Difference between revisions of "Part:BBa K4325025"
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<partinfo>BBa_K4325025 short</partinfo> | <partinfo>BBa_K4325025 short</partinfo> | ||
===Description=== | ===Description=== | ||
− | The composite part is a generator consisting of pDawn (without LVA tag) (<partinfo>BBa_K4325010 </partinfo>) and LKD (<partinfo>BBa_K4325004 </partinfo>) | + | The composite part is a generator consisting of pDawn (without LVA tag) (<partinfo>BBa_K4325010 </partinfo>) and LKD. (<partinfo>BBa_K4325004 </partinfo>) |
===Usage=== | ===Usage=== | ||
<p>We inserted the pDawn (without LVA tag) (<partinfo>BBa_K4325010 </partinfo>)blue light response system and the lysis gene LKD (<partinfo>BBa_K4325004</partinfo>) into the pSEVA331 expression vector, which was inserted into <i> E. coli</i> TOP10 screened out the colonies grew in the dark but did not grow in blue light to verify the responsiveness of pDawn (without LVA tag) to blue light.</p > | <p>We inserted the pDawn (without LVA tag) (<partinfo>BBa_K4325010 </partinfo>)blue light response system and the lysis gene LKD (<partinfo>BBa_K4325004</partinfo>) into the pSEVA331 expression vector, which was inserted into <i> E. coli</i> TOP10 screened out the colonies grew in the dark but did not grow in blue light to verify the responsiveness of pDawn (without LVA tag) to blue light.</p > | ||
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<h4> | <h4> | ||
1.Batch screening of pDawn(without LVA tag)-RBS070-LKD-T1-pSEVA331 in response to blue light lysis in <i> E. coli</i>.</h4> | 1.Batch screening of pDawn(without LVA tag)-RBS070-LKD-T1-pSEVA331 in response to blue light lysis in <i> E. coli</i>.</h4> | ||
− | [[File:K025 without LVA.png|600px|thumb|center|Figure 1 | + | [[File:K025 without LVA.png|600px|thumb|center|Figure 1 was the growth condition of pSEVA331-pDawn (without LVA tag) -RBS070-LKD-T1-TOP10 both in the dark and under the light.]]<P></P>As shown in Figure 1, four bacterial colony of pSEVA331-pDawn (without LVA tag) -RBS070-LKD-T1-TOP10 grew in the dark, but it did not grow under the light. |
<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 > | <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 > |
Revision as of 12:17, 10 October 2022
pDawn(cl)-RBS070-LKD-T1
Description
The composite part is a generator consisting of pDawn (without LVA tag) (BBa_K4325010) and LKD. (BBa_K4325004)
Usage
We inserted the pDawn (without LVA tag) (BBa_K4325010)blue light response system and the lysis gene LKD (BBa_K4325004) into the pSEVA331 expression vector, which was inserted into E. coli TOP10 screened out the colonies grew in the dark but did not grow in blue light to verify the responsiveness of pDawn (without LVA tag) 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
Characterization
1.Batch screening of pDawn(without LVA tag)-RBS070-LKD-T1-pSEVA331 in response to blue light lysis in E. coli.
As shown in Figure 1, four bacterial colony of pSEVA331-pDawn (without LVA tag) -RBS070-LKD-T1-TOP10 grew in the dark, but it did not grow under the light.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.