Reichhardt Courtney, Fong Jiunn C N, Yildiz Fitnat, Cegelski Lynette
Department of Chemistry, Stanford University, Mudd Building, Room 121, 333 Campus Drive, Stanford, CA 94305, USA.
Department of Microbiology and Environmental Toxicology, UC Santa Cruz, 1156 High Street, Santa Cruz, CA 95064, USA.
Biochim Biophys Acta. 2015 Jan;1848(1 Pt B):378-83. doi: 10.1016/j.bbamem.2014.05.030. Epub 2014 Jun 7.
Bacterial biofilms are communities of bacterial cells surrounded by a self-secreted extracellular matrix. Biofilm formation by Vibrio cholerae, the human pathogen responsible for cholera, contributes to its environmental survival and infectivity. Important genetic and molecular requirements have been identified for V. cholerae biofilm formation, yet a compositional accounting of these parts in the intact biofilm or extracellular matrix has not been described. As insoluble and non-crystalline assemblies, determinations of biofilm composition pose a challenge to conventional biochemical and biophysical analyses. The V. cholerae extracellular matrix composition is particularly complex with several proteins, complex polysaccharides, and other biomolecules having been identified as matrix parts. We developed a new top-down solid-state NMR approach to spectroscopically assign and quantify the carbon pools of the intact V. cholerae extracellular matrix using ¹³C CPMAS and ¹³C{(¹⁵N}, ¹⁵N{³¹P}, and ¹³C{³¹P}REDOR. General sugar, lipid, and amino acid pools were first profiled and then further annotated and quantified as specific carbon types, including carbonyls, amides, glycyl carbons, and anomerics. In addition, ¹⁵N profiling revealed a large amine pool relative to amide contributions, reflecting the prevalence of molecular modifications with free amine groups. Our top-down approach could be implemented immediately to examine the extracellular matrix from mutant strains that might alter polysaccharide production or lipid release beyond the cell surface; or to monitor changes that may accompany environmental variations and stressors such as altered nutrient composition, oxidative stress or antibiotics. More generally, our analysis has demonstrated that solid-state NMR is a valuable tool to characterize complex biofilm systems.
细菌生物膜是由自我分泌的细胞外基质包围的细菌细胞群落。霍乱弧菌是导致霍乱的人类病原体,其生物膜的形成有助于其在环境中的生存和传染性。对于霍乱弧菌生物膜的形成,已经确定了重要的遗传和分子要求,但尚未描述完整生物膜或细胞外基质中这些成分的组成情况。作为不溶性和非晶态的聚集体,生物膜组成的测定对传统的生化和生物物理分析构成了挑战。霍乱弧菌的细胞外基质组成特别复杂,已鉴定出几种蛋白质、复合多糖和其他生物分子作为基质成分。我们开发了一种新的自上而下的固态核磁共振方法,使用¹³C CPMAS以及¹³C{(¹⁵N}、¹⁵N{³¹P}和¹³C{³¹P}REDOR对完整的霍乱弧菌细胞外基质的碳库进行光谱分配和定量。首先对一般的糖、脂质和氨基酸库进行分析,然后进一步注释和定量为特定的碳类型,包括羰基、酰胺、甘氨酰碳和异头物。此外,¹⁵N分析显示相对于酰胺贡献有大量的胺库,这反映了带有游离胺基的分子修饰的普遍性。我们的自上而下的方法可以立即用于检查突变菌株的细胞外基质,这些突变菌株可能会改变多糖的产生或细胞表面以外的脂质释放;或者监测可能伴随环境变化和应激因素(如营养成分改变、氧化应激或抗生素)的变化。更一般地说,我们的分析表明固态核磁共振是表征复杂生物膜系统的有价值工具。