Special culture medium for strict anaerobe detection of beer
A technology of anaerobic bacteria and culture medium, which is applied in the field of special culture medium for the detection of strict anaerobic bacteria in beer
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Embodiment 1
[0008] The preparation method of embodiment 1 medium:
[0009] Weigh yeast extract: 0.5g, peptone: 0.3g, sodium lactate: 1.7g, ascorbic acid: 0.1g; sodium thiosulfate (Na2S2O4 5H2O): 0.01g, lead acetate: 0.02g, methylene blue (Methylene blue) : 0.0002g, phenylethyl alcohol (PEA): 0.2g, agar powder (ager) 1.5g.
[0010] After accurately weighing each component, put it into a conical flask with a certain volume (according to the experimental needs), add 100ml of distilled water, mix the components, heat and boil on an electric stove for 3-5 minutes (the culture medium turns from blue to colorless) , until the components are completely dissolved. When the temperature drops to about 50°C, it can be used on a flat plate. The plate must be used in a strictly anaerobic anaerobic box or anaerobic tank or anaerobic tube.
Embodiment 2
[0011] The using method of embodiment 2 culture medium:
[0012] The inoculated bacteria were two strains of Pectinatus cerevisiiphilus and Pectinatus frisingensis and lactic acid bacteria, the inoculation gradient was 10-3 gradient, and anaerobic culture was carried out at 28°C for two weeks. Lead acetate reacts with hydrogen sulfide released by pectin bacteria to form lead sulfide, forming black colonies. Since lactic acid bacteria do not produce hydrogen sulfide, their colonies remain milky white. Therefore, strict anaerobic bacteria can be clearly distinguished and identified. The specific colony color and effect can be found in the accompanying drawings of the instructions.
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