Department of Wine, Food and Molecular Biosciences, Lincoln University, New Zealand; BioBrew Ltd., PO, Box 10076, Rotorua, Mail Centre, 3046, New Zealand.
Department of Wine, Food and Molecular Biosciences, Lincoln University, New Zealand.
J Microbiol Methods. 2019 Dec;167:105778. doi: 10.1016/j.mimet.2019.105778. Epub 2019 Nov 13.
This study demonstrates an effective technique for separating and purifying viable bacteria from samples that interfere with viability staining. The viability of Bifidobacterium longum ATCC 15707 was assessed using Percoll Buoyant Density Gradient Centrifugation (PBDC) to separate bacteria from complex non-dairy food matrices and Quantitative Fluorescence Microscopy (QFM) to determine individual cells using LIVE/DEAD BacLight bacterial viability staining. Water agar (3%) was used to retain cells of B. longum and offered a lower fluorescence background with BacLight viability staining, compared with fixation on polycarbonate (PC) black membrane. The effect of drying temperatures and non-dairy foods on viability of B. longum was assessed. B. longum coated on oat, peanut or raisin was separated by filtration, low- and high-speed centrifugation, flotation and sedimentation buoyant density centrifugation. Purified cells were subsequently deposited on water agar for rehydration followed by LIVE/DEAD BacLight viability staining and enumeration. Conventional plate counting was also conducted to compare viability results. Finally, this method was applied to assess cell membrane damages of B. longum incorporated onto non-dairy foods during 24 h drying. Furthermore, viability assessment of B. longum coated onto oat, peanut, or raisin was much lower by plate counting compared to viability staining. Drying appeared to have a greater impact when viability was assessed by plate counting compared to viability staining. IMPORTANCE: Enumeration of viable beneficial bacteria from function foods presents a significant bottleneck for product development and quality control. Interference with microscopic and/or fluorescent techniques by ingredients, time required to incubate plated microbes, and the transient nature of the colony forming unit make rapid assessment of viable bacteria difficult. Viability assessment of Bifidobacterium longum ATCC 15707 by Percoll Buoyant Density Gradient Centrifugation with LIVE/DEAD BacLight viability staining on water agar (3%) was in agreement with serial dilution enumeration. Without the need for incubation viability assessment by staining provided a more rapid means to assess the impact of drying on the viability of B. longum coated onto oat, peanut or raisin.
本研究展示了一种从干扰活菌染色的样品中分离和纯化活菌的有效技术。使用聚蔗糖(Percoll)浮力密度梯度离心(PBDC)分离双歧杆菌长亚种 ATCC 15707 与复杂的非乳制品基质中的细菌,并用定量荧光显微镜(QFM)通过 LIVE/DEAD BacLight 活菌染色来测定单个细胞,以此评估双歧杆菌长亚种 ATCC 15707 的活力。水琼脂(3%)用于保留双歧杆菌的细胞,与在聚碳酸酯(PC)黑膜上固定相比,使用 BacLight 活菌染色时提供了更低的荧光背景。评估了干燥温度和非乳制品对双歧杆菌活力的影响。通过过滤、低速和高速离心、浮选和沉降浮力密度离心,将双歧杆菌长亚种 ATCC 15707 包被在燕麦、花生或葡萄干上进行分离。随后,将纯化后的细胞沉积在水琼脂上进行复水,再进行 LIVE/DEAD BacLight 活菌染色和计数。还进行了常规平板计数以比较活力结果。最后,该方法用于评估 24 小时干燥过程中双歧杆菌长亚种 ATCC 15707 包被在非乳制品上的细胞膜损伤。此外,与活菌染色相比,通过平板计数评估双歧杆菌长亚种 ATCC 15707 包被在燕麦、花生或葡萄干上的活力要低得多。与活菌染色相比,通过平板计数评估时,干燥对活力的影响似乎更大。重要性:从功能食品中对有益活菌进行计数,对产品开发和质量控制构成了重大瓶颈。成分会干扰显微镜和/或荧光技术,培养平板上微生物所需的时间,以及形成单位菌落的短暂性,使得快速评估活菌变得困难。用聚蔗糖(Percoll)浮力密度梯度离心(PBDC)结合水琼脂(3%)上的 LIVE/DEAD BacLight 活菌染色对双歧杆菌长亚种 ATCC 15707 进行活力评估,与连续稀释计数结果一致。无需孵育即可进行活力评估,通过染色提供了一种更快速的方法来评估干燥对包被在燕麦、花生或葡萄干上的双歧杆菌长亚种 ATCC 15707 活力的影响。