首页> 外文OA文献 >Pyrosequencing of Tagged 16S rRNA Gene Amplicons for Rapid Deciphering of the Microbiomes of Fermented Foods Such as Pearl Millet Slurries▿
【2h】

Pyrosequencing of Tagged 16S rRNA Gene Amplicons for Rapid Deciphering of the Microbiomes of Fermented Foods Such as Pearl Millet Slurries▿

机译:标记的16S rRNA基因扩增子的焦磷酸测序,用于快速解密诸如珍珠粟浆等发酵食品的微生物组mes

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pearl millet slurries, mixed with groundnuts or not, were chosen as a model to investigate the feasibility of obtaining a rapid overview of community structure and population dynamics of fermented foods using pyrosequencing of tagged 16S rRNA gene amplicons. From 14 fermented samples collected either in a traditional small-scale processing unit in Burkina Faso or at laboratory scale, 137,469 sequences of bacterial 16S rRNA gene amplicons were characterized. Except for a few Proteobacteria, almost all the bacterial sequences were attributed to cultivable bacteria. This approach enabled 80.7% of the sequences to be attributed to a family and 70% to a genus but did not enable identification to the species level. The bacterial sequences were assigned to four phyla, with Firmicutes representing the highest diversity, followed by Proteobacteria, Actinobacteria, and Bacteroidetes, which were found only in the slurries prepared in traditional production units. Most of the Firmicutes were lactic acid bacteria, mainly represented by members of the Lactobacillus, Pediococcus, Leuconostoc, and Weissella genera, whose ratio varied from the onset to the end of the fermentation. The other bacteria present at the beginning of fermentation were generally no longer detected at the end, which is consistent with already-known patterns in the microbial ecology of fermented foods. In conclusion, this method seems very promising for rapid and preliminary microbial characterization in many samples of an unknown food sample, by determining numerous nucleic sequences simultaneously without the need for cloning and cultivation-dependent methods.
机译:选择珍珠谷浆与花生或不与花生混合,作为模型来研究使用标记的16S rRNA基因扩增子进行焦磷酸测序来快速获得发酵食品的群落结构和种群动态的可行性。从在布基纳法索的传统小型加工装置或实验室规模收集的14个发酵样品中,鉴定了137,469个细菌16S rRNA基因扩增子序列。除了少数变形杆菌,几乎所有细菌序列均归因于可培养细菌。这种方法使80.7%的序列归因于一个科,而70%的归因于一个属,但无法对物种进行鉴定。细菌序列被分配到四个门,其中Firmicutes代表最高的多样性,其次是Proteobacteria,Actinobacteria和Bacteroidetes,它们仅在传统生产装置中制备的浆液中才能找到。大部分的Firmicutes是乳酸菌,主要以乳酸菌,Pecococcus,Leuconostoc和Weissella属为代表,其比例从发酵开始到发酵结束。通常在发酵开始时不再检测到其他在发酵开始时存在的细菌,这与发酵食品的微生物生态学中已知的模式一致。总而言之,该方法通过不需克隆和依赖培养的方法即可同时测定众多核酸序列,从而有望在未知食品样品的许多样品中进行快速和初步的微生物表征,非常有希望。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号