Sorbicillinoids are a family of hexaketide metabolites with a characteristic sorbyl side chain residue. Sixty-nine sorbicillinoids from fungi, newly identified from 2016 to 2021, are summarized in this review, including their structures and bioactivities. They are classified into monomeric, dimeric, trimeric, and hybrid sorbicillinoids according to their basic structural features, with the main groups comprising both monomeric and dimeric sorbicillinoids. Some of the identified sorbicillinoids have special structures such as ustilobisorbicillinol A, and sorbicillasins A and B. The majority of sorbicillinoids have been reported from fungi genera such as , , , and , with some sorbicillinoids exhibiting cytotoxic, antimicrobial, anti-inflammatory, phytotoxic, and α-glucosidase inhibitory activities. In recent years, marine-derived, extremophilic, plant endophytic, and phytopathogenic fungi have emerged as important resources for diverse sorbicillinoids with unique skeletons. The recently revealed biological activities of sorbicillinoids discovered before 2016 are also described in this review.
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http://dx.doi.org/10.3390/jof8010062 | DOI Listing |
Mar Drugs
November 2024
Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.
A detailed chemical study of the culture of a coral-derived fungus resulted in the isolation and identification of four new aromatic heterocycles chrysoquinazolinones A-B (-) and chrysobenzothiazoles A-B (-), along with a new sorbicillinoid 4-carboxylsorbicillin (). Chrysoquinazolinones A-B (-) combine a quinazolinone fragment with a bicyclo[2.2.
View Article and Find Full Text PDFJ Agric Food Chem
September 2024
Tobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao 266101, China.
Five new sorbicillinoid derivatives, including (±)-aspersorbicillin A [(±)-], a pair of enantiomers at C-9, and aspersorbicillins B-D (-), together with two known analogs ( and ) were isolated from the endophytic fungus TE-65L. Their structures including absolute configurations were determined by detailed spectroscopic analyses and electronic circular dichroism calculations. The herbicidal activity of sorbicillinoids on the germ and radicle elongation of various weed types was reported for the first time.
View Article and Find Full Text PDFJ Agric Food Chem
August 2024
State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Sorbicillinoids are a class of fungal polyketides with diverse structures and distinguished bioactivities. Although remarkable progress has been achieved in their chemistry and biosynthesis, the efflux of sorbicillinoids is poorly understood. Here, we found MFS transporter AcsorT was responsible for the biosynthesis of sorbicillinoids in .
View Article and Find Full Text PDFJ Infect Chemother
December 2024
Group of Peptides and Natural Products Research, School of Pharmaceutical Sciences, Southern Medical University, 1838 Guangzhou Avenue North, Guangzhou, 510515, China.
Background: Drug resistance is an important factor in the fight against influenza A virus (IAV). Natural products offer a rich source of lead compounds for the discovery of novel antiviral drugs. In a previous study, we isolated the sorbicillinoid polyketide HSL-2 from the mycelium of fungus Trichoderma sp.
View Article and Find Full Text PDFSci Rep
April 2024
AIT Austrian Institute of Technology GmbH, Center for Health and Bioresources, Konrad Lorenz Strasse 24, 3430, Tulln, Austria.
The filamentous ascomycete Trichoderma reesei, known for its prolific cellulolytic enzyme production, recently also gained attention for its secondary metabolite synthesis. Both processes are intricately influenced by environmental factors like carbon source availability and light exposure. Here, we explore the role of the transcription factor STE12 in regulating metabolic pathways in T.
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