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pH响应比色酶联免疫吸附法检测牛奶中猪霍乱沙门氏菌
引用本文:李倩影, 张抗抗, 周耀锋, 黄小林, 李响敏, 熊勇华. pH响应比色酶联免疫吸附法检测牛奶中猪霍乱沙门氏菌[J]. 食品工业科技, 2021, 42(1): 227-232. DOI: 10.13386/j.issn1002-0306.2019100100
作者姓名:李倩影  张抗抗  周耀锋  黄小林  李响敏  熊勇华
作者单位:1.1. 食品科学与技术国家重点实验室, 江西南昌 330047
基金项目:"十三五"国家重点研发计划(2018YFC1602202、2018YFC1602203、2018YFC1602505);国家自然科学基金(31760485、31901780)。
摘    要:人类常常因误食被猪霍乱沙门氏菌感染的食物而引发中毒。因此,急需构建适用于快速、灵敏检测食物中猪霍乱沙门氏菌污染的新方法。鉴于此,本文构建了一种pH响应比色酶联免疫吸附法灵敏检测牛奶中猪霍乱沙门氏菌。该方法利用葡萄糖氧化酶催化底物葡萄糖产生葡萄糖酸,导致溶液pH下降,进而引发溴甲酚紫(Bromocresol purple,BCP)溶液颜色由紫色变成亮黄色,随后通过记录BCP颜色变化(OD430/OD590)实现目标菌的定量检测。当菌浓度为2.54×103~6.17×105 CFU/mL,该方法定量检测猪霍乱沙门氏菌可用方程一表述:y1=0.1051ln (x)+0.7024(R2=0.7513);当菌浓度为6.17×105~1.67×107 CFU/mL,该方法定量检测猪霍乱沙门氏菌可用方程二表述:y2=1.3216ln (x)-15.797(R2=0.9711);当菌浓度大于1.67×107 CFU/mL时,BCP溶液呈现明显亮黄色,OD430/OD590值趋于稳定,无法实现猪霍乱沙门氏菌定量检测。将六个不同浓度的猪霍乱沙门氏菌(2.5×103~5.6×106 CFU/mL)加标至牛奶中,检测结果显示回收率介于72.16%~103.58%,相对标准偏差介于7.54%~15.30%。总之,本研究所构建的比色ELISA方法适用于牛奶中不同浓度的猪霍乱沙门氏菌快速、灵敏定量检测。

关 键 词:pH响应比色酶联免疫吸附法(pH-ELISA)  葡萄糖氧化酶  溴甲酚紫  猪霍乱沙门氏菌
收稿时间:2019-10-16

pH Responded Colorimetric ELISA for Sensitive Detection of Salmonella Choleraesuis in Milk
LI Qian-ying, ZHANG Kang-kang, ZHOU Yao-feng, HUANG Xiao-lin, LI Xiang-min, XIONG Yong-hua. pH Responded Colorimetric ELISA for Sensitive Detection of Salmonella Choleraesuis in Milk[J]. Science and Technology of Food Industry, 2021, 42(1): 227-232. DOI: 10.13386/j.issn1002-0306.2019100100
Authors:LI Qian-ying  ZHANG Kang-kang  ZHOU Yao-feng  HUANG Xiao-lin  LI Xiang-min  XIONG Yong-hua
Affiliation:1.1. State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, China
Abstract:Human maybe get poisoning after eating Salmonella choleraesuis-infected food. Thus,developing a new analytical technology for rapid and sensitive detection of Salmonella choleraesuis in food is urgently needed. Hence,a pH responded colorimetric enzyme-linked immunosorbent assay(pH-ELISA)was developed for sensitive detection of Salmonella choleraesuis in milk. In this method,glucose oxidase(GOx)was used to catalyze glucose for the generation of gluconic acid. The color of bromocresol purple(BCP)was changed from purple to bright yellow because the pH of sample solution decreased. Under the optimal conditions,the proposed method achieved two linear independent regression equations. When Salmonella choleraesuis concentration increased from 2.54×103 to 6.17×105 CFU/mL,the first regression equation was described as y1=0.1051ln(x)+0.7024(R2=0.7513). With the increase of Salmonella choleraesuis concentration from 6.17×105 to 1.67×107 CFU/mL,the second regression equation was expressed as y2=1.3216ln(x)-15.797(R2=0.9711). The average recoveries of the proposed method for spiked milk samples at Salmonella choleraesuis concentrations ranging from 2.5×103~5.6×106 CFU/mL were 72.16%~103.58% with the relative standard deviations ranging from 7.54%~15.30%. In conclusion,the developed colorimetric ELISA is suitable for the rapid and sensitive quantitation of Salmonella choleraesuis in milk.
Keywords:pH responded colorimetric enzyme-linked immunosorbent assay(pH-ELISA)  glucose oxidase  bromocresol purple  Salmonella choleraesuis
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