School of Microbiology, School of Food and Nutritional Sciences, SUSFERM Fermentation Science and Bioprocess Engineering Centre, University College Cork, T12 K8AF Cork, Ireland.
Circular Bioeconomy Research Group, Shannon Applied Biotechnology Centre, Munster Technology, V92 CX88 Tralee, Ireland.
Mar Drugs. 2023 May 21;21(5):315. doi: 10.3390/md21050315.
The present study investigates the molecular characteristics of fucoidan obtained from the brown Irish seaweed , employing hydrothermal-assisted extraction (HAE) followed by a three-step purification protocol. The dried seaweed biomass contained 100.9 mg/g of fucoidan, whereas optimised HAE conditions (solvent, 0.1N HCl; time, 62 min; temperature, 120 °C; and solid to liquid ratio, 1:30 (/)) yielded 417.6 mg/g of fucoidan in the crude extract. A three-step purification of the crude extract, involving solvents (ethanol, water, and calcium chloride), molecular weight cut-off filter (MWCO; 10 kDa), and solid-phase extraction (SPE), resulted in 517.1 mg/g, 562.3 mg/g, and 633.2 mg/g of fucoidan ( < 0.05), respectively. In vitro antioxidant activity, as determined by 1,1-diphenyl-2-picryl-hydrazyl radical scavenging and ferric reducing antioxidant power assays, revealed that the crude extract exhibited the highest antioxidant activity compared to the purified fractions, commercial fucoidan, and ascorbic acid standard ( < 0.05). The molecular attributes of biologically active fucoidan-rich MWCO fraction was characterised by quadruple time of flight mass spectrometry and Fourier-transform infrared (FTIR) spectroscopy. The electrospray ionisation mass spectra of purified fucoidan revealed quadruply ([M+4H]) and triply ([M+3H]) charged fucoidan moieties at 1376 and 1824, respectively, and confirmed the molecular mass 5444 Da (~5.4 kDa) from multiply charged species. The FTIR analysis of both purified fucoidan and commercial fucoidan standard exhibited O-H, C-H, and S=O stretching which are represented by bands at 3400 cm, 2920 cm, and 1220-1230 cm, respectively. In conclusion, the fucoidan recovered from HAE followed by a three-step purification process was highly purified; however, purification reduced the antioxidant activity compared to the crude extract.
本研究采用水热辅助提取(HAE)结合三步纯化方案,研究了从爱尔兰棕色海藻中提取的褐藻糖胶的分子特征。干燥的海藻生物质中含有 100.9mg/g 的褐藻糖胶,而优化的 HAE 条件(溶剂为 0.1N HCl;时间为 62 分钟;温度为 120°C;固液比为 1:30 (/))可从粗提取物中获得 417.6mg/g 的褐藻糖胶。对粗提取物进行三步纯化,涉及溶剂(乙醇、水和氯化钙)、分子量截止滤器(MWCO;10kDa)和固相萃取(SPE),分别得到 517.1mg/g、562.3mg/g 和 633.2mg/g 的褐藻糖胶( < 0.05)。通过 1,1-二苯基-2-苦基肼自由基清除和铁还原抗氧化能力测定法测定体外抗氧化活性表明,与纯化部分、商业褐藻糖胶和抗坏血酸标准品相比,粗提取物表现出最高的抗氧化活性( < 0.05)。用四极飞行时间质谱和傅里叶变换红外(FTIR)光谱对具有生物活性的富褐藻糖胶 MWCO 级分的分子特性进行了表征。纯化褐藻糖胶的电喷雾电离质谱显示,四重([M+4H])和三重([M+3H])带电褐藻糖胶部分分别在 1376 和 1824 处,证实了多电荷物种的分子量为 5444Da(~5.4kDa)。纯化褐藻糖胶和商业褐藻糖胶标准品的 FTIR 分析均显示 O-H、C-H 和 S=O 伸缩,分别由 3400cm、2920cm 和 1220-1230cm 处的带表示。总之,从 HAE 回收并经过三步纯化过程得到的褐藻糖胶高度纯化;然而,与粗提取物相比,纯化降低了抗氧化活性。