Enantioselective Degradation and Processing Factors of Seven Chiral Pesticides During the Processing of Wine and Rice Wine

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL
Chirality Pub Date : 2025-01-12 DOI:10.1002/chir.70018
Yuting Tan, Nuanhui Wen, Zhiqiang Lu, Wenjie Wei, Haiyan Shi, Minghua Wang
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引用次数: 0

Abstract

Chiral pesticides often undergo enantioselective degradation during food fermentation. In this study, the enantioselective fates of seven chiral pesticides during processing of wine and rice wine were investigated. The results revealed that R-metalaxyl, R-mefentrifluconazole and S-hexaconazole were preferentially degraded during wine processing with EF values of 0.57, 0.78, and 0.43, respectively, whereas S-metalaxyl and R-hexaconazole were preferentially degraded during rice wine processing with EF values of 0.44 and 0.54, respectively. Stereoselectivity was attributed to fermentative bacterial activity. The processing factor (PF) values for the five pesticides ranged from 0.04 to 0.34 during wine processing and from 0.02 to 0.29 during rice wine processing, suggesting that fermentation can mitigate pesticide exposure risks and ensure food safety. This study enhances our understanding of enantioselective fate of chiral pesticides during fermented food processing, provides guidance for the application of chiral pesticides, and enables the dietary risk of chiral pesticides in processed products to be assessed more accurately.

Abstract Image

7种手性农药在酒和黄酒加工过程中的对映选择性降解及加工因素
手性农药在食品发酵过程中经常发生对映选择性降解。研究了7种手性农药在酒和米酒加工过程中的对映选择性。结果表明,甲氨甲酯、甲苯三氟康唑和六硝康唑在黄酒加工过程中优先降解,EF值分别为0.57、0.78和0.43,而甲氨甲酯和六硝康唑在黄酒加工过程中优先降解,EF值分别为0.44和0.54。立体选择性归因于发酵细菌的活性。5种农药在白酒加工过程中的加工系数(PF)在0.04 ~ 0.34之间,在黄酒加工过程中的加工系数(PF)在0.02 ~ 0.29之间,表明发酵可以降低农药暴露风险,保证食品安全。本研究增强了我们对手性农药在发酵食品加工过程中的对手性选择命运的认识,为手性农药的应用提供了指导,并使手性农药在加工产品中的膳食风险得到更准确的评估。
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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
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