Suppr超能文献

脂多糖(LPS)内核磷酸盐对于铜绿假单胞菌 PAO1 中 LPS 的完全合成和向外膜的运输是必需的。

Lipopolysaccharide (LPS) inner-core phosphates are required for complete LPS synthesis and transport to the outer membrane in Pseudomonas aeruginosa PAO1.

机构信息

Infectious Diseases and Center for Proteomic Chemistry, Cambridge, Massachusetts, USA.

出版信息

mBio. 2011 Aug 2;2(4). doi: 10.1128/mBio.00142-11. Print 2011.

Abstract

Gram-negative outer membrane (OM) integrity is maintained in part by Mg(2+) cross-links between phosphates on lipid A and on core sugars of adjacent lipopolysaccharide (LPS) molecules. In contrast to other Gram-negative bacteria, waaP, encoding an inner-core kinase, could not be inactivated in Pseudomonas aeruginosa. To examine this further, expression of the kinases WaaP or WapP/WapQ/PA5006 was placed under the control of the arabinose-regulated pBAD promoter. Growth of these strains was arabinose dependent, confirming that core phosphorylation is essential in P. aeruginosa. Transmission electron micrographs of kinase-depleted cells revealed marked invaginations of the inner membrane. SDS-PAGE of total LPS from WaaP-depleted cells showed accumulation of a fast-migrating band. Mass spectrometry (MS) analysis revealed that LPS from these cells exhibits a unique truncated core consisting of two 3-deoxy-d-manno-octulosonic acids (Kdo), two l-glycero-d-manno-heptoses (Hep), and one hexose but completely devoid of phosphates, indicating that phosphorylation by WaaP is necessary for subsequent core phosphorylations. MS analysis of lipid A from WaaP-depleted cells revealed extensive 4-amino-4-deoxy-l-arabinose modification. OM prepared from these cells by Sarkosyl extraction of total membranes or by sucrose density gradient centrifugation lacked truncated LPS. Instead, truncated LPS was detected in the inner membrane fractions, consistent with impaired transport/assembly of this species into the OM. IMPORTANCE Gram-negative bacteria have an outer membrane (OM) comprised of a phospholipid inner leaflet and a lipopolysaccharide (LPS) outer leaflet. The OM protects cells from toxic molecules and is important for survival during infection. The LPS core kinase gene waaP can be deleted in several Gram-negative bacteria but not in Pseudomonas aeruginosa. We used a controlled-expression system to deplete WaaP directly in P. aeruginosa cells, which halted growth. WaaP depletion also caused gross changes in cell morphology and led to the accumulation of an aberrant LPS lacking several core sugars and all core phosphates. The aberrant LPS failed to reach the OM, suggesting that WaaP is essential in P. aeruginosa because it is required to produce the full-length LPS that is recognized by the OM transport/assembly machinery in this organism. Therefore, WaaP may constitute a good target for the development of novel antipseudomonal agents.

摘要

革兰氏阴性外膜 (OM) 的完整性部分由脂多糖 (LPS) 分子中脂质 A 和核心糖上的磷酸之间的镁 (Mg2+) 交联维持。与其他革兰氏阴性菌不同,编码内核心激酶的 waaP 在铜绿假单胞菌中不能失活。为了进一步研究这一点,将激酶 WaaP 或 WapP/WapQ/PA5006 的表达置于阿拉伯糖调节的 pBAD 启动子的控制之下。这些菌株的生长依赖于阿拉伯糖,这证实了核心磷酸化在铜绿假单胞菌中是必不可少的。激酶耗尽细胞的透射电子显微镜照片显示内膜明显内陷。WaaP 耗尽细胞的总 LPS 的 SDS-PAGE 显示出快速迁移带的积累。质谱 (MS) 分析表明,这些细胞的 LPS 表现出独特的截断核心,由两个 3-脱氧-d-甘露基-octulosonic 酸 (Kdo)、两个 l-甘油基-d-甘露庚糖 (Hep) 和一个己糖组成,但完全没有磷酸,表明 WaaP 的磷酸化是随后的核心磷酸化所必需的。WaaP 耗尽细胞的脂 A 的 MS 分析显示出广泛的 4-氨基-4-脱氧-l-阿拉伯糖修饰。通过总膜的 Sarkosyl 提取或通过蔗糖密度梯度离心从这些细胞制备的 OM 缺乏截断 LPS。相反,在内膜部分检测到截断 LPS,这与该物质转运/组装到 OM 中受损一致。

重要性:革兰氏阴性菌的外膜 (OM) 由磷脂内层和脂多糖 (LPS) 外层组成。OM 保护细胞免受有毒分子的侵害,并在感染期间对生存至关重要。LPS 核心激酶基因 waaP 可以在几种革兰氏阴性菌中缺失,但不能在铜绿假单胞菌中缺失。我们使用了一种受控表达系统直接在铜绿假单胞菌细胞中耗尽 WaaP,这阻止了生长。WaaP 耗尽还导致细胞形态发生严重变化,并导致异常 LPS 的积累,该 LPS 缺乏几个核心糖和所有核心磷酸。异常 LPS 未能到达 OM,这表明 WaaP 在铜绿假单胞菌中是必不可少的,因为它是产生被该生物体 OM 转运/组装机制识别的全长 LPS 所必需的。因此,WaaP 可能是开发新型抗假单胞菌药物的良好靶标。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验