Y
Yuemao Shen
Researcher at Shandong University
Publications - 338
Citations - 7235
Yuemao Shen is an academic researcher from Shandong University. The author has contributed to research in topics: Streptomyces & Chemistry. The author has an hindex of 38, co-authored 320 publications receiving 6113 citations. Previous affiliations of Yuemao Shen include Xiamen University & Kunming Institute of Botany.
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Journal ArticleDOI
Cytosporone B is an agonist for nuclear orphan receptor Nur77
Yan-yan Zhan,Xiping Du,Hang-zi Chen,Jingjing Liu,Bi-xing Zhao,Danhong Huang,Guideng Li,Qingyan Xu,Ming-Qing Zhang,Bart C. Weimer,Dong Chen,Zhe Cheng,Lianru Zhang,Qinxi Li,Shaowei Li,Zhonghui Zheng,Siyang Song,Yaojian Huang,Zhiyun Ye,Wenjin Su,Sheng-Cai Lin,Yuemao Shen,Qiao Wu +22 more
TL;DR: The octaketide cytosporone B (Csn-B) is a naturally occurring agonist for Nur77 that induced apoptosis and retarded xenograft tumor growth by inducing Nur77 expression, translocating Nur77 to mitochondria to cause cytochrome c release and may be useful as a reagent to increase understanding of Nur77 biological function.
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Biosynthesis of HSAF, a Tetramic Acid-Containing Macrolactam from Lysobacter enzymogenes
Lili Lou,Guoliang Qian,Yunxuan Xie,Jiliang Hang,Haotong Chen,Kathia Zaleta-Rivera,Yaoyao Li,Yaoyao Li,Yuemao Shen,Patrick H. Dussault,Fengquan Liu,Liangcheng Du +11 more
TL;DR: The genetic data demonstrate that the four redox genes, in addition to the PKS/NRPS gene and the sterol desaturase/fatty acid hydroxylase gene, are required for HSAF production, and reveal a previously unrecognized biosynthetic mechanism for hybrid PK/NRP in prokaryotic organisms.
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Bioactive natural products from Lysobacter.
TL;DR: A snapshot of the important work done on the lysobacterial natural products is provided to provide useful information for future biosynthetic engineering of novel antibiotics in Lysobacter.
Journal ArticleDOI
Direct evidence that the rifamycin polyketide synthase assembles polyketide chains processively.
Tin-Wein Yu,Yuemao Shen,Yukiko Doi-Katayama,Li Tang,Cheon-Seok Park,Bradley S. Moore,C. Richard Hutchinson,Heinz G. Floss +7 more
TL;DR: The structure of one of the accumulated compounds together with (18)O experiments suggests that this oxidative cyclization produces an 8-hydroxy-7, 8-dihydronaphthoquinone structure that, after the stage of proansamycin X, is dehydrogenated to an 8.hydroxynaphthOquinone.
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Nematicidal epipolysulfanyldioxopiperazines from Gliocladium roseum.
TL;DR: Five new verticillin-type epipolysulfanydioxopiperazines were isolated from wheat solid-substrate fermentation of Gliocladium roseum 1A, and all nine compounds exhibited antinematodal activity against Caenorhabditis elegans and Panagrellus redivivus.