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1.
Mar Drugs ; 21(8)2023 Jul 29.
Artigo em Inglês | MEDLINE | ID: mdl-37623712

RESUMO

New anthraquinone derivatives acruciquinones A-C (1-3), together with ten known metabolites, were isolated from the obligate marine fungus Asteromyces cruciatus KMM 4696. Acruciquinone C is the first member of anthraquinone derivatives with a 6/6/5 backbone. The structures of isolated compounds were established based on NMR and MS data. The absolute stereoconfigurations of new acruciquinones A-C were determined using ECD and quantum chemical calculations (TDDFT approach). A plausible biosynthetic pathway of the novel acruciquinone C was proposed. Compounds 1-4 and 6-13 showed a significant antimicrobial effects against Staphylococcus aureus growth, and acruciquinone A (1), dendryol B (4), coniothyrinone B (7), and ω-hydroxypachybasin (9) reduced the activity of a key staphylococcal enzyme, sortase A. Moreover, the compounds, excluding 4, inhibited urease activity. We studied the effects of anthraquinones 1, 4, 7, and 9 and coniothyrinone D (6) in an in vitro model of skin infection when HaCaT keratinocytes were cocultivated with S. aureus. Anthraquinones significantly reduce the negative impact of S. aureus on the viability, migration, and proliferation of infected HaCaT keratinocytes, and acruciquinone A (1) revealed the most pronounced effect.


Assuntos
Ascomicetos , Infecções Estafilocócicas , Staphylococcus aureus , Antraquinonas/farmacologia
2.
Plasmid ; 101: 1-9, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30465791

RESUMO

An ability to synthesize extracellular enzymes degrading a wide spectrum of plant and algae polymeric substrates makes many fungi relevant for biotechnology. The terrestrial thermophilic and marine fungal isolates capable of plant and algae degradation have been tested for antibiotic resistance for their possible use in a new genetic transformation system. Plasmids encoding the hygromycin B phosphotransferase (hph) under the control of the cauliflower mosaic virus 35S promoter, the trpC gene promoter of Aspergillus nidulans, and the Aureobasidium pullulans TEF gene promoter were delivered into the fungal cells by electroporation. The effectiveness of different promoters was compared by transformation and growth of Thermothelomyces thermophila (formerly Myceliophthora thermophila) on the selective medium and by real-time PCR analysis. A highly efficient transformation was observed at an electric-pulse of 8.5 kV/cm by using 10 µg of DNA per 1 × 105 conidia. Although all promoters were capable of hph expression in the Th. thermophila cells, the trpC promoter provided the highest level of hygromycin resistance. We further successfully applied plant binary vector pPZP for co-transformation of hph gene and enhanced green fluorescent protein gene that confirmed this transformation system could be used as an appropriate tool for gene function studies and the expression of heterologous proteins in micromycetes.


Assuntos
Organismos Aquáticos/genética , Plasmídeos/metabolismo , Saccharomycetales/genética , Esporos Fúngicos/genética , Transformação Genética , Organismos Aquáticos/classificação , Organismos Aquáticos/efeitos dos fármacos , Organismos Aquáticos/metabolismo , Aspergillus nidulans/genética , Aspergillus nidulans/metabolismo , Caulimovirus/genética , Caulimovirus/metabolismo , Cinamatos/farmacologia , Eletroporação/métodos , Temperatura Alta , Higromicina B/análogos & derivados , Higromicina B/farmacologia , Fosfotransferases (Aceptor do Grupo Álcool)/genética , Fosfotransferases (Aceptor do Grupo Álcool)/metabolismo , Filogenia , Plasmídeos/química , Regiões Promotoras Genéticas , Federação Russa , Saccharomycetales/classificação , Saccharomycetales/efeitos dos fármacos , Saccharomycetales/metabolismo , Água do Mar/microbiologia , Esporos Fúngicos/efeitos dos fármacos , Esporos Fúngicos/metabolismo
3.
J Fungi (Basel) ; 8(5)2022 Apr 27.
Artigo em Inglês | MEDLINE | ID: mdl-35628710

RESUMO

Six new polyketides acrucipentyns A-F (1-6) were isolated from the alga-derived fungus Asteromyces cruciatus KMM 4696. Their structures were established based on spectroscopic methods. The absolute configurations of acrucipentyn A was assigned by the modified Mosher's method and ROESY data analysis. Acrucipentyns A-E were identified to be the very first examples of chlorine-containing asperpentyn-like compounds. The cytotoxic and antimicrobial activities of the isolated compounds were examined. Acrucipentyns A-F were found as antimicrobial agents, which inhibited sortase A enzyme activity, bacterial growth and biofilm formation of Staphylococcus aureus and decreased LDH release from human keratinocytes HaCaT in S. aureus skin infection in an in vitro model.

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