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Mutagenesis and Adaptation of the Psychrotrophic Fungus Chrysosporium pannorum A-1 as a Method for Improving ?-pinene Bioconversion.


ABSTRACT: Mutagenesis and adaptation of the psychrotrophic fungus Chrysosporium pannorum A-1 to the toxic substrate ?-pinene were used to obtain a biocatalyst with increased resistance to this terpene and improved bioconversion properties. Mutants of the parental strain were induced with UV light and N-methyl-N'-nitro-N-nitrosoguanidine. Mutants resistant to ?-pinene were isolated using agar plates with a linear gradient of substrate concentrations. Active mutants were selected based on their general metabolic activity (GMA) expressed as oxygen consumption rate. Compared to the parental strain, the most active mutant showed an enhanced biotransformation ability to convert ?-pinene to trans-pinocarveol (315 mg per g of dry mycelium), a 4.3-fold greater biocatalytic activity, and a higher resistance to H2O2-induced oxidative stress. Biotransformation using adapted mutants yielded twice as much trans-pinocarveol as the reaction catalyzed by non-adapted mutants. The results indicate that mutagenesis and adaptation of C. pannorum A-1 is an effective method of enhancing ?-bioconversion of terpenes.

SUBMITTER: Kutyla M 

PROVIDER: S-EPMC7321369 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Mutagenesis and Adaptation of the Psychrotrophic Fungus <i>Chrysosporium pannorum</i> A-1 as a Method for Improving β-pinene Bioconversion.

Kutyła Mateusz M   Fiedurek Jan J   Gromada Anna A   Jędrzejewski Krzysztof K   Trytek Mariusz M  

Molecules (Basel, Switzerland) 20200602 11


Mutagenesis and adaptation of the psychrotrophic fungus <i>Chrysosporium pannorum</i> A-1 to the toxic substrate β-pinene were used to obtain a biocatalyst with increased resistance to this terpene and improved bioconversion properties. Mutants of the parental strain were induced with UV light and <i>N</i>-methyl-<i>N</i>'-nitro-<i>N</i>-nitrosoguanidine. Mutants resistant to β-pinene were isolated using agar plates with a linear gradient of substrate concentrations. Active mutants were selected  ...[more]

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