Research Group of Industrial Microbiology and Food Biotechnology (IMDO), Department of Bioengineering Sciences, Vrije Universiteit Brussel, Brussels, Belgium.
Laboratory for Microbiology, Ghent University, Ghent, Belgium.
Appl Environ Microbiol. 2018 Mar 19;84(7). doi: 10.1128/AEM.02846-17. Print 2018 Apr 1.
Few data have been published on the occurrence and functional role of acetic acid bacteria (AAB) in lambic beer production processes, mainly due to their difficult recovery and possibly unknown role. Therefore, a novel aseptic sampling method, spanning both the spatial and temporal distributions of the AAB and their substrates and metabolites, was combined with a highly selective medium and matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDI-TOF MS) as a high-throughput dereplication method followed by comparative gene sequencing for their isolation and identification, respectively. The AAB ( species more than species) proliferated during two phases of the lambic beer production process, represented by during a few days in the beginning of the fermentation and from 7 weeks until 24 months of maturation. Competitive exclusion tests combined with comparative genomic analysis of all genomes of strains of both species available disclosed possible reasons for this successive dominance. The spatial analysis revealed that significantly higher concentrations of acetic acid (from ethanol) and acetoin (from lactic acid) were produced at the tops of the casks, due to higher AAB counts and a higher metabolic activity of the AAB species at the air/liquid interface during the first 6 months of lambic beer production. In contrast, no differences in AAB species diversity occurred throughout the casks. Lambic beer is an acidic beer that is the result of a spontaneous fermentation and maturation process. Acidic beers are currently attracting attention worldwide. Part of the acidity of these beers is caused by acetic acid bacteria (AAB). However, due to their difficult recovery, they were never investigated extensively regarding their occurrence, species diversity, and functional role in lambic beer production. In the present study, a framework was developed for their isolation and identification using a novel aseptic sampling method in combination with matrix-assisted laser desorption ionization-time of flight mass spectrometry as a high-throughput dereplication technique followed by accurate molecular identification. The sampling method applied enabled us to take spatial differences into account regarding both enumerations and metabolite production. In this way, it was shown that more AAB were present and more acetic acid was produced at the air/liquid interface during a major part of the lambic beer production process. Also, two different AAB species were encountered, namely, at the beginning and in a later stage of the production process. This developed framework could also be applied for other fermentation processes.
关于醋酸菌(AAB)在拉比克啤酒生产过程中的发生和功能作用,只有少量数据已发表,这主要是因为它们难以回收,而且其作用可能未知。因此,我们结合了一种新颖的无菌采样方法,涵盖了 AAB 及其底物和代谢物的时空分布,并使用高选择性培养基和基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)作为高通量去重复方法,然后分别进行比较基因测序来对其进行分离和鉴定。在拉比克啤酒生产过程的两个阶段,AAB(超过 种的种)大量繁殖,发酵开始几天后的代表种为 ,发酵 7 周后至成熟 24 个月的代表种为 。竞争排除试验结合两种 AAB 所有菌株的比较基因组分析揭示了这种连续优势的可能原因。空间分析表明,由于 AAB 计数较高,以及在拉比克啤酒生产的前 6 个月中,在空气/液体界面处 AAB 物种的代谢活性更高,因此在桶的顶部会产生更高浓度的(来自乙醇)和乙酰基(来自乳酸)。相比之下,在整个桶中,AAB 物种多样性没有差异。拉比克啤酒是一种酸性啤酒,它是自发发酵和成熟过程的结果。酸性啤酒目前在全球范围内受到关注。这些啤酒的部分酸度是由醋酸菌(AAB)引起的。然而,由于它们难以回收,因此从未对其在拉比克啤酒生产中的发生、物种多样性和功能作用进行广泛研究。在本研究中,我们开发了一种使用新颖的无菌采样方法结合基质辅助激光解吸电离飞行时间质谱作为高通量去重复技术,然后进行准确分子鉴定的方法,用于它们的分离和鉴定。应用的采样方法使我们能够考虑到计数和代谢产物产生方面的空间差异。通过这种方式,结果表明在拉比克啤酒生产过程的大部分时间里,在空气/液体界面处存在更多的 AAB,并且产生了更多的乙酸。此外,在生产过程的早期和后期阶段分别遇到了两种不同的 AAB 物种,即 和 。该开发的框架也可应用于其他发酵过程。