Difference between revisions of "Team:Marburg/Labbook/Minicells"

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20 mL LB were inoculated with TB43 and TB43 HU-mCherry for flow cytometry and grown to an optical density (OD) of 0.5. We didn't see minicells.
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20 mL LB were inoculated with TB43 and TB43 HU-mCherry for flow cytometry and grown to an optical density (OD) of 0.5. No minicells could be detected.
 
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5 mL LB were inoculated with TB43, TB43 HU-mCherry, TB43 GFP and TB43 HU-mCherry GFP and incubated at 37 °C and 200 rpm.
 
5 mL LB were inoculated with TB43, TB43 HU-mCherry, TB43 GFP and TB43 HU-mCherry GFP and incubated at 37 °C and 200 rpm.
 
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</p>
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<h2>Preparation of M9 Minimal Medium</h2>
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<p>
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Two media were prepared. One according to M9 minimal medium protocol and the other without glucose.
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</p>
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<h1>15/08/24</h1>
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<h2>Plasmid Preparation</h2>
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<p>
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Cultures containing a plasmid which encodes enzymes for the biosynthesis of &beta;-carotene were treated according to the Macherey-Nagel Plasmid DNA Purification Kit protocol.
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</p>
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<h1>15/08/25</h1>
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<h2>Transformation</h2>
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<p>
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Carotinoid plasmids were transformed into chemocompetent TB43 and TB43 HU-mCherry according to Transformation into chemocompetent (RbCl) Cells protocol.
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</p>
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<h2>Plasmid Preparation</h2>
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<p>
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Cultures containing a plasmid which encodes enzymes for the biosynthesis of violacein were treated according to the Macherey-Nagel Plasmid DNA Purification Kit protocol.
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</p>
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Revision as of 17:38, 11 September 2015

15/07/07

Preparation of ONCs

Two times 5 mL LB were inoculated with TB43 and TB43 HU-mCherry and incubated at 37 °C and 200 rpm.

15/07/08

Preparation of Glycerol Stocks

Glycerol stocks of TB43 and TB43 HU-mCherry were prepared according to the glycerol stock generation protocol.

Preparation of electrocompetent Cells

Electrocompetent cells of TB43 and TB43 HU-mCherry were prepared according to the electrocompetent E.coli cells protocol.

Preparation of over-night culture (ONC)

Two times 5 mL LB were inoculated with TB43 and TB43 HU-mCherry and incubated at 37 °C and 200 rpm.

15/07/09

Preparation of electrocompetent Cells

Electrocompetent cells of TB43 and TB43 HU-mCherry were prepared according to the electrocompetent E.coli cells protocol.

15/07/10

Preparation of day culture

20 mL LB were inoculated with TB43 and TB43 HU-mCherry for flow cytometry and grown to an optical density (OD) of 0.5. No minicells could be detected.

15/07/11

Transformation

A GFP plasmid with Chloramphenicol resistance gene was transformed into TB43 and TB43 HU-mCherry via electroporation according to transformation into electrocompetent cells protocol.

15/07/13

Preparation of ONC

50 mL LB were inoculated with TB43 GFP and TB43 HU-mCherry GFP and incubated at 37 °C and 200 rpm.

15/07/15

Preparation of Minicells

TB43 GFP and TB43 HU-mCherry GFP were treated according to preparation of minicells protocol. Samples were taken and minicells could be detected via flow cytometry but only with very low yields.

15/07/27

Preparation of ONC

5 mL LB were inoculated with TB43, TB43 HU-mCherry, TB43 GFP and TB43 HU-mCherry GFP and incubated at 37 °C and 200 rpm.

15/07/28

Preparation of chemocompetent Cells

Chemocompetent cells of TB43, TB43 GFP, TB43 HU-mCherry and TB43 HU-mCherry GFP were prepared according to competent E.coli cells (RbCl) protocol.

15/08/21

Preparation of ONC

5 mL LB were inoculated with TB43, TB43 HU-mCherry, TB43 GFP and TB43 HU-mCherry GFP and incubated at 37 °C and 200 rpm.

Preparation of M9 Minimal Medium

Two media were prepared. One according to M9 minimal medium protocol and the other without glucose.

15/08/24

Plasmid Preparation

Cultures containing a plasmid which encodes enzymes for the biosynthesis of β-carotene were treated according to the Macherey-Nagel Plasmid DNA Purification Kit protocol.

15/08/25

Transformation

Carotinoid plasmids were transformed into chemocompetent TB43 and TB43 HU-mCherry according to Transformation into chemocompetent (RbCl) Cells protocol.

Plasmid Preparation

Cultures containing a plasmid which encodes enzymes for the biosynthesis of violacein were treated according to the Macherey-Nagel Plasmid DNA Purification Kit protocol.

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