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Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains

Due to its structural similarity, the α’-1′-hydroxyethyl-γ-butyrolactone obtained by reduction of (±)-α-acetyl-γ-butyrolactone may have a similar function in the body to γ-butyrolactone (GBL). In the work presented, biotransformation of α-acetyl-γ-butyrolactone by three Rhodotorula strains was perfo...

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Autores principales: Mączka, Wanda, Wińska, Katarzyna, Grabarczyk, Małgorzata, Żarowska, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073705/
https://www.ncbi.nlm.nih.gov/pubmed/30036958
http://dx.doi.org/10.3390/ijms19072106
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author Mączka, Wanda
Wińska, Katarzyna
Grabarczyk, Małgorzata
Żarowska, Barbara
author_facet Mączka, Wanda
Wińska, Katarzyna
Grabarczyk, Małgorzata
Żarowska, Barbara
author_sort Mączka, Wanda
collection PubMed
description Due to its structural similarity, the α’-1′-hydroxyethyl-γ-butyrolactone obtained by reduction of (±)-α-acetyl-γ-butyrolactone may have a similar function in the body to γ-butyrolactone (GBL). In the work presented, biotransformation of α-acetyl-γ-butyrolactone by three Rhodotorula strains was performed obtaining enantiomerically enriched alcohol. The process was carried out in growing and resting cultures. We studied how both media composition and organic solvent volume affected stereoselectivity and effectiveness of biotransformation. After 2 h, the enantiomerically pure (3R, 1′S)-α’-1′-hydroxyethyl-γ-butyrolactone was obtained using the R. marina AM77 strain in YPG (Yeast extract-Peptone-Glucose) medium enriched with 5% glycerol. To our best knowledge there is no previous information in the literature about the (±)-α-acetyl-γ-butyrolactone biotransformation performed in medium with addition of organic and deep eutectic solvents.
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spelling pubmed-60737052018-08-13 Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains Mączka, Wanda Wińska, Katarzyna Grabarczyk, Małgorzata Żarowska, Barbara Int J Mol Sci Article Due to its structural similarity, the α’-1′-hydroxyethyl-γ-butyrolactone obtained by reduction of (±)-α-acetyl-γ-butyrolactone may have a similar function in the body to γ-butyrolactone (GBL). In the work presented, biotransformation of α-acetyl-γ-butyrolactone by three Rhodotorula strains was performed obtaining enantiomerically enriched alcohol. The process was carried out in growing and resting cultures. We studied how both media composition and organic solvent volume affected stereoselectivity and effectiveness of biotransformation. After 2 h, the enantiomerically pure (3R, 1′S)-α’-1′-hydroxyethyl-γ-butyrolactone was obtained using the R. marina AM77 strain in YPG (Yeast extract-Peptone-Glucose) medium enriched with 5% glycerol. To our best knowledge there is no previous information in the literature about the (±)-α-acetyl-γ-butyrolactone biotransformation performed in medium with addition of organic and deep eutectic solvents. MDPI 2018-07-20 /pmc/articles/PMC6073705/ /pubmed/30036958 http://dx.doi.org/10.3390/ijms19072106 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mączka, Wanda
Wińska, Katarzyna
Grabarczyk, Małgorzata
Żarowska, Barbara
Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains
title Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains
title_full Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains
title_fullStr Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains
title_full_unstemmed Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains
title_short Biotransformation of α-Acetylbutyrolactone in Rhodotorula Strains
title_sort biotransformation of α-acetylbutyrolactone in rhodotorula strains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073705/
https://www.ncbi.nlm.nih.gov/pubmed/30036958
http://dx.doi.org/10.3390/ijms19072106
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