Peptidoglycan and Teichoic Acid Levels and Alterations in Staphylococcus aureus by Cell-Wall and Whole-Cell Nuclear Magnetic Resonance

被引:36
作者
Romaniuk, Joseph A. H. [1 ]
Cegelski, Lynette [1 ]
机构
[1] Stanford Univ, Dept Chem, 380 Roth Way, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
DAPTOMYCIN RESISTANCE; LYSOZYME RESISTANCE; BIOSYNTHESIS; MECHANISM; POLYMERS; ANTIBIOTICS; VANCOMYCIN; COMPLEXES; BACTERIA; BINDING;
D O I
10.1021/acs.biochem.8b00495
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gram-positive bacteria surround themselves with a multilayered macromolecular cell wall that is essential to cell survival and serves as a major target for antibiotics. The cell wall of Staphylococcus aureus is composed of two major structural components, peptidoglycan (PG) and wall teichoic acid (WTA), together creating a heterogeneous and insoluble matrix that poses a challenge to quantitative compositional analysis. Here, we present C-13 cross polarization magic angle spinning solid-state nuclear magnetic resonance (NMR) spectra of intact cell walls, purified PG, and purified WTA. The spectra reveal the clear molecular differences in the two polymers and enable quantification of PG and WTA in isolated cell walls, an attractive alternative to estimating teichoic acid content from a phosphate analysis of completely pyrolyzed cell walls. Furthermore, we discovered that unique PG and WTA spectral signatures could be identified in whole-cell NMR spectra and used to compare PG and WTA levels among intact bacterial cell samples. The distinguishing whole-cell C-13 NMR contributions associated with PG include the GlcNAc-MurNAc sugar carbons and glycyl alpha-carbons. WTA contributes carbons from the phosphoribitol backbone. Distinguishing N-15 spectral signatures include glycyl amide nitrogens in PG and the esterified D-alanyl amine nitrogens in WTA. C-13 NMR analysis was performed with samples at natural abundance and included 10 whole-cell sample comparisons. Changes consistent with altered PG and WTA content were detected in whole-cell spectra of bacteria harvested at different growth times and in cells treated with tunicamycin. This use of whole-cell NMR provides quantitative parameters of composition in the context of whole-cell activity.
引用
收藏
页码:3966 / 3975
页数:10
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