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  • References (14)
  • Citations (1)
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References14
Newest
Published on Apr 22, 2016in Journal of Natural Products 4.26
Nan Ding2
Estimated H-index: 2
,
Yi Jiang13
Estimated H-index: 13
+ 8 AuthorsChenglin Jiang6
Estimated H-index: 6
From a fermentation broth of Streptomyces albolongus obtained from Elephas maximus feces, nine bafilomycins (1–9) and seven odoriferous sesquiterpenoids (10–16) were isolated. The structures of the new compounds, including three bafilomycins, 19-methoxybafilomycin C1 amide (1), 21-deoxybafilomycin A1 (2), and 21-deoxybafilomycin A2 (3), and two sesquiterpenoid degradation products, (1β,4β,4aβ,8aα)-4,8a-dimethyloctahydronaphthalene-1,4a(2H)-diol (10) and (1β,4β,4aβ,7α,8aα)-4,8a-dimethyloctahydron...
Yuuki Yamada5
Estimated H-index: 5
(Kitasato University),
Tomohisa Kuzuyama43
Estimated H-index: 43
(UTokyo: University of Tokyo)
+ 4 AuthorsHaruo Ikeda37
Estimated H-index: 37
(Kitasato University)
Abstract Odoriferous terpene metabolites of bacterial origin have been known for many years. In genome-sequenced Streptomycetaceae microorganisms, the vast majority produces the degraded sesquiterpene alcohol geosmin. Two minor groups of bacteria do not produce geosmin, with one of these groups instead producing other sesquiterpene alcohols, whereas members of the remaining group do not produce any detectable terpenoid metabolites. Because bacterial terpene synthases typically show no significan...
Published on Jan 16, 2012in Molecules 3.06
Dan Zheng5
Estimated H-index: 5
,
Li Han7
Estimated H-index: 7
+ 6 AuthorsXueshi Huang4
Estimated H-index: 4
Two new compounds, isostreptazolin (1) and sannaphenol (2), were isolated from the culture broth of Streptomyces sannanensis and their structures elucidated on the basis of 1D and 2D NMR as well as MS, IR and UV spectroscopic data analysis. The cytotoxic activity of 1 and 2 were evaluated. Both compounds were inactive against H460 and HeLa cell lines at 100 mM.
Published on Aug 12, 2011in Journal of Biological Chemistry
Chiaki Nakano7
Estimated H-index: 7
,
Sueharu Horinouchi55
Estimated H-index: 55
,
Yasuo Ohnishi36
Estimated H-index: 36
Most terpenoids have been isolated from plants and fungi and only a few from bacteria. However, an increasing number of genome sequences indicate that bacteria possess a variety of terpenoid cyclase genes. We characterized a sesquiterpene cyclase gene (SGR2079, named gcoA) found in Streptomyces griseus. When expressed in Streptomyces lividans, gcoA directed production of a sesquiterpene, isolated and determined to be (+)-caryolan-1-ol using spectroscopic analyses. (+)-Caryolan-1-ol was also dete...
Published on Jan 23, 2009in Journal of Natural Products 4.26
Ling Ding16
Estimated H-index: 16
,
Roland Pfoh5
Estimated H-index: 5
+ 2 AuthorsHartmut Laatsch37
Estimated H-index: 37
Two new sesquiterpenes, 15-hydroxy-T-muurolol (3d) and 11,15-dihydroxy-T-muurolol (3e), along with the plant cadinenes T-muurolol (3f) and 3 alpha-hydroxy-T-muurolol (3g), were isolated from the marine-derived Streptomyces sp. M491. Their absolute configuration was established via NMR spectroscopy and X-ray crystallography of 3-oxo-T-muurolol (3a), which was reisolated from this strain. In addition, the absolute configuration of further sesquiterpenes previously reported from this strain was rev...
Published on Jan 1, 2008in Journal of the American Chemical Society 14.70
Thorben Nawrath10
Estimated H-index: 10
,
Jeroen S. Dickschat32
Estimated H-index: 32
+ 3 AuthorsStefan Schulz55
Estimated H-index: 55
(-)-Geosmin (1, blue) is an important odor component produced by many bacteria, including actinomycetes, myxobacteria, and cyanobacteria, but has also been reported for eukaryotic organisms such as fungi, liverworts, insects, and plants. Recent research has shown that the biosynthesis of 1 starts with the cyclization of farnesyl pyrophosphate to (1(10)E,5E)-germacradien-11-ol (2, yellow), the first key intermediate en route. In a retro-Prins-reaction acetone is lost, and the second key intermedi...
Published on Jan 1, 2000in Bioorganic & Medicinal Chemistry Letters 2.45
David E. Cane63
Estimated H-index: 63
(Brown University),
Ning Ke1
Estimated H-index: 1
(Brown University)
Incubation of epicubenol synthase with farnesyl pyrophosphate in the presence of 11.1 atom% H218O gave epicubenol (2 Scheme 1. Figure options Download full-size image Download high-quality image (51 K) Download as PowerPoint slide ) in which the hydroxyl oxygen atom was shown to be derived exclusively from water, as established by GC-selected ion monitoring MS of the derived TMS-epicubenol derivative (15).
Published on Oct 1, 1999in Phytochemistry 2.90
Masao Toyota31
Estimated H-index: 31
(Tokushima Bunri University),
Yumiko Yonehara1
Estimated H-index: 1
(Tokushima Bunri University)
+ 2 AuthorsYoshinori Asakawa43
Estimated H-index: 43
(Tokushima Bunri University)
Abstract The ether extract of the liverwort Porella perrottetiana afforded (−)-α-eudesmol, which showed an opposite sign of the optical rotation to that found in higher plants. Present work on the absolute configuration and an optical purity of (−)-α-eudesmol strongly suggested that the positive values (e.g.+28.5°) described in many previous papers should be revised. Since the absolute configuration of (−)-α-eudesmol was identical to that of (+)-β-eudesmol found in the higher plants, it was appa...
Published on Jan 1, 1998in Flavour and Fragrance Journal 1.38
Peter Weyerstahl24
Estimated H-index: 24
(Technical University of Berlin),
Helga Marschall21
Estimated H-index: 21
(Technical University of Berlin)
+ 1 AuthorsGyan Chandra Subba3
Estimated H-index: 3
The essential oil from the rhizomes of Hedychium gardnerianum Roscoe (‘Kahili ginger’) contains about 30% of sesquiterpenes, mainly cadinane derivatives. The following new sesquiterpenes were identified by their NMR and MS data: α-corocalene epoxide (104); 1,10;7,10-bisepoxy-1,10-seco-calamenene (68); 6,7;7,10-bisepoxy-6,7-seco-calamenene (74); 7-epi-trans- (60) and 7-epi-cis-sesquisabinene hydrate (69); 10-epi-cubenol (78); and ar-curcumen-1,10-diol (108). Copyright © 1998 John Wiley & Sons, Lt...
Cited By1
Newest
Published on Mar 1, 2018in Phytochemistry 2.90
Zhen-Zhu Zhao7
Estimated H-index: 7
(CAS: Chinese Academy of Sciences),
Kuan Zhao5
Estimated H-index: 5
(Jiangxi Science and Technology Normal University)
+ 3 AuthorsJi-Kai Liu29
Estimated H-index: 29
(SCUN/SCUEC: South Central University for Nationalities)
Abstract Molecular identification suggested an edible mushroom, which was previously named as Craterellus odoratus should be revised as Montagnula donacina . A chemical re-investigation of the culture broth of this fungus resulted in the isolation of four rare tetracyclic bergamotane-type sesquiterpenoids, namely donacinolides A and B, donacinoic acids A and B, and three cadinane-type ones, namely donacinols A–C and a meroterpenoid ( Z )-4-hydroxy-3-(3-hydroxy-3-methylbut-1-en-1-yl)benzoic acid....