首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Degradation and detection of transgenic Bacillus thuringiensis DNA and proteins in flour of three genetically modified rice events submitted to a set of thermal processes
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Degradation and detection of transgenic Bacillus thuringiensis DNA and proteins in flour of three genetically modified rice events submitted to a set of thermal processes

机译:提交一组热过程的三个转基因水稻事件中面粉中苏云金芽胞杆菌DNA和蛋白质的降解和检测

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摘要

This study aimed to investigate the degradation of three transgenic Bacillus thuringiensis (Bt) genes (Cry1Ab, Cry1Ac, and Cry1Ab/Ac) and the corresponding encoded Bt proteins in KMD1, KF6, and TT51-1 rice powder, respectively, following autoclaving, cooking, baking, or microwaving. Exogenous Bt genes were more stable than the endogenous sucrose phosphate synthase (SPS) gene, and short DNA fragments were detected more frequently than long DNA fragments in both the Bt and SPS genes. Autoclaving, cooking (boiling in water, 30 min), and baking (200 degrees C, 30 min) induced the most severe Bt protein degradation effects, and Cry1Ab protein was more stable than Cry1Ac and Cry1Ab/Ac protein, which was further confirmed by baking samples at 180 degrees C for different periods of time. Microwaving induced mild degradation of the Bt and SPS genes, and Bt proteins, whereas baking (180 degrees C, 15 min), cooking and autoclaving led to further degradation, and baking (200 degrees C, 30 min) induced the most severe degradation. The findings of the study indicated that degradation of the Bt genes and proteins somewhat correlated with the treatment intensity. Polymerase chain reaction, enzyme-linked immunosorbent assay, and lateral flow tests were used to detect the corresponding transgenic components. Strategies for detecting transgenic ingredients in highly processed foods are discussed. (C) 2015 Elsevier Ltd. All rights reserved.
机译:这项研究旨在研究高压灭菌,烹饪后分别在KMD1,KF6和TT51-1大米粉中降解三种转基因苏云金芽胞杆菌(Bt)基因(Cry1Ab,Cry1Ac和Cry1Ab / Ac)和相应的编码Bt蛋白的降解过程。 ,烘烤或微波。外源Bt基因比内源蔗糖磷酸合酶(SPS)基因更稳定,并且在Bt和SPS基因中检测到短DNA片段的频率均高于长DNA片段。高压灭菌,烹饪(在水中沸腾30分钟)和烘焙(200摄氏度,30分钟)诱导出最严重的Bt蛋白降解作用,并且Cry1Ab蛋白比Cry1Ac和Cry1Ab / Ac蛋白更稳定,这进一步得到了证实。将样品在180摄氏度下烘烤不同的时间。微波诱导了Bt和SPS基因以及Bt蛋白的轻度降解,而烘烤(180摄氏度,15分钟),蒸煮和高压灭菌导致进一步降解,而烘烤(200摄氏度,30分钟)则导致了最严重的降解。研究结果表明,Bt基因和蛋白质的降解与治疗强度有关。聚合酶链反应,酶联免疫吸附试验和侧向流动试验用于检测相应的转基因成分。讨论了检测高度加工食品中转基因成分的策略。 (C)2015 Elsevier Ltd.保留所有权利。

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