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CRISPR在消除稻曲毒素方面的创新应用:提高食品安全与质量

Innovative application of CRISPR for eliminating Ustiloxin in : Enhancing food safety and quality.

作者信息

Liu Mengqian, Wang Anning, Meng Guoliang, Liu Qing, Yang Ying, Wang Min, Wang Zheng, Wang Fen, Dong Caihong

机构信息

State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Lebensm Wiss Technol. 2024 Jul 15;204. doi: 10.1016/j.lwt.2024.116420. Epub 2024 Jul 2.

Abstract

(L.) Fr. Has long been recognized as a valuable functional food consumed in numerous countries. However, biosynthetic gene clusters of this species and safety regarding mycotoxin production remain largely unexplored. In this study, a ribosomally synthesized and post-translationally modified peptide (RiPP) cluster responsible for the production of cyclopeptide mycotoxins in was unveiled via genome mining. Ustiloxin B and a novel, predominant and specific ustiloxin I were confirmed by extraction and structural analysis. The difference between Ustiloxins I and B lied in the side chain at C19, where an additional methyl substituent in Ustiloxin I resulted in an alanine moiety substitution for glycine of Ustiloxin B. The simultaneous deletion of the two adjacent core genes, and , using a single guide RNA designed in the intergenic region, and subsequent complementation via AMA-mediated CRISPR/Cas9 system confirmed the RiPP cluster's responsibility for ustiloxin production. The cultivation of the edited strain yielded ustiloxin-free fruiting bodies without affecting agronomic characters. PCR and genome resequencing confirmed the absence of any off-target events or foreign sequence remnants. This study marks a significant advancement in utilizing CRISPR technology to control ustiloxins in food, underscoring its broader implications for food safety and quality improvement.

摘要

(L.)Fr.长期以来一直被认为是许多国家消费的一种有价值的功能性食品。然而,该物种的生物合成基因簇以及霉菌毒素产生方面的安全性在很大程度上仍未得到探索。在本研究中,通过基因组挖掘揭示了负责在 中产生环肽霉菌毒素的核糖体合成及翻译后修饰肽(RiPP)簇。通过提取和结构分析证实了玉米黑粉菌素B以及一种新型、主要且具有特异性的玉米黑粉菌素I。玉米黑粉菌素I和B之间的差异在于C19处的侧链,其中玉米黑粉菌素I中额外的甲基取代导致玉米黑粉菌素B的甘氨酸被丙氨酸部分取代。利用在基因间区域设计的单个引导RNA同时缺失两个相邻的核心基因 和 ,随后通过AMA介导的CRISPR/Cas9系统进行互补,证实了RiPP簇对玉米黑粉菌素产生的责任。编辑菌株的培养产生了不含玉米黑粉菌素的子实体,且不影响农艺性状。PCR和基因组重测序证实不存在任何脱靶事件或外源序列残留。本研究标志着利用CRISPR技术控制食品中玉米黑粉菌素方面取得了重大进展,凸显了其对食品安全和质量提升的更广泛意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba9f/11308680/090aac2a174a/nihms-2011225-f0001.jpg

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