Sulfation algae glycan oligose
一种硫酸化藻聚糖寡糖、硫酸化藻聚糖的技术,应用在低聚糖、发酵等方向
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[0049] The present invention is specifically described below with examples, but the present invention is not limited to the scope of the following examples.
[0050] The molecular weight of the sulfated alginate oligosaccharide in this example is the average molecular weight calculated from the mass analysis results.
reference example 1
[0051] Reference Example 1 Preparation of Fucoidan from Longaceae
[0052] Grind 2 kg of dried longan after breeding with a cutting machine (manufactured by Masuko Sangyo Co., Ltd.) equipped with a sieve with a pore size of 1 mm, suspend in 20 liters of 80% ethanol, stir at 25°C for 3 hours, and filter with filter paper . The resulting residue was suspended in 40 liters of 30 mM phosphate buffer (pH 6.5) containing 100 mM sodium chloride, treated at 95° C. for 2 hours, and then filtered through a stainless steel sieve with a pore size of 106 μm. 200 g of activated carbon, 4.5 liters of ethanol, and 12,000 U of alginate lyase K (manufactured by Nakaze Seika Kogyo Co., Ltd.) were added to the obtained filtrate, stirred at 25° C. for 20 hours, and centrifuged. The obtained supernatant was concentrated to 4 liters with an ultrafilter equipped with a hollow fiber having an exclusion molecular weight of 100,000, centrifuged to remove insoluble matter, and left standing at 5° C. for...
reference example 2
[0053] Reference example 2 Preparation of sulfated alginate part
[0054] 7 g of the dried fucoidan described in Reference Example 1 was dissolved in 700 ml of 20 mM imidazole hydrochloride buffer (pH 8.0) containing 50 mM sodium chloride and 10% ethanol, and the insoluble matter was removed by centrifugation. The resulting supernatant was poured into a DEAE-Cellulofine A-800 column (11.4×48 cm) equilibrated with the same buffer, washed with the same buffer, and then eluted with a concentration gradient of sodium chloride from 50 mM to 1.95 M. The eluent was taken out every 250ml. The total sugar content of each part was determined by the phenol sulfuric acid method, and the uronic acid content was determined by the carbazole sulfuric acid method. Parts 43-49, 50-55, and 56-67 were sorted according to the elution order, desalted by electrodialysis and then freeze-dried to obtain 340 mg from 43-49, 870 mg from 50-55, and 56-67. 2.64 g dry matter. The fraction obtained from f...
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