Structurally diverse polyketides and phenylspirodrimanes from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201
Four undescribed polyketide derivatives, named arthproliferins A–D ( 1 – 4 ), and one undescribed phenylspirodrimane derivative, named arthproliferin E ( 7 ), along with 11 known metabolites ( 5 , 6 , 8 – 16 ) were isolated from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201. The...
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| Published in | Journal of antibiotics Vol. 74; no. 3; pp. 190 - 198 |
|---|---|
| Main Authors | , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
London
Nature Publishing Group UK
01.03.2021
Springer Nature Nature Publishing Group |
| Subjects | |
| Online Access | Get full text |
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| Abstract | Four undescribed polyketide derivatives, named arthproliferins A–D (
1
–
4
), and one undescribed phenylspirodrimane derivative, named arthproliferin E (
7
), along with 11 known metabolites (
5
,
6
,
8
–
16
) were isolated from the soft coral-associated fungus
Stachybotrys chartarum
SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds
1
and
3
–
15
were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds
1
and
15
displayed moderate inhibitory activity against methicillin-resistant
Staphylococcus aureus
ATCC 29213 with an MIC value of 78 and 39 µg/mL, respectively. Furthermore, compound
15
displayed strong cytotoxic activities against the tested cell line with IC
50
values less than 39 nM. |
|---|---|
| AbstractList | Four undescribed polyketide derivatives, named arthproliferins A–D (
1
–
4
), and one undescribed phenylspirodrimane derivative, named arthproliferin E (
7
), along with 11 known metabolites (
5
,
6
,
8
–
16
) were isolated from the soft coral-associated fungus
Stachybotrys chartarum
SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds
1
and
3
–
15
were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds
1
and
15
displayed moderate inhibitory activity against methicillin-resistant
Staphylococcus aureus
ATCC 29213 with an MIC value of 78 and 39 µg/mL, respectively. Furthermore, compound
15
displayed strong cytotoxic activities against the tested cell line with IC
50
values less than 39 nM. Four undescribed polyketide derivatives, named arthproliferins A-D (1-4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along with 11 known metabolites (5, 6, 8-16) were isolated from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds 1 and 3-15 were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds 1 and 15 displayed moderate inhibitory activity against methicillin-resistant Staphylococcus aureus ATCC 29213 with an MIC value of 78 and 39 µg/mL, respectively. Furthermore, compound 15 displayed strong cytotoxic activities against the tested cell line with IC50 values less than 39 nM.Four undescribed polyketide derivatives, named arthproliferins A-D (1-4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along with 11 known metabolites (5, 6, 8-16) were isolated from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds 1 and 3-15 were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds 1 and 15 displayed moderate inhibitory activity against methicillin-resistant Staphylococcus aureus ATCC 29213 with an MIC value of 78 and 39 µg/mL, respectively. Furthermore, compound 15 displayed strong cytotoxic activities against the tested cell line with IC50 values less than 39 nM. Four undescribed polyketide derivatives, named arthproliferins A-D (1-4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along with 11 known metabolites (5, 6, 8-16) were isolated from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds 1 and 3-15 were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds 1 and 15 displayed moderate inhibitory activity against methicillin-resistant Staphylococcus aureus ATCC 29213 with an MIC value of 78 and 39 µg/mL, respectively. Furthermore, compound 15 displayed strong cytotoxic activities against the tested cell line with IC values less than 39 nM. Four undescribed polyketide derivatives, named arthproliferins A-D (1-4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along with 11 known metabolites (5, 6, 8-16) were isolated from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds 1 and 3-15 were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds 1 and 15 displayed moderate inhibitory activity against methicillin-resistant Staphylococcus aureus ATCC 29213 with an MIC value of 78 and 39 mu g/mL, respectively. Furthermore, compound 15 displayed strong cytotoxic activities against the tested cell line with IC50 values less than 39 nM. Four undescribed polyketide derivatives, named arthproliferins A–D (1–4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along with 11 known metabolites (5, 6, 8–16) were isolated from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201. Their structures were determined through spectroscopic methods, X-ray crystallography, and ECD analysis. Compounds 1 and 3–15 were evaluated for their cytotoxic, and antibacterial activities. Among them, compounds 1 and 15 displayed moderate inhibitory activity against methicillin-resistant Staphylococcus aureus ATCC 29213 with an MIC value of 78 and 39 µg/mL, respectively. Furthermore, compound 15 displayed strong cytotoxic activities against the tested cell line with IC50 values less than 39 nM. |
| Author | Zhou, Xuefeng Pang, Xiaoyan Li, Yunqiu Wang, Junfeng Liu, Yonghong Long, Jieyi Lin, Xiuping Liao, Shengrong Yang, Bin |
| Author_xml | – sequence: 1 givenname: Bin orcidid: 0000-0003-4748-2484 surname: Yang fullname: Yang, Bin organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 2 givenname: Jieyi surname: Long fullname: Long, Jieyi organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 3 givenname: Xiaoyan surname: Pang fullname: Pang, Xiaoyan organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 4 givenname: Xiuping surname: Lin fullname: Lin, Xiuping organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 5 givenname: Shengrong surname: Liao fullname: Liao, Shengrong organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 6 givenname: Junfeng surname: Wang fullname: Wang, Junfeng organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 7 givenname: Xuefeng orcidid: 0000-0001-9601-4869 surname: Zhou fullname: Zhou, Xuefeng organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) – sequence: 8 givenname: Yunqiu surname: Li fullname: Li, Yunqiu email: leeyq88@126.com organization: College of Pharmacy, Guilin Medical University – sequence: 9 givenname: Yonghong orcidid: 0000-0001-8327-3108 surname: Liu fullname: Liu, Yonghong email: yonghongliu@scsio.ac.cn organization: Chinese Academy of Sciences (CAS) Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, CAS, Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), University of Chinese Academy of Sciences |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33318621$$D View this record in MEDLINE/PubMed |
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| ContentType | Journal Article |
| Copyright | The Author(s), under exclusive licence to the Japan Antibiotics Research Association 2020 The Author(s), under exclusive licence to the Japan Antibiotics Research Association 2020. |
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| DOI | 10.1038/s41429-020-00386-y |
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| Keywords | SESQUITERPENES METABOLITES DITERPENOIDS COLEOPHOMONE-B SATRATOXIN-H PROTON INHIBITORS A-H SINULARIA DERIVATIVES |
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| PublicationTitle | Journal of antibiotics |
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| Snippet | Four undescribed polyketide derivatives, named arthproliferins A–D (
1
–
4
), and one undescribed phenylspirodrimane derivative, named arthproliferin E (
7
),... Four undescribed polyketide derivatives, named arthproliferins A-D (1-4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along... Four undescribed polyketide derivatives, named arthproliferins A–D (1–4), and one undescribed phenylspirodrimane derivative, named arthproliferin E (7), along... |
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| Title | Structurally diverse polyketides and phenylspirodrimanes from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201 |
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