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Clp ATPases and ClpP proteolytic complexes regulate vital biological processes in low GC, Gram-positive bacteria.Clp ATP 酶和 ClpP 蛋白酶复合体调控低 GC 含量革兰氏阳性菌中的重要生物学过程。
Mol Microbiol. 2007 Mar;63(5):1285-95. doi: 10.1111/j.1365-2958.2007.05598.x.
2
Oxygen and carbon source-regulated expression of PDC and ADH genes in the respiratory yeast Pichia anomala.氧气和碳源对呼吸型酵母异常毕赤酵母中丙酮酸脱羧酶(PDC)和乙醇脱氢酶(ADH)基因表达的调控
Yeast. 2006 Dec;23(16):1137-49. doi: 10.1002/yea.1428.
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DNA micro-array-based identification of bile-responsive genes in Lactobacillus plantarum.基于DNA微阵列技术鉴定植物乳杆菌中的胆汁反应基因。
J Appl Microbiol. 2006 Apr;100(4):728-38. doi: 10.1111/j.1365-2672.2006.02891.x.
4
Transcriptome profiling of Shewanella oneidensis gene expression following exposure to acidic and alkaline pH.嗜铁钩端螺旋菌在暴露于酸性和碱性pH值后基因表达的转录组分析
J Bacteriol. 2006 Feb;188(4):1633-42. doi: 10.1128/JB.188.4.1633-1642.2006.
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Transcriptional analysis of the acid tolerance response in Streptococcus pneumoniae.肺炎链球菌酸耐受反应的转录分析
Microbiology (Reading). 2005 Dec;151(Pt 12):3935-3946. doi: 10.1099/mic.0.28238-0.
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Unravelling the multiple effects of lactic acid stress on Lactobacillus plantarum by transcription profiling.通过转录谱分析揭示乳酸胁迫对植物乳杆菌的多重影响。
Microbiology (Reading). 2005 Dec;151(Pt 12):3881-3894. doi: 10.1099/mic.0.28304-0.
7
The cell surface of Lactobacillus reuteri ATCC 55730 highlighted by identification of 126 extracellular proteins from the genome sequence.通过从基因组序列中鉴定出126种细胞外蛋白质,揭示了罗伊氏乳杆菌ATCC 55730的细胞表面特征。
FEMS Microbiol Lett. 2005 Dec 1;253(1):75-82. doi: 10.1016/j.femsle.2005.09.042. Epub 2005 Oct 10.
8
Inducible gene expression in Lactobacillus reuteri LTH5531 during type II sourdough fermentation.罗伊氏乳杆菌LTH5531在II型酸面团发酵过程中的诱导型基因表达
Appl Environ Microbiol. 2005 Oct;71(10):5873-8. doi: 10.1128/AEM.71.10.5873-5878.2005.
9
CTXphi and Vibrio cholerae: exploring a newly recognized type of phage-host cell relationship.CTXphi噬菌体与霍乱弧菌:探索一种新发现的噬菌体-宿主细胞关系类型。
Mol Microbiol. 2005 Jul;57(2):347-56. doi: 10.1111/j.1365-2958.2005.04676.x.
10
Survival of probiotic lactobacilli in acidic environments is enhanced in the presence of metabolizable sugars.在可代谢糖存在的情况下,益生菌乳酸杆菌在酸性环境中的存活率会提高。
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罗伊氏乳杆菌对酸休克的早期反应涉及ClpL伴侣蛋白和一种假定的细胞壁改变酯酶。

The early response to acid shock in Lactobacillus reuteri involves the ClpL chaperone and a putative cell wall-altering esterase.

作者信息

Wall Torun, Båth Klara, Britton Robert A, Jonsson Hans, Versalovic James, Roos Stefan

机构信息

Department of Microbiology, Swedish University of Agricultural Sciences, Box 7025, SE-750 07 Uppsala, Sweden, and Department of Pathology, Texas Children's Hospital, Houston, TX 77030, USA.

出版信息

Appl Environ Microbiol. 2007 Jun;73(12):3924-35. doi: 10.1128/AEM.01502-06. Epub 2007 Apr 20.

DOI:10.1128/AEM.01502-06
PMID:17449683
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1932720/
Abstract

To be able to function as a probiotic, bacteria have to survive the passage through the gastrointestinal tract. We have examined survival and gene expression of Lactobacillus reuteri ATCC 55730 after a sudden shift in environmental acidity to a pH close to the conditions in the human stomach. More than 80% of the L. reuteri cells survived at pH 2.7 for 1 h. A genomewide expression analysis experiment using microarrays displayed 72 differentially expressed genes at this pH. The early response to severe acid shock in L. reuteri differed from long-term acid adaptation to milder acid stress studied in other lactic acid bacteria. The genes induced included the following: clpL, genes putatively involved in alterations of the cell membrane and the cell wall; genes encoding transcriptional regulators; phage genes; and genes of unknown function. Two genes, clpL, encoding an ATPase with chaperone activity, and lr1516, encoding a putative esterase, were selected for mutation analyses. The mutants were significantly more sensitive to acid than the wild type was. Thus, these genes could contribute to the survival of L. reuteri in the gastrointestinal tract.

摘要

为了能够发挥益生菌的功能,细菌必须在通过胃肠道的过程中存活下来。我们研究了罗伊氏乳杆菌ATCC 55730在环境酸度突然转变至接近人胃内条件的pH值后的存活情况及基因表达。超过80%的罗伊氏乳杆菌细胞在pH 2.7条件下存活了1小时。使用微阵列进行的全基因组表达分析实验显示,在此pH值下有72个差异表达基因。罗伊氏乳杆菌对严重酸休克的早期反应不同于其他乳酸菌中研究的对较温和酸应激的长期酸适应。诱导表达的基因包括:clpL、可能参与细胞膜和细胞壁改变的基因;编码转录调节因子的基因;噬菌体基因;以及功能未知的基因。选择了两个基因进行突变分析,一个是clpL,编码具有伴侣活性的ATP酶,另一个是lr1516,编码一种假定的酯酶。突变体对酸的敏感性明显高于野生型。因此,这些基因可能有助于罗伊氏乳杆菌在胃肠道中的存活。