| Literature DB >> 26611524 |
Ling Ding1, Helmar Goerls2, Katharina Dornblut1, Wenhan Lin3, Armin Maier4, Heinz-Herbert Fiebig4, Christian Hertweck1,5.
Abstract
Caryolanes are known as typical plant-derived sesquiterpenes. Here we describe the isolation and full structure elucidation of three caryolanes, bacaryolane A-C (1-3), that are produced by a bacterial endophyte (Streptomyces sp. JMRC:ST027706) of the mangrove plant Bruguiera gymnorrhiza. By 2D NMR, analysis of the first X-ray crystallographic data of a caryolane (bacaryolane C), CD spectroscopy, and comparison with data for plant-derived caryolanes, we rigorously established the absolute configuration of the bacaryolanes and related compounds from bacteria. Bacterial caryolanes appear as the mirror images of typical plant caryolanes. Apparently plant and bacteria harbor stereodivergent biosynthetic pathways, which may be used as metabolic signatures. The discovery of plant-like volatile terpenes in endophytes not only is an important addition to the bacterial terpenome but may also point to complex molecular interactions in the plant-microbe association.Entities:
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Year: 2015 PMID: 26611524 DOI: 10.1021/acs.jnatprod.5b00674
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050