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本文引用的文献

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Generation of a Uracil Auxotroph Strain of the Probiotic Yeast Saccharomyces boulardii as a Host for the Recombinant Protein Production.生成益生菌酵母布拉氏酵母菌的尿嘧啶营养缺陷型菌株作为重组蛋白生产的宿主。
Avicenna J Med Biotechnol. 2013 Jan;5(1):29-34.
2
Inhibition of tissue inflammation and bacterial translocation as one of the protective mechanisms of Saccharomyces boulardii against Salmonella infection in mice.布拉氏酵母菌抑制组织炎症和细菌易位,作为其抵抗鼠伤寒沙门氏菌感染的保护机制之一。
Microbes Infect. 2013 Apr;15(4):270-9. doi: 10.1016/j.micinf.2012.12.007. Epub 2013 Jan 30.
3
Improving health from the inside: Use of engineered intestinal microorganisms as in situ cytokine delivery system.从内部改善健康:将工程化肠道微生物用作原位细胞因子递送系统。
Bioengineered. 2013 May-Jun;4(3):172-9. doi: 10.4161/bioe.22646. Epub 2012 Oct 30.
4
Genetic characterization and construction of an auxotrophic strain of Saccharomyces cerevisiae JP1, a Brazilian industrial yeast strain for bioethanol production.酵母 JP1 的遗传特征分析及其营养缺陷型菌株的构建,酵母 JP1 是一种用于生物乙醇生产的巴西工业酵母。
J Ind Microbiol Biotechnol. 2012 Nov;39(11):1673-83. doi: 10.1007/s10295-012-1170-5. Epub 2012 Aug 15.
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New and Redesigned pRS Plasmid Shuttle Vectors for Genetic Manipulation of Saccharomycescerevisiae.新型和重新设计的 pRS 质粒穿梭载体用于酿酒酵母的遗传操作。
G3 (Bethesda). 2012 May;2(5):515-26. doi: 10.1534/g3.111.001917. Epub 2012 May 1.
6
Adhesion to the yeast cell surface as a mechanism for trapping pathogenic bacteria by Saccharomyces probiotics.黏附在酵母细胞表面作为益生菌酵母菌捕获病原菌的一种机制。
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Quantitative phenotyping of inflammatory bowel disease in the IL-10-deficient mouse by use of noninvasive magnetic resonance imaging.利用非侵入性磁共振成像对 IL-10 缺陷型小鼠的炎症性肠病进行定量表型分析。
Inflamm Bowel Dis. 2013 Jan;19(1):185-93. doi: 10.1002/ibd.23006.
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Introduction and expression of genes for metabolic engineering applications in Saccharomyces cerevisiae.用于酿酒酵母代谢工程应用的基因的引入和表达。
FEMS Yeast Res. 2012 Mar;12(2):197-214. doi: 10.1111/j.1567-1364.2011.00769.x. Epub 2012 Jan 12.
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Transformation of Saccharomyces cerevisiae and other fungi: methods and possible underlying mechanism.酿酒酵母及其他真菌的转化:方法及可能的潜在机制
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Oral treatment with Saccharomyces cerevisiae strain UFMG 905 modulates immune responses and interferes with signal pathways involved in the activation of inflammation in a murine model of typhoid fever.口服酿酒酵母菌株 UFMG 905 可调节免疫反应,并干扰参与伤寒小鼠模型中炎症激活的信号通路。
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益生菌酵母布拉酵母菌遗传转化的新见解。

Novel insights in genetic transformation of the probiotic yeast Saccharomyces boulardii.

作者信息

Douradinha Bruno, Reis Viviane C B, Rogers Matthew B, Torres Fernando A G, Evans Jared D, Marques Ernesto T A

机构信息

Fondazione Ri.MED; Palermo, Italy; University of Pittsburgh Center for Vaccine Research; Pittsburgh, PA USA.

Centro de Biotecnologia Molecular; Instituto de Ciências Biológicas; Universidade de Brasília; Brasília, Brazil.

出版信息

Bioengineered. 2014 Jan-Feb;5(1):21-9. doi: 10.4161/bioe.26271. Epub 2013 Sep 5.

DOI:10.4161/bioe.26271
PMID:24013355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4008461/
Abstract

Saccharomyces boulardii (S. boulardii) is a probiotic yeast related to Saccharomyces cerevisiae (S. cerevisiae) but with distinct genetic, taxonomic and metabolic properties. S. cerevisiae has been used extensively in biotechnological applications. Currently, many strains are available, and multiple genetic tools have been developed, which allow the expression of several exogenous proteins of interest with applications in the fields of medicine, biofuels, the food industry, and scientific research, among others. Although S. boulardii has been widely studied due to its probiotic properties against several gastrointestinal tract disorders, very few studies addressed the use of this yeast as a vector for expression of foreign genes of interest with biotechnological applications. Here we show that, despite the similarity of the two yeasts, not all genetic tools used in S. cerevisiae can be applied in S. boulardii. While transformation of the latter could be obtained using a commercial kit developed for the former, consequent screening of successful transformants had to be optimized. We also show that several genes frequently used in genetic manipulation of S. cerevisiae (e.g., promoters and resistance markers) are present in S. boulardii. Sequencing revealed a high rate of homology (> 96%) between the orthologs of the two yeasts. However, we also observed some of them are not eligible to be targeted for transformation of S. boulardii. This work has important applications toward the potential of this probiotic yeast as an expression system for genes of interest.

摘要

布拉氏酵母菌(S. boulardii)是一种益生菌酵母,与酿酒酵母(S. cerevisiae)相关,但具有独特的遗传、分类学和代谢特性。酿酒酵母已广泛应用于生物技术领域。目前,有许多菌株可供使用,并且已经开发了多种遗传工具,这使得人们能够表达几种感兴趣的外源蛋白,并应用于医学、生物燃料、食品工业和科学研究等领域。尽管布拉氏酵母菌因其对多种胃肠道疾病的益生菌特性而受到广泛研究,但很少有研究探讨将这种酵母用作表达具有生物技术应用价值的外源基因的载体。在这里,我们表明,尽管这两种酵母有相似之处,但并非所有用于酿酒酵母的遗传工具都能应用于布拉氏酵母菌。虽然可以使用为酿酒酵母开发的商业试剂盒实现后者的转化,但随后对成功转化子的筛选必须进行优化。我们还表明,酿酒酵母遗传操作中常用的几个基因(如启动子和抗性标记)在布拉氏酵母菌中也存在。测序显示这两种酵母的直系同源基因之间具有很高的同源率(> 96%)。然而,我们也观察到其中一些基因不适合用于布拉氏酵母菌的转化靶向。这项工作对于这种益生菌酵母作为感兴趣基因的表达系统的潜力具有重要应用价值。