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Fungal Genet Biol. 2018 May;114:42-52. doi: 10.1016/j.fgb.2018.03.005. Epub 2018 Mar 23.
2
Common and divergent features of galactose-1-phosphate and fructose-1-phosphate toxicity in yeast.酵母中半乳糖-1-磷酸和果糖-1-磷酸毒性的共同和差异特征。
Mol Biol Cell. 2018 Apr 15;29(8):897-910. doi: 10.1091/mbc.E17-11-0666. Epub 2018 Mar 30.
3
Polyphosphate-Accumulating Bacteria: Potential Contributors to Mineral Dissolution in the Oral Cavity.聚磷酸盐积累菌:口腔中矿物质溶解的潜在贡献者。
Appl Environ Microbiol. 2018 Mar 19;84(7). doi: 10.1128/AEM.02440-17. Print 2018 Apr 1.
4
Synthesis of Sphingolipids Impacts Survival of and the Presentation of Surface Polysaccharides.鞘脂的合成影响[具体对象未明确]的存活以及表面多糖的呈现。
Front Microbiol. 2016 Nov 29;7:1919. doi: 10.3389/fmicb.2016.01919. eCollection 2016.
5
D-Galactose as an autoinducer 2 inhibitor to control the biofilm formation of periodontopathogens.D-半乳糖作为自诱导物2抑制剂来控制牙周病原体的生物膜形成。
J Microbiol. 2016 Sep;54(9):632-637. doi: 10.1007/s12275-016-6345-8. Epub 2016 Aug 31.
6
Deletion of a 77-base-pair inverted repeat element alters the synthesis of surface polysaccharides in Porphyromonas gingivalis.删除一个77个碱基对的反向重复元件会改变牙龈卟啉单胞菌表面多糖的合成。
J Bacteriol. 2015 Apr;197(7):1208-20. doi: 10.1128/JB.02589-14. Epub 2015 Jan 26.
7
De novo assembly of bacterial transcriptomes from RNA-seq data.利用RNA测序数据对细菌转录组进行从头组装。
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8
Computational analysis of bacterial RNA-Seq data.细菌 RNA-Seq 数据的计算分析。
Nucleic Acids Res. 2013 Aug;41(14):e140. doi: 10.1093/nar/gkt444. Epub 2013 May 28.
9
Porphyromonas gingivalis: keeping the pathos out of the biont.牙龈卟啉单胞菌:让生物体内的病理因素消失。
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10
Beyond the red complex and into more complexity: the polymicrobial synergy and dysbiosis (PSD) model of periodontal disease etiology.超越红色复合体,进入更复杂的领域:牙周病病因的多微生物协同作用和失调(PSD)模型。
Mol Oral Microbiol. 2012 Dec;27(6):409-19. doi: 10.1111/j.2041-1014.2012.00663.x. Epub 2012 Sep 3.

半乳糖影响无蔗糖分解口腔病原体牙龈卟啉单胞菌的大小和细胞内组成。

Galactose Impacts the Size and Intracellular Composition of the Asaccharolytic Oral Pathobiont Porphyromonas gingivalis.

机构信息

Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA.

Department of Oral Biology, College of Dentistry, University of Florida, Gainesville, Florida, USA

出版信息

Appl Environ Microbiol. 2019 Feb 6;85(4). doi: 10.1128/AEM.02268-18. Print 2019 Feb 15.

DOI:10.1128/AEM.02268-18
PMID:30552185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6365826/
Abstract

The asaccharolytic anaerobe metabolizes proteins it encounters in the periodontal pocket, including host-derived glycoproteins such as mucins and immunoglobulins. Often, these proteins are protected by a diverse array of carbohydrates tethered to the polypeptide chain via glycolytic bonds, and produces enzymes capable of liberating these carbohydrates, exposing the proteinaceous core. In this study, we investigated the effect of individual monosaccharides, including galactose, l-fucose, mannose, and glucose, on the growth and physiology of Of the carbohydrates tested, only galactose noticeably altered the density of the bacterial culture, and we observed that cultures grown with galactose reached significantly higher densities during stationary phase. Importantly, electron micrographs and plating of in stationary phase demonstrated that the presence of galactose did not increase cell numbers; instead, the higher densities resulted from the expansion of individual cells which contained large intracellular granules. Initial attempts to characterize these granules revealed only a subtle increase in soluble carbohydrates, suggesting they are likely not composed of stored carbohydrate. Also, an analysis of major surface polysaccharides via an enzyme-linked immunosorbent assay (ELISA) did not reveal significant differences between cells grown with or without galactose. Finally, an initial investigation of the transcriptional changes elicited by galactose in late exponential phase suggested that genes important for cell shape and for the general stress response may play roles in this phenomenon. Overall, galactose, a monosaccharide commonly present on the surfaces of host proteins, substantially alters the physiology of via the production of large, currently undefined, intracellular granules. Environmental perturbations are central to the ability of pathobionts, such as , to promote the development of diseased sites. In the case of periodontal disease, increased local pH, a shift to anaerobic surroundings, and the accumulation of Gram-negative anaerobes at the expense of Gram-positive cocci are known ecological fluctuations prominently associated with progression toward disease. Importantly, in contrast, the alterations to subgingival food webs in disease sites remain poorly characterized. We hypothesized that given the dramatic shift in community structure during disease, it is possible that free carbohydrates, which would typically be readily metabolized by Gram-positive cocci after cleavage from glycoproteins, may increase in concentration locally and thereby affect the physiological state of the subgingival microbiota. In this study, we explored the impact of free monosaccharides on to gain deeper insight into the effect of dysbiotic conditions on the growth and physiology of this periodontal pathogen.

摘要

无碳水化合物可利用的厌氧菌会代谢其在牙周袋中遇到的蛋白质,包括宿主来源的糖蛋白,如粘蛋白和免疫球蛋白。这些蛋白质通常受到通过糖酵解键与多肽链连接的各种碳水化合物的保护,并且产生能够释放这些碳水化合物的酶,从而暴露出蛋白质核心。在这项研究中,我们研究了单个单糖,包括半乳糖、岩藻糖、甘露糖和葡萄糖,对生长和生理学的影响。在所测试的碳水化合物中,只有半乳糖明显改变了细菌培养物的密度,我们观察到用半乳糖培养的培养物在静止期达到明显更高的密度。重要的是,电子显微镜和静止期的平板培养表明,半乳糖的存在并没有增加细胞数量;相反,较高的密度是由于单个细胞的扩张,这些细胞含有大的细胞内颗粒。对半乳糖存在时这些颗粒的特征的初步尝试仅揭示了可溶性碳水化合物的轻微增加,表明它们可能不是由储存的碳水化合物组成的。此外,通过酶联免疫吸附测定(ELISA)对主要表面多糖的分析并未显示出用或不用半乳糖培养的细胞之间有显着差异。最后,对半乳糖在指数晚期引起的转录变化的初步研究表明,对细胞形状和一般应激反应很重要的基因可能在这种现象中起作用。总的来说,半乳糖,一种常见于宿主蛋白质表面的单糖,通过产生大的、目前未定义的细胞内颗粒,极大地改变了 的生理学特性。环境干扰是病原菌(如)促进疾病部位发展的能力的核心。就牙周病而言,局部 pH 值升高、向厌氧环境转变以及革兰氏阴性厌氧菌的积累以牺牲革兰氏阳性球菌为代价,是与疾病进展相关的已知生态波动。重要的是,相比之下,疾病部位龈下食物网的变化仍知之甚少。我们假设,鉴于疾病期间群落结构的巨大变化,原本很容易被革兰氏阳性球菌从糖蛋白上切割下来的游离碳水化合物,其浓度可能会在局部增加,从而影响龈下微生物群的生理状态。在这项研究中,我们探索了游离单糖对半乳糖的影响,以更深入地了解生态失调条件对这种牙周病原体生长和生理学的影响。