Literature DB >> 27221133

Optimizing production and evaluating biosynthesis in situ of a herbicidal compound, mevalocidin, from Coniolariella sp.

Vincent P Sica1, Mario Figueroa1,2, Huzefa A Raja1, Tamam El-Elimat1, Blaise A Darveaux3, Cedric J Pearce4, Nicholas H Oberlies5.   

Abstract

Mevalocidin is a fungal secondary metabolite produced by Coniolariella sp. It is a unique phytotoxin that demonstrates broad spectrum post-emergent herbicidal properties. With limited options for weed control, the commercialization of a natural product pesticide would be beneficial to organic farming. In this study, two mevalocidin-producing fungal strains, coded MSX56446 and MSX92917, were explored under a variety of growth conditions, including time, temperature, and media. The concentration of mevalocidin was quantitatively measured via LC-MS to determine the optimal setting for each condition. Maximum production was achieved for each condition at 20 days, at 30 °C, with YESD + agar, and with a media containing 2.5 % dextrose. Furthermore, an advanced surface sampling technique was incorporated to gain a better understanding of the fungal culture's natural ability to biosynthesize and distribute this herbicide into its environment. It was shown that both fungi actively exude mevalocidin into their environment via liquid droplet formations known as guttates.

Entities:  

Keywords:  Droplet-based liquid extraction; Fungal secondary metabolites; Herbicide; Spatial distribution

Mesh:

Substances:

Year:  2016        PMID: 27221133     DOI: 10.1007/s10295-016-1782-2

Source DB:  PubMed          Journal:  J Ind Microbiol Biotechnol        ISSN: 1367-5435            Impact factor:   3.346


  27 in total

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5.  Sampling reliability, spatial resolution, spatial precision, and extraction efficiency in droplet-based liquid microjunction surface sampling.

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10.  Polyhydroxyanthraquinones as quorum sensing inhibitors from the guttates of Penicillium restrictum and their analysis by desorption electrospray ionization mass spectrometry.

Authors:  Mario Figueroa; Alan K Jarmusch; Huzefa A Raja; Tamam El-Elimat; Jeffrey S Kavanaugh; Alexander R Horswill; R Graham Cooks; Nadja B Cech; Nicholas H Oberlies
Journal:  J Nat Prod       Date:  2014-06-09       Impact factor: 4.050

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  11 in total

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Review 4.  Droplet probe: coupling chromatography to the in situ evaluation of the chemistry of nature.

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5.  Engineering Fluorine into Verticillins (Epipolythiodioxopiperazine Alkaloids) via Precursor-Directed Biosynthesis.

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Journal:  J Nat Prod       Date:  2022-02-25       Impact factor: 4.803

7.  Mapping the Fungal Battlefield: Using in situ Chemistry and Deletion Mutants to Monitor Interspecific Chemical Interactions Between Fungi.

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Journal:  Front Microbiol       Date:  2019-02-19       Impact factor: 5.640

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10.  Media and strain studies for the scaled production of cis-enone resorcylic acid lactones as feedstocks for semisynthesis.

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