Literature DB >> 23341265

Beetles do it differently: two stereodivergent cyclisation modes in iridoid-producing leaf-beetle larvae.

Maritta Kunert1, Peter Rahfeld, Kamel H Shaker, Bernd Schneider, Anja David, Konrad Dettner, Jacques M Pasteels, Wilhelm Boland.   

Abstract

Larvae of the Chrysomelina species Phaedon cochleariae, Hydrothassa marginella, Phratora vulgatissima, Gastrophysa viridula, Gastrophysa atrocyanea, Gastrophysa cyanea and Gastrophysa polygoni produce the iridoid chrysomelidial (1) to defend themselves against predators. Feeding experiments with a deuterated precursor ([(2)H(5)]8-hydroxygeraniol 9) and in vitro isotope exchange experiments with defensive secretion in (2)H(2)O revealed differences in the cyclisation of the ultimate precursor 8-oxogeranial (8) to 1, between members of the genus Gastrophysa and all other species. In P. cochleariae, H. marginella and P. vulgatissima 1 is most likely produced by a Rauhut-Currier-type cyclisation via a "transoid dienamine", with loss of a single deuterium atom from C(4) of the precursor. In contrast, members of the genus Gastrophysa cyclise 8 via a "cisoid dienamine" intermediate, with exchange of all three deuterium atoms from the methyl group at C(3). To study whether the different cyclisation modes influence the stereochemistry of 1, the absolute configuration of 1 of the larvae was determined by GC-MS on a chiral column. In accordance with literature (J. Meinwald, T. H. Jones, J. Am. Chem. Soc. 1978, 100, 1883 and N. Shimizu, R. Yakumaru, T. Sakata, S. Shimano, Y. Kuwahara, J. Chem. Ecol. 2012, 38, 29), we found (5S,8S)-chrysomelidial (1) in H. marginella and P. vulgatissima, but P. cochleariae and all investigated members of the genus Gastrophysa synthesise (5R,8R)-chrysomelidial (1).
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2013        PMID: 23341265     DOI: 10.1002/cbic.201200689

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  4 in total

Review 1.  The Enzymology of Organic Transformations: A Survey of Name Reactions in Biological Systems.

Authors:  Chia-I Lin; Reid M McCarty; Hung-Wen Liu
Journal:  Angew Chem Int Ed Engl       Date:  2017-02-14       Impact factor: 15.336

2.  Evidence for an Enzyme-Catalyzed Rauhut-Currier Reaction during the Biosynthesis of Spinosyn A.

Authors:  Sei-Hyun Choi; Byungsun Jeon; Namho Kim; Hsin-Hui Wu; Tzu-Ping Ko; Mark W Ruszczycky; Eta A Isiorho; Yung-Nan Liu; Adrian T Keatinge-Clay; Ming-Daw Tsai; Hung-Wen Liu
Journal:  J Am Chem Soc       Date:  2021-11-23       Impact factor: 15.419

3.  A common theme in extracellular fluids of beetles: extracellular superoxide dismutases crucial for balancing ROS in response to microbial challenge.

Authors:  René R Gretscher; Priska E Streicher; Anja S Strauß; Natalie Wielsch; Magdalena Stock; Ding Wang; Wilhelm Boland; Antje Burse
Journal:  Sci Rep       Date:  2016-04-12       Impact factor: 4.379

4.  Structural determinants of reductive terpene cyclization in iridoid biosynthesis.

Authors:  Hajo Kries; Lorenzo Caputi; Clare E M Stevenson; Mohammed O Kamileen; Nathaniel H Sherden; Fernando Geu-Flores; David M Lawson; Sarah E O'Connor
Journal:  Nat Chem Biol       Date:  2015-11-09       Impact factor: 16.174

  4 in total

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