Champagne C P, Raymond Y, Gonthier J, Audet P
Agriculture and Agri-Food Canada, Food Research and Development Centre, 3600 Casavant Blvd. West, St-Hyacinthe, QC J2S 8E3, Canada.
Can J Microbiol. 2009 Apr;55(4):410-8. doi: 10.1139/w08-151.
Pasteurized and unfermented milks supplemented with probiotic bacteria are appearing on the market. It then becomes a challenge to ascertain the undesirable contamination microbiota in the presence of a largely superior population of probiotic bacteria. A method to enumerate the contaminating microbial microbiota in such probiotic-enriched milks was developed. The probiotic cultures, Lactobacillus rhamnosus Lb-Immuni-T and Bifidobacterium animalis subsp. lactis BB-12(R), were added to a pasteurized unfermented milk to reach a minimum of 1 billion CFU per 250 mL portion, as ascertained by plating on de Man - Rogosa - Sharpe (MRS) agar in anaerobic conditions. No growth of B. animalis subsp. lactis BB-12 was noted on plate count agar (PCA) or Petrifilm plates, and the presence of this culture did not affect standard plate counts (SPC) of contaminating bacteria. However, L. rhamnosus formed colonies on PCA and Petrifilm plates. Attempts were thus made to inhibit the growth of the probiotic lactobacilli in PCA. The addition of 2% sodium phosphate (SP) or 5% glycerophosphate (GP) inhibited the growth of the lactobacilli in broths, but pin-point colonies of L. rhamnosus Lb-Immuni-T nevertheless appeared on PCA supplemented with phosphates. SPC could be obtained on PCA + 2% SP by only counting the large colonies, but this resulted in a significant (4.4 fold) underestimation of SPC values. On Petrifilm AC, at dilutions 0 to 2, all colonies were considered as being contaminants, while at dilutions 3 and 4, only large colonies were counted for SPC determinations. There was a direct correlation (R2 = 0.99) between SPC values with Petrifilm in uninoculated milks and those obtained on probiotic-enriched milks. The high correlation obtained over the 102 to 106 CFU/mL range of SPC values show that this Petrifilm method is appropriate to evaluate the microbiological quality of pasteurized milks enriched with L. rhamnosus Lb-Immuni-T and B. animalis subsp. lactis BB-12.
添加了益生菌的巴氏杀菌未发酵乳正在上市。在存在大量优势益生菌的情况下,确定不良污染微生物群就成为了一项挑战。为此开发了一种方法来对这种富含益生菌的牛奶中的污染微生物群进行计数。将益生菌菌株鼠李糖乳杆菌Lb-Immuni-T和动物双歧杆菌亚种乳双歧杆菌BB-12(R)添加到巴氏杀菌未发酵乳中,使其每250毫升部分至少达到10亿CFU,这是通过在厌氧条件下接种到德氏乳酸杆菌-罗格斯-夏普(MRS)琼脂平板上确定的。在平板计数琼脂(PCA)或Petrifilm平板上未观察到动物双歧杆菌亚种乳双歧杆菌BB-12的生长,并且这种培养物的存在不影响污染细菌的标准平板计数(SPC)。然而,鼠李糖乳杆菌在PCA和Petrifilm平板上形成菌落。因此尝试在PCA中抑制益生菌乳酸杆菌的生长。添加2%的磷酸钠(SP)或5%的甘油磷酸钠(GP)可抑制肉汤中乳酸杆菌的生长,但在添加了磷酸盐的PCA上仍出现了鼠李糖乳杆菌Lb-Immuni-T的针尖状菌落。通过仅计数大菌落可在PCA + 2% SP上获得SPC,但这导致SPC值显著(4.