Literature DB >> 9351196

Degradation of the polyamine alkaloid aphelandrine by endophytic fungi isolated from Aphelandra tetragona.

C Werner1, O Petrini, M Hesse.   

Abstract

Members of the genus Aphelandra (Acanthaceae) produce rare macrocyclic polyamine alkaloids which consist of spermine acylated with two units of 3-(4-hydroxyphenyl)prop-2-enoic acid. Endophytic fungi were isolated from roots and shoots of Aphelandra tetragona and tested for their ability to metabolize the main alkaloid aphelandrine, which accumulates exclusively in the roots of the plants. Several endophytes were able to metabolize aphelandrine but only root endophytes belonging to the Nectriaceae were good metabolizers. In addition, the endophytes were grown on an agar medium containing putrescine, spermidine, or spermine as the sole nitrogen source. All fungi were able to grow on putrescine, but only the good aphelandrine metabolizers grew well on spermidine or spermine. Acremonium sp. 15, one of the most active metabolizers, grew also on a medium containing aphelandrine as sole nitrogen source. A number of strains thought to be conspecific with Acremonium sp. 15 were also tested for their ability to metabolize aphelandrine. The ability of the endophytes to metabolize aphelandrine suggests an ecological adaptation of the symbionts to their host. The possibility of using the aphelandrine metabolism as a taxonomic character is briefly discussed.

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Year:  1997        PMID: 9351196     DOI: 10.1016/s0378-1097(97)00380-7

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  6 in total

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2.  Biotransformation of 2-benzoxazolinone and 2-hydroxy-1,4-benzoxazin-3-one by endophytic fungi isolated from Aphelandra tetragona.

Authors:  M Zikmundová; K Drandarov; L Bigler; M Hesse; C Werner
Journal:  Appl Environ Microbiol       Date:  2002-10       Impact factor: 4.792

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Journal:  Folia Microbiol (Praha)       Date:  2009-08-02       Impact factor: 2.099

4.  Benzoxazolinone detoxification by N-Glucosylation: The multi-compartment-network of Zea mays L.

Authors:  Margot Schulz; Barbara Filary; Sabine Kühn; Thomas Colby; Anne Harzen; Jürgen Schmidt; Dieter Sicker; Lothar Hennig; Diana Hofmann; Ulrich Disko; Nico Anders
Journal:  Plant Signal Behav       Date:  2016

5.  Defensive properties of pyrrolizidine alkaloids against microorganisms.

Authors:  Lotte Joosten; Johannes A van Veen
Journal:  Phytochem Rev       Date:  2010-11-23       Impact factor: 5.374

6.  Effects of an Endophytic Fungus Umbelopsis dimorpha on the Secondary Metabolites of Host-Plant Kadsura angustifolia.

Authors:  Dan Qin; Ling Wang; Meijun Han; Junqi Wang; Hongchuan Song; Xiao Yan; Xiaoxiang Duan; Jinyan Dong
Journal:  Front Microbiol       Date:  2018-11-22       Impact factor: 5.640

  6 in total

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