Anraku Y, Kin E, Tanaka Y
J Biochem. 1975 Jul;78(1):165-79.
The effects of various energy poisons on oxidation of respiratory substrate, synthesis of cellular ATP, and energy transformation reaction in intact Escherichia coli cells were studied systematically. Various mutants were, therefore, used in which specific functions in the energy-transducing reactions were defective or altered. The energy poisons examined were: sodium azide. DPPA and azidebenzenes which are inhibitors of respiratory-chain phosphorylation, SF6847, and CCCP which are known to be uncouplers, zinc sulfate which is an inhibitor for certain dehydrogenases, and sodium arsenate and sodium fluoride which are inhibitors of glycolytic synthesis of ATP. The preferential inhibitions occurred in the oxidation reactions with certain respiratory substrates by energy poisons used. DPPA inhibited glycerol oxidation much more strongly than succinate oxidation. However, DPPA could inhibit the oxidation of both glycerol 3-phosphate and succinate by membrane fraction strongly while the oxidation of NADH and D-lactate slightly. It inhibited glycerol 3-phosphate dehydrogenase [EC 1.1.2.1] strongly as well as succinate dehydrogenase [EC 1.3.99.1],.but not D-lactate dehydrogenase of membrane fraction. MAB and other azidebenzene derivatives inhibited succinate oxidation preferentially. SF6847 and CCCP inhibited succinate oxidation strongly, while sodium azide inhibited it weakly and these three poisons were less inhibitory for glycerol oxidation. DPPA, sodium azide, SF6847, and CCCP inhibited the synthesis of ATP coupled with respiration but not with glycolysis. Zinc sulfate inhibited the cellular ATP synthesis coupled with either respiration or glycolysis.
系统研究了各种能量毒物对完整大肠杆菌细胞中呼吸底物氧化、细胞ATP合成及能量转化反应的影响。因此,使用了各种突变体,这些突变体在能量转导反应中的特定功能存在缺陷或改变。所检测的能量毒物有:叠氮化钠、二苯基磷酸酯(DPPA)和叠氮苯,它们是呼吸链磷酸化的抑制剂;SF6847和羰基氰间氯苯腙(CCCP),已知它们是解偶联剂;硫酸锌,是某些脱氢酶的抑制剂;以及砷酸钠和氟化钠,它们是糖酵解ATP合成的抑制剂。所使用的能量毒物在与某些呼吸底物的氧化反应中表现出优先抑制作用。DPPA对甘油氧化的抑制作用比对琥珀酸氧化的抑制作用要强得多。然而,DPPA能强烈抑制膜组分对3-磷酸甘油和琥珀酸的氧化,而对NADH和D-乳酸的氧化抑制作用较弱。它强烈抑制3-磷酸甘油脱氢酶[EC 1.1.2.1]以及琥珀酸脱氢酶[EC 1.3.99.1],但不抑制膜组分的D-乳酸脱氢酶。MAB和其他叠氮苯衍生物优先抑制琥珀酸氧化。SF6847和CCCP强烈抑制琥珀酸氧化,而叠氮化钠对其抑制作用较弱,这三种毒物对甘油氧化的抑制作用较小。DPPA、叠氮化钠、SF6847和CCCP抑制与呼吸偶联的ATP合成,但不抑制与糖酵解偶联的ATP合成。硫酸锌抑制与呼吸或糖酵解偶联的细胞ATP合成。