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本文引用的文献

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Type I signal peptidase and protein secretion in Staphylococcus aureus.金黄色葡萄球菌中的 I 型信号肽酶和蛋白质分泌。
J Bacteriol. 2012 May;194(10):2677-86. doi: 10.1128/JB.00064-12. Epub 2012 Mar 23.
2
Proteolytic cleavage inactivates the Staphylococcus aureus lipoteichoic acid synthase.蛋白水解切割使金黄色葡萄球菌脂磷壁酸合成酶失活。
J Bacteriol. 2011 Oct;193(19):5279-91. doi: 10.1128/JB.00369-11. Epub 2011 Jul 22.
3
The SLH-domain protein BslO is a determinant of Bacillus anthracis chain length.SLH 结构域蛋白 BslO 是炭疽芽孢杆菌链长的决定因素。
Mol Microbiol. 2011 Jul;81(1):192-205. doi: 10.1111/j.1365-2958.2011.07688.x. Epub 2011 May 17.
4
Location, synthesis and function of glycolipids and polyglycerolphosphate lipoteichoic acid in Gram-positive bacteria of the phylum Firmicutes.厚壁菌门中革兰氏阳性菌的糖脂和聚甘油磷酸脂质-肽聚糖的位置、合成和功能。
FEMS Microbiol Lett. 2011 Jun;319(2):97-105. doi: 10.1111/j.1574-6968.2011.02260.x. Epub 2011 Mar 25.
5
Enzymatic activities and functional interdependencies of Bacillus subtilis lipoteichoic acid synthesis enzymes.枯草芽孢杆菌脂磷壁酸合成酶的酶活性和功能相互依赖性。
Mol Microbiol. 2011 Feb;79(3):566-83. doi: 10.1111/j.1365-2958.2010.07472.x. Epub 2010 Dec 7.
6
In vitro analysis of the Staphylococcus aureus lipoteichoic acid synthase enzyme using fluorescently labeled lipids.使用荧光标记脂质对金黄色葡萄球菌脂磷壁酸合酶进行体外分析。
J Bacteriol. 2010 Oct;192(20):5341-9. doi: 10.1128/JB.00453-10. Epub 2010 Aug 13.
7
Bacillus anthracis surface-layer proteins assemble by binding to the secondary cell wall polysaccharide in a manner that requires csaB and tagO.炭疽杆菌表面层蛋白通过与二次细胞壁多糖结合进行组装,这一过程需要 csaB 和 tagO。
J Mol Biol. 2010 Sep 3;401(5):757-75. doi: 10.1016/j.jmb.2010.06.059. Epub 2010 Jul 13.
8
Two-enzyme systems for glycolipid and polyglycerolphosphate lipoteichoic acid synthesis in Listeria monocytogenes.单核细胞增生李斯特菌中用于糖脂和聚甘油磷酸脂壁酸合成的双酶系统。
Mol Microbiol. 2009 Oct;74(2):299-314. doi: 10.1111/j.1365-2958.2009.06829.x. Epub 2009 Aug 4.
9
The surface of Bacillus anthracis.炭疽杆菌的表面。
Mol Aspects Med. 2009 Dec;30(6):374-85. doi: 10.1016/j.mam.2009.07.001. Epub 2009 Jul 14.
10
Distinct and essential morphogenic functions for wall- and lipo-teichoic acids in Bacillus subtilis.枯草芽孢杆菌中壁磷壁酸和脂磷壁酸独特且重要的形态发生功能。
EMBO J. 2009 Apr 8;28(7):830-42. doi: 10.1038/emboj.2009.25. Epub 2009 Feb 19.

炭疽芽胞杆菌中脂磷壁酸的合成。

Synthesis of lipoteichoic acids in Bacillus anthracis.

机构信息

Howard Taylor Ricketts Laboratory, Argonne National Laboratory, Argonne, Illinois, USA.

出版信息

J Bacteriol. 2012 Aug;194(16):4312-21. doi: 10.1128/JB.00626-12. Epub 2012 Jun 8.

DOI:10.1128/JB.00626-12
PMID:22685279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3416223/
Abstract

Lipoteichoic acid (LTA), a glycerol phosphate polymer, is a component of the envelope of Gram-positive bacteria that has hitherto not been identified in Bacillus anthracis, the causative agent of anthrax. LTA synthesis in Staphylococcus aureus and other microbes is catalyzed by the product of the ltaS gene, a membrane protein that polymerizes polyglycerol phosphate from phosphatidyl glycerol. Here we identified four ltaS homologues, designated ltaS1 to -4, in the genome of Bacillus anthracis. Polyglycerol phosphate-specific monoclonal antibodies were used to detect LTA in the envelope of B. anthracis strain Sterne (pXO1(+) pXO2(-)) vegetative forms. B. anthracis mutants lacking ltaS1, ltaS2, ltaS3, or ltaS4 did not display defects in growth or LTA synthesis. In contrast, B. anthracis strains lacking both ltaS1 and ltaS2 were unable to synthesize LTA and exhibited reduced viability, altered envelope morphology, aberrant separation of vegetative forms, and decreased sporulation efficiency. Expression of ltaS1 or ltaS2 alone in B. anthracis as well as in other microbes was sufficient for polyglycerol phosphate synthesis. Thus, similar to S. aureus, B. anthracis employs LtaS enzymes to synthesize LTA, an envelope component that promotes bacterial growth and cell division.

摘要

脂磷壁酸(LTA)是一种甘油磷酸聚合物,是革兰氏阳性菌包膜的组成部分,迄今尚未在炭疽杆菌(炭疽病的病原体)中发现。金黄色葡萄球菌和其他微生物中的 LTA 合成由 ltaS 基因产物催化,该产物是一种膜蛋白,可将磷脂酰甘油中的多聚甘油磷酸聚合。在这里,我们在炭疽杆菌基因组中鉴定了四个 ltaS 同源物,分别命名为 ltaS1 至 ltaS4。多聚甘油磷酸特异性单克隆抗体用于检测 Sterne 株(pXO1(+) pXO2(-))炭疽杆菌营养体形式的包膜中的 LTA。缺乏 ltaS1、ltaS2、ltaS3 或 ltaS4 的炭疽杆菌突变体在生长或 LTA 合成方面没有缺陷。相比之下,同时缺乏 ltaS1 和 ltaS2 的炭疽杆菌菌株无法合成 LTA,并且表现出活力降低、包膜形态改变、营养体形式异常分离和产孢效率降低。ltaS1 或 ltaS2 在炭疽杆菌以及其他微生物中的单独表达足以合成多聚甘油磷酸。因此,与金黄色葡萄球菌类似,炭疽杆菌使用 LtaS 酶合成 LTA,这是一种促进细菌生长和细胞分裂的包膜成分。