细胞外
谷氨酸脱羧酶
谷氨酸受体
细胞内
单核细胞增生李斯特菌
流出
生物化学
生物
细胞质
细胞内pH值
化学
微生物学
细菌
酶
遗传学
受体
作者
Kimon Andreas Karatzas,Orla M. Brennan,Sinéad Heavin,John P. Morrissey,Conor P. O’Byrne
摘要
ABSTRACT It is well established that the glutamate decarboxylase (GAD) system is central to the survival of Listeria monocytogenes at low pH, both in acidic foods and within the mammalian stomach. The accepted model proposes that under acidic conditions extracellular glutamate is transported into the cell in exchange for an intracellular γ-aminobutyrate (GABA i ). The glutamate is then decarboxylated to GABA i , a reaction that consumes a proton, thereby helping to prevent acidification of the cytoplasm. In this study, we show that glutamate supplementation had no influence on either growth rate at pH 5.0 or survival at pH 2.5 when L. monocytogenes 10403S was grown in a chemically defined medium (DM). In response to acidification, cells grown in DM failed to efflux GABA, even when glutamate was added to the medium. In contrast, in brain heart infusion (BHI), the same strain produced significant extracellular GABA (GABA e ) in response to acidification. In addition, high levels of GABA i (>80 mM) were found in the cytoplasm in response to low pH in both growth media. Medium-swap and medium-mixing experiments revealed that the GABA efflux apparatus was nonfunctional in DM, even when glutamate was present. It was also found that the GadT2D2 antiporter/decarboxylase system was transcribed poorly in DM-grown cultures while overexpression of gadD1T1 and gadD3 occurred in response to pH 3.5. Interestingly, BHI-grown cells did not respond with upregulation of any of the GAD system genes when challenged at pH 3.5. The accumulation of GABA i in cells grown in DM in the absence of extracellular glutamate indicates that intracellular glutamate is the source of the GABA i . These results demonstrate that GABA production can be uncoupled from GABA efflux, a finding that alters the way we should view the operation of bacterial GAD systems.
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