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质子动力可能促使K⁺积累进入代谢中的酵母。在根据四苯基鏻分布计算酵母膜电位时需应用结合校正。

Possible energization of K+ accumulation into metabolizing yeast by the protonmotive force. Binding correction to be applied in the calculation of the yeast membrane potential from tetraphenylphosphonium distribution.

作者信息

Boxman A W, Dobbelmann J, Borst-Pauwels G W

出版信息

Biochim Biophys Acta. 1984 Apr 25;772(1):51-7. doi: 10.1016/0005-2736(84)90516-9.

Abstract

Membrane potentials of yeast cells, Saccharomyces cerevisiae, calculated from the equilibrium distribution of tetraphenylphosphonium (TPP) between cell-water and medium should be corrected for a contribution due to binding of TPP to intracellular constituents. The magnitude of this correction depends upon the way in which it is determined. In cells permeabilized by boiling, cell-binding is much higher than in cells permeabilized by repeated freezing and thawing. The binding corrections are 75 +/- 1 mV and 49 +/- 7 mV, respectively. The binding correction obtained from TPP distribution between deenergized cells and medium is much lower and amounts to 19 +/- 9 mV. The latter value is probably more reliable. It is supposed that permeabilization of the cells by boiling or repeated freezing and thawing unmasks potential TPP binding groups in the cell. The K+ accumulation into anaerobically metabolizing yeast cells can be accounted for almost quantitatively by a cotransport of protons and K+ ions if the lower binding correction is applied. This means that K+ accumulation into the yeast cell may be driven by the sum of the protonmotive force and the membrane potential.

摘要

根据四苯基鏻(TPP)在细胞内水相和培养基之间的平衡分布计算出的酿酒酵母细胞的膜电位,应针对TPP与细胞内成分结合所产生的影响进行校正。这种校正的幅度取决于其测定方式。在经煮沸通透处理的细胞中,细胞结合力远高于经反复冻融通透处理的细胞。结合校正值分别为75±1 mV和49±7 mV。通过去能细胞与培养基之间的TPP分布获得的结合校正值要低得多,为19±9 mV。后一个值可能更可靠。据推测,通过煮沸或反复冻融使细胞通透会使细胞中潜在的TPP结合基团暴露出来。如果采用较低的结合校正值,质子和钾离子的共转运几乎可以定量地解释厌氧代谢的酵母细胞中钾离子的积累。这意味着酵母细胞中钾离子的积累可能由质子动力和膜电位的总和驱动。

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