Brittneywick (Talk | contribs) |
Evan pepper (Talk | contribs) |
||
(7 intermediate revisions by 2 users not shown) | |||
Line 458: | Line 458: | ||
<div id="page"> | <div id="page"> | ||
<center> | <center> | ||
+ | <br> | ||
<br> | <br> | ||
Line 488: | Line 489: | ||
<!-- <div class="text-container"> --> | <!-- <div class="text-container"> --> | ||
<!-- <div class="paragraph-left"> --> | <!-- <div class="paragraph-left"> --> | ||
− | <p>We aim to genetically modify PCC 7942 to produce acetaminophen, a common mild anesthetic and antipyretic recognized by the WHO as an essential medicine <sup>[1]</sup>. However, in many countries with lower regulations and faulty policies regarding drug manufacturing, acetaminophen can be synthesized with lethal toxins that result in hundreds of deaths worldwide <sup>[23]</sup>. Acetaminophen is often used in conjunction with opioid pain medications postoperatively to enhance pain relief, thus reducing reliance upon opioid pharmaceuticals <sup>[24]</sup>.</p> | + | <p>We aim to genetically modify <i>S. elongatus</i> PCC 7942 to produce acetaminophen, a common mild anesthetic and antipyretic recognized by the WHO as an essential medicine<sup>[1]</sup>. However, in many countries with lower regulations and faulty policies regarding drug manufacturing, acetaminophen can be synthesized with lethal toxins that result in hundreds of deaths worldwide<sup>[23]</sup>. Acetaminophen is often used in conjunction with opioid pain medications postoperatively to enhance pain relief, thus reducing reliance upon opioid pharmaceuticals<sup>[24]</sup>.</p> |
<!-- </div> --> | <!-- </div> --> | ||
<!-- </div> --> | <!-- </div> --> | ||
Line 523: | Line 524: | ||
<!-- <div class="text-container"> | <!-- <div class="text-container"> | ||
<div class="paragraph-left"> --> | <div class="paragraph-left"> --> | ||
− | <p>We are using a previously engineered pathway in <span style="font-style: italic";>E. coli</span> as a model of acetaminophen biosynthesis to enhance PCC 7942 <sup>[26, 25]</sup>. The pathway converts chorismate, an abundant | + | <p>We are using a previously engineered pathway in <span style="font-style: italic";>E. coli</span> as a model of acetaminophen biosynthesis to enhance PCC 7942<sup>[26, 25]</sup>. The pathway converts chorismate, an abundant amino acid precursor of tryptophan, phenylalanine, and tyrosine, into acetaminophen with the addition ofthe <span style="font-style: italic";>4ABH</span> gene from <span style="font-style: italic";>A. bisporus</span>, an edible mushroom, and <span style="font-style: italic";>nhoA</span> from <span style="font-style: italic";>E. coli</span>. For more information on acetaminophen metabolics, check out <a href="https://2017.igem.org/Team:UCSC/Model">our modeling page!</a></p> |
<!-- </div> | <!-- </div> | ||
</div> --> | </div> --> | ||
Line 572: | Line 573: | ||
<a href="https://2017.igem.org/Team:UCSC/Target-Organism" class="proj-button"> | <a href="https://2017.igem.org/Team:UCSC/Target-Organism" class="proj-button"> | ||
− | <img src="https://static.igem.org/mediawiki/2017/ | + | <img src="https://static.igem.org/mediawiki/2017/8/84/Spirulinaicon.png" class="proj-button-image"> |
<div class="proj-button-desc"> | <div class="proj-button-desc"> | ||
<div class="overlap-button-text">TARGET ORGANISM</div> | <div class="overlap-button-text">TARGET ORGANISM</div> | ||
Line 578: | Line 579: | ||
</a> | </a> | ||
− | <a href="https://2017.igem.org/Team:UCSC/ | + | <a href="https://2017.igem.org/Team:UCSC/Part_Collection" class="proj-button"> |
<img src="https://static.igem.org/mediawiki/2017/9/9c/Parts_icon.png" class="proj-button-image"> | <img src="https://static.igem.org/mediawiki/2017/9/9c/Parts_icon.png" class="proj-button-image"> | ||
<div class="proj-button-desc"> | <div class="proj-button-desc"> |
Latest revision as of 01:44, 2 November 2017
ACETAMINOPHEN METABOLICS
"Antipyretic drugs, by being analgesics, reduce not only the fever but also the pain."
We aim to genetically modify S. elongatus PCC 7942 to produce acetaminophen, a common mild anesthetic and antipyretic recognized by the WHO as an essential medicine[1]. However, in many countries with lower regulations and faulty policies regarding drug manufacturing, acetaminophen can be synthesized with lethal toxins that result in hundreds of deaths worldwide[23]. Acetaminophen is often used in conjunction with opioid pain medications postoperatively to enhance pain relief, thus reducing reliance upon opioid pharmaceuticals[24].
We are using a previously engineered pathway in E. coli as a model of acetaminophen biosynthesis to enhance PCC 7942[26, 25]. The pathway converts chorismate, an abundant amino acid precursor of tryptophan, phenylalanine, and tyrosine, into acetaminophen with the addition ofthe 4ABH gene from A. bisporus, an edible mushroom, and nhoA from E. coli. For more information on acetaminophen metabolics, check out our modeling page!