Walker Michelle E, Nguyen Trung D, Liccioli Tommaso, Schmid Frank, Kalatzis Nicholas, Sundstrom Joanna F, Gardner Jennifer M, Jiranek Vladimir
School of Agriculture, Food and Wine, University of Adelaide, Urrbrae, SA 5064, Australia.
BMC Genomics. 2014 Jul 3;15(1):552. doi: 10.1186/1471-2164-15-552.
Wine fermentation is a harsh ecological niche to which wine yeast are well adapted. The initial high osmotic pressure and acidity of grape juice is followed by nutrient depletion and increasing concentrations of ethanol as the fermentation progresses. Yeast's adaptation to these and many other environmental stresses, enables successful completion of high-sugar fermentations. Earlier transcriptomic and growth studies have tentatively identified genes important for high-sugar fermentation. Whilst useful, such studies did not consider extended growth (>5 days) in a temporally dynamic multi-stressor environment such as that found in many industrial fermentation processes. Here, we identify genes whose deletion has minimal or no effect on growth, but results in failure to achieve timely completion of the fermentation of a chemically defined grape juice with 200 g L-1 total sugar.
Micro- and laboratory-scale experimental fermentations were conducted to identify 72 clones from ~5,100 homozygous diploid single-gene yeast deletants, which exhibited protracted fermentation in a high-sugar medium. Another 21 clones (related by gene function, but initially eliminated from the screen because of possible growth defects) were also included. Clustering and numerical enrichment of genes annotated to specific Gene Ontology (GO) terms highlighted the vacuole's role in ion homeostasis and pH regulation, through vacuole acidification.
We have identified 93 genes whose deletion resulted in the duration of fermentation being at least 20% longer than the wild type. An extreme phenotype, 'stuck' fermentation, was also observed when DOA4, NPT1, PLC1, PTK2, SIN3, SSQ1, TPS1, TPS2 or ZAP1 were deleted. These 93 Fermentation Essential Genes (FEG) are required to complete an extended high-sugar (wine-like) fermentation. Their importance is highlighted in our Fermentation Relevant Yeast Genes (FRYG) database, generated from literature and the fermentation-relevant phenotypic characteristics of null mutants described in the Saccharomyces Genome Database. The 93-gene set is collectively referred to as the 'Fermentome'. The fact that 10 genes highlighted in this study have not previously been linked to fermentation-related stresses, supports our experimental rationale. These findings, together with investigations of the genetic diversity of industrial strains, are crucial for understanding the mechanisms behind yeast's response and adaptation to stresses imposed during high-sugar fermentations.
葡萄酒发酵是一个恶劣的生态位,葡萄酒酵母已很好地适应了这一环境。葡萄汁最初的高渗透压和酸度,随着发酵的进行,会出现营养物质耗尽以及乙醇浓度不断增加的情况。酵母对这些以及许多其他环境压力的适应,使得高糖发酵能够成功完成。早期的转录组学和生长研究已初步确定了对高糖发酵重要的基因。虽然这些研究很有用,但它们没有考虑在许多工业发酵过程中所发现的随时间动态变化的多压力环境下的延长生长(>5天)情况。在此,我们鉴定出了这样一些基因,其缺失对生长的影响极小或没有影响,但却导致无法及时完成对含有200 g L-1总糖的化学定义葡萄汁的发酵。
进行了小规模和实验室规模的实验发酵,以从约5100个纯合二倍体单基因酵母缺失体中鉴定出72个克隆,这些克隆在高糖培养基中表现出发酵时间延长的情况。另外还纳入了21个克隆(因基因功能相关,但最初由于可能存在生长缺陷而被排除在筛选之外)。对注释到特定基因本体论(GO)术语的基因进行聚类和数值富集,突出了液泡通过液泡酸化在离子稳态和pH调节中的作用。
我们鉴定出了93个基因,其缺失导致发酵持续时间比野生型至少长20%。当DOA4、NPT1、PLC1、PTK2、SIN3、SSQ1、TPS1、TPS2或ZAP1缺失时,还观察到了一种极端表型,即“停滞”发酵。完成延长的高糖(类似葡萄酒)发酵需要这93个发酵必需基因(FEG)。它们的重要性在我们的发酵相关酵母基因(FRYG)数据库中得到了突出体现,该数据库是根据文献以及酵母基因组数据库中描述的无效突变体的发酵相关表型特征生成的。这93个基因集统称为“发酵组”。本研究中突出的10个基因此前未与发酵相关压力联系起来,这一事实支持了我们的实验原理。这些发现,连同对工业菌株遗传多样性的研究,对于理解酵母在高糖发酵过程中对压力的响应和适应背后的机制至关重要。