Team:TzuChiU Formosa/Notebook

From 2011.igem.org

(Difference between revisions)

Latest revision as of 17:19, 2 October 2011

Photopaper

2011.02.24

Discussion:

Team organization
Brain storming
- paper made by bacteria with add-ons such as colors, fragrance, etc.
- "light up" the plants for replacing lamp posts.

2011.03.04

Discussion:

Team advisory
Brain storming
- Add-ons: colorful cellulose which produced by bacteria such as beta-carotene
- information exchange with iGEM 2009 Cambridge team

2011.03.14

Discussion:

Task Allocation
Brain storming
- Avatar - "light up" the plants by transfecting symbiotic bacteria which cloned into fluorescence gene
- Eco-friendly warmer - biotic thermal pad

2011.03.23

Discussion:

- Project : paperia
- Option 1 : Culture bacteria which has pigment gene
- Option 2 : Cellulose-producing bacteria secrete pigment into the medium

2011.03.24

Discussion:

Exp. procedure:
- cloning of cellulose gene’s CDS
- the product should operate within E. coli.

2011.06.22

Discussion:

Due to some unforseen reason, the team decided to change their project.
New project: Biojenny
-economical and humane way to produce paper in large quantities.
-yeast to be our host

2011.07.01

Discussion:

Freeze > grin > genome DNA isolation > Cloning = silk protein gene

2011.07.09

Discussion:

the connections between 3 silk proteins : Fibl Fibh P25
major proteins : H-chain, L-chain, P25

2011.07.15

Discussion:

Due to limited resources and techniques required, the team decided to switch back to the previous project. Paper making !
However it would be modified to be more innovative and creative.

2011.07.18

Discussion:

Latest project : Photo paper
cyanobacteria is designed as the host, cellulose made up of the glucose produced by cyanobacteria could be one of the main attraction of the project.

2011.07.23

Discussion:

system modification to overcome the problems arises during preliminary round
Biobricks from Tokyo 2010 team will be utilized
- regulator promoter in order to regulate the secretion of cellulose to solve the aggregation of the bacteria

2011.09.07

'''Rhodobacter rudrum medium'''
K2HPO4 					1g
NaCl					0.5g
FeSO4．7H2O				0.01g
CaCl2 					0.02g
MnCl2．4H2O 				0.002g
MgSO4．7H2O				0.2g
NaMO2O4．2H2O				0.01g
ddH2O					998.258 ml
                                                   （＋
______________________________________________________
                                        1L→take100ml
		＋
Yeast Extrat				0.5g
Sodium malate
(Sodium succinate dibasic hexohydrate)	5g
NH4Cl 					1g
ddH2O 					893.5ml
                                                  （＋
______________________________________________________
                                        1L

'''Raise E. coli(PSB1C3)'''
1.50ml LB+500μl CHLORAMPHENICOL
2.37℃, overnight (14-16hrs)

2011.09.08-13

Plasmid miniprep kit

PSB1C3 plasmid

Raise Rhodobacter rubrum

1.50ml LB+500μl CHLORAMPHENICOL
2.37℃, overnight (14-16hrs)

2011.09.09

'''Raise Gluconacetobacter hansenii'''
1.50ml LB+500μl CHLORAMPHENICOL
2.37℃, overnight (14-16hrs)

2011.09.10-11

'''Digestion check of DNA'''　
PSB1C3 DNA (control)			3μl

PSB1C3/ EcoR
DNA					500ng
10×buffer				5μl
BSA					5μl
EcoRⅠ					1μl
ddH2O					29μl
                                                  （＋
______________________________________________________
                                        50μl

PSB1C3/ pstⅠ
DNA					500ng
10×buffer				5μl
BSA					5μl
pstⅠ					1μl
ddH2O					29μl
                                                  （＋
______________________________________________________
                                        50μl

PSB1C3/ EcoRⅠ+pstⅠ
DNA	                                500ng
10×buffer			        5μl
BSA				        5μl
EcoRⅠ					1μl
pstⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 30 mins

'''Digestion of DNA'''
PSB1C3/ EcoRⅠ+pstⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
EcoRⅠ					1μl
pstⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 2 hrs

'''electroelution Purification'''
PSB1C3 backbone

2011.10.14-02

'''PCR'''
template DNA                       	1μl
5×Buffer				4μl
2.5μM dNTP				1.6μl
10μM F					1μl
10μM R					1μl
Taq		                        0.2μl
ddH2O					8.8μl
                                                  （＋
______________________________________________________
                                        20μl

2011.09.15

'''Genome miniprep'''
Gluconacetobacter hansenii

2011.09.18

'''Gel/PCR DNA extraction'''
Gluconacetobacter hansenii

2011.09.21

'''Digestion of DNA'''
acsAB/ XbaⅠ+SpeⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
XbaⅠ					1μl
SpeⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 16 hr

'''Digestion of DNA'''
acsCD/ XbaⅠ+SpeⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
XbaⅠ					1μl
SpeⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 16 hr

2011.09.22

'''Ligation of DNA'''
PSB1C3-acsAB
Vector                                  3μl
Insert                                  14μl
ligase buffer                           2μl
ligase                                  1μl
ddH2O                                   -μl
                                                  （＋
______________________________________________________
                                        20μl

'''Ligation of DNA'''
PSB1A3-acsCD
Vector                                  3μl
Insert                                  14μl
ligase buffer                           2μl
ligase                                  1μl
ddH2O                                   -μl
                                                 （＋
______________________________________________________
                                        20μl

2011.09.23

'''PCR'''
PR0011 promoter                         1μl
5×Buffer				4μl
2.5μM dNTP				1.6μl
Taq		                        0.2μl
ddH2O					13.2μl
                                                  （＋
______________________________________________________
                                        20μl

2011.09.24

'''Transformation of DNA'''
PSB1C3-acsAB
Transform into E.coli
LB+CHLORAMPHENICOL

'''Transformation of DNA'''
PSB1A3-acsCD
Transform into E.coli
LB+Ampicillin

'''Transformation of DNA'''
PSB1C3-acsAB
PSB1A3-acsCD
Transform into E.coli
LB+Ampicillin+CHLORAMPHENICOL

2011.09.24

'''Ligation of DNA'''
PSB1C3-promoter
Vector                                  3μl
Insert                                  14μl
ligase buffer                           2μl
ligase                                  1μl
ddH2O                                   -μl
                                                  （＋
______________________________________________________
                                        20μl

2011.09.27

'''Digestion of DNA'''
acsCD/ XbaⅠ+SpeⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
XbaⅠ					1μl
SpeⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 16 hr

'''Ligation of DNA'''
PSB1C3-acsCD
Vector                                  3μl
Insert                                  14μl
ligase buffer                           2μl
ligase                                  1μl
ddH2O                                   -μl
                                                 （＋
______________________________________________________
                                        20μl
'''Ligation of DNA'''
PSB1C3-promoter
Vector                                  3μl
Insert                                  14μl
ligase buffer                           2μl
ligase                                  1μl
ddH2O                                   -μl
                                                  （＋
______________________________________________________
                                        20μl

2011.09.27

'''Ligation of DNA'''
PSB1C3-Cmccax-Ccp                       3μl
Insert                                  14μl
ligase buffer                           2μl
ligase                                  1μl
ddH2O                                   -μl
                                                 （＋
______________________________________________________
                                        20μl

2011.09.28

'''Digestion of DNA'''
acsCD/ XbaⅠ+SpeⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
XbaⅠ					1μl
SpeⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 16 hr


==='''2011.09.28'''===
<pre>
'''Transformation of DNA'''
PSB1C3-Cmccax-Ccp                       
Transform into E.coli
LB+CHLORAMPHENICOL

Digestion of DNA

acsAB/ XbaⅠ+SpeⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
XbaⅠ					1μl
SpeⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 16 hr

acsAB/ XbaⅠ+SpeⅠ
DNA					10μl
10×buffer				5μl
BSA					5μl
XbaⅠ					1μl
SpeⅠ					1μl
ddH2O					28μl
                                                  （＋
______________________________________________________
                                        50μl
→37℃ for 16 hr

</pre>

CO killer

2011.06.14

Today is our 1st meeting. We are a team of 9 consisting of 2 junior year students and 7 sophomore year students.

Today we discussed about team organization and task allocation. Ting-Ting was given the chance to the team leader while Steven and Li-Yi are the in-charge of system designation. We also plan our schedule so that we could make it in time.

It was quite an awkward meeting because somehow it was like when we were small going to kindergarten the 1st week. Though we study in the same campus, but due to different courses, we barely know each other. But it was very fun making new friends.

2011.06.24

It’s already end of June but we still did not get any professor to be our team advisor. Today Prof. Ingrid from Dept. of Molecular Biology and Human Genetics want to interview us before she promise us to be our team advisor. We present to her our whole project and how our idea comes up. Later on we had a little chat with her on our idea and also the whole iGEM. Finally, she accepts our invitation!

Team organization - checked !

2011.06.27

Summer is finally here! Weather is so hot and humid.

We had lunch together before we start our meeting. We were solving the problem of carbon dioxide produced by oxidation of carbon monoxide. The most ideal method is to use either plants or algae to convert the CO2 to biomass which is then processed to produce biofuels. However after long discussion with Professor Chen, we realized that we couldn’t reach that goal in such short period but we can design the host bacteria to use the Carbon Monoxide as one of the carbon source. It’s not a bad idea after all =D

2011.06.30

We all did some research on how Carbon Monoxide affects human body and what concentration level of CO is a concern. Carbon monoxide exposure levels are measured in parts per million or ppm. Steven and Joanne found out that different country has different standards. It was quite confusing because the figure is of big difference. However, after discussion with professor we knew that the risk allowance is also included in it, which is why the safety limits are not the same. Therefore, we can know conclude that, the safety standard is affected by the ppm of carbon monoxide and also the risk allowance.

We also start to do our powerpoint presentation slide which we going to show during the preliminary round.

Everyone is so focus now! Because we believed together we can achieve more. Hopefully we can keep the spirit up =D

2011.07.04

Today we had our meeting in the afternoon. The weather is so hot. It was like barbeque ourselves under the sun so we decided not to have meeting in the afternoon anymore. The topic today is the oxidation of CO to CO2 – we found out that Rhodospirillum rubrum can undergo Calvin Cycle to obtain their energy from sunlight and use CO2 as their carbon source, however cyanobacteria or other bacteria is needed for CO2 fixation and production of biofuels. But it would be much more sophiscated if we add on the cyanobacteria into the system. Hmmm … looks like we have to improve more on our system design !

2011.07.05

We talked to the microbiologist Prof. Chen CY yesterday evening and stunned us with 3 questions. The time factor, the mutation factor and the gene expression rate. The experiment of CO2 fixation requires at least half a year to complete so we probably couldn’t just simply add in our project. Besides that, we also have to think of the mutation of the gene. If the gene mutated then the product would be useless. And the most important is the rate of the protein to turn fluorescent. Lastly, if the gene size is getting bigger it would be more difficult to insert into the plasmid. Consequently, we would need more time in cloning and that would be time-costing. Uhh … we really need to find the resolution soon ! Any way, Prof. Ingrid is really very busy. We have not see her for the past 2 weeks. Gotta check out with her lab assistant.

2011.07.06

Today we had meeting in the afternoon again. Thanks god the weather is windy. We downloaded all the sequences and CDS of the gene we need. On the other hand we also search the sources of R. Rubrum which we planned to use in our project. There is a few proffesor in taiwan doing the research about R.Rubrum. So Joanne will help the letter to them to request a sample of it. And the worst case we can buy it from biotech corporation. Steven need somebody to be the in-charge of wikipedia. Leo volunteered. Found out that 2 enzymes are available : CODH–Nickel, OM5 –Molybdenum; CODH is has a higher rate of binding with CO, but OM5 can bind with CO in enormous amount at one time. Say no to procrastination ! Next meeting on Friday. A day off tomorrow =D

2011.07.09

Discussion regarding the presentation slide during the preliminary round. Task allocated to all the members. While Joanne and Steven had to write the project proposal ASAP. Not much were done today. But TGIF !! Had some photo session after the meeting. Joanne go crazy with the effect thingy on the MacBook. Stressed up after one week of intensive meeting.

2011.07.12

We are all so excited today because we having a photoshooting session this afternoon. We asked another classmate of us, Jason to be our professional photographer. It looks like all of us are good model. It started to drizzle when we were moving to another spot. Too bad we only can do indoor photoshoot. Nevermind, we can have another one in the laboratory next time. In the evening, we also had a meeting with Prof. Ingrid. We did a rehearsal about our preliminary round with her. We really have to speed up to improve our slideshow so that we could stand a chance in the coming competition.

2011.07.15

We had our second rehearsal. And we checked the email, too bad there’s no reply from the 3 professors who we send them the request letter. I think we should stalk the professor in the facebook.

2011.07.18

We had a quick briefing with Steven today. We just got the instructions to attend a meeting with our organizer on 26th of July.

Our preliminary is fixed on 22th July 12 noon. It’s only a week left, we have to work hard !!

2011.07.20

It’s the final rehearsal before our competition. Everyone is well-prepared already. Today we even wore our formal wear to the rehearsal. Steven and Leo look so smart. Practice makes perfect, now everyone can explain the slide very well. I believed that together we can achieve more.

2011.07.25

We make it to the next round! It was the big day today. The professors are impressed by our idea and really like ours creativity. However, our main problem is still the system design which is that the concentration of Carbon Monoxide which will be the inducer of the operon. Also, another problem is that we have to renew the host bacteria regularly.

2011.07.27

Finally, the deputy director of the national museum of marine biology and aquarium replied us. Too bad he doesn’t have the sample of R.Rubrum. Anyway, we’re quite motivated by his words. Thanks Prof. CS Chen

File:.jpg

Helmersi Codon

2011.02.13

Every team members propose their ideas for discussion.

3 selected project : Edible bacteria, Glowing mushrooms, Combustible bacteria.

2011.02.13

Project selected : Edible bacteria

2011.03.21

Discussion:

sequence of the soybean protein

2011.05.06

Restriction enzyme cutting site of experiment is not yet confirmed. The transport mechanism of nutrient needs more understanding.

2011.05.25

Promoter pAMJ399 of lactobacillus’s plasmid is found.

2011.06.26

The design of experiment have to discuss with team advisor. Primer have to be customized.

@@ Line 4: / Line 4: @@
 <div id="wrap">
 <div id="headerimage">
-<img src ="https://static.igem.org/mediawiki/2011/b/b3/Banner.gif" height="150" width="960">
+<img src ="https://static.igem.org/mediawiki/2011/4/47/2011banner.gif" height="150" width="960">
 </div>
@@ Line 30: / Line 30: @@
 =='''Photopaper'''==
-<gallery>
-File:Photo paper meeting(1).jpg
-File:Photo paper meeting(2).jpg
-</gallery>
 ==='''2011.02.24'''===
 '''Discussion:'''
-*Team organization
+*Team organization[[File:001.jpg|right|500px|caption]]
 *Brain storming
 **paper made by bacteria with add-ons such as colors, fragrance, etc.
 **"light up" the plants for replacing lamp posts.
 ==='''2011.03.04'''===
@@ Line 47: / Line 45: @@
 **Add-ons: colorful cellulose which produced by bacteria such as beta-carotene
 **information exchange with iGEM 2009 Cambridge team
 ==='''2011.03.14'''===
@@ Line 54: / Line 53: @@
 **Avatar - "light up" the plants by transfecting symbiotic bacteria which cloned into fluorescence gene
 **Eco-friendly warmer - biotic thermal pad
 ==='''2011.03.23'''===
@@ Line 61: / Line 61: @@
 **Option 1 : Culture bacteria which has pigment gene
 **Option 2 : Cellulose-producing bacteria secrete pigment into the medium
 ==='''2011.03.24'''===
@@ Line 68: / Line 69: @@
 ** cloning of cellulose gene’s CDS
 ** the product should operate within E. coli.
 ==='''2011.06.22'''===
@@ Line 75: / Line 77: @@
 *                -economical and humane way to produce paper in large quantities.
 *                -yeast to be our host
 ==='''2011.07.01'''===
@@ Line 80: / Line 83: @@
 * Freeze > grin > genome DNA isolation > Cloning = silk protein gene
 ==='''2011.07.09'''===
@@ Line 85: / Line 89: @@
 * the connections between 3 silk proteins : Fibl Fibh P25
 * major proteins : H-chain, L-chain, P25
 ==='''2011.07.15'''===
@@ Line 90: / Line 95: @@
 * Due to limited resources and techniques required, the team decided to switch back to the previous project. Paper making !
 * However it would be modified to be more innovative and creative.
 ==='''2011.07.18'''===
@@ Line 95: / Line 101: @@
 * Latest project : Photo paper
 * cyanobacteria is designed as the host, cellulose made up of the glucose produced by cyanobacteria could be one of the main attraction of the project.
 ==='''2011.07.23'''===
@@ Line 102: / Line 109: @@
 * Biobricks from Tokyo 2010 team will be utilized
 **regulator promoter in order to regulate the secretion of cellulose to solve the aggregation of the bacteria
 ==='''2011.09.07'''===
@@ Line 129: / Line 137: @@
 '''Raise E. coli(PSB1C3)'''
 .50ml LB+500μl CHLORAMPHENICOL
-. 37℃, overnight (14-16hrs)
+.37℃, overnight (14-16hrs)
 </pre>
 <gallery>
@@ Line 137: / Line 145: @@
 ==='''2011.09.08-13'''===
-<pre>
 '''Plasmid miniprep kit'''
-PSB1C3 plasmid
+<pre>PSB1C3 plasmid</pre>
 '''Raise Rhodobacter rubrum'''
+<pre>
 .50ml LB+500μl CHLORAMPHENICOL
 .37℃, overnight (14-16hrs)
 </pre>
 <gallery>
@@ Line 150: / Line 160: @@
 File:06.jpg
 </gallery>
 ==='''2011.09.09'''===
@@ Line 156: / Line 165: @@
 '''Raise Gluconacetobacter hansenii'''
 .50ml LB+500μl CHLORAMPHENICOL
-. 37℃, overnight (14-16hrs)
+.37℃, overnight (14-16hrs)
 </pre>
 <gallery>
@@ Line 168: / Line 177: @@
 '''Digestion check of DNA'''
 PSB1C3 DNA (control)			3μl
 PSB1C3/ EcoR
-DNA					10μl
+DNA					500ng
 ×buffer				5μl
 BSA					5μl
@@ Line 179: / Line 189: @@
 PSB1C3/ pstⅠ
-DNA					10μl
+DNA					500ng
 ×buffer				5μl
 BSA					5μl
@@ Line 189: / Line 199: @@
 PSB1C3/ EcoRⅠ+pstⅠ
-DNA	                                10μl
+DNA	                                500ng
-BSA					5μl
+×buffer			        5μl
-×buffer				5μl
+BSA				        5μl
 EcoRⅠ					1μl
 pstⅠ					1μl
@@ Line 221: / Line 231: @@
 </gallery>
+==='''2011.10.14-02'''===
-==='''2011.09.14-24'''===
 <pre>
 '''PCR'''
-template (Gluconacetobacter hansenii) 	1μl
+template DNA                       	1μl
 ×Buffer				4μl
 .5μM dNTP				1.6μl
@@ Line 258: / Line 267: @@
 <pre>
 '''Digestion of DNA'''
-acsAB/ EcoRⅠ+pstⅠ
+acsAB/ XbaⅠ+SpeⅠ
 DNA					10μl
 ×buffer				5μl
 BSA					5μl
-EcoRⅠ					1μl
+XbaⅠ					1μl
-pstⅠ					1μl
+SpeⅠ					1μl
 ddH2O					28μl
                                                    （＋
 ______________________________________________________
 μl
-→37℃ for 2 hrs
+→37℃ for 16 hr
 '''Digestion of DNA'''
-acsCD/ EcoRⅠ+pstⅠ
+acsCD/ XbaⅠ+SpeⅠ
 DNA					10μl
 ×buffer				5μl
 BSA					5μl
-EcoRⅠ					1μl
+XbaⅠ					1μl
-pstⅠ					1μl
+SpeⅠ					1μl
 ddH2O					28μl
                                                    （＋
 ______________________________________________________
 μl
-→37℃ for 2 hrs
+→37℃ for 16 hr
+</pre>
+==='''2011.09.22'''===
+<pre>
 '''Ligation of DNA'''
 PSB1C3-acsAB
@@ Line 301: / Line 313: @@
 ligase                                  1μl
 ddH2O                                   -μl
+                                                 （＋
+______________________________________________________
+μl
+</pre>
+==='''2011.09.23'''===
+<pre>
+'''PCR'''
+PR0011 promoter                         1μl
+×Buffer				4μl
+.5μM dNTP				1.6μl
+Taq		                        0.2μl
+ddH2O					13.2μl
                                                    （＋
 ______________________________________________________
@@ Line 306: / Line 332: @@
 </pre>
-==='''2011.09.22'''===
+==='''2011.09.24'''===
 <pre>
-promoter
+'''Transformation of DNA'''
+PSB1C3-acsAB
+Transform into E.coli
+LB+CHLORAMPHENICOL
+'''Transformation of DNA'''
+PSB1A3-acsCD
+Transform into E.coli
+LB+Ampicillin
+'''Transformation of DNA'''
+PSB1C3-acsAB
+PSB1A3-acsCD
+Transform into E.coli
+LB+Ampicillin+CHLORAMPHENICOL
 </pre>
-==='''2011.09.23'''===
+==='''2011.09.24'''===
 <pre>
-'''Digestion of DNA'''
+'''Ligation of DNA'''
-CmCax/ EcoRⅠ+pstⅠ
+PSB1C3-promoter
-DNA					10μl
+Vector                                  3μl
-×buffer				5μl
+Insert                                  14μl
-BSA					5μl
+ligase buffer                           2μl
-EcoRⅠ					1μl
+ligase                                  1μl
-pstⅠ					1μl
+ddH2O                                   -μl
-ddH2O					28μl
                                                    （＋
 ______________________________________________________
 μl
-→37℃ for 2 hrs
+</pre>
+==='''2011.09.27'''===
+<pre>
 '''Digestion of DNA'''
-ccp/ EcoRⅠ+pstⅠ
+acsCD/ XbaⅠ+SpeⅠ
 DNA					10μl
 ×buffer				5μl
 BSA					5μl
-EcoRⅠ					1μl
+XbaⅠ					1μl
-pstⅠ					1μl
+SpeⅠ					1μl
 ddH2O					28μl
                                                    （＋
 ______________________________________________________
 μl
-→37℃ for 2 hrs
+→37℃ for 16 hr
 '''Ligation of DNA'''
-PSB1C3-acsAB
+PSB1C3-acsCD
+Vector                                  3μl
+Insert                                  14μl
+ligase buffer                           2μl
+ligase                                  1μl
+ddH2O                                   -μl
+                                                 （＋
+______________________________________________________
+μl
+'''Ligation of DNA'''
+PSB1C3-promoter
 Vector                                  3μl
 Insert                                  14μl
@@ Line 350: / Line 402: @@
 ______________________________________________________
 μl
+</pre>
+==='''2011.09.27'''===
+<pre>
 '''Ligation of DNA'''
-PSB1A3-acsCD
+PSB1C3-Cmccax-Ccp                       3μl
-Vector                                  3μl
 Insert                                  14μl
 ligase buffer                           2μl
@@ Line 361: / Line 416: @@
 ______________________________________________________
 μl
 </pre>
-==='''2011.09.24'''===
+==='''2011.09.28'''===
+<pre>
+'''Digestion of DNA'''
+acsCD/ XbaⅠ+SpeⅠ
+DNA					10μl
+×buffer				5μl
+BSA					5μl
+XbaⅠ					1μl
+SpeⅠ					1μl
+ddH2O					28μl
+                                                  （＋
+______________________________________________________
+μl
+→37℃ for 16 hr
+==='''2011.09.28'''===
 <pre>
 '''Transformation of DNA'''
-PSB1C3-acsAB
+PSB1C3-Cmccax-Ccp
 Transform into E.coli
 LB+CHLORAMPHENICOL
+</pre>
-'''Transformation of DNA'''
+'''Digestion of DNA'''
-PSB1A3-acsCD
+<pre>
-Transform into E.coli
+acsAB/ XbaⅠ+SpeⅠ
-LB+Ampicillin
+DNA					10μl
+×buffer				5μl
+BSA					5μl
+XbaⅠ					1μl
+SpeⅠ					1μl
+ddH2O					28μl
+                                                  （＋
+______________________________________________________
+μl
+→37℃ for 16 hr
+acsAB/ XbaⅠ+SpeⅠ
+DNA					10μl
+×buffer				5μl
+BSA					5μl
+XbaⅠ					1μl
+SpeⅠ					1μl
+ddH2O					28μl
+                                                  （＋
+______________________________________________________
+μl
+→37℃ for 16 hr
+</pre>
-'''Transformation of DNA'''
-PSB1C3-acsAB
-PSB1A3-acsCD
-Transform into E.coli
-LB+Ampicillin+CHLORAMPHENICOL
 </pre>
@@ Line 394: / Line 485: @@
 File:Outdoors_shooting(3).jpg
 </gallery>
 ==='''2011.06.14'''===
@@ Line 488: / Line 577: @@
 File:Heermosi codon meeting(4).jpg
 </gallery>
 ==='''2011.02.13'''===
-'''Let the participants to propose some ideas:'''
-*To make the waste become ink after bacterial reaction.
-*Make the bacteria to produce combustible materials.
-*Make the bacteria to emit different light.
-*Edible bacteria.
-*To control the shape of bacterial.
-*To make the bacteria a fat eater.
-*Glowing mushrooms.
-*Make the bacteria to stick with dust.
-'''Poll result:'''
-Top three projects:
+'''Every team members propose their ideas for discussion. '''
-*Edible bacteria.
+*3 selected project : Edible bacteria, Glowing mushrooms, Combustible bacteria.
-*Glowing mushrooms.
-*Combustible bacteria.
-'''Conclusion:'''
-Let all participants to choose their project and make a group then check the extent of implementation.
+==='''2011.02.13'''===
-==='''2011.03.12'''===
+*Project selected : Edible bacteria
-'''Discuss the problem between the team members:'''
-*The rule of conference:
-**We can choose a chairman.
-**We can take turns by seat number then everyone has a chance to practice how to speak stable on the stage.
-'''Group report & Vote:'''
-Edible bacteria had become our determined project.
-'''Conclusion:'''
-To make three groups and search the information of soy protein, milk protein and yeast.
 ==='''2011.03.21'''===
-'''Group report:'''
-*Soy protein: There have people inject a piece of soy protein, but can’t find out the sequence.
-*The relation between milk protein and probiotics: There is both good and bad relation between milk protein and probiotics.
-*Yeast:
-Pai: Maybe we can search other organisms which have essential amino acids.  Then we can complement the lack of essential amino acids in the yeast.
-'''The application on the internet of iGEM:'''
-Huang and Celia will teach other team members how to apply it.
-'''The schedule of iGEM:'''
-.05.23:Preliminary
-'''The registration of iGEM:'''
-*Registration fee: Give it to Celia
-*Deadline: 2011.03.23 12:10-13:30
-==='''2011.04.12'''===
-'''Celiahas explain the competition system to other team members:'''
-*Everybody needs to create a new idea and search its extent of implementation.  Then design the experiment.
-*On May 23, everyone has to introduce and explain the idea through the power point.
 '''Discussion:'''
-*How to handle with our original project?
+* sequence of the soybean protein
-**We can process this project and our own project at the same time.
-**We can give the project to one of the team member.
-'''Conclusion:'''
-*We decided to give the project to Jin, but we still can process two projects at the same time if he needs our help.
-*In order to help each other and solve the problems with our ideas, we still have discussion every week.
-==='''2011.05.06'''===
-'''Share the ideas:'''
-*Sea water purification
-*Purification of factory water use
-*Bacteria for wound
-*Glowing mushroom
-'''Suggestion:'''
-*Celia: Maybe you use plant can be easier to get the same purpose.
-*Huang: Maybe you can use symbiotic bacteria of plant and inject the glowing gene into it.
-==='''2011.05.10-2011.05.12'''===
-'''Progress report:'''
-*Huanghas changed her idea and is still searching the information.
-*Tsai has an idea is about bio-battery. To create the ion concentration difference by bacteria and produce the electricity.
-**Questions:
-***Celia: If you can produce this project successfully, how do you convince the public to use your product?
-***Huang: Do you have any certification to proof that you can make this project by yeast or bacteria?
-*Zou has a new idea: To clean up our teeth by bacteria. She had find out the gene of decomposition of tartar and has the conception of teeth whitening.
-*Ting find the element that both petroleum and oil has contained.
-*Paiput out a new idea is odorless sweat.  He chooses Helicobacter pylori and Proteus mirabilis as host.
-*Jinfind the information of how Staphylococcus aureus maintain its electricity.
-*Dorrie is still searching the experiment and being revised the idea.
-*Yu has a new idea: Rust proof bacteria.  She wanted to injected the gene into aerobic bacteria.
-==='''2011.05.25'''===
-'''Progress report:'''
-*Jin: Because we have figured out the gene then we have to ask Pr. Woon to contact with the author of that paper and get the gene sequence.
-'''Homework:'''
-*To find the…
-**The performance of E.coli and Lactobacillus.
-**Protein purification.
-**The plasmid of Lactobacillus.
-**TA-cloning
-*Huang: Send the paper to team members and ask Pr. Woon help us to get the sequence.
-*Celia: Translate the conference record and store them.
+==='''2011.05.06'''===
+* Restriction enzyme cutting site of experiment is not yet confirmed. The transport mechanism of nutrient needs more understanding.
-==='''2011.06.26'''===
+==='''2011.05.25'''===
-'''Progress report:'''
+* Promoter  pAMJ399 of lactobacillus’s plasmid is found.
-Experiment design:Jinwill discuss with Pr. Woon and set for the primer.
+==='''2011.06.26'''===
-'''Homework:'''
+* The design of experiment have to discuss with team advisor. Primer have to be customized.
-*To find the farming methods of lactobacillus.
-*To find the plasmid is used by Cambridge in 2010.
-*To understand the design methods of primer.

Team:TzuChiU Formosa/Notebook

From 2011.igem.org

Latest revision as of 17:19, 2 October 2011

Contents

Photopaper

2011.02.24

2011.03.04

2011.03.14

2011.03.23

2011.03.24

2011.06.22

2011.07.01

2011.07.09

2011.07.15

2011.07.18

2011.07.23

2011.09.07

2011.09.08-13

2011.09.09

2011.09.10-11

2011.10.14-02

2011.09.15

2011.09.18

2011.09.21

2011.09.22

2011.09.23

2011.09.24

2011.09.24

2011.09.27

2011.09.27

2011.09.28

CO killer

2011.06.14

2011.06.24

2011.06.27

2011.06.30

2011.07.04

2011.07.05

2011.07.06

2011.07.09

2011.07.12

2011.07.15

2011.07.18

2011.07.20

2011.07.25

2011.07.27

Helmersi Codon

2011.02.13

2011.02.13

2011.03.21

2011.05.06

2011.05.25

2011.06.26