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Demonstration of high-affinity Mn2+ uptake in Saccharomyces cerevisiae: specificity and kinetics

机译:高亲和力MN2 +酿酒酵母中的高亲和力MN2 +摄取的演示:特异性和动力学

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The existence of multiple transport systems for Mn2+ in Saccharomyces cerevisiae has been demonstrated in this study. Mn2+ (supplied as MnCI2) was accumulated by S. cerevisiae at all Mn2+ concentrations examined (25 nM-1 mM) but a log-log plot of uptake rates and total amounts accumulated revealed the existence of at least two Mn2+ concentration-dependent transport systems. Over a low Mn2+ concentration range (25-1000 nM), high-affinity Mn2+ uptake occurred with a Km value of 0.3 μM, while transformation of kinetic data obtained over the concentration range 5-200 μM revealed another system with a Km of 62 μM. Meaningful kinetic analyses were not possible at higher Mn2+ concentrations because of toxicity: only about 30% of cells remained viable after 30 min incubation with 1000 μM MnCI2. Release of K+ accompanied Mn2+ accumulation and this increased with increasing Mn2+ concentration. However, even in non-toxic Mn2+ concentrations, the ratio of Mn2+ uptake to K+ release greatly exceeded electroneutral stoichiometric exchange. In 50 μM MnCI2, the ratio was 1: 123 and this increased to 1:2670 in 1000 μM MnCI2, a toxic concentration. External Mg2+ was found to decrease Mn2+ accumulation at all concentrations examined, but to differing extents. Over the low Mn2+ concentration range (5-200 μM), Mg2+ competitively inhibited Mn2+ uptake with a half-maximal inhibitory concentration, Ki, of 5.5 μM Mg2+. However, even in the presence of a 50-fold excess of Mg2+, inhibition of Mn2+ uptake was of the order of 72% and it appears that the cellular requirement for Mn2+ could be maintained even in the presence of such a large excess of Mg2+. Over the high Mn2+ concentration range (5-200 μM), the Ki for Mg2+ was 25.2 μM. At low Mn2+ concentrations, Zn2+ and Co2+, but not Cd2+, inhibited Mn2+ uptake, which indicated that the high-affinity Mn2+ uptake system was of low specificity, while at higher Mn2+ concentrations, where the lower-affinity Mn2+ transport system operated, inhibition was less marked. However, competition studies with potentially toxic metal cations were complicated due to toxic effects, particularly noticeable at 50 μM Co2+ and Cd2+.
机译:本研究已经证明了酿酒酵母酿酒酵母中MN2 +的多种运输系统的存在。 Mn2 +(提供为MnCl 2),在所有Mn2 +浓度(25nm-1mm)的所有Mn2 +浓度下累积,但累计的注射率和总量的对数曲线曲线表明存在至少两个Mn2 +浓度依赖的运输系统。在低Mn2 +浓度范围(25-1000nm)中,高亲和力Mn2 +摄取,km值为0.3μm,同时在浓度范围内获得的动力学数据的转化显示为千克62μm的另一个系统。由于毒性,在较高的MN2 +浓度下不可能有意义的动力学分析:30分钟孵育1000μmMNCI2后,只有约30%的细胞保持可行。释放k +伴随的Mn2 +积累,随着Mn2 +浓度的增加而增加。然而,即使在无毒的MN2 +浓度下,MN2 +摄取与K +释放的比例大大超过了电力化学计量交换。在50μMMNCl2中,该比例为1:123,这增加至1000μmmNCI2,毒性浓度增加至1:2670。发现外部Mg2 +在检查的所有浓度下降低Mn2 +积累,而是对不同的范围。在低Mn2 +浓度范围内(5-20​​0μm),Mg2 +竞争性地抑制Mn2 +摄取,半最大抑制浓度Ki为5.5μmmg2+。然而,即使在50倍过量的mg2 +存在下,Mn2 +摄取的抑制均为72%,似乎即使在这种大量过量的Mg 2 +存在下也可以保持Mn2 +的细胞要求。在高Mn2 +浓度范围(5-20​​0μm)上,Mg2 +的Ki为25.2μm。在低Mn2 +浓度下,Zn2 +和CO 2 +,但不是CD2 +,抑制Mn2 +摄取,表明高亲和力Mn2 +摄取系统具有低特异性,而在较高的Mn2 +浓度下,其中下亲和Mn2 +运输系统操作,抑制是较少标记。然而,由于毒性效应,具有潜在有毒金属阳离子的竞争研究复杂,特别是在50μmCO2+和CD2 +中特别明显。

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