Scherrer R, Louden L, Gerhardt P
J Bacteriol. 1974 May;118(2):534-40. doi: 10.1128/jb.118.2.534-540.1974.
The limiting sizes of molecules that can permeate the intact cell wall and protoplast membrane of Saccharomyces cerevisiae were determined from the inflection points in a triphasic pattern of passive equilibrium uptake values obtained with a series of inert probing molecules varying in molecular size. In the phase identified with the yeast protoplast, the uptake-exclusion threshold corresponded to a monodisperse ethylene glycol of molecular weight = 110 and Einstein-Stokes hydrodynamic radius (r(ES)) = 0.42 nm. In the cell wall phase, the threshold corresponded to a polydisperse polyethylene glycol of number-average molecular weight ( M(n)) = 620 and average radius (r(ES)) = 0.81 nm. The third phase corresponded to complete exclusion of larger molecules. The assessment of cell wall porosity was confirmed by use of a second method involving analytical gel chromatographic analyses of the molecular weight distribution for a single polydisperse polyglycol before and after uptake by the cells, which indicated a quasi-monodisperse threshold for the cell wall of M(n) = 760 and r(ES) = 0.89 nm. The results were reconciled with two situations in which much larger protein molecules previously have been reported able to penetrate the yeast cell wall.
通过一系列分子大小各异的惰性探测分子被动平衡摄取值的三相模式中的拐点,确定了能够穿透酿酒酵母完整细胞壁和原生质体膜的分子的极限大小。在与酵母原生质体对应的相中,摄取排除阈值对应于分子量为110、爱因斯坦-斯托克斯流体动力学半径(r(ES))为0.42nm的单分散乙二醇。在细胞壁相中,阈值对应于数均分子量(M(n))为620、平均半径(r(ES))为0.81nm的多分散聚乙二醇。第三相对应于更大分子的完全排除。通过使用第二种方法证实了对细胞壁孔隙率的评估,该方法涉及对细胞摄取前后单一多分散聚乙二醇的分子量分布进行分析凝胶色谱分析,结果表明细胞壁的准单分散阈值为M(n)=760和r(ES)=0.89nm。这些结果与之前报道的两种情况相协调,即更大的蛋白质分子能够穿透酵母细胞壁。