Tecson Mariel G, Abad Lucille V, Ebajo Virgilio D, Camacho Drexel H
Chemistry Department, De La Salle University, 2401 Taft Avenue, Manila 0922, Philippines.
Philippine Nuclear Research Institute, Department of Science and Technology, Commonwealth Avenue, Quezon City 1101, Philippines.
Ultrason Sonochem. 2021 May;73:105540. doi: 10.1016/j.ultsonch.2021.105540. Epub 2021 Mar 26.
Degradation of polysaccharides to afford low-molecular-weight oligosaccharides have been shown to produce new bioactivities that are not present in the starting material. The simplicity of ultrasonic treatment in the degradation of a polysaccharide, such as κ-carrageenan, offers practical advantage in producing degraded products with lower molecular weight that may have new interesting potential activities. This study embarked on investigating the effects in molecular weights and structural changes of κ-carrageenan under varying ultrasonic conditions. Molecular weight (MW) monitoring of ultrasonically-treated κ-carrageenan at various conditions were done by gel permeation chromatography. The product formed using the optimized condition was characterized using FTIR and NMR. The decrease in MW has been shown to be dependent on low concentration (5.0 mg mL), high amplitude (85%), and long treatment time (180 mins) to afford a degraded κ-carrageenan with average molecular weight (AMW) of 41,864 Da, which is a 96.33% reduction from the raw sample with initial AMW of 1,139,927 Da. Structural analysis reveals that most of the peaks of the raw κ-carrageenan was retained with minor change. 1D and 2D NMR analyses showed that the sonic process afforded a product where the sulfate group at the G4S-4 position was cleaved forming a methylene in the G4S ring. The results would be useful in the structure-activity relationship of κ-carrageenan oligosaccharides and in understanding the effect in the various potential applications of degraded κ-carrageenan.
多糖降解为低分子量的寡糖已被证明会产生起始原料中不存在的新生物活性。超声处理降解多糖(如κ-卡拉胶)的操作简便,在生产可能具有新的有趣潜在活性的低分子量降解产物方面具有实际优势。本研究着手调查不同超声条件下κ-卡拉胶的分子量和结构变化的影响。通过凝胶渗透色谱法对不同条件下超声处理的κ-卡拉胶进行分子量(MW)监测。使用优化条件形成的产物用傅里叶变换红外光谱(FTIR)和核磁共振(NMR)进行表征。结果表明,分子量的降低取决于低浓度(5.0 mg/mL)、高振幅(85%)和长时间处理(180分钟),从而得到平均分子量(AMW)为41,864 Da的降解κ-卡拉胶,与初始平均分子量为1,139,927 Da的原始样品相比,降低了96.33%。结构分析表明,原始κ-卡拉胶的大部分峰得以保留,变化较小。一维和二维核磁共振分析表明,超声处理得到的产物中,G4S-4位置的硫酸根被裂解,在G4S环中形成了一个亚甲基。这些结果将有助于研究κ-卡拉胶寡糖的构效关系,并有助于理解降解κ-卡拉胶在各种潜在应用中的效果。