Hauke Smidt
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Articles (14)
Year:
2024
Gut bacteria hold the potential to produce a broad range of metabolites that can modulate human functions, including molecules with neuroactive potential. One such molecule is γ-aminobutyric acid (GABA), the main inhibitory neurotransmitter of the central nervous system in animals. Metagenomic analyses suggest that the genomes of many gut bacteria encode glutamate decarboxylase (GAD), the enzyme that catalyzes GABA production. The genome of Akkermansia muciniphila , a mucin specialist and potential next-generation probiotic from the human gut, is predicted to encode GAD, suggesting a contributing role in GABA production in the human gut. In this study, A. muciniphila was grown in batch cultures with and without pH control. In both experiments, A. muciniphila was found to produce GABA as a response to acid (pH <5.5), although only when GABA precursors, either glutamate or glutamine, were present in the medium. Proteomic analysis comparing A. muciniphila grown with and without precursors at pH 4 did not show a difference in GAD expression, suggesting that it is expressed regardless of the presence of GABA precursors. To further investigate the function of A. muciniphila GAD, we heterologously expressed the gad gene (encoded by locus tag Amuc_0372) with a His tag in Escherichia coli and purified the GAD protein. Enzyme assays showed GAD activity in a pH range between 4 and 6, with the highest specific activity at pH 5 of 144 ± 16 µM GABA/min/mg. Overall, our results demonstrate the ability of A. muciniphila to produce GABA as an acid response and unravel the conditions under which GABA production in A. muciniphila occurs. IMPORTANCE Akkermansia muciniphila is considered to be a beneficial bacterium from the human gut, but the exact mechanisms by which A. muciniphila influences its host are not yet fully understood. To this end, it is important to identify which metabolites are produced and consumed by A. muciniphila that may contribute to a healthy gut. In the present study, we demonstrate the ability of A. muciniphila to produce γ-aminobutyric acid (GABA) when grown in an acidic environment, which often occurs in the gut. GABA is the major inhibitory neurotransmitter in the central nervous system and is present in the human gut. For this reason, it is considered an important bacterial metabolite. Our finding that A. muciniphila produces GABA in acidic environments adds to the growing body of understanding of its relationship with host health and provides an explanation on how it can survive acid stress in the human gut.
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2024
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2024
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2024
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2023
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2023
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2023
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2023
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2023
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2022
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2022
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2022
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2022
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2022
Collaborators (20)
Marie-Luise Puhlmann
Wageningen University & Research
Willem M. de Vos
-
Carel Thijs
University of Maastricht
Thijs J G Ettema
Wageningen University & Research
William Scott
Research Assistant Professor
Purdue University
Clara Belzer
-
Detmer Sipkema
Wageningen University & Research
Burak Avcı
Aarhus University
Maurizio Battino
-
Carolina de Weerth
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Marco Ventura
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Merve Atasoy
KTH Royal Institute of Technology
Erwin G. Zoetendal
-
Yuxin Wang
Rijksuniversiteit Groningen Faculty of Science and Engineering
Jasper Jan Koehorst
Wageningen University & Research
Christian Milani
University of Parma
Robert Brummer
Professor at Örebro University
Örebro university
John Penders
Associate professor
University of Maastricht
Henk A. Schols
Wageningen University & Research
David Barnett
University of Maastricht
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