Characterization of three glutamate decarboxylases from Bacillus spp. for efficient ?-aminobutyric acid production
نویسندگان
چکیده
Abstract Background Gamma-aminobutyric acid (GABA) is an important bio-product used in pharmaceuticals and functional foods as a precursor of the biodegradable plastic polyamide 4. Glutamate decarboxylase (GAD) converts l -glutamate ( -Glu) into GABA via decarboxylation. Compared with other methods, develop bioconversion platform to produce considerable interest for industrial use. Results Three GAD genes were identified from three Bacillus strains heterologously expressed Escherichia coli BL21 (DE3). The optimal reaction temperature pH values enzymes 40 °C 5.0, respectively. Of GADs, GADZ11 had highest catalytic efficiency towards -Glu (2.19 mM ? 1 s ). engineered E. strain that was whole-cell biocatalyst production GABA. After repeated use 14 times, cells produced average molar conversion rate 98.6% within h. Conclusions recombinant GADs have been conducted identification. heterologous expressing GADZ1, GADZ11, GADZ20 could accomplish biosynthesis buffer-free at high concentration. novel has potential be cost-effective biotransformation
منابع مشابه
cloning of glutamate decarboxylase and production of γ-aminobutyric acid from lactobacillus brevis
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ژورنال
عنوان ژورنال: Microbial Cell Factories
سال: 2021
ISSN: ['1475-2859']
DOI: https://doi.org/10.1186/s12934-021-01646-8