Stötzler D, Betz R, Duntze W
J Bacteriol. 1977 Oct;132(1):28-35. doi: 10.1128/jb.132.1.28-35.1977.
The biological activities of two synthetic oligopeptides (His-Trp-Leu-Gln-Leu and Trp-Leu-Gln-Leu), which represent part of the primary structure of the mating hormone alpha factor from Saccharomyces cerevisiae, were studied. The peptides did not exhibit hormonal activity by themselves. However, both intensified the mating-type-specific inhibitory effect of native alpha factor on the division of haploid cells of mating type a. Random peptides or mixtures of the corresponding amino acids did not stimulate alpha factor activity. Likewise, a synthetic peptide representing another part of the alpha factor sequence was ineffective. In addition, the activity of a factor, the mating hormone produced by a cells, was not influenced by the synthetic peptides, indicating that the compounds specifically affect the interaction between alpha factor and its target cells. The analysis of the utilization of the tetrapeptide as a source of amino acids for auxotrophic a strains suggested an extracellular site of action for the observed enhancement of alpha factor activity.
对两种合成寡肽(His-Trp-Leu-Gln-Leu和Trp-Leu-Gln-Leu)的生物活性进行了研究,这两种寡肽代表了酿酒酵母交配激素α因子一级结构的一部分。这些肽本身不表现出激素活性。然而,两者都增强了天然α因子对a型交配型单倍体细胞分裂的交配型特异性抑制作用。随机肽或相应氨基酸的混合物不会刺激α因子活性。同样,代表α因子序列另一部分的合成肽也无效。此外,a细胞产生的交配激素——一种因子的活性不受合成肽的影响,这表明这些化合物特异性地影响α因子与其靶细胞之间的相互作用。对四肽作为营养缺陷型a菌株氨基酸来源的利用分析表明,观察到的α因子活性增强作用的作用位点在细胞外。