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氯和热处理对苜蓿种子上接种的斯坦利沙门氏菌的杀灭效果以及该病原菌在发芽和储存期间的生长与存活情况

Efficacy of chlorine and heat treatment in killing Salmonella stanley inoculated onto alfalfa seeds and growth and survival of the pathogen during sprouting and storage.

作者信息

Jaquette C B, Beuchat L R, Mahon B E

机构信息

Department of Food Science and Technology, University of Georgia, Griffin 30223-1797, USA.

出版信息

Appl Environ Microbiol. 1996 Jul;62(7):2212-5. doi: 10.1128/aem.62.7.2212-2215.1996.

Abstract

The efficacy of chlorine and hot water treatments in killing Salmonella stanley inoculated onto alfalfa seeds was determined. Treatment of seeds containing 10(2) to 10(3) CFU/g in 100-micrograms/ml active chlorine solution for 5 or 10 min caused a significant (P < or = 0.05) reduction in population, and treatment in 290-micrograms/ml chlorine solution resulted in a significant reduction compared with treatment in 100 micrograms of chlorine per ml. However, concentrations of chlorine of up to 1,010 micrograms/ml failed to result in further significant reductions. Treatment of seeds containing 10(1) to 10(2) CFU of S. stanley per g for 5 min in a solution containing 2,040 micrograms of chlorine per ml reduced the population to undetectable levels (< 1 CFU/g). Treatment of seeds in water for 5 or 10 min at 54 degrees C caused a significant reduction in the S. stanley population, and treatment at > or = 57 degrees C reduced populations to < or = 1 CFU/g. However, treatment at > or = 54 degrees C for 10 min caused a substantial reduction in viability of the seeds. Treatment at 57 or 60 degrees C for 5 min appears to be effective in killing S. stanley without substantially decreasing germinability of seeds. Storage of seeds for 8 to 9 weeks at 8 and 21 degrees C resulted in reductions in populations of S. stanley of about 1 log10 and 2 log10 CFU/g, respectively. The behavior of S. stanley on seeds during soaking germination, sprouting, and refrigerated storage of sprouts was determined. An initial population of 3.29 log10 CFU/g increased slightly during 6 h of soaking, by about 10(3) CFU/g during a 24-h germination period, and by an additional 10 CFU/g during a 72-h sprouting stage. A population of 10(7) CFU/g of mature alfalfa sprouts was detected throughout a subsequent 10-day storage period at 5 degrees C. These studies indicate that while populations of S. stanley can be greatly reduced, elimination of this organism from alfalfa seeds may not be reliably achieved with traditional disinfection procedures. If S. stanley is present on seeds at the initiation of the sprout production process, populations exceeding 10(7) CFU/g can develop and survive on mature sprouts exposed to handling practices used in commercial production and marketing.

摘要

测定了氯处理和热水处理对杀灭接种在苜蓿种子上的斯坦利沙门氏菌的效果。将含有10²至10³CFU/g的种子在100微克/毫升活性氯溶液中处理5或10分钟,可使菌数显著(P≤0.05)减少,与在100微克/毫升氯溶液中处理相比,在290微克/毫升氯溶液中处理导致菌数显著减少。然而,高达1010微克/毫升的氯浓度未能导致进一步的显著减少。将含有每克10¹至10²CFU斯坦利沙门氏菌的种子在每毫升含2040微克氯的溶液中处理5分钟,可使菌数降至检测不到的水平(<1CFU/g)。将种子在54℃的水中处理5或10分钟,可使斯坦利沙门氏菌菌数显著减少,在≥57℃处理可使菌数降至≤1CFU/g。然而,在≥54℃处理10分钟会导致种子活力大幅下降。在57或60℃处理5分钟似乎能有效杀灭斯坦利沙门氏菌,而不会大幅降低种子的发芽率。将种子在8℃和21℃储存8至9周,分别使斯坦利沙门氏菌菌数减少约1个对数10和2个对数10CFU/g。测定了斯坦利沙门氏菌在种子浸泡发芽、发芽和豆芽冷藏储存期间的行为。初始菌数为3.29个对数10CFU/g,在浸泡6小时期间略有增加,在24小时发芽期增加约10³CFU/g,在72小时发芽阶段又增加10CFU/g。在随后5℃的10天储存期内,成熟苜蓿芽中检测到菌数为10⁷CFU/g。这些研究表明,虽然斯坦利沙门氏菌菌数可大幅减少,但用传统消毒程序可能无法可靠地从苜蓿种子中消除这种微生物。如果在芽苗生产过程开始时种子上存在斯坦利沙门氏菌,在商业生产和销售中采用的处理方式下,成熟芽苗上的菌数可能会超过10⁷CFU/g并存活下来。

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