LVA) blue light responsive system (<partinfo>BBa_K1075044</partinfo>) and lysis cassette LKD (<partinfo>BBa_K4325004</partinfo>) were linked with the pSEVA331 expression vector. Then these constructs were transformed into <i>. E. coli</i> TOP10 and screened for strain that grew well in dark but failed to grow under blue light. Finally, the pSEVA331-pDawn-RBS070-LKD-T1 plasmid were obtained and genomically inserted into <i>G. hansenii </i> ATCC53582 for further responsiveness verification of pDawn (CI-LVA) to blue light.</p> | ||
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=2022 SZPT-China= | =2022 SZPT-China= | ||
− | + | (<partinfo>BBa_K4325004</partinfo>).</p> | |
− | + | ||
<h3>Characterization</h3> | <h3>Characterization</h3> | ||
<h4>1.Characterization in <i>E. coli</i> TOP10</h4> | <h4>1.Characterization in <i>E. coli</i> TOP10</h4> |
Revision as of 09:07, 10 October 2022
pDawn-RBS070-LKD-T1
Description
This composite part is a generator containing pDawn (CI-LVA) (BBa_K1075044) and LKD
Usage
<p>The pDawn (CI-LVA) blue light responsive system (BBa_K1075044) and lysis cassette LKD (BBa_K4325004) were linked with the pSEVA331 expression vector. Then these constructs were transformed into . E. coli TOP10 and screened for strain that grew well in dark but failed to grow under blue light. Finally, the pSEVA331-pDawn-RBS070-LKD-T1 plasmid were obtained and genomically inserted into G. hansenii ATCC53582 for further responsiveness verification of pDawn (CI-LVA) to blue light.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2171
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE 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 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1643
Illegal BsaI.rc site found at 525
2022 SZPT-China
(BBa_K4325004).</p>
Characterization
1.Characterization in E. coli TOP10
As shown in Figure1, 14 colonies meet our expectation and one of them was picked and culture in the dark and under blue light. Growth curves shows the bacteria continue growing after 8 hours, indicating this system is not robust.
2.Characterization in G. hansenii ATCC53582
The picked plasmids from E. coli TOP10 were transformed into G. hansenii ATCC53582. It shows that these two plasmids still maintain their excellent lysis effect in G. hansenii ATCC53582.
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.