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本文引用的文献

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Exchange of aspartate and alanine. Mechanism for development of a proton-motive force in bacteria.天冬氨酸与丙氨酸的交换。细菌中质子动力产生的机制。
J Biol Chem. 1996 Feb 9;271(6):3079-84. doi: 10.1074/jbc.271.6.3079.
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Generation of a proton motive force by histidine decarboxylation and electrogenic histidine/histamine antiport in Lactobacillus buchneri.嗜布氏乳杆菌中通过组氨酸脱羧作用和生电型组氨酸/组胺反向转运产生质子动力势。
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Oxalobacter formigenes gen. nov., sp. nov.: oxalate-degrading anaerobes that inhabit the gastrointestinal tract.产甲酸草酸杆菌属,新属,新种:栖息于胃肠道的草酸降解厌氧菌。
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Oxalate:formate exchange. The basis for energy coupling in Oxalobacter.草酸盐:甲酸盐交换。草酸杆菌中能量偶联的基础。
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Purification and characterization of oxalyl-coenzyme A decarboxylase from Oxalobacter formigenes.产甲酸草酸杆菌中草酰辅酶A脱羧酶的纯化及特性研究
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一株乳酸杆菌中谷氨酸和γ-氨基丁酸的交换

Exchange of glutamate and gamma-aminobutyrate in a Lactobacillus strain.

作者信息

Higuchi T, Hayashi H, Abe K

机构信息

Soy Sauce Research Laboratory, R & D Division of Kikkoman Corporation, Noda City, Chiba, Japan.

出版信息

J Bacteriol. 1997 May;179(10):3362-4. doi: 10.1128/jb.179.10.3362-3364.1997.

DOI:10.1128/jb.179.10.3362-3364.1997
PMID:9150237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC179120/
Abstract

Lactobacillus sp. strain E1 catalyzed the decarboxylation of glutamate (Glu), resulting in a nearly stoichiometric release of the products gamma-aminobutyrate (GABA) and CO2. This decarboxylation was associated with the net synthesis of ATP. ATP synthesis was inhibited almost completely by nigericin and about 70% by N,N'-dicyclohexylcarbodiimide (DCCD), without inhibition of the decarboxylation. These findings are consistent with the possibility that a proton motive force arises from the cytoplasmic proton consumption that accompanies glutamate decarboxylation and the electrogenic Glu/GABA antiporter and the possibility that this proton motive force is coupled with ATP synthesis by DCCD-sensitive ATPase.

摘要

乳酸杆菌属菌株E1催化谷氨酸(Glu)的脱羧反应,几乎化学计量地释放出产物γ-氨基丁酸(GABA)和二氧化碳。这种脱羧反应与ATP的净合成相关。尼日利亚菌素几乎完全抑制ATP合成,N,N'-二环己基碳二亚胺(DCCD)抑制约70%,但不抑制脱羧反应。这些发现符合以下可能性:质子动力源自谷氨酸脱羧伴随的细胞质质子消耗以及电生性的Glu/GABA反向转运体;并且这种质子动力通过对DCCD敏感的ATP酶与ATP合成相偶联。