Díaz S, Zínker S, Ruiz-Herrera J
Departamento de Genética y Biología Molecular, Instituto Politécnico Nacional, México.
Antonie Van Leeuwenhoek. 1992 May;61(4):269-76. doi: 10.1007/BF00713935.
We performed experiments in parallel to study the rate of synthesis of cell wall polysaccharides and the activity of glycosyl transferases in Saccharomyces cerevisiae after arrest of a cdc 28 mutant in G1 phase by either addition of alpha-factor or transfer to the non-permissive temperature. Both effectors brought about similar time-dependent increases in the rate of synthesis and deposition of the cell wall polysaccharides chitin, glucan and mannan. These changes in cell wall composition were accompanied by an increase in the specific activities of glucan and chitin synthetases. This increase was inhibited by cycloheximide suggesting that it represented de novo enzyme biosynthesis and not enzyme activation. Our data are consistent with the notion that both alpha-factor and the cdc 28 mutation affect the same stage-specific function that controls the temporal expression of glycosyl transferases.
我们进行了平行实验,以研究通过添加α因子或转移至非允许温度使cdc 28突变体在G1期停滞之后,酿酒酵母中细胞壁多糖的合成速率和糖基转移酶的活性。两种效应物均使细胞壁多糖几丁质、葡聚糖和甘露聚糖的合成和沉积速率随时间产生相似的增加。细胞壁组成的这些变化伴随着葡聚糖合成酶和几丁质合成酶比活性的增加。这种增加被环己酰亚胺抑制,表明它代表从头酶生物合成而非酶激活。我们的数据与以下观点一致,即α因子和cdc 28突变均影响控制糖基转移酶瞬时表达的相同阶段特异性功能。