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Dioxygenases in Burkholderia ambifaria and Yersinia pestis that hydroxylate the outer Kdo unit of lipopolysaccharide.伯克霍尔德氏菌和鼠疫耶尔森氏菌中的双加氧酶,可使脂多糖的外 Kdo 单元羟化。
Proc Natl Acad Sci U S A. 2011 Jan 11;108(2):510-5. doi: 10.1073/pnas.1016462108. Epub 2010 Dec 22.
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Structural variation of glycolipids from Meiothermus taiwanensis ATCC BAA-400 under different growth temperatures.美嗜热栖热菌 ATCC BAA-400 在不同生长温度下糖脂的结构变化。
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Characterization of the six glycosyltransferases involved in the biosynthesis of Yersinia enterocolitica serotype O:3 lipopolysaccharide outer core.鉴定参与产志贺邻单胞菌 O:3 型脂多糖外核心生物合成的六种糖基转移酶。
J Biol Chem. 2010 Sep 3;285(36):28333-42. doi: 10.1074/jbc.M110.111336. Epub 2010 Jul 1.
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Characterization of the specific O-polysaccharide structure and biosynthetic gene cluster of Yersinia pseudotuberculosis serotype O:15.鉴定假结核耶尔森氏菌 O:15 血清型的特异性 O-多糖结构和生物合成基因簇。
Innate Immun. 2009 Dec;15(6):351-9. doi: 10.1177/1753425909105319.
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Identification and role of a 6-deoxy-4-keto-hexosamine in the lipopolysaccharide outer core of Yersinia enterocolitica serotype O:3.鉴定和功能的 6-脱 -4- 酮 - 己糖胺在脂多糖外核心的耶尔森氏菌 enterocolitica 血清型 O:3。
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Segregation of New Lysogenic Types during Growth of a Doubly Lysogenic Strain Derived from Escherichia Coli K12.源于大肠杆菌K12的双重溶源菌株生长过程中新溶源类型的分离
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鉴定鼠疫耶尔森菌和假结核耶尔森菌的脂多糖核心作为噬菌体 φA1122 的受体。

Identification of the lipopolysaccharide core of Yersinia pestis and Yersinia pseudotuberculosis as the receptor for bacteriophage φA1122.

机构信息

Department of Medical Biochemistry and Molecular Biology, Institute of Biomedicine, University of Turku, Turku, Finland.

出版信息

J Bacteriol. 2011 Sep;193(18):4963-72. doi: 10.1128/JB.00339-11. Epub 2011 Jul 15.

DOI:10.1128/JB.00339-11
PMID:21764935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3165662/
Abstract

φA1122 is a T7-related bacteriophage infecting most isolates of Yersinia pestis, the etiologic agent of plague, and used by the CDC in the identification of Y. pestis. φA1122 infects Y. pestis grown both at 20 °C and at 37 °C. Wild-type Yersinia pseudotuberculosis strains are also infected but only when grown at 37 °C. Since Y. pestis expresses rough lipopolysaccharide (LPS) missing the O-polysaccharide (O-PS) and expression of Y. pseudotuberculosis O-PS is largely suppressed at temperatures above 30 °C, it has been assumed that the phage receptor is rough LPS. We present here several lines of evidence to support this. First, a rough derivative of Y. pseudotuberculosis was also φA1122 sensitive when grown at 22 °C. Second, periodate treatment of bacteria, but not proteinase K treatment, inhibited the phage binding. Third, spontaneous φA1122 receptor mutants of Y. pestis and rough Y. pseudotuberculosis could not be isolated, indicating that the receptor was essential for bacterial growth under the applied experimental conditions. Fourth, heterologous expression of the Yersinia enterocolitica O:3 LPS outer core hexasaccharide in both Y. pestis and rough Y. pseudotuberculosis effectively blocked the phage adsorption. Fifth, a gradual truncation of the core oligosaccharide into the Hep/Glc (L-glycero-D-manno-heptose/D-glucopyranose)-Kdo/Ko (3-deoxy-D-manno-oct-2-ulopyranosonic acid/D-glycero-D-talo-oct-2-ulopyranosonic acid) region in a series of LPS mutants was accompanied by a decrease in phage adsorption, and finally, a waaA mutant expressing only lipid A, i.e., also missing the Kdo/Ko region, was fully φA1122 resistant. Our data thus conclusively demonstrated that the φA1122 receptor is the Hep/Glc-Kdo/Ko region of the LPS core, a common structure in Y. pestis and Y. pseudotuberculosis.

摘要

φA1122 是一种 T7 相关噬菌体,可感染鼠疫耶尔森菌(鼠疫的病原体)的大多数分离株,也被疾病预防控制中心用于鼠疫耶尔森菌的鉴定。φA1122 可感染在 20°C 和 37°C 下生长的鼠疫耶尔森菌。野生型假结核耶尔森氏菌菌株也会被感染,但仅在 37°C 下生长时才会被感染。由于鼠疫耶尔森菌表达粗糙的脂多糖(LPS),缺少 O-多糖(O-PS),而假结核耶尔森氏菌的 O-PS 表达在温度高于 30°C 时受到很大抑制,因此人们假设噬菌体的受体是粗糙的 LPS。我们在此提出了几条支持这一观点的证据。首先,当在 22°C 下生长时,假结核耶尔森氏菌的粗糙衍生物也对 φA1122 敏感。其次,细菌的过碘酸盐处理而不是蛋白酶 K 处理抑制了噬菌体的结合。第三,无法分离鼠疫耶尔森氏菌和粗糙假结核耶尔森氏菌的自发 φA1122 受体突变体,这表明在应用的实验条件下,受体对细菌的生长是必需的。第四,在鼠疫耶尔森氏菌和粗糙假结核耶尔森氏菌中异源表达肠耶尔森氏菌 O:3 LPS 外核心六糖可有效阻止噬菌体的吸附。第五,LPS 突变体中核心寡糖逐渐截短到 Hep/Glc(L-甘油-D-甘露庚糖/D-葡萄糖)-Kdo/Ko(3-去氧-D-甘露辛酮酸/D-甘油-D-塔罗辛酮酸)区域,伴随着噬菌体吸附的减少,最后,表达仅脂多糖 A 的 waaA 突变体,即也缺失 Kdo/Ko 区域,完全对 φA1122 具有抗性。因此,我们的数据明确证明了噬菌体的受体是 LPS 核心的 Hep/Glc-Kdo/Ko 区域,这是鼠疫耶尔森氏菌和假结核耶尔森氏菌的共同结构。