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对在其自然葡萄汁环境中发酵的本地菌株与商业菌株的风味生物合成基因进行比较转录分析,以及这些基因的活性与所产生的风味化合物之间的相关性。

Comparative transcriptional analysis of flavour-biosynthetic genes of a native strain fermenting in its natural must environment, vs. a commercial strain and correlation of the genes' activities with the produced flavour compounds.

作者信息

Parapouli Maria, Sfakianaki Afroditi, Monokrousos Nikolaos, Perisynakis Angelos, Hatziloukas Efstathios

机构信息

1Laboratory of Molecular Biology, Department of Biological Applications & Technologies, University of Ioannina, 451 10 Ioannina, Greece.

2Laboratory of Biochemistry, Department of Chemistry, University of Ioannina, 451 10 Ioannina, Greece.

出版信息

J Biol Res (Thessalon). 2019 Aug 5;26:5. doi: 10.1186/s40709-019-0096-8. eCollection 2019 Dec.

Abstract

BACKGROUND

During alcoholic fermentation, 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 , 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 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.

RESULTS

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 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 and in strain Z622.

CONCLUSIONS

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.

摘要

背景

在酒精发酵过程中,会合成400多种不同的化合物,其中高级醇、高级醇的乙酸酯和中链脂肪酸的乙酯是其代谢的最重要产物,决定了每种葡萄酒独特的风味特征。所产生的代谢物浓度在很大程度上取决于所使用的菌株。使用本土菌株作为起始培养物可酿造出具有优异感官特性和独特地方特色的葡萄酒,与商业菌株酿造的葡萄酒相比,品质更优。然而,这些与特定风味相关的野生型基因型与风味代谢物生物合成谱之间的关系尚未完全阐明。为此,采用qRT-PCR首次在转录水平上研究了本土酵母菌株(Z622)在其自然环境(德维纳葡萄汁)中的表现。与高级醇和酯形成相关的基因表达与所酿造葡萄酒中这些化合物的浓度相关。此外,通过应用相同的发酵条件,我们在商业菌株(VL1)中检测了相同的参数,并将其表现与菌株Z622进行了比较。

结果

菌株Z622中2-甲基丁醇、3-甲基丁醇和2-苯乙醇的浓度低于VL1,这与转氨酶和脱羧酶基因的表达水平升高相关。此外,Z622在整个发酵过程中显著高诱导,这可能解释了Z622达到的更大种群数量,并反映了该菌株对其自然环境的更好适应性。关于乙酸酯生物合成,与VL1相比,Z622产生的总乙酸酯浓度更高,这一事实与Z622菌株中两个基因的表达水平升高完全一致。

结论

本研究在转录水平上提供了证据,表明本土酵母Z622更能适应其自然环境,能够酿造出具有理想特性的葡萄酒,即高级醇浓度较低和酯含量较高,证实了其作为当地葡萄酒产业有价值起始菌株的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f4d/6683356/c264f84a1fb1/40709_2019_96_Fig1_HTML.jpg

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