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γ-氨基丁醛脱氢酶介导的 GABA 合成在谷氨酸脱羧酶和α-酮戊二酸脱羧酶基因敲除的集胞藻 PCC6803 中的作用。

GABA synthesis mediated by γ-aminobutanal dehydrogenase in Synechocystis sp. PCC6803 with disrupted glutamate and α-ketoglutarate decarboxylase genes.

机构信息

Laboratory of Cyanobacterial Biotechnology, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.

Laboratory of Cyanobacterial Biotechnology, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand; Academy of Science, Royal Society of Thailand, Bangkok 10300, Thailand.

出版信息

Plant Sci. 2020 Jan;290:110287. doi: 10.1016/j.plantsci.2019.110287. Epub 2019 Sep 27.

DOI:10.1016/j.plantsci.2019.110287
PMID:31779897
Abstract

A pathway for polyamine-derived GABA synthesis in Synechocystis sp. PCC 6803 was explored by disrupting both the glutamate decarboxylase and α-ketoglutarate decarboxylase genes. The generated Δgad:Δkgd strain had increased intracellular α-ketoglutarate and polyamine levels compared to the wild type. Gene transcript analysis using RT-PCR indicated that the Δgad:Δkgd strain had up-regulated expression of a putative gadbh whose gene product, γ-aminobutanal dehydrogenase, would catalyze the conversion of γ-aminobutanal to GABA. A strain with disrupted gabdh showed an increase in GABA, glutamate, succinate and spermidine levels. These findings provide evidence for a link between spermidine degradation and GABA synthesis in cyanobacteria. This study highlights the role of γ-aminobutanal dehydrogenase in maintaining an intact tricarboxylic acid cycle in Synechocystis.

摘要

通过敲除谷氨酸脱羧酶和α-酮戊二酸脱羧酶基因,探索了集胞藻 PCC 6803 中多胺衍生 GABA 合成的途径。与野生型相比,生成的Δgad:Δkgd 菌株具有更高的细胞内α-酮戊二酸和多胺水平。使用 RT-PCR 的基因转录分析表明,Δgad:Δkgd 菌株上调了一个假定的 gadbh 的表达,其基因产物γ-氨基丁醛脱氢酶将催化γ-氨基丁醛转化为 GABA。具有gabdh 缺失的菌株 GABA、谷氨酸、琥珀酸和亚精胺水平增加。这些发现为蓝藻中多胺降解与 GABA 合成之间的联系提供了证据。本研究强调了γ-氨基丁醛脱氢酶在维持集胞藻完整三羧酸循环中的作用。

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