Quiet day in the lab today A few…

Quiet day in the lab today!
A few of the yeast cultures i had did not grow after their first innoculation onto MEA plates. I have re-streaked Mucor, Aspergillus niger and Saccromyces spp onto fresh MEA plates and incubated them at 30C. Penicillin notatum and Aspergillus parasitucus successfully grew and i have re-streaked them onto fresh MEA plates and incubated them for two days at 30C, from this i hope to gain a pure strain of the target funghi. Confirmed Chromobacteruim CV026 and have made a broth culture so that i can make up long term storage stabs and slopes. Also made up a batch of TAE with Rosie and Fran. Now to research exactly what it is and does.

Busy day today Started the day going through…

Busy day today,
Started the day going through wednesday and thursday’s results with Rachael, so she knows where we are with our cultures, and so we can plan what we’re doing next. Taught Hammad how to do water filtration, made up 950ml of M17agar base with 10g Lactose suppliment (suspended in 100ml distilled water), both were autolaved before mixing. After lunch Rachael poured the plates. Made up 2800ml (7 x 400ml) of LB agar and poured plates with five of these. The other two were left for Nicola to add ampicillin and then pour the plates.I also made up 250ml of 0.85% w/v NaCl, this also needed to be autoclaved. Made up two stabs and slopes with the PS aeruginosa broth that i incubated overnight. Counted colony cultures from Sharon’s Brayfod water project.

Quiet day in the lab today made nutrient…

Quiet day in the lab today, made nutrient agar and MEA plates ready for tomorrow. Todays task was to try and streak plates with bacteria that looked dead. The dried bacterial sample were ‘wetted’ by adding a little Ringers solution and then streaked on nutrient agar (with the exception of the fungi, they were streaked on MEA). Once this was done, a little research was needed to find out the incubation periods for the target bacterial streak plates. On to more research to find out what each colony should look like and whether it is Gram positive or negative. Hopefully we can positively isolate and identify each bacterial culture and create stabs and slopes.

One of the most important jobs in a…

One of the most important jobs in a microbiology lab is maintaining a culture collection to ensure all the bacterial and fungal strains necessary for research are kept pure and thriving. Unfortunately, without a consistent research programme, this often doesn’t happen in our labs. I need a couple of very specific E. coli strains for my research, but I came back in at the start of this research period to plates for these strains like the first one in this picture of DH5a – almost a year old, so completely dry and, to the unobservant, useless. But, with a little encouragement, I got the few cells out alive as you can see in the second plate, and then within another day to the pure streak in the last plate.

Unfortunately, I wasn’t so lucky with my second strain, C2110, and I’ve had to revert back to a stab culture I finally unearthed, but hopefully I should see growth this morning when I get into the lab.

As a result, I’ve got some of you working on creating a culture collection of some of the random bottles of cells I’ve found lurking around in the incubator room, by creating slopes and stabs for storage. It will really be a revelation if we can get it all sorted out!!

Started the morning off by streaking nutrient agar…

Started the morning off by streaking nutrient agar plates from cultures thought to be ‘dead’ and put them in the incubator til tomrrow. Stock cultures from the lab were previously streaked on agar plates, today my task was to isolate single colonies and make up streak plates, these were placed in the incubator until tomorrow when they will hopefully have grown so they can then be gram stained and identified. Then i chose a project to conduct over the summer, If a pure sample of soya can be located then i hope to design a working PCR test to detect GM soya in non GM foods.