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首页> 外文期刊>Journal of Rapid Methods and Automation in Microbiology >INFLUENCE OF GLUCOSE OXIDASE ON THE GROWTH OF ESCHERICHIA COLI 0157:H7, LISTERIA MONOCYTOGENES, AND SALMONELLA TYPHIMURIUM IN UNIVERSAL PREENRICHMENT BROTH
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INFLUENCE OF GLUCOSE OXIDASE ON THE GROWTH OF ESCHERICHIA COLI 0157:H7, LISTERIA MONOCYTOGENES, AND SALMONELLA TYPHIMURIUM IN UNIVERSAL PREENRICHMENT BROTH

机译:葡萄糖氧化酶对大肠杆菌0157:H7、单核细胞增生李斯特菌和鼠伤寒沙门氏菌生长的影响

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Glucose oxidase (GO), a food‐grade enzyme, was compared with OxyraseTMoxygen reducing membrane fraction in Universal Preenrichment Broth (UPB) for enhancement of the growth of the facultatively anaerobic pathogens Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes Scott A. Oxidation‐reduction potential (ORP) and pH changes in UPB following the addition of GO (4 units/ml) or OxyraseTM(0.5 units/ml) were measured. Microbial growth was evaluated at 0, 3, 6, 18, and 24 h of incubation using spiral plating. Nonenzyme supplemented UPB served as the control. OxyraseTMprovided a higher oxygen scavenging action in terms of ORP decrease during the initial 6 h of incubation. However, no difference occurred in Eh between OxyraseTMand GO by 18 h, with both enzyme systems effectively reducing the Eh compared to that of the control. A 1.0 pH unit reduction was observed in GO‐supplemented UPB after 18 h, indicating production of gluconic acid. The pH decrease in OxyraseTM‐ supplemented media was 0.2 units. By 6 h, the E. coli O157:H7 population was enhanced by 0.6 and 1.4 log CFU/ml in OxyraseTM‐supplemented media, compared to the control and GO‐supplemented media, respectively. By 18 h, 0.4 and 0.9 log CFU/ml growth enhancements of the E. coli O157:H7 populations were seen in GO‐ and OxyraseTM‐supplemented media, respectively, compared to the control. By the end of 18 h, counts of S. typhimurium and L. monocytogenes increased by 0.6 and 0.2 log units, respectively, in GO‐supplemented media compar
机译:葡萄糖氧化酶 (GO) 是一种食品级酶,与通用预富集肉汤 (UPB) 中的 OxyraseTM氧还原膜组分进行了比较,以增强兼性厌氧病原体大肠杆菌 O157:H7、鼠伤寒沙门氏菌和单核细胞增生李斯特菌 Scott A. 测量添加 GO (4 单位/ml) 或 Oxyrase TM (0.5 单位/ml) 后 UPB 的氧化还原电位 (ORP) 和 pH 值变化。使用螺旋铺板在孵育 0、3、6、18 和 24 小时时评估微生物生长。补充非酶的UPB作为对照。在孵育的最初 6 小时内,Oxyrase TM 在 ORP 降低方面提供了更高的除氧作用。然而,在18小时时,Oxyrase TM和GO之间的Eh没有差异,与对照组相比,两种酶系统都有效地降低了Eh。18 小时后,在添加 GO 的 UPB 中观察到 1.0 pH 单位降低,表明葡萄糖酸的产生。添加OxyraseTM的培养基的pH值降低0.2单位。到 6 小时时,与对照和添加 GO 的培养基相比,添加 Oxyrase TM 的培养基中的大肠杆菌 O157:H7 群体分别增强了 0.6 和 1.4 log CFU/ml。到18小时时,与对照组相比,在GO和Oxyrase TM补充培养基中,大肠杆菌O157:H7群体的生长分别增强了0.4和0.9 log CFU/ml。到18 h结束时,鼠伤寒沙门氏菌和单核细胞增生李斯特菌的计数分别增加了0.6和0。2 个对数单位,分别在 GO 补充的培养基比较中

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