Vassileva Ivelina, Baev Vesselin, Yahubyan Galina, Apostolova-Kuzova Elena, Angelov Angel, Koprinarova Miglena
Institute of Molecular Biology "Acad. Roumen Tsanev", Bulgarian Academy of Sciences, Acad. G. Bonchev Str. bl. 21, 1113 Sofia, Bulgaria.
Department of Plant Physiology and Molecular Biology, Tzar Assen 24, University of Plovdiv.
Food Technol Biotechnol. 2023 Mar;61(1):138-147. doi: 10.17113/ftb.61.01.23.7796.
Sourdough is a spontaneously formed, complex microbial ecosystem of various lactic acid bacteria (LAB) and yeast which, by producing specific metabolites, determines the quality of the baked products. In order to design and control the sourdough with preferred nutritional characteristics, it is crucial that the LAB diversity of the product of interest be elucidated.
Using the opportunities of next-generation sequencing (NGS) of the V1-V3 hypervariable gene region of 16S rRNA, we studied the microbial ecosystem of a whole grain sourdough made of , originating from Southwestern Bulgaria. Since the DNA extraction method is considered crucial for the accuracy of the sequencing results, as it can introduce significant differences in the examined microbiota, we used three different commercial kits for DNA isolation and analyzed their impact on the observed bacterial diversity.
All three DNA extraction kits provided bacterial DNA which passed quality control and was successfully sequenced on Illumina MiSeq platform. The results received from the different DNA protocols showed variations in the microbial profiles. Alpha diversity indices (ACE, Chao1, Shannon, and Simpson) were also different among the three groups of results. Nevertheless, a strong dominance of phylum Firmicutes, class Bacilli, order Lactobacillales, represented mostly by family Lactobacillaceae, genus (relative abundance of 63.11-82.28%) and family Leuconostocaceae, genus (relative abundance of 3.67-36.31%) was observed. and with relative abundance of 16.15-31.24% and 6.21-16.29% respectively, were the two dominant species identified in all three DNA isolates.
The presented results give insight into the taxonomic composition of bacterial community of a specific Bulgarian sourdough. Having in mind that the sourdough is a difficult matrix for DNA isolation on the one hand, and that there is no standardized DNA extraction protocol for this matrix on the other hand, this pilot study aims to give a small contribution to the future establishment and validation of such a protocol, which will allow accurate assessment of the specific microbiota of sourdough samples.
酸面团是一种由多种乳酸菌(LAB)和酵母自发形成的复杂微生物生态系统,通过产生特定代谢产物来决定烘焙产品的质量。为了设计和控制具有理想营养特性的酸面团,阐明目标产品中LAB的多样性至关重要。
利用16S rRNA的V1-V3高变基因区域的下一代测序(NGS)技术,我们研究了源自保加利亚西南部的由[具体原料]制成的全谷物酸面团的微生物生态系统。由于DNA提取方法被认为对测序结果的准确性至关重要,因为它可能会在检测的微生物群中引入显著差异,我们使用了三种不同的商业试剂盒进行DNA分离,并分析了它们对观察到的细菌多样性的影响。
所有三种DNA提取试剂盒都提供了通过质量控制并在Illumina MiSeq平台上成功测序的细菌DNA。不同DNA提取方案得到的结果显示出微生物谱的差异。三组结果之间的α多样性指数(ACE、Chao1、香农和辛普森)也有所不同。然而,观察到厚壁菌门、芽孢杆菌纲、乳杆菌目占主导地位,主要由乳杆菌科、[属名1](相对丰度为63.11 - 82.28%)和明串珠菌科、[属名2](相对丰度为3.67 - 36.31%)代表。在所有三种DNA分离物中鉴定出的两个优势物种分别是相对丰度为16.15 - 31.24%的[物种名1]和相对丰度为6.21 - 16.29%的[物种名2]。
所呈现的结果深入了解了特定保加利亚酸面团细菌群落的分类组成。考虑到一方面酸面团是一种难以进行DNA分离的基质,另一方面针对该基质没有标准化的DNA提取方案,这项初步研究旨在为未来建立和验证这样一种方案做出一点贡献,该方案将允许准确评估酸面团样品的特定微生物群。