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固态核磁共振光谱研究山梨酸在不同pH值水平下与磷脂膜的相互作用。

Solid-state NMR spectroscopic studies on the interaction of sorbic acid with phospholipid membranes at different pH levels.

作者信息

Chu Shidong, Hawes John W, Lorigan Gary A

机构信息

Department of Chemistry and Biochemistry, Miami University, Oxford, OH 45056, USA.

出版信息

Magn Reson Chem. 2009 Aug;47(8):651-7. doi: 10.1002/mrc.2444.

Abstract

2H, 31P, and 1H-magic-angle-spinning (MAS) solid-state NMR spectroscopic methods were used to elucidate the interaction between sorbic acid, a widely used weak acid food preservative, and 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) bilayers under both acidic and neutral pH conditions. The linewidth broadening observed in the 31P NMR powder pattern spectra and the changes in the 31P longitudinal relaxation time (T1) indicate interaction with the phospholipid headgroup upon titration of sorbic acid or decanoic acid into DMPC bilayers over the pH range from 3.0 to 7.4. The peak intensities of sorbic acid decrease upon addition of paramagnetic Mn2+ ions in DMPC bilayers as recorded in the 1H MAS NMR spectra, suggesting that sorbic acid molecules are in close proximity with the membrane/aqueous surface. No significant 2H quadrupolar splitting (DeltanuQ) changes are observed in the 2H NMR spectra of DMPC-d54 upon titration of sorbic acid, and the change of pH has a slight effect on DeltanuQ, indicating that sorbic acid has weak influence on the orientation order of the DMPC acyl chains in the fluid phase over the pH range from 3.0 to 7.4. This finding is in contrast to the results of the decanoic acid/DMPC-d54 systems, where DeltanuQ increases as the concentration of decanoic acid increases. Thus, in the membrane association process, sorbic acids are most likely interacting with the headgroups and shallowly embedded near the top of the phospholipid headgroups, rather than inserting deep into the acyl chains. Thus, antimicrobial mode of action for sorbic acid may be different from that of long-chain fatty acids.

摘要

采用2H、31P和1H魔角旋转(MAS)固态核磁共振光谱方法,以阐明山梨酸(一种广泛使用的弱酸食品防腐剂)与1,2-二肉豆蔻酰-sn-甘油-3-磷酸胆碱(DMPC)双层膜在酸性和中性pH条件下的相互作用。在31P NMR粉末图谱光谱中观察到的线宽变宽以及31P纵向弛豫时间(T1)的变化表明,在pH值为3.0至7.4的范围内,将山梨酸或癸酸滴定到DMPC双层膜中时,其与磷脂头部基团发生了相互作用。如1H MAS NMR光谱所记录,在DMPC双层膜中加入顺磁性Mn2+离子后,山梨酸的峰强度降低,这表明山梨酸分子与膜/水表面紧密相邻。滴定山梨酸时,在DMPC-d54的2H NMR光谱中未观察到明显的2H四极分裂(ΔνQ)变化,且pH变化对ΔνQ有轻微影响,这表明在pH值为3.0至7.4的范围内,山梨酸对DMPC酰基链在流体相中的取向顺序影响较弱。这一发现与癸酸/DMPC-d54体系的结果相反,在该体系中,ΔνQ随癸酸浓度的增加而增大。因此,在膜缔合过程中,山梨酸很可能与头部基团相互作用,并浅埋于磷脂头部基团顶部附近,而非深入插入酰基链中。因此,山梨酸的抗菌作用模式可能与长链脂肪酸不同。

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