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Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli
γ‐Aminobutyric acid (GABA) is a kind of non‐proteinogenic amino acid which is highly soluble in water and widely used in the food and pharmaceutical industries. Enzymatic conversion is an efficient method to produce GABA, whereby glutamic acid decarboxylase (GAD) is the key enzyme that catalyzes the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071571/ https://www.ncbi.nlm.nih.gov/pubmed/37025190 http://dx.doi.org/10.1002/elsc.202200064 |
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author | Fengmin, Liu Heng, Zhang Xiangjun, Zhang Xiaobo, Wei Huiyan, Liu Haitian, Fang |
author_facet | Fengmin, Liu Heng, Zhang Xiangjun, Zhang Xiaobo, Wei Huiyan, Liu Haitian, Fang |
author_sort | Fengmin, Liu |
collection | PubMed |
description | γ‐Aminobutyric acid (GABA) is a kind of non‐proteinogenic amino acid which is highly soluble in water and widely used in the food and pharmaceutical industries. Enzymatic conversion is an efficient method to produce GABA, whereby glutamic acid decarboxylase (GAD) is the key enzyme that catalyzes the process. The activity of wild‐type GAD is usually limited by temperature, pH or biotin concentration, and hence directional modification is applied to improve its catalytic properties and practical application. GABA was produced using whole cell transformation of the recombinant strains Escherichia coli BL21(DE3)‐Gad B, E. coli BL21(DE3)‐Gad B‐T62S and E. coli BL21(DE3)‐Gad B‐Q309A. The corresponding GABA concentrations in the fermentation broth were 219.09, 238.42, and 276.66 g/L, and the transformation rates were 78.02%, 85.04%, and 98.58%, respectively. The results showed that Gad B‐T62S and Gad B‐Q309A are two effective mutation sites. These findings may contribute to ideas for constructing potent recombinant strains for GABA production. Practical Application : Enzymatic properties of the GAD from Escherichia coli and GAD site‐specific mutants were examined by analyzing their conserved sequences, substrate contacts, contact between GAD amino acid residues and mutation energy (ΔΔG) of the GAD mutants. The enzyme activity and stability of Gad B‐T62S and Gad B‐Q309A mutants were improved compared to Gad B. The kinetic parameters K(m) and V(max) of Gad B, Gad B‐T62S, and Gad B‐Q309A mutants were 11.3 ± 2.1 mM and 32.1 ± 2.4 U/mg, 7.3 ± 2.5 mM and 76.1 ± 3.1 U/mg, and 7.2 ± 3.8 mM and 87.3 ± 1.1 U/mg, respectively. GABA was produced using whole cell transformation of the recombinant strains E. coli BL21(DE3)‐Gad B, E. coli BL21(DE3)‐Gad B‐T62S, and E. coli BL21(DE3)‐Gad B‐Q309A. The corresponding GABA concentrations in the fermentation broth were 219.09, 238.42, and 276.66 g/L, and the transformation rates were 78.02%, 85.04%, and 98.58%, respectively. |
format | Online Article Text |
id | pubmed-10071571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100715712023-04-05 Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli Fengmin, Liu Heng, Zhang Xiangjun, Zhang Xiaobo, Wei Huiyan, Liu Haitian, Fang Eng Life Sci Research Articles γ‐Aminobutyric acid (GABA) is a kind of non‐proteinogenic amino acid which is highly soluble in water and widely used in the food and pharmaceutical industries. Enzymatic conversion is an efficient method to produce GABA, whereby glutamic acid decarboxylase (GAD) is the key enzyme that catalyzes the process. The activity of wild‐type GAD is usually limited by temperature, pH or biotin concentration, and hence directional modification is applied to improve its catalytic properties and practical application. GABA was produced using whole cell transformation of the recombinant strains Escherichia coli BL21(DE3)‐Gad B, E. coli BL21(DE3)‐Gad B‐T62S and E. coli BL21(DE3)‐Gad B‐Q309A. The corresponding GABA concentrations in the fermentation broth were 219.09, 238.42, and 276.66 g/L, and the transformation rates were 78.02%, 85.04%, and 98.58%, respectively. The results showed that Gad B‐T62S and Gad B‐Q309A are two effective mutation sites. These findings may contribute to ideas for constructing potent recombinant strains for GABA production. Practical Application : Enzymatic properties of the GAD from Escherichia coli and GAD site‐specific mutants were examined by analyzing their conserved sequences, substrate contacts, contact between GAD amino acid residues and mutation energy (ΔΔG) of the GAD mutants. The enzyme activity and stability of Gad B‐T62S and Gad B‐Q309A mutants were improved compared to Gad B. The kinetic parameters K(m) and V(max) of Gad B, Gad B‐T62S, and Gad B‐Q309A mutants were 11.3 ± 2.1 mM and 32.1 ± 2.4 U/mg, 7.3 ± 2.5 mM and 76.1 ± 3.1 U/mg, and 7.2 ± 3.8 mM and 87.3 ± 1.1 U/mg, respectively. GABA was produced using whole cell transformation of the recombinant strains E. coli BL21(DE3)‐Gad B, E. coli BL21(DE3)‐Gad B‐T62S, and E. coli BL21(DE3)‐Gad B‐Q309A. The corresponding GABA concentrations in the fermentation broth were 219.09, 238.42, and 276.66 g/L, and the transformation rates were 78.02%, 85.04%, and 98.58%, respectively. John Wiley and Sons Inc. 2023-03-09 /pmc/articles/PMC10071571/ /pubmed/37025190 http://dx.doi.org/10.1002/elsc.202200064 Text en © 2023 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Fengmin, Liu Heng, Zhang Xiangjun, Zhang Xiaobo, Wei Huiyan, Liu Haitian, Fang Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli |
title | Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli
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title_full | Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli
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title_fullStr | Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli
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title_full_unstemmed | Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli
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title_short | Site‐directed mutagenesis improves the practical application of L‐glutamic acid decarboxylase in Escherichia coli
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title_sort | site‐directed mutagenesis improves the practical application of l‐glutamic acid decarboxylase in escherichia coli |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071571/ https://www.ncbi.nlm.nih.gov/pubmed/37025190 http://dx.doi.org/10.1002/elsc.202200064 |
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