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从海绵共生真菌 sp. ZSDS1-F7-2 中发现的四个新型 C9 代谢物。

Four New C9 Metabolites from the Sponge-Associated Fungus sp. ZSDS1-F7-2.

机构信息

National Engineering Research Center of Navel Orange, Gannan Normal University, Ganzhou 341000, China.

Department of Chemistry, Jinan University, Guangzhou 510000, China.

出版信息

Mar Drugs. 2018 Jul 9;16(7):231. doi: 10.3390/md16070231.

DOI:10.3390/md16070231
PMID:29987219
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6071072/
Abstract

Four new structurally related metabolites, one γ-lactone named gliomasolide F (), one δ-lactone named gliomasolide G (), and two medium-chain fatty acids named gliomacids A⁻B (⁻), each containing nine carbons in total, were identified from the sponge-associated fungus sp. ZSDS1-F7-2. The planar chemical structures of these novel C9 metabolites were elucidated by nuclear magnetic resonance (NMR) spectroscopic methods, in connection with the analysis of high-resolution mass spectrometry (HRMS) and infrared (IR) data. The absolute configuration of , was determined by comparisons of experimental circular dichroism (CD) and optical rotation (OR) value with corresponding ones computed by quantum chemistry. The relative configuration of was determined by the Nuclear Overhauser effect spectroscopy (NOESY) spectrum, while its absolute configuration was tentatively determined in view of the biogenetic and biosynthetic relationships between and . Compounds ⁻, originally as an inseparable mixture, were successfully isolated after chemical modifications. The stereo-chemistries of compounds ⁻ were assumed by comparison of C NMR with those of the similar moiety reported in literature, in addition to the biogenetic and biosynthetic relationships with . The plausible biosynthetic relationships among these four C9 metabolites were supposed. Biologically, compounds ⁻ showed no cytotoxic effect against HeLa cell line at concentrations up to 25 μg/mL, while exhibited moderate antifouling activity against the settlement of larvae with IC being 12.8 μg/mL and LC > 25 μg/mL. The co-occurrence of macrolides gliomasolides A—E and four C9 metabolites in the same fermentation culture made us assume that these C9 metabolites might be biosynthetic building blocks toward the construction of more complex macrolides such as gliomasolides A—E or other unidentified polyketides.

摘要

从海绵共生真菌 sp. ZSDS1-F7-2 中鉴定出四个结构相关的新代谢物,一个 γ-内酯命名为 gliomasolide F (),一个 δ-内酯命名为 gliomasolide G (),和两个中链脂肪酸命名为 gliomacids A⁻B (⁻),每个分子总共含有九个碳原子。这些新型 C9 代谢物的平面化学结构通过核磁共振 (NMR) 光谱方法阐明,并结合高分辨率质谱 (HRMS) 和红外 (IR) 数据分析。通过比较实验圆二色性 (CD) 和旋光 (OR) 值与量子化学计算得到的相应值,确定了 的绝对构型。通过核 Overhauser 效应光谱 (NOESY) 谱确定了 的相对构型,而其绝对构型则根据 和 的生物发生和生物合成关系暂定。化合物 ⁻ 最初是一种不可分离的混合物,经过化学修饰后成功分离。通过与文献中报道的类似部分的 13C NMR 比较,假设化合物 ⁻ 的立体化学,此外还考虑了与生物发生和生物合成的关系。推测了这四个 C9 代谢物之间的可能生物合成关系。在生物学方面,化合物 ⁻ 在高达 25 μg/mL 的浓度下对 HeLa 细胞系没有细胞毒性,而 对幼虫的附着表现出中等的抗污活性,IC 为 12.8 μg/mL,LC > 25 μg/mL。在相同发酵培养物中同时存在大环内酯类化合物 gliomasolides A—E 和四个 C9 代谢物,这使我们假设这些 C9 代谢物可能是构建更复杂大环内酯类化合物(如 gliomasolides A—E 或其他未识别的聚酮类化合物)的生物合成构建块。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/c1030b2214e0/marinedrugs-16-00231-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/65e0d34ab6c7/marinedrugs-16-00231-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/952917381a62/marinedrugs-16-00231-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/5a719ec9a5eb/marinedrugs-16-00231-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/34cca69015e5/marinedrugs-16-00231-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/5dcb45ea3669/marinedrugs-16-00231-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/75d24615e6f5/marinedrugs-16-00231-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/c1030b2214e0/marinedrugs-16-00231-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/65e0d34ab6c7/marinedrugs-16-00231-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/952917381a62/marinedrugs-16-00231-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/5a719ec9a5eb/marinedrugs-16-00231-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/34cca69015e5/marinedrugs-16-00231-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/5dcb45ea3669/marinedrugs-16-00231-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/75d24615e6f5/marinedrugs-16-00231-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0f4/6071072/c1030b2214e0/marinedrugs-16-00231-g005.jpg

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