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使用肠球菌CCM 4231控制实验性污染的干发酵霍纳德萨拉米香肠中的单核细胞增生李斯特菌。

Use of enterocin CCM 4231 to control Listeria monocytogenes in experimentally contaminated dry fermented Hornád salami.

作者信息

Lauková A, Czikková S, Laczková S, Turek P

机构信息

Institute of Animal Physiology, Slovak Academy of Sciences, Kosice.

出版信息

Int J Food Microbiol. 1999 Nov 1;52(1-2):115-9. doi: 10.1016/s0168-1605(99)00125-7.

Abstract

The effectiveness of enterocin CCM 4231 in controlling Listeria monocytogenes contamination in dry fermented Hornád salami was examined. Three independent salami treatments were conducted under pilot plant and laboratory conditions. Salamis were produced according to standard technological parameters and stages with ripening for 3 weeks. The reference samples consisted of the meat mixture without either L. monocytogenes or bacteriocin addition. The control sample (CS) consisted of the meat mixture with 1% of L. monocytogenes inoculum (10(8) cfu ml(-1)) added; while the experimental sample (ES) consisted of the same mixture with enterocin CCM 4231 (12800 AU g(-1)) added. Sampling was done on the first day of the experiment, before and after bacteriocin addition for ES, on the second day and after 1, 2 and 3 weeks. The enterocin addition resulted in the reduction of L. monocytogenes by 1.67 log cycle in the ES when compared to the CS immediately after addition of the bacteriocin. Although on the second day, the growth of L. monocytogenes in ES reached 3.38 cfu g(-1) (log 10), a difference of 1.72 log was found between the ES and the CS. After 1 week of ripening, the L. monocytogenes count in the CS reached 10(7) cfu g(-1); while in the ES the count was 10(4) cfu g(-1), a difference which was maintained after 2 and 3 weeks of ripening. However, bacteriocin activity in the ES could not be detected analytically. The meat mixture used did not contain Listeria.

摘要

研究了肠球菌CCM 4231在控制干发酵霍纳德萨拉米香肠中单核细胞增生李斯特菌污染方面的有效性。在中试工厂和实验室条件下进行了三种独立的萨拉米香肠处理。萨拉米香肠按照标准工艺参数和阶段生产,成熟3周。参考样品为未添加单核细胞增生李斯特菌或细菌素的肉混合物。对照样品(CS)为添加了1%单核细胞增生李斯特菌接种物(10(8) cfu ml(-1))的肉混合物;而实验样品(ES)为添加了肠球菌CCM 4231(12800 AU g(-1))的相同混合物。在实验的第一天、添加细菌素前后(针对ES)、第二天以及1、2和3周后进行采样。与添加细菌素后立即相比,ES中添加肠球菌使单核细胞增生李斯特菌减少了1.67个对数周期。尽管在第二天,ES中单核细胞增生李斯特菌的生长达到3.38 cfu g(-1)(log 10),但ES和CS之间仍发现相差1.72个对数。成熟1周后,CS中单核细胞增生李斯特菌的数量达到10(7) cfu g(-1);而ES中的数量为10(4) cfu g(-1),这种差异在成熟2周和3周后仍然存在。然而,在ES中无法通过分析检测到细菌素活性。所用的肉混合物不含李斯特菌。

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