From 47bbe876dbd7ef2fc2b9baf0c0b0861a6a6e4176 Mon Sep 17 00:00:00 2001
From: HouTeng Chan <ht-chen21@mails.tsinghua.edu.cn>
Date: Tue, 1 Oct 2024 17:27:01 +0000
Subject: [PATCH] Update file therapy-system.html
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<h2>Design</h2>
<hr>
<div class="image-container" style="display: flex; flex-direction: column; align-items: center;">
- <img src="https://static.igem.wiki/teams/5187/wiki-therapysystem-fig/fig1.png" alt="ibd_figure" class="shadowed-image" style="width: 70%; max-width: 600px;">
+ <img src="https://static.igem.wiki/teams/5187/wiki-therapysystem-fig/fig1.png" alt="ibd_figure" class="shadowed-image" style="width: 80%; max-width: 800px;">
<p style="text-align: center; font-size: 0.9em; margin-top: 10px;">fig 1 Schematic Representation of our Experimental Design</p>
</div>
<p>We introduced muscone gas molecule receptors derived from mouse olfactory epithelial cells into chassis bioengineered bacteria. The muscone gas molecule receptor is a G protein coupled receptor in eukaryotic cells, and we chose Saccharomyces cerevisiaet as the chassis bioengineering bacterium. By modifying the mating pathway of Saccharomyces cerevisiae, the muscone gas molecule receptor is integrated into the signaling pathway of Saccharomyces cerevisiae. And downstream of the modified mating pathway, lactate dehydrogenase was introduced to alter the anaerobic metabolism pathway of Saccharomyces cerevisiae, synthesizing lactate for the treatment of IBD disease.</p>
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