Difference between revisions of "Team:US AFRL CarrollHS/Composite Part"

(Prototype team page)
 
 
(16 intermediate revisions by 4 users not shown)
Line 1: Line 1:
{{US_AFRL_CarrollHS}}
+
{{US_AFRL_CarrollHS/WikiStripDown}} {{US_AFRL_CarrollHS/Layout!}} {{US_AFRL_CarrollHS/Bootstrap1}} {{US_AFRL_CarrollHS/Bootstrap2}} {{US_AFRL_CarrollHS/Bootstrap3}} {{US_AFRL_CarrollHS/Bootstrap4}} {{US_AFRL_CarrollHS/Bootstrap8}} {{US_AFRL_CarrollHS/navbar}} {{US_AFRL_CarrollHS/hero}}
 
<html>
 
<html>
  
 +
<div class="hero">
 +
      <img src="https://static.igem.org/mediawiki/2018/0/0e/T--US_AFRL_CarrollHS--CompositePartsHeader.jpg" alt="Composite Parts" style="margin-top: 85px;">
 +
</div>
  
  
<div class="column full_size judges-will-not-evaluate">
+
<div class="background">
<h3>★  ALERT! </h3>
+
<div class="row"><h1>Part: PRhl_31_CheZ_J23117_34_RhlR</h1></div>
<p>This page is used by the judges to evaluate your team for the <a href="https://2018.igem.org/Judging/Medals">medal criterion</a> or <a href="https://2018.igem.org/Judging/Awards"> award listed below</a>. </p>
+
<div class="row"><h2><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K2594011">Bba_K2594011</a></h2></div>
<p> Delete this box in order to be evaluated for this medal criterion and/or award. See more information at <a href="https://2018.igem.org/Judging/Pages_for_Awards"> Instructions for Pages for awards</a>.</p>
+
<div class="row"><p>The plasmid senses and responds to N-butanoyl-L-Homoserine Lactone (C4-HSL), a quorum sensing molecule that is present in <i>Pseudomonas aeruginosa</i>, a common component of biofilms. The J23117 promoter constitutively expresses RhlR, which activates the PRhl promoter site when bound to C4-HSL. Once quorum sensing signals are detected, the production of CheZ, a protein responsible for chemotactic ability, begins. As the plasmid senses C4-HSL, the microbe begins moving in a straight-line path along the concentration gradient. If the microbe leaves the concentration gradient, it will begin tumbling again until it enters back into the gradient, eventually arriving at the biofilm. </p></div>
 
</div>
 
</div>
  
  
<div class="clear"></div>
+
<div class="background">
 
+
<div class="row"><h1>Part: Chitinase C-1</h1></div>
 
+
<div class="row"><h2><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K2594012">Bba_K2594012</a></h2></div>
 
+
<div class="row"><p>This plasmid contains a gene encoding for chitinase C1 fused to the N- and C-term domains of <i>Pseudomonas syringae</i> ice-nucleation protein. The fusion protein will be anchored to the <i>Escherichia coli</i> cell surface.  Chitinase is an enzyme that degrades chitin, a major component in the structure of cell walls for plant and fungi cells. In our project, the first plasmid PRhl_31_CheZ_J23117_34_RhlR allows the <i>E. coli</i> to swim next to the biofilm with ice-nucleating protein-Chitinase C-1 fusion protein on the surface. The degradation of the cell wall allows cinnamaldehyde easier access to the cell membrane and ultimately the destruction and death of the cell.  Since the ice-nucleation protein keeps Chitinase C-1 anchored to the cell membrane of the engineered <i>E. coli</i>, lower concentrations of the chitinase will be required to effectively damage and destroy the biofilm.   </p></div>
 
+
 
+
<div class="column full_size">
+
<h1>Composite Parts</h1>
+
 
+
 
+
<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.
+
</p>
+
 
+
<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>
+
 
</div>
 
</div>
  
<div class="column full_size">
+
<div class="background">
<div class="highlight decoration_background">
+
<div class="row"><h1>Part: Chitinase B4A</h1></div>
<h3>Note</h3>
+
<div class="row"><h2><a href="http://parts.igem.org/wiki/index.php?title=Part:BBa_K2594013">Bba_K2594013</a></h2></div>
<p>This page should list all the composite parts your team has made during your project. You must add all characterization information for your parts on the Registry. You should not put characterization information on this page. Remember judges will only look at the first part in the list for the Best Composite Part award, so put your best part first!</p>
+
<div class="row"><p>This plasmid contains a gene encoding for chitinase B4A originated from <i>Serratia marcescens</i> B4A fused to the N- and C-term domains of <i>Pseudomonas syringae</i> ice-nucleation protein. The fusion protein will be anchored to the  <i>Escherichia coli</i> cell surface.  Chitinase is an enzyme that degrades chitin, a major component in the structure of cell walls for plant and fungi cells.  In our project, the first plasmid PRhl_31_CheZ_J23117_34_RhlR allows the <i>E. coli</i> to swim next to the biofilm with ice-nucleating protein-Chitinase B4A fusion protein on the surface. The degradation of the cell wall allows cinnamaldehyde easier access to the cell membrane and ultimately the destruction and death of the cell.  Since the ice-nucleation protein keeps Chitinase B4A anchored to the cell membrane of the engineered <i>E. coli</i>, lower concentrations of the chitinase will be required to effectively damage and destroy the biofilm.  </p></div>
</div>
+
 
</div>
 
</div>
  
 
 
<div class="column full_size">
 
<h3>Best Composite Part Special Prize</h3>
 
 
<p>To be eligible for this award, this part must adhere to <a href="http://parts.igem.org/DNA_Submission">Registry sample submission guidelines</a> and have been sent to the Registry of Standard Biological Parts. If you have a part you wish to nominate your team for this <a href="https://2018.igem.org/Judging/Awards">special prize</a>, make sure you add your part number to your <a href="https://2018.igem.org/Judging/Judging_Form">judging form</a> and delete the box at the top of this page.
 
 
<br><br>
 
<b>Please note:</b> Judges will only look at the first part number you list, so please only enter ONE (1) part number in the judging form for this prize. </p>
 
 
</div>
 
  
 
</html>
 
</html>
 +
{{US_AFRL_CarrollHS/footer}}

Latest revision as of 02:23, 18 October 2018

Composite Parts

Part: PRhl_31_CheZ_J23117_34_RhlR

The plasmid senses and responds to N-butanoyl-L-Homoserine Lactone (C4-HSL), a quorum sensing molecule that is present in Pseudomonas aeruginosa, a common component of biofilms. The J23117 promoter constitutively expresses RhlR, which activates the PRhl promoter site when bound to C4-HSL. Once quorum sensing signals are detected, the production of CheZ, a protein responsible for chemotactic ability, begins. As the plasmid senses C4-HSL, the microbe begins moving in a straight-line path along the concentration gradient. If the microbe leaves the concentration gradient, it will begin tumbling again until it enters back into the gradient, eventually arriving at the biofilm.

Part: Chitinase C-1

This plasmid contains a gene encoding for chitinase C1 fused to the N- and C-term domains of Pseudomonas syringae ice-nucleation protein. The fusion protein will be anchored to the Escherichia coli cell surface. Chitinase is an enzyme that degrades chitin, a major component in the structure of cell walls for plant and fungi cells. In our project, the first plasmid PRhl_31_CheZ_J23117_34_RhlR allows the E. coli to swim next to the biofilm with ice-nucleating protein-Chitinase C-1 fusion protein on the surface. The degradation of the cell wall allows cinnamaldehyde easier access to the cell membrane and ultimately the destruction and death of the cell. Since the ice-nucleation protein keeps Chitinase C-1 anchored to the cell membrane of the engineered E. coli, lower concentrations of the chitinase will be required to effectively damage and destroy the biofilm.

Part: Chitinase B4A

This plasmid contains a gene encoding for chitinase B4A originated from Serratia marcescens B4A fused to the N- and C-term domains of Pseudomonas syringae ice-nucleation protein. The fusion protein will be anchored to the Escherichia coli cell surface. Chitinase is an enzyme that degrades chitin, a major component in the structure of cell walls for plant and fungi cells. In our project, the first plasmid PRhl_31_CheZ_J23117_34_RhlR allows the E. coli to swim next to the biofilm with ice-nucleating protein-Chitinase B4A fusion protein on the surface. The degradation of the cell wall allows cinnamaldehyde easier access to the cell membrane and ultimately the destruction and death of the cell. Since the ice-nucleation protein keeps Chitinase B4A anchored to the cell membrane of the engineered E. coli, lower concentrations of the chitinase will be required to effectively damage and destroy the biofilm.