Zhang Wei, Xing Fuguo, Selvaraj Jonathan Nimal, Liu Yang
Inst. of Agro-Products Processing Science and Technology, Chinese Academy of Agricultural Sciences/Key Laboratory of Agro-Products Processing, Ministry of Agriculture, Beijing, 100193, China.
J Food Sci. 2014 May;79(5):T1055-65. doi: 10.1111/1750-3841.12456. Epub 2014 Apr 23.
In order to assess the degradation of endogenous and exogenous genes during food processing, genetically modified rice with Cry1Ab was used as raw material to produce 4 processed foods: steamed rice, rice noodles, rice crackers, and sweet rice wine. The results showed various processing procedures caused different degrees of degradation of both endogenous and exogenous genes. During the processing of steamed rice and rice noodles, the procedures were so mild that only genes larger than 1500 bp were degraded, and no degradation of NOS terminator and Hpt gene was detected. For rice crackers, frying was the most severe procedure, followed by microwaving, baking, boiling, 1st drying, and 2nd drying. For sweet rice wine, fermentation had more impact on degradation of genes than the other processing procedures. All procedures in this study did not lead to degradation of genes to below 200 bp, except for NOS terminator. In the case of stability of the genes studied during processing of rice crackers and sweet rice wine, SPS gene was the most, followed by the Cry1Ab gene, Hpt gene, Pubi promoter, and NOS terminator.
In our study, we gained some information about the degradation of endogenous and exogenous genes during 4 foods processing, compared the different stabilities between endogenous and exogenous genes, and analyzed different effects of procedure on degradation of genes. In addition, the fragments of endogenous and exogenous genes about 200 bp could be detected in final products, except NOS terminator. As a result, we provided some base information about risk assessment of genetically modified (GM) food and appropriate length of fragment to detect GM component in processed foods.
为了评估食品加工过程中内源基因和外源基因的降解情况,以转Cry1Ab基因水稻为原料制作了4种加工食品:米饭、米粉、米饼和甜米酒。结果表明,不同的加工工序对内源基因和外源基因造成了不同程度的降解。在米饭和米粉的加工过程中,工序较为温和,只有大于1500 bp的基因发生降解,未检测到NOS终止子和Hpt基因的降解。对于米饼,油炸是最剧烈的工序,其次是微波处理、烘焙、水煮、一次干燥和二次干燥。对于甜米酒,发酵对基因降解的影响比其他加工工序更大。本研究中的所有工序,除了NOS终止子外,均未导致基因降解至200 bp以下。在米饼和甜米酒加工过程中所研究基因的稳定性方面,SPS基因最稳定,其次是Cry1Ab基因、Hpt基因、泛素启动子和NOS终止子。
在我们的研究中,我们获得了有关4种食品加工过程中内源基因和外源基因降解的一些信息,比较了内源基因和外源基因之间不同的稳定性,并分析了不同工序对基因降解的不同影响。此外,除了NOS终止子外,在最终产品中可以检测到约200 bp的内源基因和外源基因片段。因此,我们提供了一些关于转基因食品风险评估以及检测加工食品中转基因成分的合适片段长度的基础信息。