Difference between revisions of "Team:Reading/Protocols"

Protocols

Note: This section is an account of all laboratory protocols used by the team this year. The references at the bottom of the page provide the sources for the protocols, however we have modified several of them to our needs.

Growth of Synechocystis sp. PCC 6803

1. Thaw stock of 6803 on ice
2. 100ml of BG-11 medium added to sterile conical flask aseptically
3. Add 10µl or 5 loopfuls of 6803 to flask
4. Incubate at ~30°C and on shaker at ~58rpm, under constant illumination
5. Check growth each day by measuring OD₇₅₀

Taking optical density of culture to measure growth

We measured the OD₇₅₀ to match that used in research papers on Synechocystis¹.

1. Set spectrophotometer to measure at OD₇₅₀
2. Blank with 1ml of BG-11
3. Take OD₇₅₀ of 1ml of culture
4. If OD₇₅₀ over 1 a.u, dilute 250µl of culture in 750µl of BG-11 (1/4 dilution)

To calculate cell density, we used the equation, 1 a.u = 1.6x10⁸ cells per ml of culture².

Solar water disinfection (SODIS)

SODIS is an extremely cheap and simple method of sterilising water, requiring only sunlight, and Polyethylene terephthalate (PET) plastic bottles³. We used water from Whiteknights lakeon the University of Reading campus.

1. Pass water through a filter into a PET bottle to remove particulates
2. Seal bottle and place in sunlight. Leave bottle exposed to intense sunlight for a minimum of 6 hours

Miniprep: Isolation of plasmid DNA from bacteria

We used the Thermo Scientific GeneJET Plasmid Miniprep Kit⁴ for our miniprep. This protocol closely follows protocol A, which is detailed in the booklet included in the kit.

1. Pellet cells from 1.5ml of culture by centrifugation at 4000rpm for 2 minutes, and remove as much supernatant as possible and discard, leaving only the pellet.
2. Resuspend pellet in 250µl of Resuspension Solution by vortexing breifly until pellet no longer visable.
3. Lyse cells by adding 250µl of Lysis Solution and mixing thoroughly by inverting the tube 4-6 times until solution becomes viscous and clear
4. Add 350µl of Neutralisation Solution and mix immediately and gently until solution becomes cloudy.
5. Centrifuge for 5 minutes at 12,000rpm
6. Transfer supernatant to a GeneJET spin column. Avoid disturbing white precipitate.
7. Centrifuge for 1 minute at 12,000rpm and discard the flow-through.
8. Add 500µl of Wash Solution to GeneJET spin column, centrifuge for 1 minute at 12,000rpm, and discard flow-through.
9. Repeat step 8.
10. Discard flow-through and centrifuge for 1 minute at 12,000rpm to remove residual Wash Solution.
11. Transfer GeneJET spin column to a fresh 1.5ml microcentrifuge tube. Add 50µl of Elution Buffer, being careful not to touch the membrane with the pipette.
12. Incubate at room temperature for 2 minutes and then centrifuge for 2 minutes at 12,000rpm
13. Discard GeneJET spin column and store purified plasmid DNA at -20°C.

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References

1. Bradley, R. W., Bombelli, P., Lea-Smith, D. J. & Howe, C. J. Terminal oxidase mutants of the cyanobacterium Synechocystis sp. PCC 6803 show increased electrogenic activity in biological photo-voltaic systems. Phys. Chem. Chem. Phys. PCCP 15, 13611–13618 (2013).
2. Pojidaeva E, Zichenko V, Shestakov SV, Sokolenko A (2004) Involvement of the SppA1 peptidase in acclimation to saturating light intensities in Synechocystis sp. strain PCC 6803. J Bacteriol 186: 3991–3999.
3. SODIS. 2015. SODIS Method, Available at: href="http://www.sodis.ch/methode/index_EN
4. ThermoScientific. 2013. Thermo Scientific GeneJET PCR Purification Kit #K0701, #K0702. [Online] Available at: https://www.lifetechnologies.com/order/catalog/product/K0502?ICID=search-k0502