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链霉菌 VN1,一种产生多种代谢物的微生物,包括非天然呋喃型抗癌化合物。

Streptomyces sp. VN1, a producer of diverse metabolites including non-natural furan-type anticancer compound.

机构信息

Department of Life Science and Biochemical Engineering, SunMoon University, 70 Sunmoon-ro 221, Tangjeong-myeon, Asan-si, Chungnam, 31460, Republic of Korea.

Department of Pharmaceutical Engineering and Biotechnology, SunMoon University, 70 Sunmoon-ro 221, Tangjeong-myeon, Asan-si, Chungnam, 31460, Republic of Korea.

出版信息

Sci Rep. 2020 Feb 4;10(1):1756. doi: 10.1038/s41598-020-58623-1.

Abstract

Streptomyces sp. VN1 was isolated from the coastal region of Phu Yen Province (central Viet Nam). Morphological, physiological, and whole genome phylogenetic analyses suggested that strain Streptomyces sp. VN1 belonged to genus Streptomyces. Whole genome sequencing analysis showed its genome was 8,341,703 base pairs in length with GC content of 72.5%. Diverse metabolites, including cinnamamide, spirotetronate antibiotic lobophorin A, diketopiperazines cyclo-L-proline-L-tyrosine, and a unique furan-type compound were isolated from Streptomyces sp. VN1. Structures of these compounds were studied by HR-Q-TOF ESI/MS/MS and 2D NMR analyses. Bioassay-guided purification yielded a furan-type compound which exhibited in vitro anticancer activity against AGS, HCT116, A375M, U87MG, and A549 cell lines with IC values of 40.5, 123.7, 84.67, 50, and 58.64 µM, respectively. In silico genome analysis of the isolated Streptomyces sp. VN1 contained 34 gene clusters responsible for the biosynthesis of known and/or novel secondary metabolites, including different types of terpene, T1PKS, T2PKS, T3PKS, NRPS, and hybrid PKS-NRPS. Genome mining with HR-Q-TOF ESI/MS/MS analysis of the crude extract confirmed the biosynthesis of lobophorin analogs. This study indicates that Streptomyces sp. VN1 is a promising strain for biosynthesis of novel natural products.

摘要

从越南富安省沿海地区分离到一株链霉菌 sp. VN1。形态学、生理学和全基因组系统发育分析表明,该菌株属于链霉菌属。全基因组测序分析表明,其基因组全长 8,341,703 个碱基对,GC 含量为 72.5%。从链霉菌 sp. VN1 中分离到多种代谢产物,包括肉桂酰胺、螺缩酮抗生素 lobophorin A、二酮哌嗪环-L-脯氨酸-L-酪氨酸和一种独特的呋喃型化合物。这些化合物的结构通过 HR-Q-TOF ESI/MS/MS 和 2D NMR 分析进行了研究。基于生物活性的分离得到了一种呋喃型化合物,该化合物对AGS、HCT116、A375M、U87MG 和 A549 细胞系具有体外抗癌活性,IC 值分别为 40.5、123.7、84.67、50 和 58.64µM。从分离到的链霉菌 sp. VN1 的基因组分析中包含 34 个基因簇,负责合成已知和/或新型次级代谢产物,包括不同类型的萜类、T1PKS、T2PKS、T3PKS、NRPS 和杂合 PKS-NRPS。利用 HR-Q-TOF ESI/MS/MS 对粗提物进行的基因组挖掘证实了 lobophorin 类似物的生物合成。本研究表明,链霉菌 sp. VN1 是一种很有前途的新型天然产物生物合成菌株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c545/7000394/b8ae839aee0a/41598_2020_58623_Fig1_HTML.jpg

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