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<html lang="en"><head><meta charset="utf-8"/><meta content="width=device-width,initial-scale=1" name="viewport"/><title>Safety | SugarGain | iGEM BITS Goa</title><link href="https://2020.igem.org/Template:BITSPilani-Goa_India/css/contentCSS?action=raw&amp;ctype=text/css" rel="stylesheet"/></head><body class="theme-yellow"><nav id="main-nav"><div class="navbar navbar-expand-lg d-flex justify-content-between bg-none nav-transparent fixed-top"><a class="navbar-brand d-lg-inline-block" href="https://2020.igem.org/Team:BITSPilani-Goa_India">Sugar<span>Gain</span></a><div class="controls h-100 d-flex align-items-center"><div class="align-items-center" id="themeSwitchWrapper"><i class="icon-light"></i><div id="themeSwitch"><label class="switch" for="themeSwitchInput"><input id="themeSwitchInput" type="checkbox"/><span class="slider round"></span></label></div><i class="icon-dark"></i></div><button class="btn" id="menuSwitch"><div class="menu-icon"></div></button></div></div><div 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}</style><header class="d-flex justify-content-center"><div class="container d-flex align-items-end justify-content-between"><div id="heading"><h1>Safety</h1></div><a href="https://unsplash.com/photos/lZ4xZZuk8iA"><span data-placement="top" id="bg-attribution" title="Photo by Josh Withers on Unsplash"></span></a></div></header><main><div class="container"><div class="row"><div class="sidebar"><div class="nav" id="contents"><ul></ul></div></div><div class="content"><article><h1>Fructose Regulated Anti-Invertase Construct</h1><p>The biosensor is the crux of our genetic circuit and is composed of Frur, pFrub and the Anti-invertase gene. Frur is a transcription factor with an affinity for D-fructose. The Frur gene coding for the FruR protein prevents transcription of the regulated promoters. pFruB is the promoter region following FruR and is repressed by the FruR transcription factor, in the absence of D-Fructose.</p><div class="image"><img alt="Fructose regulated Anti-Invertase Construct in the absence of Fructose-1-phosphate" src="https://static.igem.org/mediawiki/2020/6/6d/T--BITSPilani-Goa_India--img--Design--AIwoFruc.png"/><p>Figure 1: Fructose regulated Anti-Invertase Construct in the absence of Fructose-1-phosphate</p></div><p>This prevents any further transcription, and no Anti-invertase protein is released. If D-Fructose is present in the cell, the FruR transcription factor will bind preferentially to it and thus be inactivated. This means that the repression of the related promoter pFruB will be released, enabling the transcription of the anti-invertase protein. Which can then act on invertase and stop sucrose loss.</p><div class="image"><img alt="hello" src="https://static.igem.org/mediawiki/2020/4/47/T--BITSPilani-Goa_India--img--Description--calgary.jpg"/><p>Figure 2: hello</p></div><h1>Killswitch</h1><p>It is very important for us to have a robust biosafety model for our project because it is associated with a widely consumed edible product, sugar. The most important parts of the killswitch construct are the FNR promoter, the toxin ccdB responsible for binding and impairing the functioning of bacterial Gyrase and it’s antitoxin ccda. The ccda is under the FNR promoter whereas the ccdb is under a commonly used T7 constitutive promoter. Both promoters are supplemented by conserved and strong Ribosomal Binding Sites (RBS). The FNR promoter is only active in an anaerobic environment and inactivates in an aerobic environment. It forms the crux of the construct because it controls the antitoxin expression.</p><p>The killswitch function can also be best explained with the help of two different cases. One where the bacterial cell is in an aerobic environment and one in an anaerobic environment.</p><h2>Anaerobic</h2><p>This Diagram portrays the behaviour of the killswitch genetic circuit inside the sugarcane stem which is an anaerobic environment.</p><div class="image"><img alt="hello" src="https://static.igem.org/mediawiki/2020/4/47/T--BITSPilani-Goa_India--img--Description--calgary.jpg"/><p>Figure 3: hello</p></div><p>The ccdb toxin is under a constitutive promoter which constantly expresses the toxin inside the cell. Due to the nature of the surrounding, the FNR promoter will be active and hence ccda antitoxin will also be produced in the cell. Since both ccda and ccdb is present in the cell, they will make a toxin-antitoxin complex and be degraded. This way the bacteria is able to survive inside the sugarcane stem.</p><h2>Aerobic</h2><p>This diagram portrays the behaviour of the killswitch genetic circuit outside the sugarcane stem which is an aerobic environment.</p><div class="image"><img alt="Killswitch Genetic Circut outside sugarcane stem" src="https://static.igem.org/mediawiki/2020/0/07/T--BITSPilani-Goa_India--img--Design--KSAero.png"/><p>Figure 4: Killswitch Genetic Circut outside sugarcane stem</p></div><p>In this case, too, ccdb is expressed constitutively with the help of the T7 promoter. But due to the presence of oxygen, the FNR promoter is switched off. This leads to an increase in the levels of ccdb in the cell. Which in turn leads to a complete halt in cell division and death. This ensures that the bacteria will not be able to survive outside the sugarcane environment.</p><div class="image"><img alt="Anti-Invertase Modelled Protein Structure" src="https://static.igem.org/mediawiki/2020/d/db/T--BITSPilani-Goa_India--img--Design--AI.gif"/><p>Figure 5: Anti-Invertase Modelled Protein Structure</p></div></article><div class="d-flex justify-content-between my-5"><a class="button prev flex justify-content-end long" href="https://2020.igem.org/Team:BITSPilani-Goa_India/Description"><span aria-hidden="" class="circle"><span class="icon arrow"></span></span><span class="button-text">Description</span></a><a class="button next short" href="https://2020.igem.org/Team:BITSPilani-Goa_India/Model"><span aria-hidden="" class="circle"><span class="icon arrow"></span></span><span class="button-text">Model</span></a></div></div></div></div></main><footer><div id="footerNav"><div class="container"><div class="row justify-content-between"><div class="col-sm-6 col-md-4 col-lg-3 py-2"><a class="footer-heading">Project</a><ul><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Description">Description</a></li><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Design">Design</a></li><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Model">Model</a></li><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Engineering">Engineering</a></li><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Safety">Safety</a></li><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Implementation">Implementation</a></li></ul></div><div class="col-sm-6 col-md-4 col-lg-3 py-2"><a class="footer-heading">Human Practices</a><ul><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Human_Practices">Human-Centered Design</a></li><li class="py-1"><a href="https://2020.igem.org/Team:BITSPilani-Goa_India/Education">Science 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<h1> Safety </h1>
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<p>Please visit the <a href="https://2020.igem.org/Safety">Safety Hub</a> to find this year's safety requirements & deadlines, and to learn about safe & responsible research in iGEM.</p>
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<p>On this page of your wiki, you should write about how you are addressing any safety issues in your project. The wiki is a place where you can <strong>go beyond the questions on the safety forms</strong>, and write about whatever safety topics are most interesting in your project. (You do not need to copy your safety forms onto this wiki page.)</p>
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<h3>Safe Project Design</h3>
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<p>Does your project include any safety features? Have you made certain decisions about the design to reduce risks? Write about them here! For example:</p>
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<li>Choosing a non-pathogenic chassis</li>
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<li>Choosing parts that will not harm humans / animals / plants</li>
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<li>Substituting safer materials for dangerous materials in a proof-of-concept experiment</li>
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<li>Including an "induced lethality" or "kill-switch" device</li>
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<h3>Safe Lab Work</h3>
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<p>What safety procedures do you use every day in the lab? Did you perform any unusual experiments, or face any unusual safety issues? Write about them here!</p>
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Revision as of 00:04, 21 September 2020

Safety | SugarGain | iGEM BITS Goa

Safety

Fructose Regulated Anti-Invertase Construct

The biosensor is the crux of our genetic circuit and is composed of Frur, pFrub and the Anti-invertase gene. Frur is a transcription factor with an affinity for D-fructose. The Frur gene coding for the FruR protein prevents transcription of the regulated promoters. pFruB is the promoter region following FruR and is repressed by the FruR transcription factor, in the absence of D-Fructose.

Fructose regulated Anti-Invertase Construct in the absence of Fructose-1-phosphate

Figure 1: Fructose regulated Anti-Invertase Construct in the absence of Fructose-1-phosphate

This prevents any further transcription, and no Anti-invertase protein is released. If D-Fructose is present in the cell, the FruR transcription factor will bind preferentially to it and thus be inactivated. This means that the repression of the related promoter pFruB will be released, enabling the transcription of the anti-invertase protein. Which can then act on invertase and stop sucrose loss.

hello

Figure 2: hello

Killswitch

It is very important for us to have a robust biosafety model for our project because it is associated with a widely consumed edible product, sugar. The most important parts of the killswitch construct are the FNR promoter, the toxin ccdB responsible for binding and impairing the functioning of bacterial Gyrase and it’s antitoxin ccda. The ccda is under the FNR promoter whereas the ccdb is under a commonly used T7 constitutive promoter. Both promoters are supplemented by conserved and strong Ribosomal Binding Sites (RBS). The FNR promoter is only active in an anaerobic environment and inactivates in an aerobic environment. It forms the crux of the construct because it controls the antitoxin expression.

The killswitch function can also be best explained with the help of two different cases. One where the bacterial cell is in an aerobic environment and one in an anaerobic environment.

Anaerobic

This Diagram portrays the behaviour of the killswitch genetic circuit inside the sugarcane stem which is an anaerobic environment.

hello

Figure 3: hello

The ccdb toxin is under a constitutive promoter which constantly expresses the toxin inside the cell. Due to the nature of the surrounding, the FNR promoter will be active and hence ccda antitoxin will also be produced in the cell. Since both ccda and ccdb is present in the cell, they will make a toxin-antitoxin complex and be degraded. This way the bacteria is able to survive inside the sugarcane stem.

Aerobic

This diagram portrays the behaviour of the killswitch genetic circuit outside the sugarcane stem which is an aerobic environment.

Killswitch Genetic Circut outside sugarcane stem

Figure 4: Killswitch Genetic Circut outside sugarcane stem

In this case, too, ccdb is expressed constitutively with the help of the T7 promoter. But due to the presence of oxygen, the FNR promoter is switched off. This leads to an increase in the levels of ccdb in the cell. Which in turn leads to a complete halt in cell division and death. This ensures that the bacteria will not be able to survive outside the sugarcane environment.

Anti-Invertase Modelled Protein Structure

Figure 5: Anti-Invertase Modelled Protein Structure