Chiba/Goal

From 2007.igem.org

< Chiba(Difference between revisions)
(→A test to confirm a limit of size)
m
 
(124 intermediate revisions not shown)
Line 2: Line 2:
[[Image:chiba_logo.png|center]]
[[Image:chiba_logo.png|center]]
__NOTOC__
__NOTOC__
-
{| style="border:0;width:100%;" cellpadding="20px" cellspacing="0"
+
{| style="border:0;width:100%;font-family:'Trebuchet MS'" cellpadding="20px" cellspacing="0"
| align="center" |
| align="center" |
-
[[Chiba|Introduction]] | [[Chiba/Project_Design|Project Design]] | [[Chiba/Engeneering_Flagella|Engeneering Flagella]] | [[Chiba/Quorum_Sensing|Quorum Sensing]] | [[Chiba/Goal|Our Goal]] || [[Chiba/Team_Members|Team Members]] | [[Chiba/Members_Only|メンバ連絡簿]]
+
[[Chiba|Home]]<br>
 +
<span style="font-size:120%;font-weight:bold;">[[Chiba/Introduction|Introduction]] | [[Chiba/Project_Design|Project Design]] ( [[Chiba/Engeneering_Flagella|1.Affinity Tag]] | [[Chiba/Communication|2.Communication Module]] | [[Chiba/Quorum_Sensing|3.Size Control]] ) | [[Chiba/Making Marimo|Making Marimos]] |  [[Chiba/Goal|Our Goal]]</span><br>
 +
[[Chiba/Acknowledgements|Acknowledgements]] | [[Chiba/Team_Members|Team Members]] | [http://chem.tf.chiba-u.jp/igem/ iGEM Chiba Website] | [[Chiba/Members_Only|メンバ連絡簿]]  
|}
|}
-
==Our Goal:Making Marimo==
+
==Our Goal: Yet To Be Done==
 +
As Final-Construction, we  will carry out four experiments.
*A test of adsorption between flagella
*A test of adsorption between flagella
*A test to confirm a limit of size
*A test to confirm a limit of size
*A test to form Marimo
*A test to form Marimo
-
(As Final-Construction, we carry out three experiments.
+
*A test of size control
-
First, a test of adsorption between flagella. The purpose of this test is confirming adsorption between senders and receivers with His-Tag.
+
 
-
Second, a test to confirm a limit of size. The purpose of this test is to confirm that  Marimo has a limit of size.
+
-
Third, a test to form Marimo!)
+
===A test of adsorption between flagella===
===A test of adsorption between flagella===
-
senderとreceiver同士がHis-Tagで吸着しているかを確認するためのテストである。
+
[[Image:Imida2.gif|frame|'''Fig. 28''' A test of adsorption between flagella]]
 +
====Purpose====
 +
Confirm adsorption between senders and receivers with His-Tag.
-
1.Senderとreceiverをそれぞれ培養し、receiverの培養液の中に、senderを１滴加える。
+
====Method====
-
2.その中に金属イオンを加えると、senderとreceiverが鞭毛同士で吸着し始める。
+
#Culture senders and receivers in a test tube.  
-
3.ある程度吸着したら、imidazolを加えたものとそうでないものをプレートにまく。
+
#Drop senders into receivers tube and mix cobalt ion. <!-- They start to aggregate because of they have His-Tag. -->
-
4.imidazolを加えたものはばらばらのコロニーができ、imidazolなしのものは、senderとreceiverが
+
#<!-- After aggregation, we -->Divide it into two groups. One is added imidazole and the other is non imidazole. Inoculate them on the plates.
-
  くっついているので、くっついたコロニーができる。
+
#Check the colony.
-
(First, we carry out a test of adsorption between flagella.
+
=====Prediction=====
-
We culture senders and receivers in a test tube. Then, we drop senders into receivers and mix cobalt ion. They start to aggregate because of they have His-Tag.
+
If succeeded, cultures which is added imidazole will form a indipendent colony of senders&receivers. The other (non imidazole) will form colonies of adsorbed senders and receivers.
-
After aggregation, we divide it into two groups. One is added imidazole and the other is non imidazole. We inoculate them on the plates.
+
-
Cultures added imidazole form sender’s colony and receiver’s colony. The other (non imidazole) form colonies adsorbed senders and receivers.
+
-
If we succeed, we show that senders and receivers aggregate with His-Tag.)
+
===A test to confirm a limit of size===
===A test to confirm a limit of size===
-
マリモを作る前の段階として、マリモの成長が有限の大きさで止まるか２次元で確認するためのテストである。
 
-
1.senderとreceiverを試験管でそれぞれ培養する。
+
<br>[[Image:ugen.gif|frame|'''Fig. 29''' A test to confirm a limit of size]]<br>
-
2.receiverをプレートに均一にまき、senderを真ん中に少量スポットし一晩培養する。
+
====Purpose====
-
3.senderの近く（GFPを発現している)、中間、遠く（GFPを発現していない）から数箇所ずつ菌をとってそれぞれ希釈液を作る。
+
The purpose of this test is to confirm that Marimo has a limit of size on a plate.
-
4.希釈した菌にCo2+を加えてプレートにまく。
+
 
-
5.FliCを発現していなかったreceiverは、ばらばらのコロニーを作り、FliCを発現していたreceiverは塊になったコロニーを作る。
+
====Method====
 +
 
 +
 
 +
#Culture senders and receivers in a test tube.  
 +
#Inoculate receivers equally on the plate, and drop senders at the center of it.
 +
#After over night,pick colonies which are near the senders (colonies express GFP), the end of the circle expressed GFP, and out of the green circle.
 +
#Dilute them.
 +
#Mix cobalt ion into dilutions and inoculate on the plates.
 +
#Check the colony.
 +
=====Prediction=====
 +
If succeeded,receivers which don’t express FliC (they didn’t sense AHL and express GFP) form colonies one by one. <br>And receivers expressed FliC (they sensed AHL and expressed GFP) form aggregated colonies.)
 +
 
 +
===A test to form Marimo===
 +
 
 +
[[Image:Howto.gif|frame|'''Fig. 30''' A test to form Marimo]]
 +
====Purpose====
 +
Actually we make Marimo.
 +
*AHL diffuse fast because it is very small molecule.
 +
*Packed senders into a very thin capillary . AHL from it diffuse slowly and form concentrate gradients. AHL gradients enable Marimos to aggregate like a real ball.
 +
 
 +
====Method====
 +
#Culture senders and receivers in each test tube and mix Cobalt ions in receiver's tube.
 +
#Add senders to receivers with a capillary.
 +
#Check Marimos.
 +
=====Prediction=====
 +
If succeeded,AHL from senders spreads.<br>
 +
Receivers express GFP and FliC-His,and besides,bond with cobalt ions.
 +
<br>Finnally,form marimos.<br><br><br><br><br><br><br><br><br>
-
(First, we culture senders and receivers in a test tube. Next, we inoculate receivers equally on the plate, and drop senders at the center of it.
+
===A test of size control===
-
After over night, we pick colonies which are near the senders (colonies express GFP), the end of the circle expressed GFP, and out of the green circle.
+
[[Image:size.gif|frame|'''Fig. 31''' A test of size control]]
-
Then, we dilute them .
+
====Purpose====
-
Next, we mix cobalt ion into dilutions and inoculate on the plates.
+
Control marimo's size by changing　the ratio of amount of senders and receivers.
-
Receivers which don’t express FliC (they didn’t sense AHL and express GFP) form colonies one by one.
+
-
Receivers expressed FliC (they sensed AHL and expressed GFP) form aggregated colonies.)
+
-
　
+
====Method====
 +
#Culture senders and receivers in each test tube.
 +
#Observe marimo's size by changing the amount of receivers and their types.(const.senders)
 +
#Observe marimo's size by changing the amount of senders.(const.receivers)
-
===りんご飴アッセイ===
+
=====Prediction=====
-
ついに毬藻を作る！！！
+
Low concentration of senders or  receivers : Mini Marimo<br>
-
*AHLはとても小さな分子で、自由度が高いので、拡散するのが早い。
+
High concentration of senders or receivers : Big Marimo<br><br>
-
キャピラリーを利用することによって、senderが生産するAHLの拡散を遅くし、AHLの濃度勾配を作ることができる。濃度勾配によってより球体に近いマリモができる。
+
 +
==In the Long Run==
 +
*Make Marimo which cross section is colorful. Receivers form layers and express various fluorescent proteins. When we cut Marimo, We will be able to observe beautiful gradation.
 +
*Bacteria Marimo grows like Real Marimo!
 +
Bacteria Marimo grows when it is lighted as if performing photosynthesis like natural Marimo.
-
1.receiverとsenderを一晩培養する。Receiverの培養液の中にはコバルトイオンをまぜておく。
+
'''Light triggered marino growth'''<br>
-
2.キャピラリーでsenderを吸い取り、receiverの培養液の中に加える。
+
[[Image:Light sensing sender.jpg]]
-
3.Senderの出したAHLが拡散し始める。
+
-
4.ReceiverはAHLを感じてGFPを発現する。また鞭毛を生やし、Ni２＋を介してHisタグ同士で吸着し始める。
+
-
5.集合が成長してマリモになる。
+
-
==Discussion==
+
This gene circuit contains light sensor gene. LuxI represses light senser.
 +
#Prepare mixture of Senders, Receivers(AHL -> FliC-His and GFP), and Co<sup>2+</sup>. 
 +
#Senders express FliC-His but do not synthesize AHL. Senders aggregate FliC-His and Co ions.
 +
#When the culture is lighted, senders express LuxI and synthesize AHL.
 +
#Receivers express FliC-His and GFP.
 +
#Receivers aggregate around the Senders core.
-
==Future==
+
Other than that, we have many FUTURE IDEAS (very far future...far enough we can leave CHIBA University happy) such as Marimo-mediated polous materials/ gels. Also presented are the other ways to make marimo in completely different strategies. To check those out, please visit our [http://chem.tf.chiba-u.jp/igem/ official website] (keep updated; never get frozen)
-
===サイズ制御===
+
-
*senderとreceiverの量を変えて様々なサイズのマリモを作る
+
-
===motto Future!!!!!===
+
<!--ゲル化した細胞を利用した，バイオクロマトグラフフィ-->
-
*サイズをもっと大きくしてマリモでキャッチボールがしたい
+
<!--collect ion ? by tahiro-->
-
*リポソームの中でマリモを作る
+
-
*大腸菌マリモをえびちゃんと共生
+

Latest revision as of 06:43, 27 October 2007

Chiba logo.png

Home
Introduction | Project Design ( 1.Affinity Tag | 2.Communication Module | 3.Size Control ) | Making Marimos | Our Goal
Acknowledgements | Team Members | [http://chem.tf.chiba-u.jp/igem/ iGEM Chiba Website] | メンバ連絡簿


Our Goal: Yet To Be Done

As Final-Construction, we will carry out four experiments.

  • A test of adsorption between flagella
  • A test to confirm a limit of size
  • A test to form Marimo
  • A test of size control


A test of adsorption between flagella

Fig. 28 A test of adsorption between flagella

Purpose

Confirm adsorption between senders and receivers with His-Tag.

Method

  1. Culture senders and receivers in a test tube.
  2. Drop senders into receivers tube and mix cobalt ion.
  3. Divide it into two groups. One is added imidazole and the other is non imidazole. Inoculate them on the plates.
  4. Check the colony.
Prediction

If succeeded, cultures which is added imidazole will form a indipendent colony of senders&receivers. The other (non imidazole) will form colonies of adsorbed senders and receivers.

A test to confirm a limit of size


Fig. 29 A test to confirm a limit of size

Purpose

The purpose of this test is to confirm that Marimo has a limit of size on a plate.

Method

  1. Culture senders and receivers in a test tube.
  2. Inoculate receivers equally on the plate, and drop senders at the center of it.
  3. After over night,pick colonies which are near the senders (colonies express GFP), the end of the circle expressed GFP, and out of the green circle.
  4. Dilute them.
  5. Mix cobalt ion into dilutions and inoculate on the plates.
  6. Check the colony.
Prediction

If succeeded,receivers which don’t express FliC (they didn’t sense AHL and express GFP) form colonies one by one.
And receivers expressed FliC (they sensed AHL and expressed GFP) form aggregated colonies.)

A test to form Marimo

Fig. 30 A test to form Marimo

Purpose

Actually we make Marimo.

  • AHL diffuse fast because it is very small molecule.
  • Packed senders into a very thin capillary . AHL from it diffuse slowly and form concentrate gradients. AHL gradients enable Marimos to aggregate like a real ball.

Method

  1. Culture senders and receivers in each test tube and mix Cobalt ions in receiver's tube.
  2. Add senders to receivers with a capillary.
  3. Check Marimos.
Prediction

If succeeded,AHL from senders spreads.
Receivers express GFP and FliC-His,and besides,bond with cobalt ions.
Finnally,form marimos.








A test of size control

Fig. 31 A test of size control

Purpose

Control marimo's size by changing　the ratio of amount of senders and receivers.

Method

  1. Culture senders and receivers in each test tube.
  2. Observe marimo's size by changing the amount of receivers and their types.(const.senders)
  3. Observe marimo's size by changing the amount of senders.(const.receivers)
Prediction

Low concentration of senders or receivers : Mini Marimo
High concentration of senders or receivers : Big Marimo

In the Long Run

  • Make Marimo which cross section is colorful. Receivers form layers and express various fluorescent proteins. When we cut Marimo, We will be able to observe beautiful gradation.
  • Bacteria Marimo grows like Real Marimo!

Bacteria Marimo grows when it is lighted as if performing photosynthesis like natural Marimo.

Light triggered marino growth
Light sensing sender.jpg

This gene circuit contains light sensor gene. LuxI represses light senser.

  1. Prepare mixture of Senders, Receivers(AHL -> FliC-His and GFP), and Co2+.
  2. Senders express FliC-His but do not synthesize AHL. Senders aggregate FliC-His and Co ions.
  3. When the culture is lighted, senders express LuxI and synthesize AHL.
  4. Receivers express FliC-His and GFP.
  5. Receivers aggregate around the Senders core.

Other than that, we have many FUTURE IDEAS (very far future...far enough we can leave CHIBA University happy) such as Marimo-mediated polous materials/ gels. Also presented are the other ways to make marimo in completely different strategies. To check those out, please visit our [http://chem.tf.chiba-u.jp/igem/ official website] (keep updated; never get frozen)


Retrieved from "http://2007.igem.org/wiki/index.php/Chiba/Goal"