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对 88 份泡菜发酵过程中细菌生态变化的大规模靶向宏基因组学分析。

Large-scale targeted metagenomics analysis of bacterial ecological changes in 88 kimchi samples during fermentation.

机构信息

Microbiology and Functionality Research Group, World Institute of Kimchi, Gwangju, 61755, Republic of Korea.

Microbiology and Functionality Research Group, World Institute of Kimchi, Gwangju, 61755, Republic of Korea.

出版信息

Food Microbiol. 2017 Sep;66:173-183. doi: 10.1016/j.fm.2017.05.002. Epub 2017 May 6.

DOI:10.1016/j.fm.2017.05.002
PMID:28576366
Abstract

The microbial communities in kimchi vary widely, but the precise effects of differences in region of origin, ingredients, and preparation method on the microbiota are unclear. We analyzed the bacterial community composition of household (n = 69) and commercial (n = 19) kimchi samples obtained from six Korean provinces between April and August 2015. Samples were analyzed by barcoded pyrosequencing targeting the V1-V3 region of the 16S ribosomal RNA gene. The initial pH of the kimchi samples was 5.00-6.39, and the salt concentration was 1.72-4.42%. Except for sampling locality, all categorical variables, i.e., salt concentration, major ingredient, fermentation period, sampling time, and manufacturing process, influenced the bacterial community composition. Particularly, samples were highly clustered by sampling time and salt concentration in non-metric multidimensional scaling plots and an analysis of similarity. These results indicated that the microbial community differed according to fermentation conditions such as salt concentration, major ingredient, fermentation period, and sampling time. Furthermore, fermentation properties, including pH, acidity, salt concentration, and microbial abundance differed between kimchi samples from household and commercial sources. Analyses of changes in bacterial ecology during fermentation will improve our understanding of the biological properties of kimchi, as well as the relationships between these properties and the microbiota of kimchi.

摘要

泡菜中的微生物群落差异很大,但起源地、成分和制备方法的差异对微生物群的确切影响尚不清楚。我们分析了 2015 年 4 月至 8 月期间从韩国六个省采集的家庭(n=69)和商业(n=19)泡菜样本的细菌群落组成。通过针对 16S 核糖体 RNA 基因 V1-V3 区的条形码焦磷酸测序对样本进行了分析。泡菜样本的初始 pH 值为 5.00-6.39,盐浓度为 1.72-4.42%。除采样地点外,所有分类变量,即盐浓度、主要成分、发酵时间、采样时间和生产工艺,都影响了细菌群落组成。特别是,在非度量多维尺度图和相似性分析中,采样时间和盐浓度高度聚类了样本。这些结果表明,微生物群落根据盐浓度、主要成分、发酵时间和采样时间等发酵条件而有所不同。此外,家庭和商业来源的泡菜样本的发酵特性(包括 pH 值、酸度、盐浓度和微生物丰度)存在差异。分析发酵过程中细菌生态学的变化将有助于我们了解泡菜的生物学特性,以及这些特性与泡菜微生物群之间的关系。

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