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Inhibition of Listeria monocytogenes on the surface of individually packaged hot dogs with a packaging film coating containing nisin

机译:用含乳链菌肽的包装膜包衣抑制单包装热狗中的单核细胞增生李斯特菌

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摘要

The objective of this study was to determine the effectiveness of packaging films coated with a methylcellulose/hydroxypropyl methylcellulose-based solution containing 10,000, 7,500, 2,500, or 156.3 IU/ml nisin for controlling Listeria monocytogenes on the surfaces of vacuum-packaged hot dogs. Barrier film coated with a methylcellulose/hydroxypropyl methylcellulose-based solution containing nisin or no nisin (control) was heat sealed to form individual pouches. Hot dogs were placed in control and nisin-containing pouches and inoculated with a five-strain L monocytogenes cocktail (approximately 5 log CFU per package), vacuum sealed, and stored for intervals of 2 It and 7, 15, 21, 28, and 60 d at 4degreesC. After storage, hot dogs and packages were rinsed with 0.1% peptone water. Diluent was spiral plated on modified oxford agar and tryptic soy agar and incubated to obtain counts (CFU per package). L. monocytogenes counts on hot dogs packaged in films coated with 156.3 IU/ml nisin decreased slightly (similar to0.5-log reduction) through day 15 of refrigerated storage but was statistically the same (P > 0.05) as hot dogs packaged in films without nisin after 60 d of storage. Packaging films coated with a cellulose-based solution containing 10,000 and 7,500 IU/ml nisin significantly decreased (P < 0.05) L. monocytogenes populations on the surface of hot dogs by greater than 2 log CFU per package throughout the 60-d study. Similar results were observed for hot dogs packaged in films coated with 2,500 IU/ml nisin; however, L. monocytogenes populations were observed to be approximately 4 log CFU per package after 60 d of refrigerated storage from plate counts on tryptic soy and modified oxford agars.
机译:这项研究的目的是确定用含有10,000、7,500、2,500或156.3 IU / ml乳酸链球菌素的甲基纤维素/羟丙基甲基纤维素基溶液涂覆的包装膜对控制真空包装热狗表面单核细胞增生李斯特菌的有效性。加热涂覆有包含乳链菌肽或不含乳链菌肽的甲基纤维素/羟丙基甲基纤维素基溶液的屏障膜(对照)以形成单独的袋。将热狗放在对照组和含乳链菌肽的小袋中,并接种五株L单核细胞增生李斯特氏菌鸡尾酒(每个包装约5 log CFU),真空密封,并以2 It和7、15、21、28和7的间隔存储4摄氏度60 d。储存后,热狗和包装用0.1%蛋白ept水冲洗。将稀释剂螺旋接种在改良的牛津琼脂和胰蛋白酶大豆琼脂上并孵育以获得计数(每包CFU)。在冷藏后的第15天,用156.3 IU / ml乳链菌肽包被的薄膜包装的热狗中的单核细胞增生李斯特菌计数略有下降(约减少0.5-log),但与包装在薄膜中的热狗统计上相同(P> 0.05)存放60天后不含乳链菌肽。在整个60天的研究中,用含有10,000和7,500 IU / ml乳酸链球菌素的纤维素基溶液涂布的包装膜,每包热狗表面的单核细胞增生李斯特氏菌数量显着降低(P <0.05)单核细胞增生李斯特菌种群,每包装超过2 log CFU。对于包装在涂有2,500 IU / ml乳链菌肽的薄膜中的热狗,观察到了相似的结果。然而,在冷藏储存60天后,从胰蛋白酶大豆和改良牛津琼脂上的平板计数中观察到,单核细胞增生李斯特氏菌种群大约为每个包装4 log CFU。

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