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	<id>https://wiki.fkkt.uni-lj.si/index.php?action=history&amp;feed=atom&amp;title=Acetil_koencim_A</id>
	<title>Acetil koencim A - Revision history</title>
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	<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;action=history"/>
	<updated>2026-04-18T18:17:20Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;diff=4771&amp;oldid=prev</id>
		<title>Sara Drvarič Talian at 19:18, 12 December 2010</title>
		<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;diff=4771&amp;oldid=prev"/>
		<updated>2010-12-12T19:18:49Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 19:18, 12 December 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l1&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=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Acetil koencim A&amp;#039;&amp;#039;&amp;#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocetne kisline]] &amp;lt;ref&amp;gt;S. P. Stanforth, Natural Product Chemistry at a Glance, stran 8&amp;lt;/ref&amp;gt;, ki je sestavljen iz acetila, ß-merkaptoetilaminske enote, enote pantotenata ([[vitamini B|vitamin B]]&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;), fosfata in 3&amp;#039;,5&amp;#039;-adenozin difosfata &amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 451&amp;lt;/ref&amp;gt;. Njena kemijska formula je C&amp;lt;sub&amp;gt;23&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;38&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;7&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;17&amp;lt;/sub&amp;gt;P&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;S, molska masa pa 809,57 g/mol. &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Acetil koencim A&amp;#039;&amp;#039;&amp;#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocetne kisline]] &amp;lt;ref&amp;gt;S. P. Stanforth, Natural Product Chemistry at a Glance, stran 8&amp;lt;/ref&amp;gt;, ki je sestavljen iz acetila, ß-merkaptoetilaminske enote, enote pantotenata ([[vitamini B|vitamin B]]&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;), fosfata in 3&amp;#039;,5&amp;#039;-adenozin difosfata &amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 451&amp;lt;/ref&amp;gt;. Njena kemijska formula je C&amp;lt;sub&amp;gt;23&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;38&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;7&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;17&amp;lt;/sub&amp;gt;P&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;S, molska masa pa 809,57 g/mol. &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Acetil koencim A nastane, ko se acetilna skupina (CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;CO-) poveže s sulfhidrilno (tiolno) skupino (-SH) molekule [[koencim A|koencima A]] z visokoenergijsko (nestabilno) vezjo &amp;lt;ref&amp;gt;Oxford dictionary of chemistry, stran 5&amp;lt;/ref&amp;gt;. Spojina je pomembna za [[pregled metabolizma|metabolizem]], deluje kot koencim v mnogih bioloških reakcijah acetilacije in kot intermediat v razgradnji snovi pridobljenih iz hrane [http://www.ncbi.nlm.nih.gov/books/NBK28401/figure/A195/?report=objectonly (shematski prikaz)], hkrati pa je iz nje možen nastanek maščobnih kislin, holesterola in ketonskih teles &amp;lt;ref&amp;gt;American Heritage Stedman&amp;#039;s Medical Dictionary&amp;lt;/ref&amp;gt;. &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot; data-marker=&quot;+&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Acetil koencim A nastane, ko se acetilna skupina (CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;CO-) poveže s sulfhidrilno (tiolno) skupino (-SH) molekule [[koencim A|koencima A]] z visokoenergijsko (nestabilno) vezjo &amp;lt;ref&amp;gt;Oxford dictionary of chemistry, stran 5&amp;lt;/ref&amp;gt;. Spojina je pomembna za [[pregled metabolizma|metabolizem]], deluje kot koencim v mnogih bioloških reakcijah acetilacije in kot intermediat v razgradnji snovi pridobljenih iz hrane [http://www.ncbi.nlm.nih.gov/books/NBK28401/figure/A195/?report=objectonly (shematski prikaz)], hkrati pa je iz nje možen nastanek maščobnih kislin, holesterola in &lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;[[ketonska telesa|&lt;/ins&gt;ketonskih teles&lt;ins style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;]] &lt;/ins&gt;&amp;lt;ref&amp;gt;American Heritage Stedman&amp;#039;s Medical Dictionary&amp;lt;/ref&amp;gt;. &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Služi kot prenašalec ogljikovih atomov acetilne skupine, ki izhaja iz: &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;Služi kot prenašalec ogljikovih atomov acetilne skupine, ki izhaja iz: &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Sara Drvarič Talian</name></author>
	</entry>
	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;diff=4749&amp;oldid=prev</id>
		<title>Sara Drvarič Talian at 14:39, 12 December 2010</title>
		<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;diff=4749&amp;oldid=prev"/>
		<updated>2010-12-12T14:39:30Z</updated>

		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;table style=&quot;background-color: #fff; color: #202122;&quot; data-mw=&quot;interface&quot;&gt;
				&lt;col class=&quot;diff-marker&quot; /&gt;
				&lt;col class=&quot;diff-content&quot; /&gt;
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				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;← Older revision&lt;/td&gt;
				&lt;td colspan=&quot;2&quot; style=&quot;background-color: #fff; color: #202122; text-align: center;&quot;&gt;Revision as of 14:39, 12 December 2010&lt;/td&gt;
				&lt;/tr&gt;&lt;tr&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-lineno&quot; id=&quot;mw-diff-left-l1&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=&quot;diff-marker&quot; data-marker=&quot;−&quot;&gt;&lt;/td&gt;&lt;td style=&quot;color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&lt;del style=&quot;font-weight: bold; text-decoration: none;&quot;&gt;==Acetil koencim A==&lt;/del&gt;&lt;/div&gt;&lt;/td&gt;&lt;td colspan=&quot;2&quot; class=&quot;diff-side-added&quot;&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Acetil koencim A&amp;#039;&amp;#039;&amp;#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocetne kisline]] &amp;lt;ref&amp;gt;S. P. Stanforth, Natural Product Chemistry at a Glance, stran 8&amp;lt;/ref&amp;gt;, ki je sestavljen iz acetila, ß-merkaptoetilaminske enote, enote pantotenata ([[vitamini B|vitamin B]]&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;), fosfata in 3&amp;#039;,5&amp;#039;-adenozin difosfata &amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 451&amp;lt;/ref&amp;gt;. Njena kemijska formula je C&amp;lt;sub&amp;gt;23&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;38&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;7&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;17&amp;lt;/sub&amp;gt;P&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;S, molska masa pa 809,57 g/mol. &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Acetil koencim A&amp;#039;&amp;#039;&amp;#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocetne kisline]] &amp;lt;ref&amp;gt;S. P. Stanforth, Natural Product Chemistry at a Glance, stran 8&amp;lt;/ref&amp;gt;, ki je sestavljen iz acetila, ß-merkaptoetilaminske enote, enote pantotenata ([[vitamini B|vitamin B]]&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;), fosfata in 3&amp;#039;,5&amp;#039;-adenozin difosfata &amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 451&amp;lt;/ref&amp;gt;. Njena kemijska formula je C&amp;lt;sub&amp;gt;23&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;38&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;7&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;17&amp;lt;/sub&amp;gt;P&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;S, molska masa pa 809,57 g/mol. &amp;lt;br&amp;gt;&lt;/div&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;tr&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;td class=&quot;diff-marker&quot;&gt;&lt;/td&gt;&lt;td style=&quot;background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;&quot;&gt;&lt;br/&gt;&lt;/td&gt;&lt;/tr&gt;
&lt;/table&gt;</summary>
		<author><name>Sara Drvarič Talian</name></author>
	</entry>
	<entry>
		<id>https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;diff=4748&amp;oldid=prev</id>
		<title>Sara Drvarič Talian: New page: ==Acetil koencim A== &#039;&#039;&#039;Acetil koencim A&#039;&#039;&#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocet...</title>
		<link rel="alternate" type="text/html" href="https://wiki.fkkt.uni-lj.si/index.php?title=Acetil_koencim_A&amp;diff=4748&amp;oldid=prev"/>
		<updated>2010-12-12T14:38:32Z</updated>

		<summary type="html">&lt;p&gt;New page: ==Acetil koencim A== &amp;#039;&amp;#039;&amp;#039;Acetil koencim A&amp;#039;&amp;#039;&amp;#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocet...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;==Acetil koencim A==&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Acetil koencim A&amp;#039;&amp;#039;&amp;#039; je organska spojina [http://library.med.utah.edu/NetBiochem/FattyAcids/2_4.html (strukturna formula)], tioesterski derivat [[ocetna kislina|ocetne kisline]] &amp;lt;ref&amp;gt;S. P. Stanforth, Natural Product Chemistry at a Glance, stran 8&amp;lt;/ref&amp;gt;, ki je sestavljen iz acetila, ß-merkaptoetilaminske enote, enote pantotenata ([[vitamini B|vitamin B]]&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;), fosfata in 3&amp;#039;,5&amp;#039;-adenozin difosfata &amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 451&amp;lt;/ref&amp;gt;. Njena kemijska formula je C&amp;lt;sub&amp;gt;23&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;38&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;7&amp;lt;/sub&amp;gt;O&amp;lt;sub&amp;gt;17&amp;lt;/sub&amp;gt;P&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;S, molska masa pa 809,57 g/mol. &amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Acetil koencim A nastane, ko se acetilna skupina (CH&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;CO-) poveže s sulfhidrilno (tiolno) skupino (-SH) molekule [[koencim A|koencima A]] z visokoenergijsko (nestabilno) vezjo &amp;lt;ref&amp;gt;Oxford dictionary of chemistry, stran 5&amp;lt;/ref&amp;gt;. Spojina je pomembna za [[pregled metabolizma|metabolizem]], deluje kot koencim v mnogih bioloških reakcijah acetilacije in kot intermediat v razgradnji snovi pridobljenih iz hrane [http://www.ncbi.nlm.nih.gov/books/NBK28401/figure/A195/?report=objectonly (shematski prikaz)], hkrati pa je iz nje možen nastanek maščobnih kislin, holesterola in ketonskih teles &amp;lt;ref&amp;gt;American Heritage Stedman&amp;#039;s Medical Dictionary&amp;lt;/ref&amp;gt;. &amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Služi kot prenašalec ogljikovih atomov acetilne skupine, ki izhaja iz: &amp;lt;br&amp;gt;&lt;br /&gt;
-razgradnje aminokislin, &amp;lt;br&amp;gt;&lt;br /&gt;
-razgradnje maščob skozi [[beta oksidacija|beta oksidacijo]] maščobnih kislin&amp;lt;ref&amp;gt; N. A. Campbell, Biology, stran 180&amp;lt;/ref&amp;gt; ter &amp;lt;br&amp;gt; &lt;br /&gt;
-[[piruvat|piruvata]], ki nastane skozi [[glikoliza|glikolizo]] enostavnih sladkorjev v procesu razgradnje ogljikovih hidratov &amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 514&amp;lt;/ref&amp;gt;.  &amp;lt;br&amp;gt;&lt;br /&gt;
Acetil koencim A nato vstopi v cikel citronske kisline ([[Krebsov cikel]]), ta pa je predpogoj, da poteče [[oksidativna fosforilacija]], ki proizvaja energijo ([[ATP]]). &amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Iz treh molekul acetil koencima A se lahko tvori 3-hidroksi-3-metilglutaril koencim A, ki je prekurzor [[holesterol|holesterola]] in ketonskih teles. Za namen sinteze maščobnih kislin se acetil koencim A pretvori v citrat in izstopi v citosol&amp;lt;ref&amp;gt;L. Stryer, Biochemistry, stran 770&amp;lt;/ref&amp;gt;. Spojina igra pomembno vlogo tudi pri sintezi živčnega prenašalca [[acetilholin|acetilholina]]. Pri določenih bakterijah je možen tudi anaeroben reverzibilen nastanek acetil koencima A iz piruvata, ki ga katalizira piruvat format liaza, pri sesalcih pa pretvorba acetil koencima A nazaj v piruvat ni možna. &amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Viri ==&lt;br /&gt;
&amp;lt;references/&amp;gt;&lt;br /&gt;
* [http://en.wikipedia.org/wiki/Acetyl_coenzyme_A  Acetyl-CoA, Wikipedia] &amp;lt;br&amp;gt;&lt;br /&gt;
* [http://en.wikipedia.org/wiki/Pyruvate_formate_lyase Pyruvate formate lyase, Wikipedia] &amp;lt;br&amp;gt;&lt;br /&gt;
== Zunanje povezave ==&lt;br /&gt;
* [http://www.chm.bris.ac.uk/motm/acetylcoa/acoah.htm Acetyl Coenzyme A – Molecule of the month for May 2007]&lt;br /&gt;
* [http://library.med.utah.edu/NetBiochem/FattyAcids/2_1.html Acetyl CoA – The Center of Lipid Metabolism]&lt;br /&gt;
[[Category:LEX]]&lt;/div&gt;</summary>
		<author><name>Sara Drvarič Talian</name></author>
	</entry>
</feed>