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Kvasny Prum. 1978; 24(11): 246-249 | DOI: 10.18832/kp1978041
The article deals with the cultivation in test tubes on semisolid beer medium (P3) of microorganisms rapidly spoiling beer. Beer must be treated as follows: carbon dioxide should be expelled by shaking, the amount of dissolved oxygen reduced by introducing nitrogen stream under 1,5mg of O2 in 1 litre, bottles filled, capped with crown corks and pasteurized. The storage period of beer so treated can be improved by applyingsome stabilizing adsorption preparation. Prior to inoculation 30ml of 0,7% hot water solution of agar must be mixed with 100ml of stored beer and this mixture poured in test tubes with 0,1 - 1,0ml samples or strips of membrane filter holding microorganisms. Microorganisms quickly spoiling beer can be identified after 4 days of cultivation at 28 °C. Slowly propagating microorganisms can be identified later. Tetracycline (50µg/ml) suppresses selectively propagation of bacteria, whereas actidion (30µg/ml) of yeast. Comparison of the numbers of lactobacilli in cask beer, in highly nutritive medium and in P3 indicates, that only a certain part of lactobacilli present in beer is responsible for its rapid spoilage. There is a corrrelation between the numbers of quick-spoiling microorganisms and storage quality of beer. Microorganisms multiplied in samples of benn in P3 were morphologically identical with those multiplied in stored, bottled beer. The described method being simple and requiring little time is suitable for routine checking.
(In Czech, English summary only)
Published: November 1, 1978