Riou C, Nicaud J M, Barre P, Gaillardin C
Laboratoire de Microbiologie et Technologie des Fermentations, INRA-IPV, Montpellier, France.
Yeast. 1997 Aug;13(10):903-15. doi: 10.1002/(SICI)1097-0061(199708)13:10<903::AID-YEA145>3.0.CO;2-1.
Genetic engineering of wine yeast strains requires the identification of gene promoters specifically activated under wine processing conditions. In this study, transcriptional activation of specific genes was followed during the time course of wine fermentation by quantifying mRNA levels in a haploid wine strain of Saccharomyces cerevisiae grown on synthetic or natural winery musts. Northern analyses were performed using radioactive probes from 19 genes previously described as being expressed under laboratory growth conditions or on molasses in S. cerevisiae during the stationary phase and/or under nitrogen starvation. Nine genes, including members of the HSP family, showed a transition-phase induction profile. For three of them, mRNA transcripts could be detected until the end of the fermentation. Expression of one of these genes, HSP30, was further studied using a HSP30::lacZ fusion on both multicopy and monocopy expression vectors. The production of beta-galactosidase by recombinant cells was measured during cell growth and fermentation on synthetic and natural winery musts. We showed that the HSP30 promoter can induce high gene expression during late stationary phase and remains active until the end of the wine fermentation process. Similar expression profiles were obtained on five natural winery musts.
葡萄酒酵母菌株的基因工程需要鉴定在葡萄酒酿造条件下特异性激活的基因启动子。在本研究中,通过定量在合成或天然酒厂葡萄汁上生长的酿酒酵母单倍体葡萄酒菌株中的mRNA水平,跟踪葡萄酒发酵过程中特定基因的转录激活。使用来自19个基因的放射性探针进行Northern分析,这些基因先前被描述为在实验室生长条件下或在酿酒酵母的静止期和/或氮饥饿期间在糖蜜上表达。包括热休克蛋白(HSP)家族成员在内的9个基因显示出过渡阶段诱导模式。其中3个基因的mRNA转录本在发酵结束前都能检测到。使用多拷贝和单拷贝表达载体上的HSP30::lacZ融合进一步研究了其中一个基因HSP30的表达。在合成和天然酒厂葡萄汁上的细胞生长和发酵过程中,测量重组细胞产生的β-半乳糖苷酶。我们表明,HSP30启动子可以在静止后期诱导高基因表达,并在葡萄酒发酵过程结束前保持活性。在五种天然酒厂葡萄汁上获得了类似的表达谱。