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本文引用的文献

1
Synthesis of the antigenic tetrasaccharide side chain from the major glycoprotein of Bacillus anthracis exosporium.炭疽芽孢杆菌外孢子主要糖蛋白抗原性四糖侧链的合成。
J Org Chem. 2007 Aug 17;72(17):6513-20. doi: 10.1021/jo070750s. Epub 2007 Jul 28.
2
Bacillus anthracis spores of the bclA mutant exhibit increased adherence to epithelial cells, fibroblasts, and endothelial cells but not to macrophages.bclA突变型炭疽芽孢杆菌孢子对上皮细胞、成纤维细胞和内皮细胞的黏附性增强,但对巨噬细胞的黏附性未增强。
Infect Immun. 2007 Sep;75(9):4498-505. doi: 10.1128/IAI.00434-07. Epub 2007 Jul 2.
3
Immunogens related to the synthetic tetrasaccharide side chain of the Bacillus anthracis exosporium.与炭疽芽孢杆菌外孢子囊合成四糖侧链相关的免疫原。
Bioorg Med Chem. 2007 Jun 15;15(12):4283-310. doi: 10.1016/j.bmc.2007.03.057. Epub 2007 Mar 23.
4
The complete genome sequence of Bacillus thuringiensis Al Hakam.苏云金芽孢杆菌Al Hakam的全基因组序列。
J Bacteriol. 2007 May;189(9):3680-1. doi: 10.1128/JB.00241-07. Epub 2007 Mar 2.
5
Synthesis and antigenic analysis of the BclA glycoprotein oligosaccharide from the Bacillus anthracis exosporium.炭疽芽孢杆菌外孢子囊BclA糖蛋白寡糖的合成与抗原分析
Chemistry. 2006 Dec 13;12(36):9136-49. doi: 10.1002/chem.200601245.
6
Anti-carbohydrate antibodies for the detection of anthrax spores.用于检测炭疽芽孢的抗碳水化合物抗体。
Angew Chem Int Ed Engl. 2006 Oct 6;45(39):6581-2. doi: 10.1002/anie.200602048.
7
Bacillus anthracis multiplication, persistence, and genetic exchange in the rhizosphere of grass plants.炭疽芽孢杆菌在禾本科植物根际的增殖、存活及基因交换
Appl Environ Microbiol. 2006 May;72(5):3168-74. doi: 10.1128/AEM.72.5.3168-3174.2006.
8
Monoclonal antibodies for Bacillus anthracis spore detection and functional analyses of spore germination and outgrowth.用于炭疽芽孢杆菌孢子检测以及孢子萌发和生长功能分析的单克隆抗体。
J Immunol. 2006 May 15;176(10):6076-84. doi: 10.4049/jimmunol.176.10.6076.
9
Pathogenomic sequence analysis of Bacillus cereus and Bacillus thuringiensis isolates closely related to Bacillus anthracis.与炭疽芽孢杆菌密切相关的蜡样芽孢杆菌和苏云金芽孢杆菌分离株的病原体基因组序列分析。
J Bacteriol. 2006 May;188(9):3382-90. doi: 10.1128/JB.188.9.3382-3390.2006.
10
From genomics to chemical genomics: new developments in KEGG.从基因组学到化学基因组学:KEGG的新进展
Nucleic Acids Res. 2006 Jan 1;34(Database issue):D354-7. doi: 10.1093/nar/gkj102.

炭疽芽孢杆菌的蒽糖生物合成操纵子。

Anthrose biosynthetic operon of Bacillus anthracis.

作者信息

Dong Shengli, McPherson Sylvia A, Tan Li, Chesnokova Olga N, Turnbough Charles L, Pritchard David G

机构信息

University of Alabama at Birmingham, Department of Biochemistry and Molecular Genetics, 1530 3rd Ave. S, Birmingham, AL 35294-2170, USA.

出版信息

J Bacteriol. 2008 Apr;190(7):2350-9. doi: 10.1128/JB.01899-07. Epub 2008 Feb 1.

DOI:10.1128/JB.01899-07
PMID:18245286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2293201/
Abstract

The exosporium of Bacillus anthracis spores consists of a basal layer and an external hair-like nap. The nap is composed primarily of the glycoprotein BclA, which contains a collagen-like region with multiple copies of a pentasaccharide side chain. This oligosaccharide possesses an unusual terminal sugar called anthrose, followed by three rhamnose residues and a protein-bound N-acetylgalactosamine. Based on the structure of anthrose, we proposed an enzymatic pathway for its biosynthesis. Examination of the B. anthracis genome revealed six contiguous genes that could encode the predicted anthrose biosynthetic enzymes. These genes are transcribed in the same direction and appear to form two operons. We introduced mutations into the B. anthracis chromosome that either delete the promoter of the putative upstream, four-gene operon or delete selected genes in both putative operons. Spores produced by strains carrying mutations in the upstream operon completely lacked or contained much less anthrose, indicating that this operon is required for anthrose biosynthesis. In contrast, inactivation of the downstream, two-gene operon did not alter anthrose content. Additional experiments confirmed the organization of the anthrose operon and indicated that it is transcribed from a sigma(E)-specific promoter. Finally, we demonstrated that anthrose biosynthesis is not restricted to B. anthracis as previously suggested.

摘要

炭疽芽孢杆菌孢子的芽孢外膜由一个基底层和外部毛发状绒毛组成。该绒毛主要由糖蛋白BclA构成,其包含一个具有多个五糖侧链拷贝的类胶原区域。这种寡糖拥有一种名为蒽糖的不寻常末端糖,接着是三个鼠李糖残基和一个与蛋白质结合的N-乙酰半乳糖胺。基于蒽糖的结构,我们提出了其生物合成的酶促途径。对炭疽芽孢杆菌基因组的研究揭示了六个相邻基因,它们可能编码预测的蒽糖生物合成酶。这些基因按相同方向转录,似乎形成两个操纵子。我们在炭疽芽孢杆菌染色体中引入突变,要么删除假定的上游四基因操纵子的启动子,要么删除两个假定操纵子中的选定基因。在上游操纵子中携带突变的菌株产生的孢子完全缺乏蒽糖或蒽糖含量大幅降低,这表明该操纵子是蒽糖生物合成所必需的。相比之下,下游两基因操纵子的失活并未改变蒽糖含量。进一步的实验证实了蒽糖操纵子的结构,并表明它是从一个σ(E)特异性启动子转录的。最后,我们证明蒽糖生物合成并不像之前所认为的那样仅限于炭疽芽孢杆菌。