Cardinali G, Vollenbroich V, Jeon M S, de Graaf A A, Hollenberg C P
Institut für Mikrobiologie, Heinrich Heine Universität Düsseldorf, Germany.
Mol Cell Biol. 1997 Mar;17(3):1722-30. doi: 10.1128/MCB.17.3.1722.
The induction process of the galactose regulon has been intensively studied, but until now the nature of the inducer has remained unknown. We have analyzed a delta gal7 mutant of the yeast Kluyveromyces lactis, which lacks the galactotransferase activity and is able to express the genes of the Gal/Lac regulon also in the absence of galactose. We found that this expression is semiconstitutive and undergoes a strong induction during the stationary phase. The gal1-209 mutant, which has a reduced kinase activity but retains its positive regulatory function, also shows a constitutive expression of beta-galactosidase, suggesting that galactose is the inducer. A gal10 deletion in delta gal7 or gal1-209 mutants reduces the expression to under wild-type levels. The presence of the inducer could be demonstrated in both delta gal7 crude extracts and culture medium by means of a bioassay using the induction in gal1-209 cells. A mutation in the transporter gene LAC12 decreases the level of induction in gal7 cells, indicating that galactose is partly released into the medium and then retransported into the cells. Nuclear magnetic resonance analysis of crude extracts from delta gal7 cells revealed the presence of 50 microM galactose. We conclude that galactose is the inducer of the Gal/Lac regulon and is produced via UDP-galactose through a yet-unknown pathway.
半乳糖调节子的诱导过程已得到深入研究,但迄今为止,诱导剂的本质仍不清楚。我们分析了乳酸克鲁维酵母的一个Δgal7突变体,该突变体缺乏半乳糖转移酶活性,并且在没有半乳糖的情况下也能够表达Gal/Lac调节子的基因。我们发现这种表达是半组成型的,并且在稳定期会经历强烈的诱导。gal1-209突变体的激酶活性降低但保留其正调控功能,其也显示出β-半乳糖苷酶的组成型表达,这表明半乳糖是诱导剂。在Δgal7或gal1-209突变体中缺失gal10会使表达降低至野生型水平以下。通过使用gal1-209细胞中的诱导进行生物测定,可以在Δgal7粗提物和培养基中证明诱导剂的存在。转运蛋白基因LAC12中的突变会降低gal7细胞中的诱导水平,这表明半乳糖部分释放到培养基中,然后再转运到细胞中。对Δgal7细胞粗提物的核磁共振分析揭示了存在50微摩尔的半乳糖。我们得出结论,半乳糖是Gal/Lac调节子的诱导剂,并且是通过UDP-半乳糖经由一条未知途径产生的。