Team:HUNGENIOUS

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Revision as of 15:16, 11 April 2014

This is a template page. READ THESE INSTRUCTIONS.

You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki. You can find some examples HERE.

You MUST have the following information on your wiki:

a team description
project description
safety information (did your team take a safety training course? were you supervised in the lab?)
team attribution (who did what part of your project?)

You may also wish to add other page such as:

lab notebook
sponsor information
other information

REMEMBER, keep all of your pages within your teams namespace.
Example: 2013hs.igem.org/Team:HUNGENIOUS/Our_Pets

You can write a background of your team here. Give us a background of your team, the members, etc. Or tell us more about something of your choosing.
Tell us more about your project. Give us background. Use this as the abstract of your project. Be descriptive but concise (1-2 paragraphs)	File:HUNGENIOUS team.png Your team picture
	Team HUNGENIOUS

Official Team Profile

Our team is from the hungarian Radnóti Miklós High School, and it is made up of seven students from a biology class and one who comes from a maths class. We have interest in Molecular Biology. The team consist of sixteen and seventeen years old students in their 10th and 11th years of a state school. We will cooperate with the Biological Research Centre of Hungarian Academy of Sciences.

Project

We decided to start two projects. Both of them is coconnected with nutrition and he gastrointestinal tract. In the first project our main aim is tocreate a bacterium which produces chitinase enzyme to treat Crohn's disease, the other is an Amanitin-biosensor. Our aim is to detect the toxin of the poisonous death cap. Crohn’s disease is a chronic, festering, inflammatory intestinal disease, which causes diarrhoea, ulcerous wounds in the mid-intestines. It is unknown how it develops in pour body and its cure is unknown as well. Researches have proved that the N-acetylglucosamine is able to ease the symptoms. The polymer form of N-acetylglucosamine is chitin. The chitinase enzyme converts chitin to its monomers.We plan to insert the chitinase coding gene into bacteria. Thus taking the bacteria as a probiotic they can produce their effect locally and for longer time.

Notebook

We have weekly sessions on tuesdays where we discuss what we have done so far, and what to do afterwards. Every member of the team gets new tasks to do until the next meeting. We have lessons in the mornings during the weekdays, so we can only work on our project in the afternoons and on weekends.

Results/Conclusions

What did you achieve over the course of your semester?

Safety

What safety precautions did your team take? Did you take a safety training course? Were you supervised at all times in the lab?

Attributions

We have split into two groups. One is working on the Amanitin-biosensor, the other one is doing research on Crohn's disease. Our specialists on the disease are: Petra, Réka, Andris and Martin. The subteam making the biosensor consists of Miklós, Gergő, Márk and Ákos. The leader of the team is our teacher, Mr Sándor Bán.

Human Practices

The Crohn's disease is a chronical, festering, intestinal disease. The whole intesine is sappurated, it's incurable. Our aim with the second project is protection in simple and cheap way with N-acetylglucosamine. Animal cells doesn't have a periplast, only an extracellular matrix surrounds the cells in order to protect them. The N-acetylglucosamine connects to this matrix increasing its protective effect. As the N-acetylglucosamine's polymer form is the chitin, therefore we can produce chitinase enzyme with a bacterium which is also an intestinal one which can disassemble the chitin to N-acetylglucosamine.

Nowadays, death cap (Amanita phalloides) is one the most responsible species worldwide, which cause poisoning and significant rate of these toxications (mostly those which occur far from the necessary medical attendance) has lethal outcome. In Califonia, for example, 6300 poisonings were registered between 1993 and 1997. The main cause of these accidents is that the death cap may be confused with Agaricus species, due to their similar apperance, thus threatening verdant and negligent people. With our project it would become easier to distinguish Amanita from other species, so ensuring the mushroom we eat is not toxic.

Fun!

What was your favorite team snack?? Have a picture of your team mascot?

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@@ Line 56: / Line 56: @@
 ===Project===
-We decided to start two projects.
+We decided to start two projects. Both of them is coconnected with nutrition and he gastrointestinal tract.
-One of them is the Amanitin-biosensor. Our aim is to detect the toxin of the poisonous death cap.
+In the first project our main aim is tocreate a bacterium which produces chitinase enzyme to treat Crohn's disease, the other is an Amanitin-biosensor. Our aim is to detect the toxin of the poisonous death cap.
-The other one is a bacterium which produces chitinase enzyme to treat Crohn's disease.
+Crohn’s disease is a chronic, festering, inflammatory intestinal disease, which causes diarrhoea, ulcerous wounds in the mid-intestines. It is unknown how it develops in pour body and its cure is unknown as well. Researches have proved that the N-acetylglucosamine is able to ease the symptoms.
+The polymer form of N-acetylglucosamine is chitin. The chitinase enzyme converts chitin to its monomers.We plan to insert the chitinase coding gene into bacteria. Thus taking the bacteria as a probiotic they can produce their effect locally and for longer time.
 ===Notebook===