Edinburgh/Yoghurt/Applications
From 2007.igem.org
(→Self Flavouring Yoghurt) |
(→Self Flavouring Yoghurt) |
||
| Line 15: | Line 15: | ||
Figure 1, shows how a sugar inducible promoter (in this case arabinose) could be used to induce gene expression, which would result in the yoghurt colour changing from red to orange. | Figure 1, shows how a sugar inducible promoter (in this case arabinose) could be used to induce gene expression, which would result in the yoghurt colour changing from red to orange. | ||
| + | |||
| + | '''Possible sugar inducible promoters''' | ||
| + | |||
| + | We identified three promoters, which are activated by three different sugars, these are: | ||
| + | * Trehalose (see fig. 2) | ||
| + | * Maltose (see fig. 3) | ||
| + | * Arabinose (promoter may be found in registry under [http://partsregistry.org/Part:BBa_I0500 BBa_I0500] | ||
===Why Vanillin?=== | ===Why Vanillin?=== | ||
Revision as of 20:46, 22 October 2007
Introduction | Applications | Design | Modelling | Wet Lab | Proof of concept | References
Contents |
Self Flavouring Yoghurt
The original idea from this project has some root in simplifying the process for making yoghurt and consumer choice.
One of the ideas we came up with was to create Lactic acid bacteria (LAB), which contained several flavour and colour biosynthetic pathways, each induced by a different molecule. We hit upon the idea of using sugar (trehalose, maltose, arabinose ect) inducible operons to initiate the synthesis of a particular flavour or colour biosynthesis pathway. This way the consumer could chose what colour and flavour yoghurt they wanted to eat that day, and make it by adding the sugar to induce the desired biosynthesis pathway.
The reason for chosing sugar inducible promoters was to potentially enable the final product to be consumer friendly, i.e. safe enough to be eaten by the general public. Thereby cancelling out the possibility of using the majority of inducible promoters already present in the registry (such as the Ptet promoter). The use of the Plac promoter was also cancelled out, as milk contains high levels of lactose, which would result in the Plac promoter being continually active.
Figure 1, shows how a sugar inducible promoter (in this case arabinose) could be used to induce gene expression, which would result in the yoghurt colour changing from red to orange.
Possible sugar inducible promoters
We identified three promoters, which are activated by three different sugars, these are:
- Trehalose (see fig. 2)
- Maltose (see fig. 3)
- Arabinose (promoter may be found in registry under [http://partsregistry.org/Part:BBa_I0500 BBa_I0500]
Why Vanillin?
|
|
| Vanilla planifolia |
Vanillin is the major contributer to vanilla flavouring, which is utilised in a multitude of different products. These range from scents and fragrances, to cakes, orange juice and ice cream!
Vanilla flavouring is traditionally extracted from the orchid Vanilla planifolia, first discovered in Mexico, and now widely grown throughout the Americas and tropics.
The world market for natural vanilla flavouring is currently worth over $1 billion per annum, and each kilogram of vanilla extract can fetch as much as $3000!
Our project will enable the natural synthesis of vanillin (the major constituent of vanillia flavouring), from the amino acid tyrosine.
We chose tyrosine as our starting point for vanillin biosynthesis for the following reasons:
- endogenously produced by many bacteria, so there is no need to add a starter substrate
- present within milk proteins, will provide an additional tyrosine source for our yoghurt producing LAB
- required one less enzymatic step than phenylalanine
- several papers report the possibility of upregulating the tyrosine biosynthesis pathway. This could be utilised to increase vanillin production
As vanillin will be produced by a living organism, and not chemical synthesis, our novel pathway constites a natural source of vanillin, and the final product could be marketed as such. Potentially, the successful and efficient production of vanillin from a natural metabolite (tyrosine) could lead to a much cheaper industrial scale method of natural vanilla flavour production.
More information about vanilla flavouring and its production may be found on [http://en.wikipedia.org/wiki/Vanilla wikipedia]
Potential Medical Benefits of GM Food
Bonus's of Zeaxanthanin Pathway
The carotenoids produced by the zeaxanthin pathway are not just pretty pigments as they also have several world renound health benefits!
The properties of both B-carotene and lycopene have been avidly studied by scientists, a few examples of these are given below. By encorporating these carotenoids into our yoghurt, we are not only using healthy food colourings, but we are also helping to protect future consumers from diseases such as cancer, heart disease and nyctalopia (poor dark adaptation).
B-carotene
B-carotene is converted into vitamin A by the body. Vitamin A is essential for vision, immune response, epithelial cell growth and repair, bone growth, reproduction and maintenance of the surface linings of the eyes, to name a few examples.
Deficiency in vitamin A can cause:
- Abnormal dark adaptation
- dry skin, hair & broken fingernails
- decreased resistance to infections
Lycopene
Lycopene a carotenoid, with red pigmentation, is an intermediate in the zeaxanthin pathway. Several studies have reported the benifits of having a high dietry intake of lycopene, a few examples of which are given below.
Lycopene is reported to be an extremally benificial antioxident:
| "its unique structural and biologic properties enable lycopene to prevent free-radical damage to cells caused by reactive oxygen species, thus acting as a potent antioxidant" (Ansari & Ansari, 2005) |
Lycopene has also been inversely related with the risk of chronic disease, including prostate cancer and heart disease:
| "Dietary intakes of tomatoes and tomato products containing lycopene have been shown to be associated with decreased risk of chronic diseases such as cancer and cardiovascular diseases in several recent studies" (A Venket Rao, 2000) |
Introduction | Applications | Design | Modelling | Wet Lab | Proof of concept | References
