Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces and Trichoderma Species
The importance of bioactive natural compounds in pharmacology and other biotechnological fields has stimulated the scientific community to explore new environmental contexts and their associated microbial diversity. As the largest frontier in biological discovery, the sea represents a significant so...
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Format: | Electronic Book Chapter |
Language: | English |
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MDPI - Multidisciplinary Digital Publishing Institute
2019
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Online Access: | DOAB: download the publication DOAB: description of the publication |
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024 | 7 | |a 10.3390/books978-3-03897-981-4 |c doi | |
041 | 0 | |a eng | |
042 | |a dc | ||
072 | 7 | |a PS |2 bicssc | |
100 | 1 | |a Nicoletti, Rosario |4 auth | |
700 | 1 | |a Vinale, Francesco |4 auth | |
245 | 1 | 0 | |a Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces and Trichoderma Species |
260 | |b MDPI - Multidisciplinary Digital Publishing Institute |c 2019 | ||
300 | |a 1 electronic resource (134 p.) | ||
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338 | |a online resource |b cr |2 rdacarrier | ||
506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
520 | |a The importance of bioactive natural compounds in pharmacology and other biotechnological fields has stimulated the scientific community to explore new environmental contexts and their associated microbial diversity. As the largest frontier in biological discovery, the sea represents a significant source of organisms producing novel secondary metabolites with interesting bioactivities. Of the available biological material, fungi have received increasing consideration, both due to their pervasive occurrence in varying habitats as well as their aptitude to develop symbiotic associations with higher organisms in numerous contexts. In many cases, fungal strains have been reported as the real producers of drugs originally extracted from marine plants and animals. Due to the constantly increasing number of marine-derived fungi yielding valuable bioactive products, it is now appropriate to present these findings to a recipient audience in a more organized form. This Special Issue of Marine Drugs, entitled "Bioactive Compounds from Marine-Derived Aspergillus, Penicillium, Talaromyces, and Trichoderma Species"" is specifically focused on a few genera of ascomycetous fungi which are widespread regarding marine contexts and are particularly inclined to establishing symbiotic relationships. For this project, we welcome submissions of full research papers, short notes, and review articles reporting the discovery and characterization of products showing antibiotic, antitumor, antiviral, insecticidal, antimalarial, antifouling, antioxidant, plant growth-promoting and/or resistance-inducing, as well as other less-exploited activities. | ||
540 | |a Creative Commons |f https://creativecommons.org/licenses/by-nc-nd/4.0/ |2 cc |4 https://creativecommons.org/licenses/by-nc-nd/4.0/ | ||
546 | |a English | ||
650 | 7 | |a Biology, life sciences |2 bicssc | |
653 | |a antibacterial activity | ||
653 | |a n/a | ||
653 | |a Talaromyces purpurogenus | ||
653 | |a lapatinib | ||
653 | |a antibacterial | ||
653 | |a hydroxypyrrolidine | ||
653 | |a bis-indolyl benzenoids | ||
653 | |a penitrem A | ||
653 | |a cytotoxicities | ||
653 | |a sesquiterpenoid | ||
653 | |a secondary metabolites | ||
653 | |a drug discovery | ||
653 | |a sponge-associated fungus | ||
653 | |a candidusin | ||
653 | |a Penicillium sp. TJ403-1 | ||
653 | |a coumarin | ||
653 | |a gefitinib | ||
653 | |a bioactive products | ||
653 | |a Aspergillaceae | ||
653 | |a indole-diterpenoids | ||
653 | |a mangroves | ||
653 | |a diterpenoid | ||
653 | |a Penicillium raistrickii | ||
653 | |a ECD calculations | ||
653 | |a Talaromyces | ||
653 | |a marine-derived fungi | ||
653 | |a BK (Maxi-K) channel | ||
653 | |a polyketides | ||
653 | |a EGFR | ||
653 | |a chromone | ||
653 | |a aspetritone | ||
653 | |a Aspergillus | ||
653 | |a breviane spiroditerpenoid | ||
653 | |a endophytic fungi | ||
653 | |a cytotoxic | ||
653 | |a cytotoxicity | ||
653 | |a breast cancer | ||
653 | |a mangrove endophytic fungus | ||
653 | |a IDH1 inhibitory activity | ||
653 | |a NMR data calculations | ||
653 | |a antifungal activity | ||
653 | |a Aspergillus candidus | ||
653 | |a diastereomers | ||
653 | |a TNF-? | ||
653 | |a sterone | ||
653 | |a Aspergillus clavatus | ||
653 | |a HER2 | ||
653 | |a thermo-change strategy | ||
856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/1317 |7 0 |z DOAB: download the publication |
856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/42129 |7 0 |z DOAB: description of the publication |