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Improving the safety and quality of raw tuna fillets by X-ray irradiation

机译:X射线辐照提高金枪鱼生鱼片的安全性和质量

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In this study, raw tuna fillet (25 g) samples were inoculated by immersing in 0.1% peptone water that contained 10(8-9) CFU ml(-1) of a three-strain mixture of Salmonella enterica for 1 min. The samples were then air dried at 22 degrees C for 30 min (to allow bacterial attachment) in the biosafety cabinet and were packaged separately in sterilized bags prior to X-ray treatments (0.0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6 kGy). The surviving Salmonella populations on raw tuna fillets samples were evaluated using a nonselective medium (tryptic soy agar) for 6 h with xylose lysine desoxycholate (XLD) selective medium overlay. The plates were then incubated for an additional 18 h at 37 degrees C. Finally, the colonies were counted and the results were expressed as log CFU g(-1). Furthermore, un-inoculated tuna samples (25 g) were packaged separately in sterilized bags and exposed to the lowest and highest X-ray doses (0.0 and 6.0 kGy), then stored at 5 degrees C, 10 degrees C or 25 degrees C for 25, 15 or 5 days, respectively. On the testing-dates, samples were withdrawn and microflora (psychrotrophic and mesophilic) counts, quality [color (using Hunter colorimeter) and texture (using Instron machine)] were evaluated. The results indicated that more than a 6 log CFU reduction of Salmonella population being achieved with 0.6 kGy X-ray treatment. Furthermore, treatment with X-ray significantly reduced the initial inherent microbiota on raw tuna fillets and inherent levels were significantly (p 0.05) lower than the control samples throughout the shelf-life storage at 5, 10 or 25 degrees C for 25, 15 or 5 days, respectively. There was a significant effect of X-ray treatment on tuna color after treatment (day 0). However, no significant differences (p > 0.05) in color or texture of control and treated samples were observed after (day 0). These results indicated that X-ray is a good preservative technology for seafood products intended to be consumed raw. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在这项研究中,将生金枪鱼片(25 g)样品浸泡在0.1%的蛋白in水中进行接种,其中该蛋白contained包含10(8-9)CFU ml(-1)的三株肠炎沙门氏菌混合物1分钟。然后将样品在生物安全柜中于22摄氏度空气干燥30分钟(以使细菌附着),并在进行X射线处理(0.0、0.1、0.2、0.3、0.4、0.5、0.6)之前分别包装在灭菌袋中kGy)。使用非选择性培养基(胰蛋白酶大豆琼脂)与木糖赖氨酸脱氧胆酸盐(XLD)选择性培养基覆盖,评估生金枪鱼鱼片样品上尚存的沙门氏菌种群。然后将板在37℃下再孵育18小时。最后,计数菌落,结果表示为log CFU g(-1)。此外,将未接种的金枪鱼样品(25 g)分别包装在灭菌袋中,并暴露于最低和最高X射线剂量(0.0和6.0 kGy)下,然后分别在5摄氏度,10摄氏度或25摄氏度下保存25、15或5天。在测试日期,取出样品并评估菌群(精神营养和嗜温菌)计数,质量[颜色(使用Hunter比色计)和质地(使用Instron机)]。结果表明,采用0.6 kGy X射线治疗,沙门氏菌种群的CFU减少量超过6 log。此外,在5、10或25摄氏度,25、15和25的保质期内,X射线处理显着减少了生金枪鱼鱼片的初始固有菌群,并且固有水平显着低于对照样品(p <0.05)。或5天。处理后(第0天),X射线处理对金枪鱼色有显着影响。然而,在第0天之后,在对照和处理的样品的颜色或质地上没有观察到显着差异(p> 0.05)。这些结果表明,X射线是打算以生食方式消费的海鲜产品的良好防腐技术。 (C)2015 Elsevier Ltd.保留所有权利。

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