The rate of lactic fermentation can be measured readily with centrifuged cells in glucose solution. Virtanen and associates have done this with cells of Streptococcus lactis and Lactobacillus casei, mostly with dried or toluene-treated cells, but one series (1927) deals with living cells. Their results in regard to the optimal pH differ widely from ours. Several other factors are reported here which Virtanen and his associates did not study.
METHODOur studies are limited to strains 14 (isolated from plants) and 125 (from milk) of S. lactis. Virtanen grew his bacteria in whey, i.e., in a lactose medium. We used a broth made of 5 grams peptone, 5 grams tryptone, 10 grams glucose, 36.6 grams Na2HPO4.12H20 and 4.2 grams KH2PO4 per liter. This same medium plus 15 grams agar was used for plate counts. Inoculation was heavy, 5 to 10 cc. of a young culture per liter. The cells were centrifuged when the culture was 12 to 14 hours old. The sedimented cells were re-suspended in a phosphate buffer of the same concentration as given above. This suspension was added to the test medium in such quantity that the cells from 250 cc. of culture were condensed in 50 cc. of the test medium. Thus, we hoped to avoid growth.The test medium consisted of the same 2 per cent buffer (36.6 grams Na2HP04.12H20 = 15.8 grams anhydrous, plus 4.2 grams KH2PO4) to which 3 or 5 grams peptone and 20 grams glucose per liter were added. The peptone is essential. All cultivation and all fermentation tests were carried out at 300C. 547 on July 31, 2020 by guest