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Synthesis of versatile neuromodulatory molecules by a gut microbial glutamate decarboxylase.
Dadi, Pavani; Pauling, Clint W; Shrivastava, Abhishek; Shah, Dhara D.
Afiliação
  • Dadi P; Biodesign Center for Fundamental and Applied Microbiomics, Arizona State University, Tempe, AZ 85281.
  • Pauling CW; School of Life Sciences, Arizona State University, Tempe, AZ 85281.
  • Shrivastava A; Biodesign Center for Fundamental and Applied Microbiomics, Arizona State University, Tempe, AZ 85281.
  • Shah DD; School of Mathematical and Natural Sciences, Arizona State University, Glendale, AZ 85306.
bioRxiv ; 2024 Jun 14.
Article em En | MEDLINE | ID: mdl-38915512
ABSTRACT
Dysbiosis of the microbiome correlates with many neurological disorders, yet very little is known about the chemistry that controls the production of neuromodulatory molecules by gut microbes. Here, we found that an enzyme glutamate decarboxylase (BfGAD) of a gut microbe Bacteroides fragilis forms multiple neuromodulatory molecules such as γ-aminobutyric acid (GABA), hypotaurine, taurine, homotaurine, and ß-alanine. We evolved BfGAD and doubled its taurine productivity. Additionally, we increased its specificity towards the substrate L-glutamate. Here, we provide a chemical strategy via which the BfGAD activity could be fine-tuned. In future, this strategy could be used to modulate the production of neuromodulatory molecules by gut microbes.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article