Difference between revisions of "Team:SBS SH 112144"
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| − | <p> | + | <p>Cyanobacteria release microcystin LR(MCLR), the most common of microcystin(MC), which is toxic to human and can lead to severe diseases such as liver cancer(Shimizu 2011). Massive reproduction of cyanobacteria has occurred throughout the world and caused serious water quality problem, such as the case of Taihu Lake in 2007. MCLR are structurally stable to withstand physicochemical and biological stresses, including pH, temperature, sunlight and common enzymes, under natural conditions (Harada 1996; Okano et al. 2006). Neither can common water filtering process successfully get rid of it, meaning that only those natural MC-degrading bacterias is capable of degrading MCLR. Studying the degradation process is thus critical to address the water quality problem brought by MCLR. Among 10-more species of such bacteria, our group intends to research on the strand Sphingomonas sp, which possess a MC-degrading pathway that involves 3 genes: mrl A mrl B mrl C that works in a sequential chain reaction(Shimizu 2011) and an additional gene, mrl D, whose product is speculated to aid the transport of MCLR or its degradation process(Bourne, 2001). The MRL A enzyme first linearize the ring-form MCLR, then MRLB cut it into Tetrapeptide, following by the further hydrolysis of Tetra-Peptide into smaller peptides, such as Adda, illustrated by the graph below.(Bourne, 2001). Previous studies have also shown that MCLR can induce the expression of all 3 genes, while linearized MCLR,tetrapeptide and Adda only stimulate the expression of mlr A and mlrB (Shimizu 2011). Being familiar with these information, our group aims to explore on how different combination of these genes can affect the MCLR degradation rates, so that a more efficient degrading model mabe be established.</p> |
<ul> | <ul> | ||
<li> <a href="https://2018.igem.org/Competition">Competition Hub</a> </li> | <li> <a href="https://2018.igem.org/Competition">Competition Hub</a> </li> | ||
Revision as of 03:07, 28 June 2018
Welcome to iGEM 2018!
Your team has been approved and you are ready to start the iGEM season!
Project Description
Cyanobacteria release microcystin LR(MCLR), the most common of microcystin(MC), which is toxic to human and can lead to severe diseases such as liver cancer(Shimizu 2011). Massive reproduction of cyanobacteria has occurred throughout the world and caused serious water quality problem, such as the case of Taihu Lake in 2007. MCLR are structurally stable to withstand physicochemical and biological stresses, including pH, temperature, sunlight and common enzymes, under natural conditions (Harada 1996; Okano et al. 2006). Neither can common water filtering process successfully get rid of it, meaning that only those natural MC-degrading bacterias is capable of degrading MCLR. Studying the degradation process is thus critical to address the water quality problem brought by MCLR. Among 10-more species of such bacteria, our group intends to research on the strand Sphingomonas sp, which possess a MC-degrading pathway that involves 3 genes: mrl A mrl B mrl C that works in a sequential chain reaction(Shimizu 2011) and an additional gene, mrl D, whose product is speculated to aid the transport of MCLR or its degradation process(Bourne, 2001). The MRL A enzyme first linearize the ring-form MCLR, then MRLB cut it into Tetrapeptide, following by the further hydrolysis of Tetra-Peptide into smaller peptides, such as Adda, illustrated by the graph below.(Bourne, 2001). Previous studies have also shown that MCLR can induce the expression of all 3 genes, while linearized MCLR,tetrapeptide and Adda only stimulate the expression of mlr A and mlrB (Shimizu 2011). Being familiar with these information, our group aims to explore on how different combination of these genes can affect the MCLR degradation rates, so that a more efficient degrading model mabe be established.
Styling your wiki
You may style this page as you like or you can simply leave the style as it is. You can easily keep the styling and edit the content of these default wiki pages with your project information and completely fulfill the requirement to document your project.
While you may not win Best Wiki with this styling, your team is still eligible for all other awards. This default wiki meets the requirements, it improves navigability and ease of use for visitors, and you should not feel it is necessary to style beyond what has been provided.
Uploading pictures and files
You must upload any pictures and files to the iGEM 2018 server. Remember to keep all your pictures and files within your team's namespace or at least include your team's name in the file name.
When you upload, set the "Destination Filename" to T--YourOfficialTeamName--NameOfFile.jpg. (If you don't do this, someone else might upload a different file with the same "Destination Filename", and your file would be erased!)
Wiki template information
We have created these wiki template pages to help you get started and to help you think about how your team will be evaluated. You can find a list of all the pages tied to awards here at the Pages for awards link. You must edit these pages to be evaluated for medals and awards, but ultimately the design, layout, style and all other elements of your team wiki is up to you!
Editing your wiki
On this page you can document your project, introduce your team members, document your progress and share your iGEM experience with the rest of the world!
Use WikiTools - Edit in the black menu bar to edit this page
Tips
This wiki will be your team’s first interaction with the rest of the world, so here are a few tips to help you get started:
- State your accomplishments! Tell people what you have achieved from the start.
- Be clear about what you are doing and how you plan to do this.
- You have a global audience! Consider the different backgrounds that your users come from.
- Make sure information is easy to find; nothing should be more than 3 clicks away.
- Avoid using very small fonts and low contrast colors; information should be easy to read.
- Start documenting your project as early as possible; don’t leave anything to the last minute before the Wiki Freeze. For a complete list of deadlines visit the iGEM 2018 calendar
- Have lots of fun!
Inspiration
You can also view other team wikis for inspiration! Here are some examples: