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		<title>User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Ecoli:PhotoReceptorComponent - Revision history</title>
		<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;action=history</link>
		<description>Revision history for this page on the wiki</description>
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			<title>Etienne Robillard: /* Misc purine/pyrimidine agonists */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=656043&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;Misc purine/pyrimidine agonists&lt;/span&gt;&lt;/p&gt;

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				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;←Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 08:40, 15 November 2012&lt;/td&gt;
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		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 85:&lt;/td&gt;
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&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* [http://en.wikibooks.org/wiki/Principles_of_Biochemistry/Nucleic_acid_III:_Sythesis_of_nucleotides Principles of Biochemistry/Nucleic acid III: Synthesis of nucleotides]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* [http://en.wikibooks.org/wiki/Principles_of_Biochemistry/Nucleic_acid_III:_Sythesis_of_nucleotides Principles of Biochemistry/Nucleic acid III: Synthesis of nucleotides]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** Notice: Further connections towards elucidating the metabolic regulation of Scooby Doo based restriction endonucleases suggests Imidazole may be synthetized with or without formaldehyde, thus supporting the hypothesis of Imidazole derived adducts as orthogonal '''nucleic acid inhibitors'''.&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** Notice: Further connections towards elucidating the metabolic regulation of Scooby Doo based restriction endonucleases suggests Imidazole may be synthetized with or without formaldehyde, thus supporting the hypothesis of Imidazole derived adducts as orthogonal '''nucleic acid inhibitors'''.&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** &amp;quot;What is a &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;'''&lt;/del&gt;Purine'''? The name was invented by the German chemist Emil Fischer in 1884. A purine is a nucleotide (a nucleoside + phosphate group) that is amine based and planar, aromatic, and heterocyclic. The structure of purine is that of a cyclohexane(pyrimidine group) and cyclopentane('''imidazole''' group) attached to one another; the Nitrogen atoms are at positions 1,3,7,9. Adenine(A) and Guanine(G) are examples of purines which are involved in the construction of the backbone of the DNA and RNA. They are also a part of the structures for Adenosine disphosphate (ADP), triphosphate(ATP), and other enzymes. Purines form bonds with pentoses exclusively through the 9th Nitrogen atom.&amp;quot; [http://en.wikibooks.org/wiki/Structural_Biochemistry/Nucleic_Acid/Nitrogenous_Bases/Purines 1]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'''&lt;/ins&gt;&amp;quot;What is a Purine'''? The name was invented by the German chemist Emil Fischer in 1884. A purine is a nucleotide (a nucleoside + phosphate group) that is amine based and planar, aromatic, and &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'''&lt;/ins&gt;heterocyclic&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;'''&lt;/ins&gt;. The structure of purine is that of a cyclohexane(pyrimidine group) and cyclopentane('''imidazole''' group) attached to one another; the Nitrogen atoms are at positions 1,3,7,9. Adenine(A) and Guanine(G) are examples of purines which are involved in the construction of the backbone of the DNA and RNA. They are also a part of the structures for Adenosine disphosphate (ADP), triphosphate(ATP), and other enzymes. Purines form bonds with pentoses exclusively through the 9th Nitrogen atom.&amp;quot; [http://en.wikibooks.org/wiki/Structural_Biochemistry/Nucleic_Acid/Nitrogenous_Bases/Purines 1]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** [http://www.bioinfo.org.cn/book/biochemistry/chapt21/bio8.htm Degradation of Purines and Pyrimidines Leads to Uric Acid and Urea, Respectively]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** [http://www.bioinfo.org.cn/book/biochemistry/chapt21/bio8.htm Degradation of Purines and Pyrimidines Leads to Uric Acid and Urea, Respectively]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;del style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;===== cAMP (Cyclic adenosine monophosphate) notes ===== &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;===== cAMP (Cyclic adenosine monophosphate) notes ===== &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&lt;/table&gt;</description>
			<pubDate>Thu, 15 Nov 2012 08:40:15 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
		<item>
			<title>Etienne Robillard: /* Engineering Deceit with the Clouds: The H3 receptor site is an inducible metabolic promoter for orthogonal drug delivery and prokariotic gene regulation using Lactose derived repressors: An hypothesis.... */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=640650&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;Engineering Deceit with the Clouds: The H3 receptor site is an inducible metabolic promoter for orthogonal drug delivery and prokariotic gene regulation using Lactose derived repressors: An hypothesis....&lt;/span&gt;&lt;/p&gt;

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				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 11:49, 24 October 2012&lt;/td&gt;
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		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 17:&lt;/td&gt;
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&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* &amp;quot;The former name elective mutism indicates a widespread misconception among psychologists that selective mute people choose to be silent in certain situations, while the truth is that they often wish to speak but cannot. To reflect the involuntary nature of this disorder, the name was changed to selective mutism in 1994.&amp;quot; [http://en.wikipedia.org/wiki/Selective_mutism 1]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* &amp;quot;The former name elective mutism indicates a widespread misconception among psychologists that selective mute people choose to be silent in certain situations, while the truth is that they often wish to speak but cannot. To reflect the involuntary nature of this disorder, the name was changed to selective mutism in 1994.&amp;quot; [http://en.wikipedia.org/wiki/Selective_mutism 1]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;=== &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;Engineering Deceit &lt;/del&gt;with &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;the Clouds&lt;/del&gt;: The &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;H3 receptor site &lt;/del&gt;is an inducible &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;metabolic promoter &lt;/del&gt;for orthogonal &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;drug &lt;/del&gt;delivery and prokariotic gene regulation using Lactose derived repressors&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;: An hypothesis.... &lt;/del&gt;===&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;=== &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Light induced phosphoramidate antiviral protein expression &lt;/ins&gt;with &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;dual-input OmpR-(P-N) and LacZ promoters&lt;/ins&gt;: The &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;histidine kinase (EnvZ) &lt;/ins&gt;is an inducible &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;enzymatic catalyst &lt;/ins&gt;for orthogonal &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;prodrug &lt;/ins&gt;delivery and prokariotic gene regulation using Lactose derived repressors &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;and phosphonates derived nucleotides &lt;/ins&gt;===&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* '''Must read!''' [http://pathman.smpdb.ca/pathways/SMP00044/pathway Histidine Metabolism] (Serine/Threonine related?)&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* '''Must read!''' [http://pathman.smpdb.ca/pathways/SMP00044/pathway Histidine Metabolism] (Serine/Threonine related?)&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&lt;/table&gt;</description>
			<pubDate>Wed, 24 Oct 2012 11:49:51 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
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			<title>Etienne Robillard: User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Buzz moved to User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Ecoli:PhotoReceptorComponent</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=640637&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;a href=&quot;/wiki/User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Buzz&quot; title=&quot;User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Buzz&quot;&gt;User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Buzz&lt;/a&gt; moved to &lt;a href=&quot;/wiki/User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&quot; title=&quot;User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Ecoli:PhotoReceptorComponent&quot;&gt;User:Etienne Robillard/Notebook/Chemtrails911 notebook/Agent Ecoli:PhotoReceptorComponent&lt;/a&gt;&lt;/p&gt;

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				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 10:57, 24 October 2012&lt;/td&gt;
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			<pubDate>Wed, 24 Oct 2012 10:57:02 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
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			<title>Etienne Robillard: /* More BZ notes */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=640598&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;More BZ notes&lt;/span&gt;&lt;/p&gt;

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				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 09:12, 24 October 2012&lt;/td&gt;
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		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL: a C6-hexanoyl '''phosphoramidate''' based ester; ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;autophosphorylation &lt;/del&gt;of the LacZ::LuxR kinase; Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. [see also Acyclic nucleoside phosphonates; purine nucleotide analogs; cidofovir; tenofovir; adefovir; acetonitrile])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL: a C6-hexanoyl '''phosphoramidate''' based ester; ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;&amp;lt;span style=&amp;quot;color:red&amp;quot;&amp;gt;autoPhosphorylation&amp;lt;/span&amp;gt; &lt;/ins&gt;of the LacZ::LuxR kinase; Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. [see also Acyclic nucleoside phosphonates; purine nucleotide analogs; cidofovir; tenofovir; adefovir; acetonitrile])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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			<pubDate>Wed, 24 Oct 2012 09:12:48 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
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			<title>Etienne Robillard: /* More BZ notes */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=639621&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;More BZ notes&lt;/span&gt;&lt;/p&gt;

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				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 12:02, 23 October 2012&lt;/td&gt;
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		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;
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&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL: a C6-&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;hexanol &lt;/del&gt;'''phosphoramidate''' based ester; ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of autophosphorylation of the LacZ::LuxR kinase&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;) &lt;/del&gt;Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. [see also Acyclic nucleoside phosphonates; purine nucleotide analogs; cidofovir; tenofovir; adefovir; acetonitrile])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL: a C6-&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;hexanoyl &lt;/ins&gt;'''phosphoramidate''' based ester; ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of autophosphorylation of the LacZ::LuxR kinase&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;; &lt;/ins&gt;Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. [see also Acyclic nucleoside phosphonates; purine nucleotide analogs; cidofovir; tenofovir; adefovir; acetonitrile])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;!-- diff generator: internal 2013-06-20 06:05:37 --&gt;
&lt;/table&gt;</description>
			<pubDate>Tue, 23 Oct 2012 12:02:16 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
		<item>
			<title>Etienne Robillard: /* More BZ notes */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=639600&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;More BZ notes&lt;/span&gt;&lt;/p&gt;

			&lt;table style=&quot;background-color: white; color:black;&quot;&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;←Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 11:51, 23 October 2012&lt;/td&gt;
			&lt;/tr&gt;
		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL: a C6-hexanol '''phosphoramidate''' based ester&lt;del class=&quot;diffchange diffchange-inline&quot;&gt;: &lt;/del&gt;ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of autophosphorylation of the LacZ::LuxR kinase) Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. [])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL: a C6-hexanol '''phosphoramidate''' based ester&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;; &lt;/ins&gt;ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of autophosphorylation of the LacZ::LuxR kinase) Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. [&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;see also Acyclic nucleoside phosphonates; purine nucleotide analogs; cidofovir; tenofovir; adefovir; acetonitrile&lt;/ins&gt;])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;!-- diff generator: internal 2013-06-20 06:05:37 --&gt;
&lt;/table&gt;</description>
			<pubDate>Tue, 23 Oct 2012 11:51:36 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
		<item>
			<title>Etienne Robillard: /* More BZ notes */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=639568&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;More BZ notes&lt;/span&gt;&lt;/p&gt;

			&lt;table style=&quot;background-color: white; color:black;&quot;&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;←Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 11:23, 23 October 2012&lt;/td&gt;
			&lt;/tr&gt;
		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 139:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde degrading enzyme = benzaldehyde &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* cyanide + benzaldehyde = BZ&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL)&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* BZ (cAMP) + arabinose = '''LuxR''' (device input is 30C6HSL&lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;: a C6-hexanol '''phosphoramidate''' based ester: ie a synthetic nucleoside coupled to a imidazolium molecule used for horizontal gene transfer by binding to the L-histidine ligand, a neurotransmitter, as the result of autophosphorylation of the LacZ::LuxR kinase) Note that I also found out that phosphoramidate based phosphonates are classified as potent insecticides with recombinant properties in bacterias such a ''P.aeruginosa''. []&lt;/ins&gt;)&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** thus we have: A + B &amp;lt;=&amp;gt; C + D &amp;nbsp;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;** where C=N-(3-oxo-hexanoyl)-L-homoserine lactone is an autoinducer and D is a protein (luxR) implicated in gene transcriptional activation. ([http://en.wikipedia.org/wiki/Autoinducer#Vibrio_fischeri:_bioluminescence 1])&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;!-- diff generator: internal 2013-06-20 06:05:37 --&gt;
&lt;/table&gt;</description>
			<pubDate>Tue, 23 Oct 2012 11:23:17 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
		<item>
			<title>Etienne Robillard: /* Imidazole pornography: Nitrogenous-derived nerve gas precursor agents linked as prime suspects in the spraying of experimental aerosols over unaware and disinformed Quebec population */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=633751&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;Imidazole pornography: Nitrogenous-derived nerve gas precursor agents linked as prime suspects in the spraying of experimental aerosols over unaware and disinformed Quebec population&lt;/span&gt;&lt;/p&gt;

			&lt;table style=&quot;background-color: white; color:black;&quot;&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
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			&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;←Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 14:05, 8 October 2012&lt;/td&gt;
			&lt;/tr&gt;
		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 2:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 2:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;'''&amp;quot;The synthesis of several complex organic compounds follows a multistep synthesis. &amp;quot;Multistep synthesis&amp;quot; refers to the procedure in which the product of one reaction serves as the starting material in the subsequent reaction. The multistep synthesis of benzilic acid begins with a conversion benzaldehyde to benzoin through a condensation reaction. The benzoin then oxidizes into benzil, which undergoes rearrangement to give benzilic acid.&amp;quot;''' [http://www.ehow.com/info_10059172_explanation-multistep-synthesis-benzilic-acid.html 1]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;'''&amp;quot;The synthesis of several complex organic compounds follows a multistep synthesis. &amp;quot;Multistep synthesis&amp;quot; refers to the procedure in which the product of one reaction serves as the starting material in the subsequent reaction. The multistep synthesis of benzilic acid begins with a conversion benzaldehyde to benzoin through a condensation reaction. The benzoin then oxidizes into benzil, which undergoes rearrangement to give benzilic acid.&amp;quot;''' [http://www.ehow.com/info_10059172_explanation-multistep-synthesis-benzilic-acid.html 1]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;Moreover, on wikipedia we can read the following excerpt:&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;'''&amp;quot;The benzoin condensation is a reaction (often called a condensation reaction, for historical reasons) between two aromatic aldehydes, particularly benzaldehyde. The reaction is catalyzed by a nucleophile such as the cyanide anion or an N-heterocyclic carbene. The reaction product is an aromatic acyloin with benzoin as the parent compound.[1] An early version of the reaction was developed in 1832 by Justus von Liebig and Friederich Woehler during their research on bitter almond oil.[2] The catalytic version of the reaction was developed by Nikolay Zinin in the late 1830s,[3][4] and the reaction mechanism for this organic reaction was proposed in 1903 by A. J. Lapworth.[5]&amp;quot;''' [http://en.wikipedia.org/wiki/Benzoin_condensation 2]&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;=== A mental prison is still a prison: The Histamine H3 receptor is possibly implicated in unrational behavior and selective mutism disorders in healthy middle-age adults ===&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;=== A mental prison is still a prison: The Histamine H3 receptor is possibly implicated in unrational behavior and selective mutism disorders in healthy middle-age adults ===&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;!-- diff generator: internal 2013-06-20 06:05:37 --&gt;
&lt;/table&gt;</description>
			<pubDate>Mon, 08 Oct 2012 14:05:44 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
		<item>
			<title>Etienne Robillard: /* Heterocyclic carbenes as low-level chemical warfare agents */</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=633746&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;Heterocyclic carbenes as low-level chemical warfare agents&lt;/span&gt;&lt;/p&gt;

			&lt;table style=&quot;background-color: white; color:black;&quot;&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
			&lt;col class='diff-marker' /&gt;
			&lt;col class='diff-content' /&gt;
			&lt;tr valign='top'&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;←Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 13:33, 8 October 2012&lt;/td&gt;
			&lt;/tr&gt;
		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 31:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 31:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;NB: [http://en.wikipedia.org/wiki/Threonine &amp;quot;Tyrosine is not an alcohol but a phenol, since its hydroxyl group is bonded directly to an aromatic ring, giving it different acid/base and oxidative properties).&amp;quot;]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;NB: [http://en.wikipedia.org/wiki/Threonine &amp;quot;Tyrosine is not an alcohol but a phenol, since its hydroxyl group is bonded directly to an aromatic ring, giving it different acid/base and oxidative properties).&amp;quot;]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt;-&lt;/td&gt;&lt;td style=&quot;background: #ffa; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;==== Heterocyclic &lt;del class=&quot;diffchange diffchange-inline&quot;&gt;carbenes &lt;/del&gt;as low-level chemical warfare agents&amp;nbsp; ====&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;==== &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;N-&lt;/ins&gt;Heterocyclic &lt;ins class=&quot;diffchange diffchange-inline&quot;&gt;Carbenes (NHC) &lt;/ins&gt;as low-level chemical warfare agents&amp;nbsp; ====&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* Lactose (Lac operon): [[http://www.pstcc.edu/mfhicks/biol2120/prokaryoticregulation.html 1]]&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;* Lactose (Lac operon): [[http://www.pstcc.edu/mfhicks/biol2120/prokaryoticregulation.html 1]]&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
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&lt;/table&gt;</description>
			<pubDate>Mon, 08 Oct 2012 13:33:03 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
		<item>
			<title>Etienne Robillard at 13:19, 8 October 2012</title>
			<link>http://www.openwetware.org/index.php?title=User:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent&amp;diff=633745&amp;oldid=prev</link>
			<description>&lt;p&gt;&lt;/p&gt;

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				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;←Older revision&lt;/td&gt;
				&lt;td colspan='2' style=&quot;background-color: white; color:black;&quot;&gt;Revision as of 13:19, 8 October 2012&lt;/td&gt;
			&lt;/tr&gt;
		&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 1:&lt;/td&gt;
&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot;&gt;Line 1:&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;== Imidazole pornography: Nitrogenous-derived nerve gas precursor agents linked as prime suspects in the spraying of experimental aerosols over unaware and disinformed Quebec population ==&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;== Imidazole pornography: Nitrogenous-derived nerve gas precursor agents linked as prime suspects in the spraying of experimental aerosols over unaware and disinformed Quebec population ==&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td colspan=&quot;2&quot;&gt;&amp;nbsp;&lt;/td&gt;&lt;td class='diff-marker'&gt;+&lt;/td&gt;&lt;td style=&quot;background: #cfc; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;&lt;ins style=&quot;color: red; font-weight: bold; text-decoration: none;&quot;&gt;'''&amp;quot;The synthesis of several complex organic compounds follows a multistep synthesis. &amp;quot;Multistep synthesis&amp;quot; refers to the procedure in which the product of one reaction serves as the starting material in the subsequent reaction. The multistep synthesis of benzilic acid begins with a conversion benzaldehyde to benzoin through a condensation reaction. The benzoin then oxidizes into benzil, which undergoes rearrangement to give benzilic acid.&amp;quot;''' [http://www.ehow.com/info_10059172_explanation-multistep-synthesis-benzilic-acid.html 1]&lt;/ins&gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;=== A mental prison is still a prison: The Histamine H3 receptor is possibly implicated in unrational behavior and selective mutism disorders in healthy middle-age adults ===&lt;/div&gt;&lt;/td&gt;&lt;td class='diff-marker'&gt; &lt;/td&gt;&lt;td style=&quot;background: #eee; color:black; font-size: smaller;&quot;&gt;&lt;div&gt;=== A mental prison is still a prison: The Histamine H3 receptor is possibly implicated in unrational behavior and selective mutism disorders in healthy middle-age adults ===&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;!-- diff generator: internal 2013-06-20 06:05:37 --&gt;
&lt;/table&gt;</description>
			<pubDate>Mon, 08 Oct 2012 13:19:53 GMT</pubDate>			<dc:creator>Etienne Robillard</dc:creator>			<comments>http://www.openwetware.org/wiki/User_talk:Etienne_Robillard/Notebook/Chemtrails911_notebook/Agent_Ecoli:PhotoReceptorComponent</comments>		</item>
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