pH-stat: Culture of Synechocystis sp. PCC 6803

Objectives of the culture

General

By introducing a culture of Synechocystis sp cianobaceria. PCC 6803 we intent to ensure that the pH changes resulting from growth and proliferation function as a switch in order to activate the colicins, so that in the artificial system created, as time passes, the colicins produced by Escherichia coli will increase their concentration in their habitat, being inactive until the pH reaches the optimum range of activation, which is when they ´ll get activated and will produce cell lysis and kill the pathogens.

Specific

To develop what we have stated above, we need to know:

• How to establish the culture at the laboratory

• The temporal evolution of the pH in the culture.

Establishing the culture under laboratory conditions.

The material and methods needed are :

• 18 Watts fluorescent tubes of white light, special tubes for aquariums that divide the spectrum mostly between the peaks of the visible red and blue light, which stimulate the photosynthesis.

• Volumetric flasks, 100 ml and 200 ml

• Air Pumps

• Commercial Fertilizer Brand COMPO

• Distilled, tap and analytical water (Type II)

The first experiment consisted of a series of six cultures in which environmental conditions varied so as to know the habitat preferences of the cyanobacterium. We distinguished two different groups:

The first, consisting of C1, C2 and C3, which have tap , distilled and analytical water respectively. It also uses a reflector box, which increases the irradiation of light on the culture, and a magnetic stirrer, which prevents the deposition of cells on the bottom

The second group , which are C4, C5 and C6, without reflector or magnetic stirrer, but we kept the water in the same order as before.

Results and discussion

The other conditions remained constant in both cases, as are detailed in the following table:

The day after having inoculated the culture, the absorbency data were collected and the cells / ml counted with a camera Neubawer. The absorbancy was measured at 440 nm and 750 nm as the first was the highest value according to the spectrophotometer after a sweep, and the second was taken according to references (Burrows, EH, et. Al., 2009, JF Allen, 2008). In the account we distinguished between simple cells, ie those which are not in the reproductive period, and those which are.

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For technical reasons, a power cut for an entire weekend, on our arrival the following Monday, the cultures showed a transparent colour which had nothing to do with their usual blue-green algae colour ( cyanobacteria).So, we got rid of the remains and started a new culture. This time we chose the least contaminated water which still showed a good margin of survival, analytical water, to which we added a higher concentration of fertilizer to stimulate growth. Besides ,we decided to stop using the reflector box as we had evidence that such a bright light caused photo-inhibition. The volumes and other conditions kept constant.