Difference between revisions of "Team:Paris Bettencourt/Design"
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<h1 class="date two">Safety & Regulations</h1> | <h1 class="date two">Safety & Regulations</h1> | ||
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the forms of B12 present in food and supplements. | the forms of B12 present in food and supplements. | ||
<br>The same is not true of vitamin A, though: most vitamin pills contain retinol, which is the form | <br>The same is not true of vitamin A, though: most vitamin pills contain retinol, which is the form | ||
− | of vitamin A that is used by the human body. | + | of vitamin A that is used by the human body, and which can be toxic at very high dose. The ß-carotene produced by our yeast though is not toxic, since the body only converts what it need into retinol. |
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<br>The vitamin B2 that our micro-organism is producing is riboflavin, which can be toxic at very | <br>The vitamin B2 that our micro-organism is producing is riboflavin, which can be toxic at very | ||
high dose. However it is very unlikely that we will produce more that the daily requirement (about | high dose. However it is very unlikely that we will produce more that the daily requirement (about | ||
1.2mg/day), contrarily to the vitamin pills that we can buy on the market and that often contain a | 1.2mg/day), contrarily to the vitamin pills that we can buy on the market and that often contain a | ||
− | lot more, from 10 to 100 mg. | + | lot more, from 10 to 100 mg. |
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− | <h2>European Regulations</h2> | + | <h2>European and Indian Regulations</h2> |
− | + | In order to evaluate the feasibility of our product’s implementation, we researched the european and indian regulations concerning the production and distribution of genetically engineered micro-organisms. | |
− | + | <br>We found that the EU directive 90/219/EC of the EC relative to the contained use of GMO would allow production of this product within the european market. This directive is enforced in each of the EU member’s national regulations. | |
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− | + | In India, the FSSIE (Food Safety and Standard Authority in India) told us the safety needed to be established in order for our product to be authorized. Both Dr. A. K. Sharma from the FSSAI and Dr. Sunita Grover the Dairy Microbiology Division at the National Dairy Research Institute advised us to chose micro-organisms that were already present in the fermented foods we were targeting, which we did. These organisms are all in Risk Group 1 (Unlikely to cause human disease.), and have the GRAS status (Generally Considered As Safe). | |
− | + | <br>We also found out that the Indian law currently doesn’t allow GM microorganisms because of the use of antibiotic markers that makes them unsafe to eat. But according to Samir K. Brahmachari, former director of the Council of Scientific and Industrial Research in India, our product has a greater chance to be authorized if there is no more live bacteria in the final form of the dish, that is actually eaten. Since the idli is steamed for 10 to 15 minutes before it is eaten, we made an experiment to assess the presence of yeasts and bacteria in the steamed idli, and found out that the steaming process effectively sterilizes the idli and eliminates the microbes present in the batter. | |
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− | <h1 class="date three"> | + | <h1 class="date three">Continuity</h1> |
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Revision as of 03:54, 19 September 2015