<?xml version="1.0"?>
<feed xmlns="http://www.w3.org/2005/Atom" xml:lang="en">
		<id>http://gcat.davidson.edu/GcatWiki/index.php?action=history&amp;feed=atom&amp;title=Describe_different_design_architectures</id>
		<title>Describe different design architectures - Revision history</title>
		<link rel="self" type="application/atom+xml" href="http://gcat.davidson.edu/GcatWiki/index.php?action=history&amp;feed=atom&amp;title=Describe_different_design_architectures"/>
		<link rel="alternate" type="text/html" href="http://gcat.davidson.edu/GcatWiki/index.php?title=Describe_different_design_architectures&amp;action=history"/>
		<updated>2026-06-09T23:50:32Z</updated>
		<subtitle>Revision history for this page on the wiki</subtitle>
		<generator>MediaWiki 1.28.2</generator>

	<entry>
		<id>http://gcat.davidson.edu/GcatWiki/index.php?title=Describe_different_design_architectures&amp;diff=6994&amp;oldid=prev</id>
		<title>BoCool at 15:18, 28 October 2008</title>
		<link rel="alternate" type="text/html" href="http://gcat.davidson.edu/GcatWiki/index.php?title=Describe_different_design_architectures&amp;diff=6994&amp;oldid=prev"/>
				<updated>2008-10-28T15:18:45Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Davidson XOR Biological Design ==&lt;br /&gt;
[http://partsregistry.org/AHL '''List of auto-inducers and their catalog numbers.''']&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
&amp;lt;center&amp;gt;'''Davidson Approach'''&amp;lt;br&amp;gt;&lt;br /&gt;
'''Here is an idea Malcolm and Laurie developed.''' &amp;lt;br&amp;gt;&lt;br /&gt;
'''Everyone please look at this and ask questions and find holes in it now so we don't waste time building something that won't work.'''&amp;lt;br&amp;gt;&amp;lt;/center&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;center&amp;gt; [[Image:XOR_AMC1b.jpg]]&amp;lt;br&amp;gt;&amp;lt;/center&amp;gt;&lt;br /&gt;
The idea is to have two mirrored halves of the system. LasR is regulated by PAI-1 {3-oxododecanoyl-HSL (3OC12HSL)} and LuxR is activated by AI-1 {3-oxohexanoyl-homoserine lactone ([http://partsregistry.org/3OC6HSL 3OC6HSL])}. There is a potential problem in that the Lux half is more likely to get positive feedback than the Las half. This MAY not be a problem because 0/0 is leaky so we put a weak RBS to minimize leaky protein production. Also, if we add AI-2 and AI-1 is produced by leak, then the entire system shuts down. The repressor site is located between -35 and -10 of the promoter. The activator binding site is upstream of -35. This has been documented [http://www.bio.davidson.edu/courses/synthetic/papers/LuxR.pdf by Egland and Greenberg]&lt;br /&gt;
&lt;br /&gt;
[[Oligos_to_Build]]: Sequences we will need to make this XOR gate.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Missouri Western XOR Biological Design 1==&lt;br /&gt;
&lt;br /&gt;
These two XOR circuits are designed to complement each other. Each recieves a cell-to-cell signal (AI-1 or AI-2) and a chemical signal (IPTG or AHL) and processes it into a cell-to-cell signal.  Colonies that output AI-1 would alternate with colonies that produce AI-2.  The input message to be hashed could be encoded by the presence or absence of the chemical signals, which would also alternate.  &lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:XOR DR AI2.PNG]]&lt;br /&gt;
&lt;br /&gt;
'''Above '''- Input of AI-1 or IPTG turns on production of AI-2 by LuxS.  Input by both AI-1 and IPTG allows production of the repressors cI and Mnt, which repress both transcription units.  LuxR and LacI are constitutively expressed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Image:XOR DR AI1b.PNG]]&amp;lt;br&amp;gt;&lt;br /&gt;
'''Above''' - Input of AI-2 or aTc turns on production of AI-1 by LuxI.  Input by both AI-2 and aTc allows production of the repressors cI and Mnt, which repress both transcription units.  LsrK, LsrR and TetR are constitutively expressed.&lt;/div&gt;</summary>
		<author><name>BoCool</name></author>	</entry>

	</feed>