Genomic and Metabolomic Analyses of the Marine Fungus Emericellopsis cladophorae: Insights into Saltwater Adaptability Mechanisms and Its Biosynthetic Potential

被引:23
作者
Goncalves, Micael F. M. [1 ]
Hilario, Sandra [1 ]
van de Peer, Yves [2 ,3 ,4 ,5 ]
Esteves, Ana C. [1 ]
Alves, Artur [1 ]
机构
[1] Univ Aveiro, Dept Biol, CESAM, P-3810193 Aveiro, Portugal
[2] Univ Ghent, Dept Plant Biotechnol & Bioinformat, B-9052 Ghent, Belgium
[3] VIB, Ctr Plant Syst Biol, B-9052 Ghent, Belgium
[4] Univ Pretoria, Dept Biochem Genet & Microbiol, ZA-0028 Pretoria, South Africa
[5] Nanjing Agr Univ, Acad Adv Interdisciplinary Studies, Coll Hort, Nanjing 210095, Peoples R China
关键词
antimicrobial; anticancer; marine fungi; metabolites; whole genome sequencing; ANTIFUNGAL PEPTAIBOL; ACID; TRANSPORTER; ADAPTATION; LEUCINOSTATIN; BERGOFUNGIN; RIBOFLAVIN; ANNOTATION; PATHWAY; PROTEIN;
D O I
10.3390/jof8010031
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genus Emericellopsis is found in terrestrial, but mainly in marine, environments with a worldwide distribution. Although Emericellopsis has been recognized as an important source of bioactive compounds, the range of metabolites expressed by the species of this genus, as well as the genes involved in their production are still poorly known. Untargeted metabolomics, using UPLC- QToF-MS/MS, and genome sequencing (Illumina HiSeq) was performed to unlock E. cladophorae MUM 19.33 chemical diversity. The genome of E. cladophorae is 26.9 Mb and encodes 8572 genes. A large set of genes encoding carbohydrate-active enzymes (CAZymes), secreted proteins, transporters, and secondary metabolite biosynthetic gene clusters were identified. Our analysis also revealed genomic signatures that may reflect a certain fungal adaptability to the marine environment, such as genes encoding for (1) the high-osmolarity glycerol pathway; (2) osmolytes' biosynthetic processes; (3) ion transport systems, and (4) CAZymes classes allowing the utilization of marine polysaccharides. The fungal crude extract library constructed revealed a promising source of antifungal (e.g., 9,12,13-Trihydroxyoctadec-10-enoic acid, hymeglusin), antibacterial (e.g., NovobiocinA), anticancer (e.g., daunomycinone, isoreserpin, flavopiridol), and anti-inflammatory (e.g., 2'-O-Galloylhyperin) metabolites. We also detected unknown compounds with no structural match in the databases used. The metabolites' profiles of E. cladophorae MUM 19.33 fermentations were salt dependent. The results of this study contribute to unravel aspects of the biology and ecology of this marine fungus. The genome and metabolome data are relevant for future biotechnological exploitation of the species.
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页数:20
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