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Team:Uppsala/metabolic-engineering
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<!-- Contains sub-logo picture --> | <!-- Contains sub-logo picture --> | ||
| - | <div id="igem_logo"><a href="https://2013.igem.org/ | + | <div id="igem_logo"><a href="https://2013.igem.org/Team:Uppsala"><img class="igem_logo" src="https://static.igem.org/mediawiki/2013/e/e0/Uppsala2013_IGEMlogo.png"></a></div> |
| - | <div id="igem"><a href="https://2013.igem.org/Main_Page"><img class="igem" src="https://static.igem.org/mediawiki/2013/ | + | <div id="igem"><a href="https://2013.igem.org/Main_Page"><img class="igem" src="https://static.igem.org/mediawiki/2013/b/b8/Uppsala2013_Uppsala_IGEM_log_blue.png"></a></div> |
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| + | <img class="slogan" src="https://static.igem.org/mediawiki/2013/a/ad/Uppsala2013_Header.png"> | ||
</div> | </div> | ||
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<li><a href="https://2013.igem.org/Team:Uppsala/project" id="list_type1"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/a/aa/Uppsala2013_Project.png"></a> | <li><a href="https://2013.igem.org/Team:Uppsala/project" id="list_type1"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/a/aa/Uppsala2013_Project.png"></a> | ||
<ul> | <ul> | ||
| - | + | ||
<li><a href="https://2013.igem.org/Team:Uppsala/chassi">Chassi</a> | <li><a href="https://2013.igem.org/Team:Uppsala/chassi">Chassi</a> | ||
<ul> | <ul> | ||
| Line 50: | Line 74: | ||
<li><a href="https://2013.igem.org/Team:Uppsala/promoters">Promoters</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/promoters">Promoters</a></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/reporter-genes">Reporter genes</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/reporter-genes">Reporter genes</a></li> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/toxin-antitoxin-system">Toxin-antitoxin system</a></li> |
<li><a href="https://2013.igem.org/Team:Uppsala/vectors">Vectors</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/vectors">Vectors</a></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/signal-peptide">Signal peptide</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/signal-peptide">Signal peptide</a></li> | ||
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<li><a href="https://2013.igem.org/Team:Uppsala/metabolic-engineering">Metabolic engineering</a> | <li><a href="https://2013.igem.org/Team:Uppsala/metabolic-engineering">Metabolic engineering</a> | ||
<ul> | <ul> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/p-coumaric-acid"> | + | <li><a href="https://2013.igem.org/Team:Uppsala/p-coumaric-acid">p-Coumaric acid</a></li> |
<li><a href="https://2013.igem.org/Team:Uppsala/resveratrol">Resveratrol</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/resveratrol">Resveratrol</a></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/lycopene">Lycopene</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/lycopene">Lycopene</a></li> | ||
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<li><a | <li><a | ||
href="https://2013.igem.org/Team:Uppsala/saffron">Saffron</a></li> | href="https://2013.igem.org/Team:Uppsala/saffron">Saffron</a></li> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/astaxanthin">Astaxanthin</a></li> |
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/zeaxanthin">Zeaxanthin</a></li> |
</ul></li> | </ul></li> | ||
</li> | </li> | ||
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href="https://2013.igem.org/Team:Uppsala/miraculin">Miraculin</a></li> | href="https://2013.igem.org/Team:Uppsala/miraculin">Miraculin</a></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/chromoproteins">Chromoproteins</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/chromoproteins">Chromoproteins</a></li> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/safety">Safety experiment</a></li> | + | <li><a href="https://2013.igem.org/Team:Uppsala/safety-experiment">Safety experiment</a></li> |
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/results">Results</a></li> |
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<li><a href="https://2013.igem.org/Team:Uppsala/modeling" id="list_type1"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/6/63/Uppsala2013_Modeling.png"></a> | <li><a href="https://2013.igem.org/Team:Uppsala/modeling" id="list_type1"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/6/63/Uppsala2013_Modeling.png"></a> | ||
<ul> | <ul> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/P-Coumaric-acid-pathway">Kinetic model</a></li> |
<li><a href="https://2013.igem.org/Team:Uppsala/modeling-tutorial">Modeling tutorial </a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/modeling-tutorial">Modeling tutorial </a></li> | ||
| + | |||
| + | <li><a href="https://2013.igem.org/Team:Uppsala/toxicity-model">Toxicity model</a></li> | ||
</ul></li> | </ul></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/parts" id="list_type2"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/e/eb/Uppsala2013_parts.png"></a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/parts" id="list_type2"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/e/eb/Uppsala2013_parts.png"></a></li> | ||
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<li><a href="https://2013.igem.org/Team:Uppsala/carotenoid-group">Carotenoid group</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/carotenoid-group">Carotenoid group</a></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/chassi-group">Chassi group</a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/chassi-group">Chassi group</a></li> | ||
| - | + | <li><a href="https://2013.igem.org/Team:Uppsala/advisors">Advisors</a></li> | |
| + | |||
</ul></li> | </ul></li> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/human-practice" id="list_type3"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/b/b8/Uppsala2013_HP.png"></a> |
<ul> | <ul> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/yoghurt">Yoghurt +</a></li> |
| - | <li><a href="https://2013.igem.org/Team:Uppsala/synbioday"> | + | <li><a href="https://2013.igem.org/Team:Uppsala/synbioday">SynBioDay</a></li> |
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/biosafety-and-ethics">Biosafety and ethics</a></li> |
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/public-opinion">Public opinion </a></li> |
| - | + | <li><a href="https://2013.igem.org/Team:Uppsala/Outreach">High school & media </a></li> | |
| - | + | <li><a href="https://2013.igem.org/Team:Uppsala/bioart">BioArt</a></li> | |
| + | <li><a href="https://2013.igem.org/Team:Uppsala/LactonutritiousWorld">A LactoWorld</a></li> | ||
| + | <li><a href="https://2013.igem.org/Team:Uppsala/killswitches">Killswitches</a></li> | ||
| + | <li><a href="https://2013.igem.org/Team:Uppsala/realization">Patent</a></li> | ||
</ul></li> | </ul></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/attribution" id="list_type4"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/5/5d/Uppsala2013_Attributions.png"></a></li> | <li><a href="https://2013.igem.org/Team:Uppsala/attribution" id="list_type4"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/5/5d/Uppsala2013_Attributions.png"></a></li> | ||
<li><a href="https://2013.igem.org/Team:Uppsala/notebook" id="list_type3"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/3/36/Uppsala2013_Notebook.png"></a> | <li><a href="https://2013.igem.org/Team:Uppsala/notebook" id="list_type3"><img class="nav-text" src="https://static.igem.org/mediawiki/2013/3/36/Uppsala2013_Notebook.png"></a> | ||
<ul> | <ul> | ||
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/safety-form">Safety form</a></li> |
| - | <li><a href="https://2013.igem.org/Team:Uppsala/ | + | <li><a href="https://2013.igem.org/Team:Uppsala/protocols">Protocols</a></li> |
</ul></li> | </ul></li> | ||
</ul> | </ul> | ||
| - | </div> | + | </div> |
</div> | </div> | ||
| - | |||
<div id="main_content"> <!-- Put content here --> | <div id="main_content"> <!-- Put content here --> | ||
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<div id="chassi_pic_container_a"> | <div id="chassi_pic_container_a"> | ||
| - | <div id="metabolic_pic_lycopene"> < | + | <div id="metabolic_pic_lycopene"> <a href="https://2013.igem.org/Team:Uppsala/lycopene"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/3/39/Uppsala2013_Lycopene2.png" onmouseover="this.src='https://static.igem.org/mediawiki/2013/b/b4/Uppsala2013_LycopenePushed.png'" onmouseout="this.src='https://static.igem.org/mediawiki/2013/3/39/Uppsala2013_Lycopene2.png'"> </div> |
| - | <div id="metabolic_pic_zeaxanthin"> < | + | |
| - | <div id="metabolic_pic_astaxanthin"> < | + | <div id="metabolic_pic_zeaxanthin"> <a href="https://2013.igem.org/Team:Uppsala/zeaxanthin"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/0/0b/Uppsala2013_Zeaxantin2.png" onmousemove="this.src='https://static.igem.org/mediawiki/2013/0/07/Uppsala2013_Zeaxantin2Pushed.png'" onmouseout="this.src='https://static.igem.org/mediawiki/2013/0/0b/Uppsala2013_Zeaxantin2.png'"> </div> |
| + | |||
| + | <div id="metabolic_pic_astaxanthin"><a href="https://2013.igem.org/Team:Uppsala/astaxanthin"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/3/3a/Uppsala2013_Astaxanthin2.png" onmouseover="this.src='https://static.igem.org/mediawiki/2013/0/0d/Uppsala2013_Astaxanthin2Pushed.png'" onmouseout="this.src='https://static.igem.org/mediawiki/2013/3/3a/Uppsala2013_Astaxanthin2.png'"> </div> | ||
| + | |||
</div> | </div> | ||
<div id="chassi_pic_container_b"> | <div id="chassi_pic_container_b"> | ||
| - | <div id="metabolic_pic_beta_carotene"> < | + | <div id="metabolic_pic_beta_carotene"><a href="https://2013.igem.org/Team:Uppsala/betacarotene"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/3/3c/Uppsala2013_beta-carotene2.png" onmouseover="this.src='https://static.igem.org/mediawiki/2013/0/04/Uppsala2013_beta-carotene2Pushed.png'" onmouseout="this.src='https://static.igem.org/mediawiki/2013/3/3c/Uppsala2013_beta-carotene2.png'"> </div> |
</div> | </div> | ||
<div id="chassi_pic_container_c"> | <div id="chassi_pic_container_c"> | ||
| - | <div id="metabolic_pic_saffron"> < | + | <div id="metabolic_pic_saffron"><a href="https://2013.igem.org/Team:Uppsala/saffron"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/7/7a/Uppsala2013_Saffron2.png" onmouseover="this.src='https://static.igem.org/mediawiki/2013/8/8f/Uppsala2013_Saffron2Pushed.png'" |
| - | <div id="metabolic_pic_coumeric"> < | + | onmouseout="this.src='https://static.igem.org/mediawiki/2013/7/7a/Uppsala2013_Saffron2.png'"> </div> |
| - | <div id="metabolic_pic_resveratrol"> < | + | |
| + | <div id="metabolic_pic_coumeric"><a href="https://2013.igem.org/Team:Uppsala/p-coumaric-acid"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/0/02/Uppsala2013_P-coumaric_acid2.png" onmouseover="this.src='https://static.igem.org/mediawiki/2013/4/4a/Uppsala2013_0P-coumaric_acid2Pushed.png'" onmouseout="this.src='https://static.igem.org/mediawiki/2013/0/02/Uppsala2013_P-coumaric_acid2.png'"> </div> | ||
| + | |||
| + | <div id="metabolic_pic_resveratrol"><a href="https://2013.igem.org/Team:Uppsala/resveratrol"><img class="metabolic_pic" src="https://static.igem.org/mediawiki/2013/0/08/Uppsala2013_Resveratrol2.png" onmouseover="this.src='https://static.igem.org/mediawiki/2013/0/04/Uppsala2013_Resveratrol2Pushed.png'" onmouseout="this.src='https://static.igem.org/mediawiki/2013/0/08/Uppsala2013_Resveratrol2.png'"> </div> | ||
</div> | </div> | ||
</div> <!-- Closing div for shortcut_pic --> | </div> <!-- Closing div for shortcut_pic --> | ||
| + | |||
<div id="container_mini_pic"> | <div id="container_mini_pic"> | ||
| - | <div id="coumeric_div"> | + | <div class="text_box_in_the_box" id="coumeric_div"> |
| - | <div id="substance_title"> <h3> P- | + | <a href="https://2013.igem.org/Team:Uppsala/p-coumaric-acid"> |
| + | <div id="substance_title"> <h3> P-coumaric acid </h3> </div> | ||
<div class="coumeric_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/0/02/20130924122324%21Uppsala2013_P-coumaric_acid3.png"> </div> | <div class="coumeric_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/0/02/20130924122324%21Uppsala2013_P-coumaric_acid3.png"> </div> | ||
| - | <div id="substance_text"> <p> P-coumaric acid is an antioxidant that is produced from tyrosin by the | + | |
| + | </a> | ||
| + | <div id="substance_text"> <p> P-coumaric acid is an antioxidant that is produced from tyrosin by the enzyme Tyrosine ammonia lyase (TAL). This antioxidant has been shown to have many health benefits. For example studies have shown that it can reduce the risk of atherosclerosis and also reduce the risk of stomach cancer. P-coumaric acid can be found in foods such as peanuts, garlic, wine and vinegar. </p> | ||
| + | |||
| + | |||
| + | <div id="substance_plasmid"> <a href="https://2013.igem.org/Team:Uppsala/p-coumaric-acid#b1"> <img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/1/18/Uppsala2013_P-coumaric_plasmid.png"></a> </div> | ||
| + | |||
| + | </div> | ||
</div> | </div> | ||
| - | <div id="resveratrol_div"> | + | |
| + | |||
| + | <div class="text_box_in_the_box" id="resveratrol_div"> | ||
| + | <a href="https://2013.igem.org/Team:Uppsala/resveratrol"> | ||
<div id="substance_title"> <h3> Resveratrol </h3> </div> | <div id="substance_title"> <h3> Resveratrol </h3> </div> | ||
<div class="resveratrol_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/b/bb/Uppsala2013_ResveratrolSymbol.png"> </div> | <div class="resveratrol_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/b/bb/Uppsala2013_ResveratrolSymbol.png"> </div> | ||
| - | <div id="substance_text"> <p> Resveratrol belongs to a group of molecules known as Phyloalexin which is used by many plants to battle infections of all sorts. Many studies have been done on resveratrol showing it has a wide range of beneficial properties ranging from skin cancer reduction to anti-inflamatory effects and antioxidant properties. Perhaps the most interesting property is that of life extension. | + | |
| + | </a> | ||
| + | <div id="substance_text"> <p>Resveratrol belongs to a group of molecules known as Phyloalexin which is used by many plants to battle infections of all sorts. Many studies have been done on resveratrol showing it has a wide range of beneficial properties ranging from skin cancer reduction to anti-inflamatory effects and antioxidant properties. Perhaps the most interesting property is that of life extension.</p> | ||
| + | |||
| + | <div id="substance_plasmid"> <a href="https://2013.igem.org/Team:Uppsala/resveratrol#b1"> <img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/c/c5/Uppsala2013_Resveratrol_plasmid.png"></a> </div> | ||
| + | |||
| + | </div> | ||
</div> | </div> | ||
| - | <div id="lycopene_div"> | + | |
| + | <div class="text_box_in_the_box" id="lycopene_div"> | ||
| + | <a href="https://2013.igem.org/Team:Uppsala/lycopene"> | ||
<div id="substance_title"> <h3> Lycopene </h3> </div> | <div id="substance_title"> <h3> Lycopene </h3> </div> | ||
<div class="lycopene_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/8/8f/Uppsala2013_LycopeneSymbol.png"> </div> | <div class="lycopene_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/8/8f/Uppsala2013_LycopeneSymbol.png"> </div> | ||
| - | <div id="substance_text"> <p> Lycopene is a carotenoid that primarily derives from the xanthophyll group. The precursor responsible for | + | </a> |
| + | <div id="substance_text"> <p> Lycopene is a carotenoid that primarily derives from the xanthophyll group. The precursor responsible for Lycopene production is phytoene, when present together with the enzyme CrtE a catalytic reaction takes place and Lycopene is produced. Lycopene is an antioxidant that can be found in both vegetables and fruits, it is mostly known for its characteristic red color in tomatoes. </p> | ||
| + | |||
| + | |||
| + | <div id="substance_plasmid"> <a href="https://2013.igem.org/Team:Uppsala/lycopene#b1"> <img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/2/24/Uppsala2013_Lycopen_plasmid.png"></a> </div> | ||
| + | |||
| + | </div> | ||
</div> | </div> | ||
| - | <div id="beta_carotene_div"> | + | <div class="text_box_in_the_box" id="beta_carotene_div"> |
| + | <a href="https://2013.igem.org/Team:Uppsala/betacarotene"> | ||
<div id="substance_title"> <h3> β-carotene </h3> </div> | <div id="substance_title"> <h3> β-carotene </h3> </div> | ||
<div class="beta_carotene_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/0/00/Uppsala2013_beta-caroteneSymbol.png"> </div> | <div class="beta_carotene_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/0/00/Uppsala2013_beta-caroteneSymbol.png"> </div> | ||
| - | <div id="substance_text"> <p> β-carotene is a precursor of | + | |
| + | </a> | ||
| + | <div id="substance_text"> <p> β-carotene is a precursor of substances such as Vitamin A, zeaxanthine and asthaxanthine. β-carotene is a derive from Lycopene and is commonly known for its characteristic orange color, it is found in fruits and vegetables. Vitamin A which is a derive from β-carotene has important health aspects for our skin, different membranes and for our eyes. </p> | ||
| + | |||
| + | |||
| + | <div id="substance_plasmid"> <a href="https://2013.igem.org/Team:Uppsala/betacarotene#b1"><img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/a/ac/Uppsala2013_Beta-caroten_Plasmid.png"></a> </div> | ||
| + | |||
| + | </div> | ||
</div> | </div> | ||
| - | <div id="astaxanthin_div"> | + | <div class="text_box_in_the_box" id="astaxanthin_div"> |
| + | <a href="https://2013.igem.org/Team:Uppsala/astaxanthin"> | ||
<div id="substance_title"> <h3> Astaxanthin </h3> </div> | <div id="substance_title"> <h3> Astaxanthin </h3> </div> | ||
<div class="astaxanthin_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/d/d8/Uppsala2013_AstaxanthinSymbol.png"> </div> | <div class="astaxanthin_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/d/d8/Uppsala2013_AstaxanthinSymbol.png"> </div> | ||
| - | <div id="substance_text"> <p> Astaxanthin is a carotenoid pigment that derives from the xanthophyll group | + | </a> |
| + | <div id="substance_text"> <p> Astaxanthin is a carotenoid pigment that derives from the xanthophyll group and is most known for giving the red color of salmon, lobster and shrimp. Astaxanthin is a very strong antioxidant and is produced using the microalgae Haematococcus or synthetically. The substance costs around 2500 US dollars per kg and is often used in fishfarming to give salmon its red color.</p> | ||
| + | |||
| + | |||
| + | <div id="substance_plasmid"> <a href="https://2013.igem.org/Team:Uppsala/astaxanthin#b1"> <img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/5/50/Uppsala2013_Astaxanthin_plasmid.png"> </a> </div> | ||
| + | |||
| + | </div> | ||
</div> | </div> | ||
| - | <div id="zeaxanthin_div"> | + | <div class="text_box_in_the_box" id="zeaxanthin_div"> |
| + | <a href="https://2013.igem.org/Team:Uppsala/zeaxanthin"> | ||
<div id="substance_title"> <h3> Zeaxanthin </h3> </div> | <div id="substance_title"> <h3> Zeaxanthin </h3> </div> | ||
| - | <div class="zeaxanthin_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/ | + | <div class="zeaxanthin_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/e/e5/Uppsala2013_Zeaxantin2symbol.png"> </div> |
| - | <div id="substance_text"> Zeaxanthin is a yellow carotenoid | + | </a> |
| + | <div id="substance_text"> Zeaxanthin is a yellow carotenoid derived from the precursor ß-carotene by the enzyme ”Beta-carotene hydroxylase”. Zeaxanthin acts as an antioxidant and can be found in for example peppers, yolk and maize. According to studies zeaxanthin has positive effects on both undamaged and impaired vision and it may prevent age-related macular degeneration (AMD). | ||
| + | |||
| + | |||
| + | <div id="substance_plasmid"><a href="https://2013.igem.org/Team:Uppsala/zeaxanthin#b1"> <img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/0/01/Uppsala2013_Zeaxanthin_Plasmid.png"></a> </div> | ||
| + | |||
| + | </div> | ||
</div> | </div> | ||
| - | <div id="saffron_div"> | + | <div class="text_box_in_the_box" id="saffron_div"> |
| + | <a href="https://2013.igem.org/Team:Uppsala/saffron"> | ||
<div id="substance_title"> <h3> Saffron </h3> </div> | <div id="substance_title"> <h3> Saffron </h3> </div> | ||
<div class="saffron_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/5/5f/Uppsala2013_Saffronmini.png"> </div> | <div class="saffron_pic"> <img class="metabolic_mini_pic" src="https://static.igem.org/mediawiki/2013/5/5f/Uppsala2013_Saffronmini.png"> </div> | ||
| - | <div id="substance_text"> <p> Saffron is | + | |
| + | </a> | ||
| + | <div id="substance_text"> <p>Saffron is the most expensive spice in the world. It is extracted from the stigmata of Crocus Sativus. The flower can be cultivated in the Mediterranean and Middle East area. The spice is a combination of over 150 different compounds, but the main components are picrocrocin (taste), safranal (aroma) and crocin (colour). These components are all derivatives of zeaxanthin. </p> | ||
| + | |||
| + | <div id="substance_plasmid"><a href="https://2013.igem.org/Team:Uppsala/saffron#b1"><img class="substance_plasmid" src="https://static.igem.org/mediawiki/2013/c/c7/Saffron_plasmid.png"></a> </div> | ||
| + | </div> | ||
| + | |||
</div> | </div> | ||
| Line 201: | Line 291: | ||
<div id="bottom-pic"> | <div id="bottom-pic"> | ||
| - | + | ||
</div> | </div> | ||
Latest revision as of 19:46, 27 October 2013
Metabolic Engineering
We have aimed our project at producing food nutrients in bacteria. These nutrients normally exists in for example carrots, tomatoes, garlic, grapes and several other important food. By transferring genes from plants and fruits we can make our bacteria produce vital nutrients and commercially attractive supplements. We alter the metabolic pathways of our bacteria by introducing new genes or by modifying existing pathways.
Organic materia produced by nature is one of our main sources of energy. For billions of years, nature has perfected its machinery. We get fuel from both fossilized organisms and renewable biomateria. All life on earth is dependent of getting the right amount of food and nutrition. As we become more and more people on earth, we need to optimize our techniques for food and nutritional production. This is where we can step in and alter natures machinery.
P-coumaric acid
P-coumaric acid is an antioxidant that is produced from tyrosin by the enzyme Tyrosine ammonia lyase (TAL). This antioxidant has been shown to have many health benefits. For example studies have shown that it can reduce the risk of atherosclerosis and also reduce the risk of stomach cancer. P-coumaric acid can be found in foods such as peanuts, garlic, wine and vinegar.
Resveratrol
Resveratrol belongs to a group of molecules known as Phyloalexin which is used by many plants to battle infections of all sorts. Many studies have been done on resveratrol showing it has a wide range of beneficial properties ranging from skin cancer reduction to anti-inflamatory effects and antioxidant properties. Perhaps the most interesting property is that of life extension.
Lycopene
Lycopene is a carotenoid that primarily derives from the xanthophyll group. The precursor responsible for Lycopene production is phytoene, when present together with the enzyme CrtE a catalytic reaction takes place and Lycopene is produced. Lycopene is an antioxidant that can be found in both vegetables and fruits, it is mostly known for its characteristic red color in tomatoes.
β-carotene
β-carotene is a precursor of substances such as Vitamin A, zeaxanthine and asthaxanthine. β-carotene is a derive from Lycopene and is commonly known for its characteristic orange color, it is found in fruits and vegetables. Vitamin A which is a derive from β-carotene has important health aspects for our skin, different membranes and for our eyes.
Astaxanthin
Astaxanthin is a carotenoid pigment that derives from the xanthophyll group and is most known for giving the red color of salmon, lobster and shrimp. Astaxanthin is a very strong antioxidant and is produced using the microalgae Haematococcus or synthetically. The substance costs around 2500 US dollars per kg and is often used in fishfarming to give salmon its red color.
Zeaxanthin
Zeaxanthin is a yellow carotenoid derived from the precursor ß-carotene by the enzyme ”Beta-carotene hydroxylase”. Zeaxanthin acts as an antioxidant and can be found in for example peppers, yolk and maize. According to studies zeaxanthin has positive effects on both undamaged and impaired vision and it may prevent age-related macular degeneration (AMD).
Saffron
Saffron is the most expensive spice in the world. It is extracted from the stigmata of Crocus Sativus. The flower can be cultivated in the Mediterranean and Middle East area. The spice is a combination of over 150 different compounds, but the main components are picrocrocin (taste), safranal (aroma) and crocin (colour). These components are all derivatives of zeaxanthin.
