School of Chemical Sciences and School of Biological Sciences, University of Auckland, Auckland 1142, New Zealand.
G3 (Bethesda). 2021 Apr 15;11(4). doi: 10.1093/g3journal/jkab061.
It is standard practice to ferment white wines at low temperatures (10-18°C). However, low temperatures increase fermentation duration and risk of problem ferments, leading to significant costs. The lag duration at fermentation initiation is heavily impacted by temperature; therefore, identification of Saccharomyces cerevisiae genes influencing fermentation kinetics is of interest for winemaking. We selected 28 S. cerevisiae BY4743 single deletants, from a prior list of open reading frames (ORFs) mapped to quantitative trait loci (QTLs) on Chr. VII and XIII, influencing the duration of fermentative lag time. Five BY4743 deletants, Δapt1, Δcgi121, Δclb6, Δrps17a, and Δvma21, differed significantly in their fermentative lag duration compared to BY4743 in synthetic grape must (SGM) at 15 °C, over 72 h. Fermentation at 12.5°C for 528 h confirmed the longer lag times of BY4743 Δcgi121, Δrps17a, and Δvma21. These three candidates ORFs were deleted in S. cerevisiae RM11-1a and S288C to perform single reciprocal hemizygosity analysis (RHA). RHA hybrids and single deletants of RM11-1a and S288C were fermented at 12.5°C in SGM and lag time measurements confirmed that the S288C allele of CGI121 on Chr. XIII, encoding a component of the EKC/KEOPS complex, increased fermentative lag phase duration. Nucleotide sequences of RM11-1a and S288C CGI121 alleles differed by only one synonymous nucleotide, suggesting that intron splicing, codon bias, or positional effects might be responsible for the impact on lag phase duration. This research demonstrates a new role of CGI121 and highlights the applicability of QTL analysis for investigating complex phenotypic traits in yeast.
在低温(10-18°C)下发酵白葡萄酒是标准做法。然而,低温会延长发酵时间并增加问题发酵的风险,导致成本显著增加。发酵起始时的滞后时间受温度影响很大;因此,鉴定影响发酵动力学的酿酒酵母基因对于酿酒具有重要意义。我们从先前映射到 Chr. VII 和 XIII 上的数量性状位点(QTL)的开放阅读框(ORF)列表中选择了 28 个酿酒酵母 BY4743 单缺失体,影响发酵滞后时间的持续时间。在 15°C 的合成葡萄汁(SGM)中,与 BY4743 相比,五个 BY4743 缺失体(Δapt1、Δcgi121、Δclb6、Δrps17a 和 Δvma21)在发酵滞后时间上有显著差异,持续时间为 72 小时。在 12.5°C 下发酵 528 小时,证实了 BY4743 Δcgi121、Δrps17a 和 Δvma21 的滞后时间更长。这三个候选 ORF 在酿酒酵母 RM11-1a 和 S288C 中缺失,以进行单顺反子杂合性分析(RHA)。在 SGM 中,在 12.5°C 下发酵 RM11-1a 和 S288C 的 RHA 杂种和单缺失体,并确认滞后时间测量结果表明,在 Chr. XIII 上编码 EKC/KEOPS 复合物组成部分的 S288C CGI121 等位基因,延长了发酵滞后阶段的持续时间。RM11-1a 和 S288C CGI121 等位基因的核苷酸序列仅相差一个同义核苷酸,这表明内含子剪接、密码子偏向或位置效应可能是影响滞后时间的原因。这项研究展示了 CGI121 的新作用,并强调了 QTL 分析在研究酵母中复杂表型特征方面的适用性。