Difference between revisions of "Part:BBa K5136042"
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<center><html><img src="https://static.igem.wiki/teams/4907/wiki/parts/haoxihuan/and-gate.png" width="700px"></html></center>
 
<center><html><img src="https://static.igem.wiki/teams/4907/wiki/parts/haoxihuan/and-gate.png" width="700px"></html></center>
 
<center><b>Fig. 1 Gene circuits of verification system for <i>hrp</i> AND gate. </b></center>
 
<center><b>Fig. 1 Gene circuits of verification system for <i>hrp</i> AND gate. </b></center>
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<br/>If we use CspA Cold-responsive elements to express proteins at low temperatures, there will be a risk of gene leakage at a higher temperature than we expected because the response temperature has a broad range. To solve this problem, we plan to combine a logic AND gate with the CspA CRE. Based on it, we designed an AND gate to respond to low temperature, namely, <i>hrp</i> AND gate. In this system, the <i>hrpR</i> and <i>hrpS</i> genes are regulated by the CspA CRE (Fig. 2). Under low-temperature conditions, only when both proteins are expressed, can the expression of downstream genes be induced, reducing the leaky expression.
 
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<center><html><img src="https://static.igem.wiki/teams/4907/wiki/parts/haoxihuan/cspa-and-gate.png" width="700px"></html></center>
 
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<center><b>Fig. 2 Gene circuits of <i>hrp</i> system regulated by the CspA CRE.</b></center>
 
  
 
===Characterization===
 
===Characterization===
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When we were building this circuit, colony PCR was used to certify the plasmid was correct. We got the target fragment-****bp(Fig. 3).
 
When we were building this circuit, colony PCR was used to certify the plasmid was correct. We got the target fragment-****bp(Fig. 3).
  
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<center><html><img src="https://static.igem.wiki/teams/4907/wiki/parts/haoxihuan/cspa-and-gate.png" width="700px"></html></center>
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<center><b>Fig. 2 Gene circuits of <i>hrp</i> system regulated by the CspA CRE.</b></center>
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Revision as of 11:18, 30 September 2024


LexRO

Biology

LexRO is a synthetic light-switchable repressor, based on a novel LOV light sensor domain, RsLOV. In the darkness, LexRO dimerizes and binds to its cognate operator sequence to repress promoter activity. Upon light exposure, the LexRO dimer dissociates, causing dissociation from the operator sequence, and initiates gene expression.

Usage and design

In the darkness, LexRO dimerizes and binds to the cognate operator sequence to repress the activity of pColE408. Upon blue light exposure, the LexRO dimer dissociates, causing dissociation from the operator sequence, and initiates the expression of ccdB， eventually leading to cell death. We used LexRO, pHybrid 2)-114 version, SD7, ccdA, and ccdB to construct the regulation system and obtained the composite part BBa_K5136231, which was assembled on the expression vector pSB4A5.

Fig. 1 Gene circuits of verification system for hrp AND gate.

Characterization

Agarose gel electrophoresis (AGE)

When we were building this circuit, colony PCR was used to certify the plasmid was correct. We got the target fragment-****bp(Fig. 3).

Fig. 2 Gene circuits of hrp system regulated by the CspA CRE.

Sequence and Features