单月桂酸蔗糖单独和与有机酸联合对单核增生李斯特菌和金黄色葡萄球菌的抑制作用。

J D Monk, L R Beuchat, A K Hathcox
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引用次数: 49

摘要

研究了脂肪酸蔗糖酯单独和与乙二胺四乙酸(EDTA)、乙酸、乳酸和柠檬酸联合使用对单核细胞增生李斯特菌和金黄色葡萄球菌存活、生长和热失活的影响。在胰蛋白酶磷酸酯(TPB)和胰蛋白酶豆汤(TSB)中添加400微克ml-1的蔗糖,对单核增生乳杆菌和葡萄球菌的生长没有抑制作用。分别为葡萄球菌。然而,在对数生长期,与不含单月桂酸蔗糖(SML)的TPB相比,在含有100微克ml-1单月桂酸蔗糖(SML)的TPB中检测到的单核增生乳杆菌数量显著减少(P <或= 0.05)。当浓度为400微克ml-1时,SML对单核增生乳杆菌具有致死性。葡萄球菌的抑制作用不明显。葡萄球菌。在含SML的肉汤中添加EDTA对这两种微生物具有协同抑制作用。单独的螯合剂在100微克ml-1浓度下对两种病原体都没有作用,但在200微克ml-1浓度下有抑制作用。当孵育温度从30℃降低到15℃或5℃时,对单核增生乳杆菌的抑制作用更为明显。在孵育前32小时,在TPB中添加0.1%的乙酸或乳酸,使100和200微克ml-1 SML的抑制作用最小化。在TSB中单独添加SML或SML和有机酸培养时,金黄色葡萄球菌对单核细胞增生乳杆菌的表现类似,但没有那么明显。SML和EDTA对单核增生乳杆菌热失活有明显的协同抑制作用,而对葡萄球菌热失活则相反。葡萄球菌。SML对单核增生乳杆菌和葡萄球菌生长的控制效果。应进一步调查最有可能被这些病原体污染的食品中的金黄色葡萄球菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory effects of sucrose monolaurate, alone and in combination with organic acids, on Listeria monocytogenes and Staphylococcus aureus.

The effects of sucrose esters of fatty acids, alone and in combination with ethylenediaminetetraacetic acid (EDTA), acetic acid, lactic acid and citric acid, on survival, growth and thermal inactivation of Listeria monocytogenes and Staphylococcus aureus were determined. The presence of sucrose monocaprate (400 micrograms ml-1) in tryptose phosphate broth (TPB) or tryptic soy broth (TSB) did not inhibit the growth of L. monocytogenes or Staph. aureus, respectively. However, significantly (P < or = 0.05) lower populations of L. monocytogenes were detected in TPB containing as little as 100 micrograms ml-1 sucrose monolaurate (SML) during the logarithmic growth phase compared to populations detected in TPB containing no SML. At 400 micrograms ml-1, SML was lethal to L. monocytogenes. Less marked inhibitory effects were observed with Staph. aureus. The addition of EDTA to broth containing SML had a synergistic effect on the inhibition of both organisms. The chelator alone had no effect at 100 micrograms ml-1 on either pathogen but was inhibitory at 200 micrograms ml-1. Inhibition of L. monocytogenes was more pronounced as the incubation temperature was decreased from 30 degrees C to 15 or 5 degrees C. The addition of 0.1% acetic or lactic acid to TPB minimized the inhibitory effect of 100 and 200 micrograms ml-1 SML during the first 32 h of incubation. Staphylococcus aureus behaved similarly, but not as dramatically, to L. monocytogenes when cultured in TSB supplemented with SML alone or SML and organic acids. A synergistic inhibitory effect of SML and EDTA on heat inactivation of L. monocytogenes was evident but the reverse phenomenon was observed with Staph. aureus. The effectiveness of SML in controlling the growth of L. monocytogenes and Staph. aureus in foods most likely to be contaminated with these pathogens should be further investigated.

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