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首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >EVIDENCE FOR TRANSMEMBRANE ELECTRON TRANSFER COUPLED TO PROTON SECRETION IN PLASMA MEMBRANE VESICLES LOADED BY ELECTROPORATION
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EVIDENCE FOR TRANSMEMBRANE ELECTRON TRANSFER COUPLED TO PROTON SECRETION IN PLASMA MEMBRANE VESICLES LOADED BY ELECTROPORATION

机译:静电加载等离子体膜囊中质子分泌的跨膜电子转移证据

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We demonstrate an in vitro trans plasma membrane electron transport from an encapsulated nucleotide to an external electron acceptor. Right-side-out vesicles prepared from soybean hypocotyls by aqueous two-phase partitioning were loaded with NADH by electroporation. Absence of calcium ions and an electric field strength of over 2 kV/cm was necessary for opening of the vesicles and importation of NADH. The presence of calcium ions was necessary for vesicle sealing. External NADH was removed with oxalacetate and malate dehydrogenase. If an impermeable electron acceptor was added to the exterior of the sealed vesicles, the oxidation of encapsulated NADH was increased, indicating a transmembrane electron transfer from an internal e(-) donor to the external e(-) acceptor analogous to that observed with intact cells. The ratio of NADH oxidized to hexacyanoferrat III reduced was 0.67. This indicates that NADH oxidation with oxygen as acceptor still occurred. Oxidation of the internal NADH was not affected by actinomycin D. Inhibition was also observed by the auxin 2,4-D, but by the inactive analog 2,3-D too. Oxidation of internal NADH both in absence and presence of the external acceptor, HCF III, showed a rapid decline in activity, which is relieved by the detergent Triton X-100, or the protonophore FCCP. Maximum NADH oxidation both with and without HCF III required an internal acidic pH gradient across the vesicle membrane. The results are consistent with a proton-gradient driving transplasma membrane NADH dehydrogenase which can transfer electrons to oxygen or an external impermeable oxidant. [References: 52]
机译:我们证明了体外反式质膜电子运输从封装的核苷酸到外部电子受体。由大豆下胚轴通过水两相分配制备的右侧出囊泡通过电穿孔加载NADH。缺少钙离子和超过2 kV / cm的电场强度对于打开囊泡和导入NADH是必要的。钙离子的存在对于囊泡密封是必要的。用草酰乙酸和苹果酸脱氢酶除去外部NADH。如果将不可渗透的电子受体添加到密封囊泡的外部,则封装的NADH的氧化会增加,这表明跨膜电子从内部e(-)供体到外部e(-)受体的转移类似于完整观察到的转移。细胞。氧化的NADH与还原的六氰基铁酸酯的比例为0.67。这表明仍然发生了用氧作为受体的NADH氧化。内部NADH的氧化不受放线菌素D的影响。生长素2,4-D也被抑制,但无活性的类似物2,3-D也被抑制。在不存在和存在外部受体HCF III的情况下,内部NADH的氧化均显示出活性的快速下降,这可以通过去污剂Triton X-100或质子载体FCCP缓解。在有和没有HCF III的情况下,最大的NADH氧化都需要整个囊泡膜的内部酸性pH梯度。结果与质子梯度驱动质膜NADH脱氢酶一致,后者可以将电子转移到氧气或外部不可渗透的氧化剂上。 [参考:52]

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