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Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst

Phenylacetylcarbinol (PAC) is a precursor for the synthesis of several pharmaceuticals, including ephedrine, pseudoephedrine, and norephedrine. PAC is commonly produced through biotransformation using microbial pyruvate decarboxylase (PDC) in the form of frozen–thawed whole cells. However, the lack...

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Autores principales: Kumar, Anbarasu, Techapun, Charin, Sommanee, Sumeth, Mahakuntha, Chatchadaporn, Feng, Juan, Htike, Su Lwin, Khemacheewakul, Julaluk, Porninta, Kritsadaporn, Phimolsiripol, Yuthana, Wang, Wen, Zhuang, Xinshu, Qi, Wei, Jantanasakulwong, Kittisak, Nunta, Rojarej, Leksawasdi, Noppol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533076/
https://www.ncbi.nlm.nih.gov/pubmed/37755036
http://dx.doi.org/10.3390/jof9090928
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author Kumar, Anbarasu
Techapun, Charin
Sommanee, Sumeth
Mahakuntha, Chatchadaporn
Feng, Juan
Htike, Su Lwin
Khemacheewakul, Julaluk
Porninta, Kritsadaporn
Phimolsiripol, Yuthana
Wang, Wen
Zhuang, Xinshu
Qi, Wei
Jantanasakulwong, Kittisak
Nunta, Rojarej
Leksawasdi, Noppol
author_facet Kumar, Anbarasu
Techapun, Charin
Sommanee, Sumeth
Mahakuntha, Chatchadaporn
Feng, Juan
Htike, Su Lwin
Khemacheewakul, Julaluk
Porninta, Kritsadaporn
Phimolsiripol, Yuthana
Wang, Wen
Zhuang, Xinshu
Qi, Wei
Jantanasakulwong, Kittisak
Nunta, Rojarej
Leksawasdi, Noppol
author_sort Kumar, Anbarasu
collection PubMed
description Phenylacetylcarbinol (PAC) is a precursor for the synthesis of several pharmaceuticals, including ephedrine, pseudoephedrine, and norephedrine. PAC is commonly produced through biotransformation using microbial pyruvate decarboxylase (PDC) in the form of frozen–thawed whole cells. However, the lack of microorganisms capable of high PDC activity is the main factor in the production of PAC. In addition, researchers are also looking for ways to utilize agro-industrial residues as an inexpensive carbon source through an integrated biorefinery approach in which sugars can be utilized for bioethanol production and frozen–thawed whole cells for PAC synthesis. In the present study, Candida tropicalis, Saccharomyces cerevisiae, and the co-culture of both strains were compared for their biomass and ethanol concentrations, as well as for their volumetric and specific PDC activities when cultivated in a sugarcane bagasse (SCB) hydrolysate medium (SCBHM). The co-culture that resulted in a higher level of PAC (8.65 ± 0.08 mM) with 26.4 ± 0.9 g L(−1) ethanol production was chosen for further experiments. Biomass production was scaled up to 100 L and the kinetic parameters were studied. The biomass harvested from the bioreactor was utilized as frozen–thawed whole cells for the selection of an initial pyruvate (Pyr)-to-benzaldehyde (Bz) concentration ([Pyr]/[Bz]) ratio suitable for the PAC biotransformation in a single-phase emulsion system. The initial [Pyr]/[Bz] at 100/120 mM resulted in higher PAC levels with 10.5 ± 0.2 mM when compared to 200/240 mM (8.60 ± 0.01 mM). A subsequent two-phase emulsion system with Pyr in the aqueous phase, Bz in the organic phase, and frozen–thawed whole cells of the co-culture as the biocatalyst produced a 1.46-fold higher PAC level when compared to a single-phase emulsion system. In addition, the cost analysis strategy indicated preliminary costs of USD 0.82 and 1.01/kg PAC for the single-phase and two-phase emulsion systems, respectively. The results of the present study suggested that the co-culture of C. tropicalis and S. cerevisiae can effectively produce bioethanol and PAC from SCB and would decrease the overall production cost on an industrial scale utilizing the two-phase emulsion system with the proposed multiple-pass strategy.
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spelling pubmed-105330762023-09-28 Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst Kumar, Anbarasu Techapun, Charin Sommanee, Sumeth Mahakuntha, Chatchadaporn Feng, Juan Htike, Su Lwin Khemacheewakul, Julaluk Porninta, Kritsadaporn Phimolsiripol, Yuthana Wang, Wen Zhuang, Xinshu Qi, Wei Jantanasakulwong, Kittisak Nunta, Rojarej Leksawasdi, Noppol J Fungi (Basel) Article Phenylacetylcarbinol (PAC) is a precursor for the synthesis of several pharmaceuticals, including ephedrine, pseudoephedrine, and norephedrine. PAC is commonly produced through biotransformation using microbial pyruvate decarboxylase (PDC) in the form of frozen–thawed whole cells. However, the lack of microorganisms capable of high PDC activity is the main factor in the production of PAC. In addition, researchers are also looking for ways to utilize agro-industrial residues as an inexpensive carbon source through an integrated biorefinery approach in which sugars can be utilized for bioethanol production and frozen–thawed whole cells for PAC synthesis. In the present study, Candida tropicalis, Saccharomyces cerevisiae, and the co-culture of both strains were compared for their biomass and ethanol concentrations, as well as for their volumetric and specific PDC activities when cultivated in a sugarcane bagasse (SCB) hydrolysate medium (SCBHM). The co-culture that resulted in a higher level of PAC (8.65 ± 0.08 mM) with 26.4 ± 0.9 g L(−1) ethanol production was chosen for further experiments. Biomass production was scaled up to 100 L and the kinetic parameters were studied. The biomass harvested from the bioreactor was utilized as frozen–thawed whole cells for the selection of an initial pyruvate (Pyr)-to-benzaldehyde (Bz) concentration ([Pyr]/[Bz]) ratio suitable for the PAC biotransformation in a single-phase emulsion system. The initial [Pyr]/[Bz] at 100/120 mM resulted in higher PAC levels with 10.5 ± 0.2 mM when compared to 200/240 mM (8.60 ± 0.01 mM). A subsequent two-phase emulsion system with Pyr in the aqueous phase, Bz in the organic phase, and frozen–thawed whole cells of the co-culture as the biocatalyst produced a 1.46-fold higher PAC level when compared to a single-phase emulsion system. In addition, the cost analysis strategy indicated preliminary costs of USD 0.82 and 1.01/kg PAC for the single-phase and two-phase emulsion systems, respectively. The results of the present study suggested that the co-culture of C. tropicalis and S. cerevisiae can effectively produce bioethanol and PAC from SCB and would decrease the overall production cost on an industrial scale utilizing the two-phase emulsion system with the proposed multiple-pass strategy. MDPI 2023-09-14 /pmc/articles/PMC10533076/ /pubmed/37755036 http://dx.doi.org/10.3390/jof9090928 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kumar, Anbarasu
Techapun, Charin
Sommanee, Sumeth
Mahakuntha, Chatchadaporn
Feng, Juan
Htike, Su Lwin
Khemacheewakul, Julaluk
Porninta, Kritsadaporn
Phimolsiripol, Yuthana
Wang, Wen
Zhuang, Xinshu
Qi, Wei
Jantanasakulwong, Kittisak
Nunta, Rojarej
Leksawasdi, Noppol
Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst
title Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst
title_full Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst
title_fullStr Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst
title_full_unstemmed Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst
title_short Production of Phenylacetylcarbinol via Biotransformation Using the Co-Culture of Candida tropicalis TISTR 5306 and Saccharomyces cerevisiae TISTR 5606 as the Biocatalyst
title_sort production of phenylacetylcarbinol via biotransformation using the co-culture of candida tropicalis tistr 5306 and saccharomyces cerevisiae tistr 5606 as the biocatalyst
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533076/
https://www.ncbi.nlm.nih.gov/pubmed/37755036
http://dx.doi.org/10.3390/jof9090928
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