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钠负荷酵母中的钠转运与磷代谢:体内用钠-23和磷-31核磁共振波谱法同步观察

Sodium transport and phosphorus metabolism in sodium-loaded yeast: simultaneous observation with sodium-23 and phosphorus-31 NMR spectroscopy in vivo.

作者信息

Höfeler H, Jensen D, Pike M M, Delayre J L, Cirillo V P, Springer C S, Fossel E T, Balschi J A

机构信息

NMR Laboratory, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Biochemistry. 1987 Aug 11;26(16):4953-62. doi: 10.1021/bi00390a011.

DOI:10.1021/bi00390a011
PMID:3311159
Abstract

Simultaneous 23Na and 31P NMR spectra were obtained from a number of yeast suspensions. Prior to NMR spectroscopy, the yeast cells were Na-loaded: this replaced some of the intracellular K+ with Na+. These cells were also somewhat P-deficient in that they had no polyphosphate species visible in the 31P NMR spectrum. In the NMR experiments, the Na-loaded cells were suspended in media which contained inorganic phosphate, very low Na+, and a shift reagent for the Na+ NMR signal. The media differed as to whether dioxygen, glucose, or K+ was present individually or in combinations and as to whether the medium was buffered or not. The NMR spectra revealed that the cells always lost Na+ and gained phosphorus. However, the nature of the Na+ efflux time course and the P metabolism differed depending on the medium. The Na+ efflux usually proceeded linearly until the amount of Na+ extruded roughly equalled the amount of NH4+ and orthophosphate initially present in the medium (external phosphate was added as NH4H2PO4). Thus, we presume this first phase reflects a Na+ for NH4+ exchange. The Na+ efflux then entered a transition phase, either slowing, ceasing, or transiently reversing, before resuming at about the same value as that of the first phase. We presume that this last phase involves the simultaneous extrusion of intracellular anions as reported in the literature. The phosphorus metabolism was much more varied. In the absence of exogenous glucose, the P taken up accumulated first as intracellular inorganic phosphate; otherwise, it accumulated first in the "sugar phosphate" pool. In most cases, at least some of the P left the sugar phosphate pool and entered the polyphosphate reservoir in the vacuole. However, this never happened until the phase probably representing Na+ for NH4+ exchange was completed, and the P in the polyphosphate pool never remained there permanently but always eventually reverted back to the sugar phosphate pool. These changes are interpreted in terms of hierarchical energy demands on the cells under the different conditions. In particular, the energy for the Na+ for NH4+ exchange takes precedence over that required to produce and store polyphosphate. This conclusion is supported by the fact that when the cells are "forced" to exchange K+, as well as NH4+, for Na+ (by the addition of 5 times as much K+ to the NH4+-containing medium), polyphosphates are never significantly formed, and the initial linear Na+ efflux phase persists possibly 6 times as long.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

从多个酵母悬液中获取了同时的23Na和31P核磁共振谱。在进行核磁共振光谱分析之前,对酵母细胞进行了钠加载:这用Na+取代了一些细胞内的K+。这些细胞也有点缺磷,因为在31P核磁共振谱中看不到多聚磷酸盐。在核磁共振实验中,钠加载的细胞悬浮在含有无机磷酸盐、极低Na+以及用于Na+核磁共振信号的位移试剂的培养基中。培养基的不同之处在于是否单独或组合存在氧气、葡萄糖或K+,以及培养基是否缓冲。核磁共振谱显示细胞总是失去Na+并获得磷。然而,Na+外流的时间进程和磷代谢的性质因培养基而异。Na+外流通常呈线性进行,直到挤出的Na+量大致等于培养基中最初存在的NH4+和正磷酸盐的量(外部磷酸盐以NH4H2PO4的形式添加)。因此,我们推测第一阶段反映了Na+与NH4+的交换。然后Na+外流进入一个过渡阶段,要么减慢、停止,要么短暂逆转,然后恢复到与第一阶段大致相同的值。我们推测最后一个阶段涉及如文献报道的细胞内阴离子的同时挤出。磷代谢则更为多样。在没有外源葡萄糖的情况下,摄取的磷首先作为细胞内无机磷酸盐积累;否则,它首先在“糖磷酸盐”池中积累。在大多数情况下,至少一些磷离开糖磷酸盐池并进入液泡中的多聚磷酸盐储存库。然而,直到可能代表Na+与NH4+交换的阶段完成之前,这种情况从未发生过,并且多聚磷酸盐池中的磷从未永久留在那里,而是最终总是回到糖磷酸盐池。这些变化根据不同条件下细胞的分级能量需求来解释。特别是,Na+与NH4+交换所需的能量优先于产生和储存多聚磷酸盐所需的能量。当细胞“被迫”用K+以及NH4+交换Na+(通过向含NH4+的培养基中添加5倍量的K+)时,多聚磷酸盐从未大量形成以及最初的线性Na+外流阶段可能持续6倍长的事实支持了这一结论。(摘要截断于400字)

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