"
Team:TzuChiU Formosa/Notebook/photopaper
From 2011.igem.org
(→2011.09.07) |
(→2011.09.07) |
||
| Line 129: | Line 129: | ||
'''Rhodobacter rudrum medium''' | '''Rhodobacter rudrum medium''' | ||
<br> | <br> | ||
| - | <br>K2HPO4 | + | <br>K2HPO4 1g |
| - | <br>NaCl 0.5g | + | <br>NaCl 0.5g |
| - | <br>FeSO4．7H2O | + | <br>FeSO4．7H2O 0.01g |
| - | <br>CaCl2 | + | <br>CaCl2 0.02g |
| - | <br>MnCl2．4H2O | + | <br>MnCl2．4H2O 0.002g |
| - | <br>MgSO4．7H2O | + | <br>MgSO4．7H2O 0.2g |
| - | <br>NaMO2O4．2H2O | + | <br>NaMO2O4．2H2O 0.01g |
| - | <br>ddH2O 998. | + | <br>ddH2O 998.258ml |
<br>________________________________________ | <br>________________________________________ | ||
<br> 1L →take100ml | <br> 1L →take100ml | ||
| Line 142: | Line 142: | ||
＋ | ＋ | ||
| - | <br>Yeast Extrat | + | <br>Yeast Extrat 0.5g |
<br>Sodium malate | <br>Sodium malate | ||
| - | <br>(Sodium succinate dibasic hexohydrate) | + | <br>(Sodium succinate dibasic hexohydrate) 5g |
<br>NH4Cl 1g | <br>NH4Cl 1g | ||
| - | <br>ddH2O | + | <br>ddH2O 893.5ml |
<br>_________________________________________________ | <br>_________________________________________________ | ||
<br> 1L | <br> 1L | ||
Revision as of 14:55, 3 October 2011
Contents |
Photopaper
Meeting Notes
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
2011.09.15
Genome miniprep
Gluconacetobacter hansenii
2011.09.18
Gel/PCR DNA extraction
Gluconacetobacter hansenii
Protocols
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 998.258ml
________________________________________
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/EcoRI]
DNA 500ng
10×buffer 5μl
BSA 5μl
EcoRⅠ 1μl
ddH2O 29μl
_______________________________
total 50μl
[pSB1C3/PstⅠ]
DNA 500ng
10×buffer 5μl
BSA 5μl
pstⅠ 1μl
ddH2O 29μl
_________________________________
total 50μl
[PSB1C3/EcoRⅠ+PstⅠ]
DNA 500ng
10×buffer 5μl
BSA 5μl
EcoRⅠ 1μl
pstⅠ 1μl
ddH2O 28μl
__________________________________
total 50μl
→37℃ for 30 mins
Digestion of DNA
[PSB1C3/EcoRⅠ+pstⅠ]
DNA 10μl
10×buffer 5μl
BSA 5μl
EcoRⅠ 1μl
pstⅠ 1μl
ddH2O 28μl
____________________________________
total 50μl
→37℃ for 2 hrs
electroelution Purification
PSB1C3 backbone
2011.09.14-24
PCRtemplate DNA 1μl
5×Buffer 4μl
2.5μM dNTP 1.6μl
10μM F 1μl
10μM R 1μl
Taq 0.2μl
ddH2O 8.8μl
_______________________________
total 20μl
2011.09.21
Digestion of DNA
[acsAB/ XbaⅠ+SpeⅠ]
DNA 10μl
10×buffer 5μl
BSA 5μl
EcoRⅠ 1μl
pstⅠ 1μl
ddH2O 28μl
____________________________
total 50μl
→37℃ for 16 hr
Digestion of DNA
[acsCD/XbaⅠ+SpeⅠ]
DNA 10μl
10×buffer 5μl
BSA 5μl
EcoRⅠ 1μl
pstⅠ 1μl
ddH2O 28μl
__________________________________
total 50μl
→37℃ for 16 hr
2011.09.22
Ligation of DNA
[PSB1C3-acsAB]
Vector 3μl
Insert 14μl
ligase buffer 2μl
ligase 1μl
ddH2O -μl
________________________________
total 20μl
Ligation of DNA
[PSB1A3-acsCD]
Vector 3μl
Insert 14μl
ligase buffer 2μl
ligase 1μl
ddH2O -μl
_________________________________
total 20μl
2011.09.23
PCR
PR0011 promoter 1μl
5×Buffer 4μl
2.5μM dNTP 1.6μl
Taq 0.2μl
ddH2O 13.2μl
_____________________________________
total 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
________________________________
total 20μl
