Noble Jessica, Sanchez Isabelle, Blondin Bruno
Lallemand SAS, Blagnac, 31700, France.
Institut Coopératif du Vin, Lattes, 34970, France.
Microb Cell Fact. 2015 May 8;14:68. doi: 10.1186/s12934-015-0245-1.
Wine yeasts can produce undesirable sulfur compounds during alcoholic fermentation, such as SO2 and H2S, in variable amounts depending mostly on the yeast strain but also on the conditions. However, although sulfur metabolism has been widely studied, some of the genetic determinants of differences in sulfite and/or sulfide production between wine yeast strains remain to be identified. In this study, we used an integrated approach to decipher the genetic determinants of variation in the production of undesirable sulfur compounds.
We examined the kinetics of SO2 production by two parental strains, one high and one low sulfite producer. These strains displayed similar production profiles but only the high-sulfite producer strain continued to produce SO2 in the stationary phase. Transcriptomic analysis revealed that the low-sulfite producer strain overexpressed genes of the sulfur assimilation pathway, which is the mark of a lower flux through the pathway consistent with a lower intracellular concentration in cysteine. A QTL mapping strategy then enabled us to identify MET2 and SKP2 as the genes responsible for these phenotypic differences between strains and we identified new variants of these genes in the low-sulfite producer strain. MET2 influences the availability of a metabolic intermediate, O-acetylhomoserine, whereas SKP2 affects the activity of a key enzyme of the sulfur assimilation branch of the pathway, the APS kinase, encoded by MET14. Furthermore, these genes also affected the production of propanol and acetaldehyde. These pleiotropic effects are probably linked to the influence of these genes on interconnected pathways and to the chemical reactivity of sulfite with other metabolites.
This study provides new insight into the regulation of sulfur metabolism in wine yeasts and identifies variants of MET2 and SKP2 genes, that control the activity of both branches of the sulfur amino acid synthesis pathway and modulate sulfite/sulfide production and other related phenotypes. These results provide novel targets for the improvement of wine yeast strains.
葡萄酒酵母在酒精发酵过程中会产生不同数量的不良含硫化合物,如二氧化硫(SO₂)和硫化氢(H₂S),其产量主要取决于酵母菌株,但也受发酵条件影响。然而,尽管对硫代谢已进行了广泛研究,但葡萄酒酵母菌株之间亚硫酸盐和/或硫化物产量差异的一些遗传决定因素仍有待确定。在本研究中,我们采用综合方法来解读不良含硫化合物产量变化的遗传决定因素。
我们检测了两个亲本菌株(一个亚硫酸盐高产菌株和一个亚硫酸盐低产菌株)产生SO₂的动力学。这些菌株表现出相似的产量曲线,但只有亚硫酸盐高产菌株在稳定期继续产生SO₂。转录组分析表明,亚硫酸盐低产菌株中硫同化途径的基因过表达,这表明该途径通量较低,与细胞内较低的半胱氨酸浓度一致。然后,一种数量性状基因座(QTL)定位策略使我们能够确定MET2和SKP2是导致菌株间这些表型差异的基因,并且我们在亚硫酸盐低产菌株中鉴定出了这些基因的新变体。MET2影响代谢中间体O - 乙酰高丝氨酸的可用性,而SKP2影响该途径硫同化分支的关键酶(由MET14编码的APS激酶)的活性。此外,这些基因还影响丙醇和乙醛的产量。这些多效性效应可能与这些基因对相互关联途径的影响以及亚硫酸盐与其他代谢物的化学反应性有关。
本研究为葡萄酒酵母中硫代谢的调控提供了新的见解,并鉴定出MET2和SKP2基因的变体,这些变体控制硫氨基酸合成途径两个分支的活性,并调节亚硫酸盐/硫化物的产生以及其他相关表型。这些结果为改良葡萄酒酵母菌株提供了新的靶点。