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本文引用的文献

1
Diversity in Mycobacterium tuberculosis mannosylated cell wall determinants impacts adaptation to the host.分枝杆菌 Mannosylated 细胞壁决定因素的多样性影响其对宿主的适应。
Tuberculosis (Edinb). 2010 Mar;90(2):84-93. doi: 10.1016/j.tube.2010.02.003. Epub 2010 Mar 3.
2
Chapter 2: Biogenesis of the cell wall and other glycoconjugates of Mycobacterium tuberculosis.第2章:结核分枝杆菌细胞壁及其他糖缀合物的生物合成
Adv Appl Microbiol. 2009;69:23-78. doi: 10.1016/S0065-2164(09)69002-X.
3
Role of phosphatidylinositol mannosides in the interaction between mycobacteria and DC-SIGN.磷脂酰肌醇甘露糖苷在分枝杆菌与DC-SIGN相互作用中的作用
Infect Immun. 2009 Oct;77(10):4538-47. doi: 10.1128/IAI.01256-08. Epub 2009 Aug 3.
4
New insights into the early steps of phosphatidylinositol mannoside biosynthesis in mycobacteria: PimB' is an essential enzyme of Mycobacterium smegmatis.分枝杆菌中磷脂酰肌醇甘露糖苷生物合成早期步骤的新见解:PimB' 是耻垢分枝杆菌的一种必需酶。
J Biol Chem. 2009 Sep 18;284(38):25687-96. doi: 10.1074/jbc.M109.030593. Epub 2009 Jul 28.
5
Substrate-induced conformational changes in the essential peripheral membrane-associated mannosyltransferase PimA from mycobacteria: implications for catalysis.分枝杆菌中必需的外周膜相关甘露糖基转移酶PimA的底物诱导构象变化:对催化作用的影响
J Biol Chem. 2009 Aug 7;284(32):21613-25. doi: 10.1074/jbc.M109.003947. Epub 2009 Jun 11.
6
Bioinformatics identification of MurJ (MviN) as the peptidoglycan lipid II flippase in Escherichia coli.生物信息学鉴定MurJ(MviN)为大肠杆菌中的肽聚糖脂质II翻转酶。
Proc Natl Acad Sci U S A. 2008 Oct 7;105(40):15553-7. doi: 10.1073/pnas.0808352105. Epub 2008 Oct 1.
7
Solution structure of Alg13: the sugar donor subunit of a yeast N-acetylglucosamine transferase.Alg13的溶液结构:酵母N-乙酰葡糖胺转移酶的糖供体亚基。
Structure. 2008 Jun;16(6):965-75. doi: 10.1016/j.str.2008.03.010.
8
The immunomodulatory lipoglycans, lipoarabinomannan and lipomannan, are exposed at the mycobacterial cell surface.免疫调节性脂多糖、脂阿拉伯甘露聚糖和脂甘露聚糖暴露于分枝杆菌细胞表面。
Tuberculosis (Edinb). 2008 Nov;88(6):560-5. doi: 10.1016/j.tube.2008.04.002. Epub 2008 Jun 9.
9
Glycosyltransferases: structures, functions, and mechanisms.糖基转移酶:结构、功能及作用机制
Annu Rev Biochem. 2008;77:521-55. doi: 10.1146/annurev.biochem.76.061005.092322.
10
Mutations in pimE restore lipoarabinomannan synthesis and growth in a Mycobacterium smegmatis lpqW mutant.pimE 基因的突变可恢复耻垢分枝杆菌 lpqW 突变体中脂阿拉伯甘露聚糖的合成及生长。
J Bacteriol. 2008 May;190(10):3690-9. doi: 10.1128/JB.00200-08. Epub 2008 Mar 14.

分枝杆菌中磷酯酰肌醇甘露糖脂生物合成与调控的分子基础。

Molecular basis of phosphatidyl-myo-inositol mannoside biosynthesis and regulation in mycobacteria.

机构信息

Unidad de Biofisica, Centro Mixto Consejo Superior de Investigaciones Cientificas-Universidad del País Vasco/Euskal Herriko Unibertsitatea, Leioa, Bizkaia 48940, Spain.

出版信息

J Biol Chem. 2010 Oct 29;285(44):33577-83. doi: 10.1074/jbc.R110.168328. Epub 2010 Aug 27.

DOI:10.1074/jbc.R110.168328
PMID:20801880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2962455/
Abstract

Phosphatidyl-myo-inositol mannosides (PIMs) are unique glycolipids found in abundant quantities in the inner and outer membranes of the cell envelope of all Mycobacterium species. They are based on a phosphatidyl-myo-inositol lipid anchor carrying one to six mannose residues and up to four acyl chains. PIMs are considered not only essential structural components of the cell envelope but also the structural basis of the lipoglycans (lipomannan and lipoarabinomannan), all important molecules implicated in host-pathogen interactions in the course of tuberculosis and leprosy. Although the chemical structure of PIMs is now well established, knowledge of the enzymes and sequential events leading to their biosynthesis and regulation is still incomplete. Recent advances in the identification of key proteins involved in PIM biogenesis and the determination of the three-dimensional structures of the essential phosphatidyl-myo-inositol mannosyltransferase PimA and the lipoprotein LpqW have led to important insights into the molecular basis of this pathway.

摘要

磷酸肌醇甘露糖脂(PIMs)是一种独特的糖脂,在所有分枝杆菌物种的细胞包膜的内外膜中大量存在。它们基于带有一个到六个甘露糖残基和多达四个酰基链的磷酸肌醇脂质锚。PIMs 不仅被认为是细胞包膜的重要结构组成部分,也是糖脂(甘露聚糖和阿拉伯半乳聚糖)的结构基础,所有这些在结核分枝杆菌和麻风分枝杆菌的宿主-病原体相互作用过程中都是重要的分子。尽管 PIMs 的化学结构现在已经确定,但对导致其生物合成和调节的酶和顺序事件的了解仍然不完整。最近在鉴定参与 PIM 生物发生的关键蛋白方面的进展以及确定必需的磷酸肌醇甘露糖基转移酶 PimA 和脂蛋白 LpqW 的三维结构,使人们对该途径的分子基础有了重要的了解。