Literature DB >> 26100667

Production of (15)N-labeled α-amanitin in Galerina marginata.

Hong Luo1, Brandon DuBois2, R Michael Sgambelluri3, Evan R Angelos2, Xuan Li4, Daniel Holmes5, Jonathan D Walton6.   

Abstract

α-Amanitin is the major causal constituent of deadly Amanita mushrooms that account for the majority of fatal mushroom poisonings worldwide. It is also an important biochemical tool for the study of its target, RNA polymerase II. The commercial supply of this bicyclic peptide comes from Amanita phalloides, the death cap mushroom, which is collected from the wild. Isotopically labeled amanitin could be useful for clinical and forensic applications, but α-amanitin has not been chemically synthesized and A. phalloides cannot be cultured on artificial medium. Using Galerina marginata, an unrelated saprotrophic mushroom that grows and produces α-amanitin in culture, we describe a method for producing (15)N-labeled α-amanitin using growth media containing (15)N as sole nitrogen source. A key to success was preparing (15)N-enriched yeast extract via a novel method designated "glass bead-assisted maturation." In the presence of the labeled yeast extract and (15)N-NH4Cl, α-amanitin was produced with >97% isotope enrichment. The labeled product was confirmed by HPLC, high-resolution mass spectrometry, and NMR.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Amanita; Galerina; Isotope labeling; LC-MS; NMR; α-Amanitin

Mesh:

Substances:

Year:  2015        PMID: 26100667      PMCID: PMC4526342          DOI: 10.1016/j.toxicon.2015.06.018

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  24 in total

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Review 4.  The application of stable isotopes in biomedical research.

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8.  1H, 13C and 15N chemical shift referencing in biomolecular NMR.

Authors:  D S Wishart; C G Bigam; J Yao; F Abildgaard; H J Dyson; E Oldfield; J L Markley; B D Sykes
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Journal:  Toxins (Basel)       Date:  2014-08-05       Impact factor: 4.546

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