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Ursodeoxycholic acid production by Gibberella zeae mutants
Ursodeoxycholic acid (UDCA) is a highly demanded pharmaceutical steroid widely used in medicine. An ascomycete Gibberella zeae VKM F-2600 is capable of producing UDCA by 7β-hydroxylation of lithocholic acid (LCA). The present study is aimed at the improvement of the fungus productivity. The original...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360310/ https://www.ncbi.nlm.nih.gov/pubmed/35939125 http://dx.doi.org/10.1186/s13568-022-01446-2 |
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author | Kollerov, Vyacheslav Donova, Marina |
author_facet | Kollerov, Vyacheslav Donova, Marina |
author_sort | Kollerov, Vyacheslav |
collection | PubMed |
description | Ursodeoxycholic acid (UDCA) is a highly demanded pharmaceutical steroid widely used in medicine. An ascomycete Gibberella zeae VKM F-2600 is capable of producing UDCA by 7β-hydroxylation of lithocholic acid (LCA). The present study is aimed at the improvement of the fungus productivity. The original procedures for the protoplast obtaining followed by UV mutagenesis and screening of ketoconazole-resistant mutant clones have been applied. The highest yield of G. zeae protoplasts was obtained when using the mycelium in the active growth phase, ammonium chloride as an osmotic stabilizer and treatment of the fungal cells by the lytic enzymes cocktail from Trichoderma hurzanium. The conditions for effective protoplast regeneration and the UV-mutagenesis were found to provide 6–12% survival rate of the protoplasts with superior number of possible mutations. Three of 27 ketoconazole-resistant mutant clones obtained have been selected due to their increased biocatalytic activity towards LCA. The mutant G. zeae M23 produced 26% more UDCA even at relatively high LCA concentration (4 g/L) as compared with parent fungal strain, and the conversion reached 88% (w/w). The yield of UDCA reached in this study prefers those ever reported. The results contribute to the knowledge on ascomycete mutagenesis, and are of importance for biotechnological production of value added cholic acids. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9360310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-93603102022-08-10 Ursodeoxycholic acid production by Gibberella zeae mutants Kollerov, Vyacheslav Donova, Marina AMB Express Original Article Ursodeoxycholic acid (UDCA) is a highly demanded pharmaceutical steroid widely used in medicine. An ascomycete Gibberella zeae VKM F-2600 is capable of producing UDCA by 7β-hydroxylation of lithocholic acid (LCA). The present study is aimed at the improvement of the fungus productivity. The original procedures for the protoplast obtaining followed by UV mutagenesis and screening of ketoconazole-resistant mutant clones have been applied. The highest yield of G. zeae protoplasts was obtained when using the mycelium in the active growth phase, ammonium chloride as an osmotic stabilizer and treatment of the fungal cells by the lytic enzymes cocktail from Trichoderma hurzanium. The conditions for effective protoplast regeneration and the UV-mutagenesis were found to provide 6–12% survival rate of the protoplasts with superior number of possible mutations. Three of 27 ketoconazole-resistant mutant clones obtained have been selected due to their increased biocatalytic activity towards LCA. The mutant G. zeae M23 produced 26% more UDCA even at relatively high LCA concentration (4 g/L) as compared with parent fungal strain, and the conversion reached 88% (w/w). The yield of UDCA reached in this study prefers those ever reported. The results contribute to the knowledge on ascomycete mutagenesis, and are of importance for biotechnological production of value added cholic acids. GRAPHICAL ABSTRACT: [Image: see text] Springer Berlin Heidelberg 2022-08-08 /pmc/articles/PMC9360310/ /pubmed/35939125 http://dx.doi.org/10.1186/s13568-022-01446-2 Text en © The Author(s) 2022 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/) . |
spellingShingle | Original Article Kollerov, Vyacheslav Donova, Marina Ursodeoxycholic acid production by Gibberella zeae mutants |
title | Ursodeoxycholic acid production by Gibberella zeae mutants |
title_full | Ursodeoxycholic acid production by Gibberella zeae mutants |
title_fullStr | Ursodeoxycholic acid production by Gibberella zeae mutants |
title_full_unstemmed | Ursodeoxycholic acid production by Gibberella zeae mutants |
title_short | Ursodeoxycholic acid production by Gibberella zeae mutants |
title_sort | ursodeoxycholic acid production by gibberella zeae mutants |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360310/ https://www.ncbi.nlm.nih.gov/pubmed/35939125 http://dx.doi.org/10.1186/s13568-022-01446-2 |
work_keys_str_mv | AT kollerovvyacheslav ursodeoxycholicacidproductionbygibberellazeaemutants AT donovamarina ursodeoxycholicacidproductionbygibberellazeaemutants |