首页> 外文期刊>Journal of Biological Research >Comparative transcriptional analysis of flavour-biosynthetic genes of a native Saccharomyces cerevisiae strain fermenting in its natural must environment, vs. a commercial strain and correlation of the genes activities with the produced flavour compounds
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Comparative transcriptional analysis of flavour-biosynthetic genes of a native Saccharomyces cerevisiae strain fermenting in its natural must environment, vs. a commercial strain and correlation of the genes activities with the produced flavour compounds

机译:对天然酿酒酵母菌株发酵的对比转录分析,其天然酿酒酵母菌菌菌株与生产的香料化合物的商业菌株和基因活性的相关性和基因活性的相关性

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During alcoholic fermentation, Saccharomyces cerevisiae synthesizes more than 400 different compounds with higher alcohols, acetate esters of higher alcohols and ethyl esters of medium-chain fatty acids being the most important products of its metabolism, determining the particular flavour profile of each wine. The concentration of the metabolites produced depends to a large extent on the strain used. The use of indigenous strains as starting cultures can lead to the production of wines with excellent organoleptic characteristics and distinct local character, superior in quality when compared to their commercial counterparts. However, the relationship of these wild-type genotypes, linked to specific terroirs, with the biosynthetic profiles of flavour metabolites is not completely clarified and understood. To this end, qRT-PCR was employed to examine, for the first time on the transcriptional level, the performance of an indigenous Saccharomyces cerevisiae strain (Z622) in its natural environment (Debina grape must). The expression of genes implicated in higher alcohols and esters formation was correlated with the concentrations of these compounds in the produced wine. Furthermore, by applying the same fermentation conditions, we examined the same parameters in a commercial strain (VL1) and compared its performance with the one of strain Z622. Strain Z622, exhibited lower concentrations of 2-methylbutanol, 3-methylbutanol and 2-phenyl ethanol, than VL1 correlating with the elevated expression levels of transaminase and decarboxylase genes. Furthermore, the significantly high induction of ADH3 throughout fermentation of Z622 probably explains the larger population numbers reached by Z622 and reflects the better adaptation of the strain to its natural environment. Regarding acetate ester biosynthesis, Z622 produced higher concentrations of total acetate esters, compared with VL1, a fact that is in full agreement with the elevated expression levels of both ATF1 and ATF2 in strain Z622. This study provides evidence on the transcriptional level that indigenous yeast Z622 is better adapted to its natural environment able to produce wines with desirable characteristics, i.e. lower concentrations of higher alcohol and higher ester, verifying its potential as a valuable starter for the local wine-industry.
机译:在酒精发酵期间,酿酒酵母酿酒酵母合成400多种不同的醇,高级醇的乙酸酯和中链脂肪酸的乙酯是其新陈代谢的最重要产物,确定每种葡萄酒的特定风味概况。所产生的代谢物的浓度在很大程度上取决于所用的菌株。本土菌株作为起始培养物可以导致生产具有优异的感官特性和不同局部性质的葡萄酒,与其商业对应物相比,质量优异。然而,这些野生型基因型的关系与特定的陶纱有关,具有风味代谢物的生物合成谱并不完全阐明和理解。为此,使用QRT-PCR在其自然环境中首次进行分析水平,首次进行分析水平,其在其自然环境中的酿酒酵母菌株(Z622)的性能(Debina葡萄必须)。将含有较高醇和酯形成的基因的表达与生产的酒中这些化合物的浓度相关。此外,通过施加相同的发酵条件,我们在商业菌株(VL1)中检查了相同的参数,并将其与菌株Z622中的一种进行了比较。菌株Z622,表现出低浓度的2-甲基丁醇,3-甲基丁醇和2-苯基乙醇,而不是与转氨酶和脱羧酶基因的高表达水平相关的VL1。此外,在Z622发酵过程中显着高的ADH3诱导可能解释了Z622达到的较大的人口数,并反映了对其自然环境的菌株更好地调整。关于醋酸酯生物合成,与VL1相比,Z622产生了更高的总乙酸酯酯,这是与菌株Z622中ATF1和ATF2的升高的表达水平完全一致。本研究提供了有关土着酵母Z622的转录水平的证据,该分析水平更好地适应其能够生产具有所需特性的葡萄酒的天然环境,即较低浓度的高级酒精和更高的酯,验证其作为当地葡萄酒行业的有价值的起动器的潜力。

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