Difference between revisions of "Team:Tsinghua/Composite Part"

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<div class="highlightBox">
+
<p>
<h4>Note</h4>
+
<br />
<p>In order to be considered for the <a href="https://2015.igem.org/Judging/Awards#SpecialPrizes">Best New Composite Part award</a>, you must fill out this page. Please give links to the Registry entries for the Composite parts you have made. Please see the Registry's <a href="http://parts.igem.org/Help:Parts#Basic_and_Composite_Parts"> Help:Parts page</a> for more information on part types.</p>
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</p>
 +
<div style="border:none;padding:0cm 0cm 2.0pt 0cm;">
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<span style="font-size:18px;"><strong>Part:BBa_K1797000</strong></span>
 +
</p>
 
</div>
 
</div>
 
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<p style="text-align:center;margin-left:0cm;background:white;">
 +
<b><span style="font-size:16px;">Blue
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Light Sensing System with GFP Reporter</span></b>
 +
</p>
 +
<p style="background:white;">
 +
This
 +
part is a combination of B0034-YF1-B0034-FixJ(BBa_K592016), FixK2
 +
promoter(BBa_K592006), and amilGFP(BBa_K592010) in that order. We also add a
 +
constitutive promoter(BBa_J23119) so that teams can use this part to test the
 +
blue light system easily. When the cells are kept in dark, they will express
 +
amilGFP, a yellow chromoprotein. This protein causes the cells to have a yellow
 +
color. When the cells are exposed to blue light, the amilGFP won't be expressed
 +
and the yellow color can't be seen.
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
<div style="border:none;padding:0cm 0cm 2.0pt 0cm;">
 +
<h1 style="text-align:center;margin-left:0cm;">
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<span style="font-size:18px;">Part:BBa_K1797001</span>
 +
</h1>
 +
</div>
 +
<p class="MsoNormal" style="text-align:center;">
 +
<b><span style="font-size:16px;">Red Light Sensing System</span></b>
 +
</p>
 +
<p class="MsoNormal">
 +
This part is mainly composed of
 +
Cph8(BBa_K592018), ho1(BBa_I15008) and PcyA(BBa_I15009), which form the red
 +
light sensing system in E.coli. Cph8 is a synthetic red light sensor,
 +
consisting of Cph1, a natural red light sensor, and EnvZ, a histidine kinase.
 +
The most important part of the light sensor is PCB(phycocyanobilin), without
 +
which the red light sensor cannot work. However, PCB is not generated by E.coli
 +
naturally. So we need to introduce ho1 and PcyA into E.coli. Actually we've
 +
also submitted the PCB generation system(BBa_K1797008). These two enzymes can
 +
change heme into PCB. Here we combine the three main parts- Cph8, ho1 and PcyA-
 +
together to facilitate parts users.
 +
</p>
 +
<p class="MsoNormal">
 +
<br />
 +
</p>
 +
<p class="MsoNormal">
 +
<br />
 +
</p>
 +
<div style="border:none;padding:0cm 0cm 2.0pt 0cm;">
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<strong><span style="font-size:18px;">Part:BBa_K1797003</span></strong>
 +
</p>
 +
</div>
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<b><span style="font-size:16px;">Blue Light Sensing System with GFP and RFP Reporter</span></b>
 +
</p>
 +
<p class="MsoNormal" align="left">
 +
This part is one of the many bio-bricks used to test the
 +
blue-light system in our project. Specifically, it contains an entire
 +
blue-light system, including a light sensor YF1 and a response regulator FixJ,
 +
and two Fixk2 promoter regulated reporters. We used this part to test the
 +
efficacy and efficiency of the blue-light system in E. coli. If the bacteria
 +
carrying this plasmid is provided with blue light, two reporters cannot be
 +
synthesized. On the contrary, if it is kept in dark, then the bacteria colony
 +
will display a mixture color from RFP and GFP.
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
<p>
 +
<p class="MsoNormal" align="left">
 +
<br />
 +
</p>
 +
<div style="border:none;padding:0cm 0cm 2.0pt 0cm;">
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<strong><span style="font-size:18px;">Part:BBa_K1797004</span></strong>
 +
</p>
 +
</div>
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<b><span style="font-size:16px;">Blue Light Sensing System With GFP And BFP Reporter</span></b>
 +
</p>
 +
<p class="MsoNormal" align="left">
 +
This part is an improved part based on BBa_K1797000.
 +
Except for the GFP reporter system, we introduced cI repressor and
 +
corresponding BFP. In the absence of blue light, GFP but not BFP will be
 +
expressed. With blue light, BFP but not GFP will be expressed.
 +
</p>
 +
<p class="MsoNormal" align="left">
 +
<br />
 +
</p>
 +
<p class="MsoNormal" align="left">
 +
<br />
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
<div style="border:none;padding:0cm 0cm 2.0pt 0cm;">
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<span style="font-size:18px;"><strong>Part:BBa_K1797008</strong></span>
 +
</p>
 +
</div>
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<b><span style="font-size:16px;">PCB generation system</span></b>
 +
</p>
 +
<p class="MsoNormal">
 +
This part includes ho1 and PcyA, both of which
 +
are needed in converting heme into PCB(phycocyanobilin). PCB is an important
 +
part of the Cph1, a red light sensor. Since PCB cannot be generated naturally
 +
by E.coli. This part can be used to produce PCB and make sure the E.coli can
 +
sense red light.
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
<div style="border:none;padding:0cm 0cm 2.0pt 0cm;">
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<span style="font-size:18px;"><strong>Part:BBa_K1797009</strong></span>
 +
</p>
 +
</div>
 +
<p class="MsoNormal" align="left" style="text-align:center;">
 +
<b><span style="font-size:16px;">Red light sensing system with mRFP reporter</span></b>
 +
</p>
 +
<p class="MsoNormal" align="left">
 +
This part consists of a red light sensing
 +
system(BBa_K1797001) and an RFP reporter system. When bacterial colonies are
 +
exposed to red light, the OmpR promoter is not activated, preventing the
 +
expression of RFP. When colonies are kept in dark, the corresponding
 +
transcription factor of mpR promoter is activated and RFP is expressed, making
 +
the colonies red.
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 +
<p>
 +
<br />
 +
</p>
 
<p>
 
<p>
A composite part is a functional unit of DNA consisting of two or more basic parts assembled together. <a href="http://parts.igem.org/wiki/index.php/Part:BBa_I13507">BBa_I13507</a> is an example of a composite part, consisting of an RBS, a protein coding region for a red fluorescent protein, and a terminator.
+
<br />
 
</p>
 
</p>
 
+
<h1 style="text-align:center;margin-left:0cm;">
<p>New composite BioBrick devices can be made by combining existing BioBrick Parts (like Inverters, Amplifiers, Smell Generators, Protein Balloon Generators, Senders, Receivers, Actuators, and so on).</p>
+
<br />
 +
</h1>
  
  

Revision as of 01:48, 19 September 2015

Composite Parts


Part:BBa_K1797000

Blue Light Sensing System with GFP Reporter

This part is a combination of B0034-YF1-B0034-FixJ(BBa_K592016), FixK2 promoter(BBa_K592006), and amilGFP(BBa_K592010) in that order. We also add a constitutive promoter(BBa_J23119) so that teams can use this part to test the blue light system easily. When the cells are kept in dark, they will express amilGFP, a yellow chromoprotein. This protein causes the cells to have a yellow color. When the cells are exposed to blue light, the amilGFP won't be expressed and the yellow color can't be seen.



Part:BBa_K1797001

Red Light Sensing System

This part is mainly composed of Cph8(BBa_K592018), ho1(BBa_I15008) and PcyA(BBa_I15009), which form the red light sensing system in E.coli. Cph8 is a synthetic red light sensor, consisting of Cph1, a natural red light sensor, and EnvZ, a histidine kinase. The most important part of the light sensor is PCB(phycocyanobilin), without which the red light sensor cannot work. However, PCB is not generated by E.coli naturally. So we need to introduce ho1 and PcyA into E.coli. Actually we've also submitted the PCB generation system(BBa_K1797008). These two enzymes can change heme into PCB. Here we combine the three main parts- Cph8, ho1 and PcyA- together to facilitate parts users.



Part:BBa_K1797003

Blue Light Sensing System with GFP and RFP Reporter

This part is one of the many bio-bricks used to test the blue-light system in our project. Specifically, it contains an entire blue-light system, including a light sensor YF1 and a response regulator FixJ, and two Fixk2 promoter regulated reporters. We used this part to test the efficacy and efficiency of the blue-light system in E. coli. If the bacteria carrying this plasmid is provided with blue light, two reporters cannot be synthesized. On the contrary, if it is kept in dark, then the bacteria colony will display a mixture color from RFP and GFP.



Part:BBa_K1797004

Blue Light Sensing System With GFP And BFP Reporter

This part is an improved part based on BBa_K1797000. Except for the GFP reporter system, we introduced cI repressor and corresponding BFP. In the absence of blue light, GFP but not BFP will be expressed. With blue light, BFP but not GFP will be expressed.




Part:BBa_K1797008

PCB generation system

This part includes ho1 and PcyA, both of which are needed in converting heme into PCB(phycocyanobilin). PCB is an important part of the Cph1, a red light sensor. Since PCB cannot be generated naturally by E.coli. This part can be used to produce PCB and make sure the E.coli can sense red light.



Part:BBa_K1797009

Red light sensing system with mRFP reporter

This part consists of a red light sensing system(BBa_K1797001) and an RFP reporter system. When bacterial colonies are exposed to red light, the OmpR promoter is not activated, preventing the expression of RFP. When colonies are kept in dark, the corresponding transcription factor of mpR promoter is activated and RFP is expressed, making the colonies red.





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