Joho M, Yamanaka C, Murayama T
Microbios. 1986;45(184-185):169-79.
The Cd2+ accommodation mechanism of S. cerevisiae has been examined. In a synthetic medium containing 1 microM CdSO4, cell proliferation was observed following a time lag period of approximately 18 h. During the time lag period, the cell number and viable cell count did not change and the cells did not excrete organic acid as a Cd-chelator, neither did they produce inorganic sulphide in the form of CdS. Whereas approximately 30% of Cd2+ taken up by Cd-accommodated cells was distributed in the cytosol, only a small percentage of Cd2+ was found in the cytosol of unaccommodated cells following 1 h incubation in 1 microM Cd-medium. Furthermore, some Cd2+ in the soluble fraction from Cd-accommodated cells was bound to low molecular weight (less than 30,000) protein(s), while unaccommodated cells only contained small amounts of these proteins. Therefore, it is proposed that Cd2+ binds to the low molecular weight protein(s) present in the cytosol, resulting in a decrease of Cd-toxicity, although the exact mechanism of accommodation is not clear.
已经对酿酒酵母的Cd2+容纳机制进行了研究。在含有1 microM CdSO4的合成培养基中,经过约18小时的延迟期后观察到细胞增殖。在延迟期内,细胞数量和活细胞计数没有变化,细胞既没有分泌作为Cd螯合剂的有机酸,也没有产生CdS形式的无机硫化物。虽然被Cd容纳的细胞摄取的Cd2+中约30%分布在细胞质中,但在1 microM Cd培养基中孵育1小时后,未被容纳的细胞的细胞质中仅发现少量Cd2+。此外,来自被Cd容纳的细胞的可溶部分中的一些Cd2+与低分子量(小于30,000)蛋白质结合,而未被容纳的细胞仅含有少量这些蛋白质。因此,有人提出Cd2+与细胞质中存在的低分子量蛋白质结合,导致Cd毒性降低,尽管确切的容纳机制尚不清楚。