Team:Tsinghua

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Welcome to iGEM08 Tsinghua's wiki page


Contents

Intro of Our Project

News

GF taq is recommended in our PCR reactions. 2008.June.25

The first plasmid is successfully constrcuted. 2008.Jul.20

The gene we need is at synthesis in Geneart. 2008.Jul.24

The standard vector pSB1A3 lost in the transformation. 2008.Jul.28

Then it finally succeeds. 2008.Jul.31

Template of one of the receptors are still in vacancy.

New edition of project interpretation are in process.

Intro of Tsinghua University

Tsinghua University was established in 1911, originally under the name “Tsinghua Xuetang”. The school was renamed "Tsinghua School" in 1912. The university section was founded in 1925. The name “National Tsinghua University” was adopted in 1928.

The educational philosophy of Tsinghua is to "train students with integrity." Among over 120,000 students who have graduated from Tsinghua since its founding are many outstanding scholars, eminent entrepreneurs and great statesmen remembered and respected by their fellow Chinese citizens.

With the motto of “Self-Discipline and Social Commitment” and the spirit of “Actions Speak Louder than Words”, Tsinghua University is dedicated to the well-being of Chinese society and to world development.

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Our Team

Campus

Library2.jpg

Medicine.jpg

West Stadium2.jpg

Soul of Tsinghua.jpg

Astro.jpg

== Team Roster ==

Guoqiang Chen	 Professor	 chengq@mail.tsinghua.edu.cn 
Shao Li	 Professor	 shaoli@tsinghua.edu.cn
Zhirong Sun	 Professor	 sunzhr@mail.tsinghua.edu.cn 
Syna Gao	 Ph.D	         synagao@gmail.com
Tao  Ma	 Ph.D	         mat07@mails.thu.edu.cn
Yanchao Han	 Ph.D	         haytcb@gmail.com
Feng Liu	 Undergraduate	 liufeng04@mails.tsinghua.edu.cn
Junjie Luo	 Undergraduate	 jjluo54@163.com
Yaxuan Yang	 Undergraduate	 yangyx04@mails.tsinghua.edu.cn
Jun Wang	 Undergraduate	 wj-cn@163.com
Chao Wang	 Undergraduate	 wangchao05@mails.tsinghua.edu.cn
Qi   Liu	 Undergraduate	 q-liu05@mails.tsinghua.edu.cn
Shiqing Wang	 Undergraduate	 wangsq05@mails.thu.edu.cn
Tong  Si	 Undergraduate	 sit05@mails.thu.edu.cn
Shan Lin	 Undergraduate	 coolls03@163.com
Yilong Zou	 Undergraduate	 ylzouyilong@yahoo.cn 
Ziying Liu	 Undergraduate	 liuzy05@mails.tsinghua.edu.cn
Xing Rong	 Undergraduate	 rongx05@mails.thu.edu.cn
Yicheng Long	 Undergraduate	 longyc05@mails.tsinghua.edu.cn
Luying Jia	 Undergraduate	 jialy05@mails.tsinghua.edu.cn
Yuemeng Wang	 Undergraduate	 wym05@mails.tsinghua.edu.cn
Junya Peng	 Undergraduate	 junya.peng@gmail.com
Xiaoxi Yuan	 Undergraduate	 tangbf1983@gmail.com
Chong Wang	 Undergraduate	 wangchongxn@yahoo.com.cn
Feng  Tian	 Undergraduate	 tianf06@mails.tsinghua.edu.cn
Yuanfan  Yang	 Undergraduate	 yangyf06@mails.tsinghua.edu.cn
Liang Zheng	 Undergraduate	 1000zhengliang@sina.com
Yongqiang Gou	 Undergraduate	 gouyongqiang007@163.com
He  Yang	 Undergraduate	 yanghemary@gmail.com 
Zi  Wang	 Undergraduate	 fiona99988@yahoo.com.cn
Gechong  Ruan    Undergraduate   rgc06@mails.tsinghua.edu.cn
Bing  Xing       Undergraduate   binxing1987@gmail.com


== Team Members ==

         Yaxuan Yang Yaxuan Yang.jpg    Chao Wang  Chao Wang.jpg   Qi LiuQi Liu2.jpg       

Shiqing WangShiqing Wang2.jpg Yilong ZouYilong Zou.jpg     Yicheng Long Yicheng Long.jpg  

 Luying JiaLuying Jia2.jpg    Yuemeng WangYuemeng Wang2.jpg Feng Tian Feng Tian.jpg  
Yuanfan YangYuanfan Yang2.jpg   He Yang  He Yang2.jpg   Zi WangZi Wang3.jpg    

 Gechong RuanGechong Ruan2.jpg     Bin XingBin Xing.jpg

== Our Schedule ==

  Time	                      Events
Dec. 15, 2007	              Team of Tsinghua University Founded
Dec. 31, 2007	              Brain Storm(1)
Jan-Feb, 2008	              Backgroud Investigation
Feb.25, 2008	              Brain Storm(2)
Mar., 2008	              Experimental procedure design;
                             Modeling in silico Started  
Apr.1,2008	              Wet Lab work started
Apr.-Aug.,2008	              Wet Lab Work
May.1, 2008	              Team Registry
May.25, 2008	              Students’ Association of Synthetic Biology(SASB) Founded
June.21, 2008	              “Teach the teacher “workshop, in Kyoto, Japan
Sept.-Oct., 2008	      Inspection and Revision     
Oct.20,2008	              Summary, Presentation Preparation
Nov.8-9,2008	              Jamboree In MIT


Project

== Abstract ==

  This year we are trying to work at the motility of bacteria. E.coli senses some chemicals and moves toward

or stays still, this behavior is called chemotaxis. Any modification of the pathway from the sensor to the motile apparatus will cause into different chemotactic effcts.

 Moreover,most of the biosensors today are designed for a specific target signal, and they can not 

substitute each other in most cases. By structural analysis we find that most receptors for the same type of ligands exhibits great similarity, both in sequence information and characteristics. Our project

is designed toward an "Interchangeable Biosensor". The strategy is almost trial and error, to find

an appropriate pathway between chemical molecules and corresponding reactions. Signals other than

chemicals are much harder to manipulate, and to integrate together the signals seems even more

challenging,we are trying to isolate the elements and standardise them.

== Background ==

Motile bacteria can respond to chemical gradients in their environment. Such directed movement in response to special chemicals is defined as chemotaxis. If organisms detect substances beneficial for surviving, positive chemotaxis occurs and cells will move in the direction of increasing concentration. In contrast, negative chemotaxis occurs when motile bacteria move away from a repellant. Both kinds of responses adjust the behaviors of organisms to the environment, thus improve their ability of surviving. One typical chemotactic behavior is the response of Escherichia coli toward certain nutritions, which plays a key role in seeking food. Researchers have investigated thoroughly into the molecular mechanism of it. Motility in prokaryotes is accomplished by flagellum, a complex structure moving the cell by rotation, much like the propeller in a motor boat. In E.coli, counterclockwise rotation moves the cell in a direction called a run, while clockwise rotation results in tumbling of the cell. The direction of rotation is controlled by phosphorylation of CheY, a signaling protein in the chemotaxis pathway of E.coli. Low level of phosphorylation results in counterclockwise rotation of flagella and makes the cell move forward. In contrast, phosphorylated CheY favors tumbling. The level of protein phosphorylation is regulated by certain attractant or repellent, which can bind specific receptors on the cell surface. Signals are then passed through a series of intracellular biochemical reactions, in which phosphorylation of CheY is controlled. In this way bacteria accomplish chemotactic behavior.

Escherichia coli is a common kind of engineer bacteria, which is convenient for genetic manipulation. It is likely that we make use of the chemotactic pathway in E.coli, making them detect and move toward a special chemical substance, maybe a certain kind of pollutant. If the genetic engineering strain also has the ability of degrading aimed chemicals, efficiency of pollution treatment can be hopefully improved a lot. However, the natural ligands concerning chemotaxis in E.coli are limited in several kinds of nutrition, such as carbohydrate and amino acids. Strains that can detecting more kinds of organic substances and even heavy metal ions is planed to be got through the reconstruction of chemotaxis system.



== Design ==

== Predicted Result ==

== Related literature ==

Modeling

Laboratory Work

== Scheme ==

== Lab Log ==

== Protocols ==

== == Molecular cloning == ==

  1   PCR
    
 1.1 Gold Faster 	Taq system:
   Reagent	           Concentration/Activity	50ul 	100ul
   GF taq buffer     	    10x	                         5       10
   GF taq		                                 0.5	  0.5
   dNTPmix	            10mM each	                 1	  2
   Primer 1 	            10uM	                 1	  2
   Primer 2	            10um	                 1	  2
   Template DNA	      changeable	                 0.5	  1
   MgCl2	            0.2M	                 0.5	  1
   ddH2O	                ---	                40.5	 81
 1.2 The program under Gold faster taq system
   Progress	     Program I	                 Program 2
   Predenaturing    95℃         2-5 min	         95℃   2-5 min
   Denaturing	     95℃        10-20sec	         95℃   10-20sec
   Annealing	     (Tm-5) ℃   2-5 sec	         68℃   10-15sec/1kb
   Extension	     72℃        10-15sec/1kb	

25-30cycle 25-30cycle

   Last extension	  1-2min or skipped	       1-2min or skipped
   2 	Restriction cut:
           Reagent	        Concentration/Activity	 Volume(50ul system)
           Restriction cut buffer	10x	           5ul
           Enzyme 1	                --	           2.5ul
           Enzyme 2	                --	           2.5ul
 Incubate at 37℃, 1.5 hrs or longer
 (Enzymes from Takara Co., Ltd)
     3  Ligation:
              Reagent	    Volume(10ul system)
              Solution I	5ul
              DNA fragment	3.5ul
              Vector	        1.5ul
   Incubate at 16-18℃,1hr or longer
   (Ligation kit from Takara)




== == Bacteria behavior == ==

Devices and Parts

== Parts ==

== == Protein Coding == ==

== == Regulatory == ==

== == Vectors == ==

== == Others == ==

== Devices ==

Communication

== Meet up ==

   2007.Dec.1          With Peking University team leaders.
   2007.Dec.15         With all the students from different academies.
   2008. Feb           With candidate instructors in Our Department.
   2008. March         With Faculties from Professor Lee's lab.
   2008. April         With Drew Endy in Peking University.
   2008. April         With Peking University.
   2008. June.21-22    On Teachers' Workshop, with most Asia teams.
   2008. July.17       With Beijing Normal University Team
   2008.July.25        With Invitrogen.Co. Ltd.

== Phone ==

== E-mails ==

  2008. July          With ETH_Zurich by E-mail

Doodle Board

           Friends.jpg

The organism grew on the plate was not bacteria,but fungi. 2008.July .23

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   Contact us: sasbthu@yahoo.cn