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Microfiltration of Enzyme Treated Egg Whites for Accelerated Detection of Viable Salmonella

机译:酶处理蛋清的微滤技术可快速检测沙门氏菌

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We report detection of <13 CFU of Salmonella per 25 g egg white within 7 h by concentrating the bacteria using microfiltration through 0.2-mu m cutoff polyethersulfone hollow fiber membranes. A combination of enzyme treatment, controlled cross-flow on both sides of the hollow fibers, and media selection were key to controlling membrane fouling so that rapid concentration and the subsequent detection of low numbers of microbial cells were achieved. We leveraged the protective effect of egg white proteins and peptone so that the proteolytic enzymes did not attack the living cells while hydrolyzing the egg white proteins responsible for fouling. The molecular weight of egg white proteins was reduced from about 70 kDa to 15 kDa during hydrolysis. This enabled a 50-fold concentration of the cells when a volume of 525 mL of peptone and egg white, containing 13 CFU of Salmonella, was decreased to a 10 mL volume in 50 min. A 10-min microcentrifugation step further concentrated the viable Salmonella cells by 10x. The final cell recovery exceeded 100%, indicating that microbial growth occurred during the 3-h processing time. The experiments leading to rapid concentration, recovery, and detection provided further insights on the nature of membrane fouling enabling fouling effects to be mitigated. Unlike most membrane processes where protein recovery is the goal, recovery of viable microorganisms for pathogen detection is the key measure of success, with modification of cell-free proteins being both acceptable and required to achieve rapid microfiltration of viable microorganisms. (C) 2016 American Institute of Chemical Engineers
机译:我们报告通过使用0.2微米的截留聚醚砜中空纤维膜微滤浓缩细菌,在7小时内检测到每25克蛋白中沙门氏菌<13 CFU。酶处理,控制中空纤维两侧的错流以及选择培养基的组合是控制膜结垢的关键,因此可以快速浓缩并随后检测到少量的微生物细胞。我们利用蛋清蛋白和蛋白ept的保护作用,使蛋白水解酶在水解造成结垢的蛋清蛋白时不会攻击活细胞。在水解过程中,蛋清蛋白的分子量从约70 kDa降至15 kDa。当将含有13 CFU沙门氏菌的525 mL蛋白ept和蛋清的体积在50分钟内降至10 mL时,可使细胞浓度提高50倍。 10分钟的微量离心步骤进一步将存活的沙门氏菌细胞浓缩了10倍。最终细胞回收率超过100%,表明在3小时的处理时间内发生了微生物生长。导致快速浓缩,回收和检测的实验为膜污染的性质提供了进一步的见解,从而减轻了污染的影响。与大多数以蛋白质回收为目标的膜法不同,回收用于病原体检测的活微生物是成功的关键指标,对无细胞蛋白质的修饰既可以接受,也需要进行修饰以实现活微生物的快速微滤。 (C)2016美国化学工程师学会

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