Cargando…
Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production
The growing world needs commodity amino acids such as L‐glutamate and L‐lysine for use as food and feed, and specialty amino acids for dedicated applications. To meet the supply a paradigm shift regarding their production is required. On the one hand, the use of sustainable and cheap raw materials i...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328739/ https://www.ncbi.nlm.nih.gov/pubmed/35488805 http://dx.doi.org/10.1111/1751-7915.14067 |
_version_ | 1784757784221319168 |
---|---|
author | Irla, Marta Wendisch, Volker F. |
author_facet | Irla, Marta Wendisch, Volker F. |
author_sort | Irla, Marta |
collection | PubMed |
description | The growing world needs commodity amino acids such as L‐glutamate and L‐lysine for use as food and feed, and specialty amino acids for dedicated applications. To meet the supply a paradigm shift regarding their production is required. On the one hand, the use of sustainable and cheap raw materials is necessary to sustain low production cost and decrease detrimental effects of sugar‐based feedstock on soil health and food security caused by competing uses of crops in the feed and food industries. On the other hand, the biotechnological methods to produce functionalized amino acids need to be developed further, and titres enhanced to become competitive with chemical synthesis methods. In the current review, we present successful strain mutagenesis and rational metabolic engineering examples leading to the construction of recombinant bacterial strains for the production of amino acids such as L‐glutamate, L‐lysine, L‐threonine and their derivatives from methanol as sole carbon source. In addition, the fermentative routes for bioproduction of N‐methylated amino acids are highlighted, with focus on three strategies: partial transfer of methylamine catabolism, S‐adenosyl‐L‐methionine dependent alkylation and reductive methylamination of 2‐oxoacids. |
format | Online Article Text |
id | pubmed-9328739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93287392022-07-30 Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production Irla, Marta Wendisch, Volker F. Microb Biotechnol Minireview The growing world needs commodity amino acids such as L‐glutamate and L‐lysine for use as food and feed, and specialty amino acids for dedicated applications. To meet the supply a paradigm shift regarding their production is required. On the one hand, the use of sustainable and cheap raw materials is necessary to sustain low production cost and decrease detrimental effects of sugar‐based feedstock on soil health and food security caused by competing uses of crops in the feed and food industries. On the other hand, the biotechnological methods to produce functionalized amino acids need to be developed further, and titres enhanced to become competitive with chemical synthesis methods. In the current review, we present successful strain mutagenesis and rational metabolic engineering examples leading to the construction of recombinant bacterial strains for the production of amino acids such as L‐glutamate, L‐lysine, L‐threonine and their derivatives from methanol as sole carbon source. In addition, the fermentative routes for bioproduction of N‐methylated amino acids are highlighted, with focus on three strategies: partial transfer of methylamine catabolism, S‐adenosyl‐L‐methionine dependent alkylation and reductive methylamination of 2‐oxoacids. John Wiley and Sons Inc. 2022-04-30 /pmc/articles/PMC9328739/ /pubmed/35488805 http://dx.doi.org/10.1111/1751-7915.14067 Text en © 2022 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Minireview Irla, Marta Wendisch, Volker F. Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production |
title | Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production |
title_full | Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production |
title_fullStr | Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production |
title_full_unstemmed | Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production |
title_short | Efficient cell factories for the production of N‐methylated amino acids and for methanol‐based amino acid production |
title_sort | efficient cell factories for the production of n‐methylated amino acids and for methanol‐based amino acid production |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328739/ https://www.ncbi.nlm.nih.gov/pubmed/35488805 http://dx.doi.org/10.1111/1751-7915.14067 |
work_keys_str_mv | AT irlamarta efficientcellfactoriesfortheproductionofnmethylatedaminoacidsandformethanolbasedaminoacidproduction AT wendischvolkerf efficientcellfactoriesfortheproductionofnmethylatedaminoacidsandformethanolbasedaminoacidproduction |