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通过毛细管电泳分离内含子剪接位点图谱研究德克氏酵母/布鲁塞尔酒香酵母的种内变异。

Intraspecific variations of Dekkera/Brettanomyces bruxellensis genome studied by capillary electrophoresis separation of the intron splice site profiles.

机构信息

Dipartimento di Scienze e Tecnologie Alimentari e Microbiologiche, Università degli Studi di Milano, via Celoria 2, 20133, Milan, Italy.

出版信息

Int J Food Microbiol. 2012 Jun 15;157(1):6-15. doi: 10.1016/j.ijfoodmicro.2012.02.017. Epub 2012 Mar 3.

Abstract

In enology, "Brett" character refers to the wine spoilage caused by the yeast Dekkera/Brettanomyces bruxellensis and its production of volatile phenolic off-flavours. However, the spoilage potential of this yeast is strain-dependent. Therefore, a rapid and reliable recognition at the strain level is a key point to avoid serious economic losses. The present work provides an operative tool to assess the genetic intraspecific variation in this species through the use of introns as molecular targets. Firstly, the available partial D./B. bruxellensis genome sequence was investigated in order to build primers annealing to introns 5' splice site sequence (ISS). This analysis allowed the detection of a non-random vocabulary flanking the site and, exploiting this feature, the creation of specific probes for strain discrimination. Secondly, the separation of the intron splice site PCR fragments was obtained throughout the set up of a capillary electrophoresis protocol, giving a 94% repeatability threshold in our experimental conditions. The comparison of results obtained with ISS-PCR/CE versus the ones performed by mtDNA RFLP revealed that the former protocol is more discriminating and allowed a reliable identification at strain level. Actually sixty D./B. bruxellensis isolates were recognised as unique strains, showing a level of similarity below 79% and confirming the high genetic polymorphism existing within the species. Two main clusters were grouped at similarity levels of about 46% and 47%, respectively, showing a poor correlation with the geographic area of isolation. Moreover, from the evolutionary point of view, the proposed technique could determine the frequency of the genome rearrangements that can occur in D./B. bruxellesis populations.

摘要

在酿酒学中,“布雷特”特征是指酵母德克特拉酵母(Dekkera/Brettanomyces bruxellensis)及其产生的挥发性酚类异味污染葡萄酒而导致的葡萄酒变质。然而,这种酵母的变质潜力取决于菌株。因此,在菌株水平上快速、可靠地识别是避免严重经济损失的关键。本工作通过使用内含子作为分子靶标,为评估该物种的种内遗传变异提供了一种可行的工具。首先,研究了现有的部分德克特拉酵母/布雷特酵母基因组序列,以便构建退火到内含子 5'剪接位点序列(ISS)的引物。该分析允许检测到侧翼序列的非随机词汇,并利用该特征,创建了用于菌株鉴别专用的探针。其次,通过建立毛细管电泳方案,获得了内含子剪接位点 PCR 片段的分离,在我们的实验条件下,重复性阈值达到 94%。将 ISS-PCR/CE 与 mtDNA RFLP 获得的结果进行比较表明,前者方案更具鉴别力,能够可靠地在菌株水平上进行鉴定。实际上,60 株德克特拉酵母/布雷特酵母分离株被识别为独特的菌株,其相似度低于 79%,证实了该物种内存在高度的遗传多态性。两个主要聚类分别在相似度水平约为 46%和 47%聚类,与分离的地理区域相关性较差。此外,从进化的角度来看,该技术可以确定德克特拉酵母/布雷特酵母种群中基因组重排的发生频率。

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