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利用条码焦磷酸测序技术分析十种代表性泡菜发酵过程中的细菌群落结构。

Bacterial community analysis during fermentation of ten representative kinds of kimchi with barcoded pyrosequencing.

机构信息

Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul 130-701, Republic of Korea.

出版信息

Food Microbiol. 2012 May;30(1):197-204. doi: 10.1016/j.fm.2011.10.011. Epub 2011 Oct 19.

Abstract

Kimchi, a food made of fermented vegetables, is densely populated by indigenous microorganisms that originate from the raw ingredients under normal conditions. Most microbiological studies on kimchi have been on the most popular dish, baechu-kimchi (Chinese cabbage kimchi). Therefore, relatively little is known about the various other kinds of kimchi (depending on the region, season, main ingredient, starter culture inoculation and recipe). In this study, we collected 100 samples periodically during the fermentation of ten representative kinds of kimchi (including starter-inoculated kimchi) that were stored in the refrigerator (4 °C) during the 30-35 days fermentation period. The multiplex barcoded pyrosequencing of a hypervariable V1-V3 region of the 16S ribosomal RNA (rRNA) gene tagged with sample-specific barcodes for multiplex identifiers was employed for bacterial community profiling. We found that bacterial communities differed between starter-inoculated and non-inoculated kimchi at the early stages of fermentation, but overall there were no significant differences in the late phases. Also, the diversity and richness of bacterial communities varied depending on the various types of kimchi, and these differences could largely be explained by the major ingredients and the manufacture processes of each types of kimchi. This study provides the comprehensive understanding of the factors influencing the biodiversity of the kimchi ecosystem.

摘要

泡菜是一种由发酵蔬菜制成的食物,在正常条件下,其原料中就密集存在着土著微生物。大多数泡菜的微生物学研究都集中在最受欢迎的菜肴,白菜泡菜(Chinese cabbage kimchi)上。因此,对于各种其他类型的泡菜(取决于地区、季节、主要成分、起始培养接种和配方),人们了解相对较少。在这项研究中,我们在 30-35 天的发酵期间定期收集了 100 个样本,这些样本来自十种具有代表性的泡菜(包括起始接种的泡菜),在发酵期间将这些泡菜储存在冰箱(4°C)中。使用带有样品特异性多路复用标识符的 16S 核糖体 RNA(rRNA)基因 V1-V3 区的超变区的多重条形码焦磷酸测序技术用于细菌群落分析。我们发现,在发酵的早期阶段,接种和未接种的泡菜之间的细菌群落存在差异,但在后期阶段总体上没有显著差异。此外,细菌群落的多样性和丰富度取决于各种类型的泡菜,这些差异在很大程度上可以用每种泡菜的主要成分和制造工艺来解释。本研究提供了对影响泡菜生态系统生物多样性因素的全面了解。

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