A Hydrolase Produced by Rhodococcus erythropolis HQ Is Responsible for the Detoxification of Zearalenone
文献类型： 外文期刊
作者： Hu, Junqiang 1 ; Du, Shilong 1 ; Qiu, Han 1 ; Wu, Yuzhuo 3 ; Hong, Qing 1 ; Wang, Gang 2 ; Mohamed, Sherif Ramzy 4 ; Lee, Yin-Won 2 ; Xu, Jianhong 1 ;
作者机构： 1.Nanjing Agr Univ, Coll Life Sci, Key Lab Agr Environm Microbiol, Minist Agr, Nanjing 210095, Peoples R China
2.Jiangsu Acad Agr Sci, Minist Agr & Rural Affairs, Minist Sci & Technol, Jiangsu Key Lab Food Qual & Safety-State Key Lab C, Nanjing 210014, Peoples R China
3.Jiangsu Univ, Sch Food & Biol Engn, Zhenjiang 212013, Peoples R China
4.Natl Res Ctr, Food Ind & Nutr Res Inst, Food Toxicol & Contaminants Dept, Tahreer St, Dokki 12411, Giza, Egypt
5.Seoul Natl Univ, Dept Agr Biotechnol, Seoul 08826, South Korea
关键词： zearalenone; Rhodococcus erythropolis; biodegradation; hydrolase
期刊名称：TOXINS （ 影响因子：4.2； 五年影响因子：4.7 ）
ISSN：
年卷期： 2023 年 15 卷 12 期
页码：
收录情况： SCI
摘要： Zearalenone (ZEN), an estrogenic mycotoxin, is one of the prevalent contaminants found in food and feed, posing risks to human and animal health. In this study, we isolated a ZEN-degrading strain from soil and identified it as Rhodococcus erythropolis HQ. Analysis of degradation products clarified the mechanism by which R. erythropolis HQ degrades ZEN. The gene zenR responsible for degrading ZEN was identified from strain HQ, in which zenR is the key gene for R. erythropolis HQ to degrade ZEN, and its expression product is a hydrolase named ZenR. ZenR shared 58% sequence identity with the hydrolase ZenH from Aeromicrobium sp. HA, but their enzymatic properties were significantly different. ZenR exhibited maximal enzymatic activity at pH 8.0-9.0 and 55(degrees)C, with a Michaelis constant of 21.14 mu M, and its enzymatic activity is 2.8 times that of ZenH. The catalytic triad was identified as S132-D157-H307 via molecular docking and site-directed mutagenesis. Furthermore, the fermentation broth of recombinant Bacillus containing ZenR can be effectively applied to liquefied corn samples, with the residual amount of ZEN decreased to 0.21 mu g/g, resulting in a remarkable ZEN removal rate of 93%. Thus, ZenR may serve as a new template for the modification of ZEN hydrolases and a new resource for the industrial application of biological detoxification. Consequently, ZenR could potentially be regarded as a novel blueprint for modifying ZEN hydrolases and as a fresh resource for the industrial implementation of biological detoxification.
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