Department of Microbiology and Immunology, Emory University School of Medicine, 1510 Clifton Road, RRC 3070, Atlanta, GA 30322, United States.
Department of Biology, Eastern Washington University, 1175 Washington St. Science 226, Cheney, WA 99004, United States.
Lett Appl Microbiol. 2024 Jun 3;77(6). doi: 10.1093/lambio/ovae051.
γ-Aminobutyric acid (GABA) is an inhibitory neurotransmitter of the central nervous system that impacts physical and mental health. Low GABA levels have been documented in several diseases, including multiple sclerosis and depression, and studies suggest that GABA could improve disease outcomes in those conditions. Probiotic bacteria naturally produce GABA and have been engineered to enhance its synthesis. Strains engineered thus far use inducible expression systems that require the addition of exogenous molecules, which complicates their development as therapeutics. This study aimed to overcome this challenge by engineering Lactococcus lactis with a constitutive GABA synthesis gene cassette. GABA synthesizing and transport genes (gadB and gadC) were cloned onto plasmids downstream of constitutive L. lactis promoters [P2, P5, shortened P8 (P8s)] of different strengths and transformed into L. lactis. Fold increase in gadCB expression conferred by these promoters (P2, P5, and P8s) was 322, 422, and 627, respectively, compared to the unmodified strain (P = 0.0325, P8s). GABA synthesis in the highest gadCB expressing strain, L. lactis-P8s-glutamic acid decarboxylase (GAD), was dependent on media supplementation with glutamic acid and significantly higher than the unmodified strain (P < 0.0001, 125 mM, 200 mM glutamic acid). Lactococcus lactis-P8s-GAD is poised for therapeutic testing in animal models of low-GABA-associated disease.
γ-氨基丁酸(GABA)是中枢神经系统的抑制性神经递质,影响身心健康。几种疾病中都记录到 GABA 水平降低,包括多发性硬化症和抑郁症,研究表明 GABA 可以改善这些疾病的预后。益生菌自然产生 GABA,并且已经被设计来增强其合成。迄今为止,用于工程改造的菌株使用诱导表达系统,需要添加外源分子,这使它们作为治疗剂的开发复杂化。本研究旨在通过用组成型 GABA 合成基因盒工程改造乳酸乳球菌来克服这一挑战。GABA 合成和转运基因(gadB 和 gadC)被克隆到质粒上,位于不同强度的组成型乳球菌启动子(P2、P5、缩短的 P8(P8s))的下游,并转化为乳酸乳球菌。与未修饰的菌株相比,这些启动子(P2、P5 和 P8s)赋予 gadCB 表达的倍数增加分别为 322、422 和 627(P = 0.0325,P8s)。在表达最高 gadCB 的菌株,即乳酸乳球菌-P8s-谷氨酸脱羧酶(GAD)中,GABA 的合成依赖于培养基中谷氨酸的补充,并且明显高于未修饰的菌株(P < 0.0001,125 mM、200 mM 谷氨酸)。Lactococcus lactis-P8s-GAD 有望在与 GABA 水平降低相关的疾病动物模型中进行治疗测试。