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Innovative application of CRISPR for eliminating Ustiloxin in Cordyceps militaris: Enhancing food safety and quality.
Liu, Mengqian; Wang, Anning; Meng, Guoliang; Liu, Qing; Yang, Ying; Wang, Min; Wang, Zheng; Wang, Fen; Dong, Caihong.
Affiliation
  • Liu M; State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.
  • Wang A; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Meng G; State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.
  • Liu Q; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Yang Y; State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.
  • Wang M; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Wang Z; State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.
  • Wang F; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Dong C; State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing, 100101, China.
Lebensm Wiss Technol ; 2042024 Jul 15.
Article in En | MEDLINE | ID: mdl-39119199
ABSTRACT
Cordyceps militaris (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 Cordyceps was unveiled via genome mining. Ustiloxin B and a novel, predominant and Cordyceps 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, CmustYb and CmustYa, using a single guide RNA designed in the intergenic region, and subsequent in-situ 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Lebensm Wiss Technol Year: 2024 Document type: Article Affiliation country: China Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Lebensm Wiss Technol Year: 2024 Document type: Article Affiliation country: China Country of publication: Reino Unido