Difference between revisions of "Team:Reading/Notebook"
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<p> LB BG-11 Kan plates and LB BG-11 plates made up to plate the competition assay on </p> | <p> LB BG-11 Kan plates and LB BG-11 plates made up to plate the competition assay on </p> | ||
<title2> <b> 01/09/15 </b> </title2> | <title2> <b> 01/09/15 </b> </title2> | ||
− | <p> Competition | + | <p> Competition assay</p> |
+ | </br> |
Revision as of 12:54, 18 September 2015
This page is an account of the daily events in our lab and project. Dates are in the UK format DD/MM/YY. 6803 refers to the cyanobacterium used - Synechocystis sp. PCC 6803
All placed on the windowsill in our lab under natural light and at room temperature (~25°C)
2 Litres of water collected from Whiteknights Lake on campus for SODIS, method outlines in protocols.
Estimating the Cells per ml for the flask from 29/06 1 a.u at 750nm = 1.6x108
OD750 measurement and cells per ml estimated for flasks cultured on 02/07
The lamp safety testing completed so flasks placed under the bright white light bulb
Flasks are getting very green, definitely a good sign!
Flask 2 discarded as it is not showing growth, and has signs of contamination. We received most of the lab equipment we have ordered.
Miniprep of plasmid DNA: We carried out extraction of biobrick construct plasmids from E.coli NEB-5α glycerol stocks.
We extracted pSB1K3 plasmid backbones combined with biobricks containing the following genes:
- PilA1
- PsaD
- PetF
- PilT
This gave us 4 samples of plasmid DNA, which were placed in the freezer at -20°C.
-
BG-11 cultures: We added ~200ml of BG-11 to two sterile 500ml conical flasks. We inoculated them as follows;
- Flask 5 - 1ml of Wild type 6803 from flask 3 as this flask had the best growth.
- Flask 6 - 10µl of stock Howe Lab triple mutant 6803.
- SODIS lakewater cultures: We added ~200ml of SODIS lakewater to three sterile 500ml conical flasks. We inoculated them as follows;
- SODIS 1 and 2 - 1ml of Wild type 6803 from flask 3 as this flask had the best growth.
- SODIS 3 - 1ml of stock Howe Lab triple mutant 6803.
All flasks cultured today were placed in the incubator, being shaken at 58rpm, 30°C, and under bright white light
200ml of BG-11 was added to flasks 3 and 4 which already contained ~100ml of ~2 a.u density 6803 WT.
Competition Assay
200ml of BG-11 added to a new sterile conical flask
added 10ul of WT 6803 and 10ul of MT3 6803
Flask was placed in the incubator, being shaken at 58rpm, 30°C, and under bright white light
DNA concentration from miniprep
- PilA1 = 11.16ns/ul
- PsaD = 13.01ns/ul
- PetF = 0.38ns/ul
- PilT = 8.58ns/ul
*no DNA due to miniprep from Glycerol Stock
Made LB Agar tranplates for culturing
- PilA1
- PsaD
- PetF
- PilT
No growth on plates from 07/08
Cultured plates of LB Agar from all stocks (glycerol stocks)
Growth on many the stocks from 10/08, replated onto LB kan 50 plates
Competition Assay had begun to turn a light green colour.
Stock growth onto LB kan 50 plates unsuccessful.
Potassium ferricyanide reagent arrives, protocols start being drawn up
Nanowires concluded to be a non-fruitful venture
Our lab becomes engulfed in the tides of cuvettes arriving
Competition assay starting to reach log phase
LB BG-11 Kan plates and LB BG-11 plates made up to plate the competition assay on
Competition assay