Team:HokkaidoU Japan/Notebook/plastic protocols
From 2012.igem.org
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(→Culture and harvest) |
(→Polymer producing media) |
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|2×LB | |2×LB | ||
- | | | + | |10 ml |
|- | |- | ||
|●50% Glucose | |●50% Glucose | ||
- | | | + | |800 ul |
|- | |- | ||
|●1M pantothenic acid Ca | |●1M pantothenic acid Ca | ||
- | | | + | |200 ul |
|- | |- | ||
|Amp(100mg/ml) | |Amp(100mg/ml) | ||
- | | | + | |20 ul |
|- | |- | ||
|ROwater | |ROwater | ||
- | |8. | + | |8.98 ml |
|- | |- | ||
|} | |} | ||
- | Put 1. | + | Put 1.5 ml each into the test tube. |
Line 33: | Line 33: | ||
|- | |- | ||
|ROwater | |ROwater | ||
- | | | + | |7 ml |
|- | |- | ||
|Glucose | |Glucose | ||
- | | | + | |10 g....Heat and stir until it melts. |
|- | |- | ||
|ROwater | |ROwater | ||
- | |up to | + | |up to 20 ml |
|- | |- | ||
|} | |} | ||
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|- | |- | ||
|ROwater | |ROwater | ||
- | | | + | |7 ml |
|- | |- | ||
|pantothenic acid Ca | |pantothenic acid Ca | ||
- | |4. | + | |4.77 g....Heat and stir until it melts. |
|- | |- | ||
|ROwater | |ROwater | ||
- | |up to | + | |up to 10 ml |
|- | |- | ||
|} | |} |
Revision as of 05:35, 19 August 2012
Bold text
Polymer producing media
polymer producing media (LB:2%Glc+ 10mM pantothenic acid Ca + Amp100mg/l) 20ml
2×LB | 10 ml |
●50% Glucose | 800 ul |
●1M pantothenic acid Ca | 200 ul |
Amp(100mg/ml) | 20 ul |
ROwater | 8.98 ml |
Put 1.5 ml each into the test tube.
●50%gulcose
ROwater | 7 ml |
Glucose | 10 g....Heat and stir until it melts. |
ROwater | up to 20 ml |
Filter sterilize.
●1M pantothenic acid Ca
ROwater | 7 ml |
pantothenic acid Ca | 4.77 g....Heat and stir until it melts. |
ROwater | up to 10 ml |
Filter sterilize.
Culture and harvest
- Preculture transformed media 1.5ml for 10~14 hours, 180rpm/30℃.
- Culture 15μl preculture media in polymer producing media for 48hours, 180rpm/30℃.
- Centrifuge for 10min, 5000rpm.
- Remove supernatant and add 500ml ROwater and suspend it.
- Centrifuge again for 10min, 5000rpm and remove its supernatant.
- Freeze in -80℃ for more than 3hours.
- Freeze-dry for more than 48hours.
Polymer extraction and purification
- Move dried up bacteria into test tube.
- Break up them to separate and add 10ml chloroform.
- Incubate for 48hour at 60C.
- Make it filtered through PTFE and move it into another test tube.
- Volatilize organic solvent by exposing air and separate polymer.
- Add 5ml hexane and voltex for a minute. After centrifuging (1,500rpm, 10min), remove the clear layer.
- Volatilize chloroform by exposing air again.
- Add 5ml MtOH, voltex for a minute, centrifuge (1,500rpm, 10min), and remove the clear layer.
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