JÄRVIK's method for counting of Leuconostoc organisms was examined and modified. The modified agar medium is a selective one for use in the plate procedure for counting and isolation of Leuconostoc organisms in milk, mixed-strain starter culture, and dairy products. It was prepared as follows:
1) Basal medium:
Glucose, 5g. Peptone, 5g.
Na
2HPO
4•12H
2O. 3g. (Eurocidine, 0.1g.)
Yeast-extract, 5g. Malt-extract, 10g.
Agar, 15g. Distilled water, 1000
mlAdjust the pH of the medium to 6.5.
Sterilize at 120°C for 10 minutes.
2) Acetate buffer solution:
Sodium acetate•3H
2O. 14.1g. Acetic acid, 14.1g.
Make the volume to 1000
ml with distilled water.
Sterilize at 120°C for 10 minutes.
3) 0.1Nα-bromopropionic acid solution:
α-Bromopropionic acid, 15.299g, per 1000
ml of solution,
Sterilize at 120°C for 10 minutes.
The best results were obtained when 7.5
ml of acetate buffer solution and 1.0
ml of 0.1N α-bromopropionic acid solution were added to 100
ml of basal medium, and when the plates were incubated at 21°C for 4-5 days.
The modified medium inhibited the growth of Streptococcus strains, but supported the normal growth of Leuconostoc strains in mixed lactic starter culture.
The results of isolation tests of Leuconostoc organisms indicate that it is necessary to eliminate the Lactobacillus count by microscopic examination in order to obtain an exact count of Leuconostoc organisms when the medium is applied to cheese, because only a few Lactobacillus strains begin to grow within 5 days.
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