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罗伊氏乳杆菌对酸面团环境的全局转录反应

Global transcriptional response of Lactobacillus reuteri to the sourdough environment.

作者信息

Hüfner Eric, Britton Robert A, Roos Stefan, Jonsson Hans, Hertel Christian

机构信息

Institute of Food Science and Biotechnology, Section Food Microbiology, University of Hohenheim, Stuttgart, Germany.

出版信息

Syst Appl Microbiol. 2008 Oct;31(5):323-38. doi: 10.1016/j.syapm.2008.06.005. Epub 2008 Aug 30.

DOI:10.1016/j.syapm.2008.06.005
PMID:18762399
Abstract

Lactobacillus reuteri is a lactic acid bacterium that is highly adapted to the sourdough environment. It is a dominant member of industrial type II sourdoughs, and is also able to colonize the intestinal tract of mammals, including humans, and birds. In this study, the transcriptional response of L. reuteri ATCC 55730 was investigated during sourdough fermentation by using whole-genome microarrays. Significant changes of mRNA levels were found for 101 genes involved in diverse cellular processes, such as carbohydrate and energy metabolism, cell envelope biosynthesis, exopolysaccharide production, stress responses, signal transduction and cobalamin biosynthesis. The results showed extensive changes of the organism's gene expression during growth in sourdough as compared with growth in chemically defined medium, and, thus, revealed pathways involved in the adaptation of L. reuteri to the ecological niche of sourdough. The utilization of starch and non-starch carbohydrates, the remodelling of the cell wall, characterized by reduced D-alanylation, and increased amounts of cell wall-associated polysaccharides, as well as the regulatory function of two component systems for cell wall biogenesis and metabolism were suggested by the gene expression data as being important for growth in sourdough. The impact of several L. reuteri genes for effective growth in sourdough was shown by implementation of mutant strains in sourdough fermentation. This study contributes to the understanding of the molecular fundamentals of L. reuteri's ecological competitiveness, and provides a basis for further exploration of genetic traits involved in adaptation to the food environment.

摘要

罗伊氏乳杆菌是一种高度适应酸面团环境的乳酸菌。它是工业II型酸面团的主要成员,也能够定殖于包括人类在内的哺乳动物以及鸟类的肠道中。在本研究中,通过使用全基因组微阵列研究了罗伊氏乳杆菌ATCC 55730在酸面团发酵过程中的转录反应。发现参与多种细胞过程(如碳水化合物和能量代谢、细胞包膜生物合成、胞外多糖产生、应激反应、信号转导和钴胺素生物合成)的101个基因的mRNA水平发生了显著变化。结果表明,与在化学成分确定的培养基中生长相比,该生物体在酸面团中生长期间基因表达发生了广泛变化,从而揭示了罗伊氏乳杆菌适应酸面团生态位所涉及的途径。基因表达数据表明,淀粉和非淀粉碳水化合物的利用、以减少D-丙氨酰化和增加细胞壁相关多糖量为特征的细胞壁重塑,以及双组分系统对细胞壁生物合成和代谢的调节功能,对于在酸面团中生长很重要。通过在酸面团发酵中使用突变菌株,显示了几个罗伊氏乳杆菌基因对在酸面团中有效生长的影响。本研究有助于理解罗伊氏乳杆菌生态竞争力的分子基础,并为进一步探索参与适应食品环境的遗传特性提供了基础。

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