Cargando…

Phosphonates enantiomers receiving with fungal enzymatic systems

BACKGROUND: Phosphonates derivatives are in the area of interests because of their unique chemical-physical features. These compounds manifest variety of biological interactions within the sensitive living cells, including impact on particular enzymes activities. Biological “cause and effect” intera...

Descripción completa

Detalles Bibliográficos
Autores principales: Serafin-Lewańczuk, Monika, Brzezińska-Rodak, Małgorzata, Lubiak-Kozłowska, Katarzyna, Majewska, Paulina, Klimek-Ochab, Magdalena, Olszewski, Tomasz K., Żymańczyk-Duda, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028800/
https://www.ncbi.nlm.nih.gov/pubmed/33827578
http://dx.doi.org/10.1186/s12934-021-01573-8
_version_ 1783676009203105792
author Serafin-Lewańczuk, Monika
Brzezińska-Rodak, Małgorzata
Lubiak-Kozłowska, Katarzyna
Majewska, Paulina
Klimek-Ochab, Magdalena
Olszewski, Tomasz K.
Żymańczyk-Duda, Ewa
author_facet Serafin-Lewańczuk, Monika
Brzezińska-Rodak, Małgorzata
Lubiak-Kozłowska, Katarzyna
Majewska, Paulina
Klimek-Ochab, Magdalena
Olszewski, Tomasz K.
Żymańczyk-Duda, Ewa
author_sort Serafin-Lewańczuk, Monika
collection PubMed
description BACKGROUND: Phosphonates derivatives are in the area of interests because of their unique chemical-physical features. These compounds manifest variety of biological interactions within the sensitive living cells, including impact on particular enzymes activities. Biological “cause and effect” interactions are based upon the specific matching between the structures and/or compounds and this is usually the result of proper optical configurations of particular chiral moieties. Presented research is targeted to the phosphonates with the heteroatom incorporated in their side functionalities. Such molecules are described as possible substrates of bioconversion for the first time lately and this field is not fully explored. RESULTS: Presented research is targeted to the synthesis of pure hetero-phosphonates enantiomers. The catalytic activity of yeasts and moulds were tested towards two substrates: the thienyl and imidazole phosphonates to resolve their racemic mixtures. Biotransformations conditions differed depending on the outcome, what included changing of following parameters: type of cultivation media, bioprocess duration (24–72 h), additional biocatalyst pre-treatment (24–48 h starvation step triggering the secondary metabolism). (S)-1-amino-1-(3-thienyl)methylphosphonate was produced with the assistance of R. mucilaginosa or A. niger (e.e. up to 98% and yield up to 100%), starting from the 3 mM of substrate racemic mixture. Bioconversion of racemic mixture of 3 mM of (1-amino-1-(4-imidazole)methylphosphonic acid) resulted in the synthesis of S-isomer (up to 95% of e.e.; 100% of yield) with assistance of R. mucilaginosa. 24 h biotransformation was conducted with biomass preincubated under 48-hour starvation conditions. Such stereoselective resolution of the racemic mixtures of substrates undergoes under kinetic control with the conversion of one from the enantiomers. CONCLUSIONS: Composition of the culturing media and pre-incubation in conditions of nutrient deficiency were significant factors influencing the results of kinetic resolution of racemic mixtures of phosphonic substrates and influencing the economic side of the biocatalysis e.g. by determining the duration of whole biocatalytic process. GRAPHICAL ABSTRACT: [Image: see text]
format Online
Article
Text
id pubmed-8028800
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-80288002021-04-09 Phosphonates enantiomers receiving with fungal enzymatic systems Serafin-Lewańczuk, Monika Brzezińska-Rodak, Małgorzata Lubiak-Kozłowska, Katarzyna Majewska, Paulina Klimek-Ochab, Magdalena Olszewski, Tomasz K. Żymańczyk-Duda, Ewa Microb Cell Fact Review BACKGROUND: Phosphonates derivatives are in the area of interests because of their unique chemical-physical features. These compounds manifest variety of biological interactions within the sensitive living cells, including impact on particular enzymes activities. Biological “cause and effect” interactions are based upon the specific matching between the structures and/or compounds and this is usually the result of proper optical configurations of particular chiral moieties. Presented research is targeted to the phosphonates with the heteroatom incorporated in their side functionalities. Such molecules are described as possible substrates of bioconversion for the first time lately and this field is not fully explored. RESULTS: Presented research is targeted to the synthesis of pure hetero-phosphonates enantiomers. The catalytic activity of yeasts and moulds were tested towards two substrates: the thienyl and imidazole phosphonates to resolve their racemic mixtures. Biotransformations conditions differed depending on the outcome, what included changing of following parameters: type of cultivation media, bioprocess duration (24–72 h), additional biocatalyst pre-treatment (24–48 h starvation step triggering the secondary metabolism). (S)-1-amino-1-(3-thienyl)methylphosphonate was produced with the assistance of R. mucilaginosa or A. niger (e.e. up to 98% and yield up to 100%), starting from the 3 mM of substrate racemic mixture. Bioconversion of racemic mixture of 3 mM of (1-amino-1-(4-imidazole)methylphosphonic acid) resulted in the synthesis of S-isomer (up to 95% of e.e.; 100% of yield) with assistance of R. mucilaginosa. 24 h biotransformation was conducted with biomass preincubated under 48-hour starvation conditions. Such stereoselective resolution of the racemic mixtures of substrates undergoes under kinetic control with the conversion of one from the enantiomers. CONCLUSIONS: Composition of the culturing media and pre-incubation in conditions of nutrient deficiency were significant factors influencing the results of kinetic resolution of racemic mixtures of phosphonic substrates and influencing the economic side of the biocatalysis e.g. by determining the duration of whole biocatalytic process. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2021-04-07 /pmc/articles/PMC8028800/ /pubmed/33827578 http://dx.doi.org/10.1186/s12934-021-01573-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Serafin-Lewańczuk, Monika
Brzezińska-Rodak, Małgorzata
Lubiak-Kozłowska, Katarzyna
Majewska, Paulina
Klimek-Ochab, Magdalena
Olszewski, Tomasz K.
Żymańczyk-Duda, Ewa
Phosphonates enantiomers receiving with fungal enzymatic systems
title Phosphonates enantiomers receiving with fungal enzymatic systems
title_full Phosphonates enantiomers receiving with fungal enzymatic systems
title_fullStr Phosphonates enantiomers receiving with fungal enzymatic systems
title_full_unstemmed Phosphonates enantiomers receiving with fungal enzymatic systems
title_short Phosphonates enantiomers receiving with fungal enzymatic systems
title_sort phosphonates enantiomers receiving with fungal enzymatic systems
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8028800/
https://www.ncbi.nlm.nih.gov/pubmed/33827578
http://dx.doi.org/10.1186/s12934-021-01573-8
work_keys_str_mv AT serafinlewanczukmonika phosphonatesenantiomersreceivingwithfungalenzymaticsystems
AT brzezinskarodakmałgorzata phosphonatesenantiomersreceivingwithfungalenzymaticsystems
AT lubiakkozłowskakatarzyna phosphonatesenantiomersreceivingwithfungalenzymaticsystems
AT majewskapaulina phosphonatesenantiomersreceivingwithfungalenzymaticsystems
AT klimekochabmagdalena phosphonatesenantiomersreceivingwithfungalenzymaticsystems
AT olszewskitomaszk phosphonatesenantiomersreceivingwithfungalenzymaticsystems
AT zymanczykdudaewa phosphonatesenantiomersreceivingwithfungalenzymaticsystems