Ali Md A, Hui Wang, Lin Guangen, Dang Fang F, Wu Shuang, Man Chaoxin, Jiang Yujun
Northeast Agricultural University, College of Food Science, Key Laboratory of Dairy Science, Ministry of Education, Harbin, China 150030.
J AOAC Int. 2019 Mar 1;102(2):532-538. doi: 10.5740/jaoacint.18-0216. Epub 2018 Aug 22.
subsp. HN019 is widely used as a probiotic in various dairy preparations. To ensure optimal health benefits, an adequate number of probiotics should be viable in products, but the culture-based methods require longer periods to account for the strain. Develop a standard curve to account viable load of subsp. HN019 by real-time PCR. The growth curve was developed according to plate count method, and cycle threshold (C) curve was prepared using C values. These two curves were then combined to construct the standard curve. To validate the method, the strain was proliferated in whole milk, and viable loads were enumerated by plate counting and relative PCR counting followed by determining the SEM between the two counts. The growth curve and C curve, respectively, showed the highest viable load (2.13 × 10 CFU/mL) and lowest C value (18.29) after 18 h, and during the entire growth phase (0-18 h), viable loads are inversely proportional to the C values. The standard curve revealed the model = 2E + 18e ( = cells/mL, = C value; ² = 0.992). In validation, the highest SEM (± 0.70 × 10) was found between the plate count (1.15 × 10 cells/mL) and relative PCR count (1.29 × 10 cells/mL) after cultivating for 14 h. The method could be readily used in dairy industries to quantify viable subsp. HN019 by a shorter period. Culture-independent enumeration of viable subsp. HN019 by real-time PCR.
亚种HN019在各种乳制品制剂中被广泛用作益生菌。为确保最佳健康效益,产品中应有足够数量的活益生菌,但基于培养的方法需要更长时间来鉴定菌株。通过实时荧光定量PCR绘制标准曲线以测定亚种HN019的活菌数。根据平板计数法绘制生长曲线,并使用循环阈值(C)值绘制C曲线。然后将这两条曲线合并以构建标准曲线。为验证该方法,将该菌株在全脂牛奶中增殖,并通过平板计数和相对PCR计数确定活菌数,随后测定两次计数之间的标准误。生长曲线和C曲线分别在18小时后显示出最高活菌数(2.13×10 CFU/mL)和最低C值(18.29),并且在整个生长阶段(0-18小时),活菌数与C值成反比。标准曲线显示模型 = 2E + 18e( = 细胞数/mL, = C值;² = 0.992)。在验证过程中,培养14小时后,平板计数(1.15×10细胞/mL)和相对PCR计数(1.29×10细胞/mL)之间的标准误最高(± 0.70×10)。该方法可在乳制品行业中轻松用于在较短时间内定量亚种HN019的活菌数。通过实时荧光定量PCR对亚种HN019进行不依赖培养的活菌计数。