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作 者:李鑫[1] 顾夕梅 绳敖楠 张丽[1] 陈晓佩[1] 勇强[1]
机构地区:[1]南京林业大学化学工程学院,江苏南京210037
出 处:《林产化学与工业》2015年第5期93-97,共5页Chemistry and Industry of Forest Products
基 金:江苏省高校自然科学研究重大项目(14KJA220003);江苏省自然科学基金项目(BK20131426);江苏高校优势学科建设工程项目资助项目(无编号)
摘 要:采用聚乙二醇6000/柠檬酸钠的双水相木聚糖酶水解体系制备木二糖,以10 g/L桦木木聚糖为底物,木聚糖酶的酶用量为20 IU/g(以木聚糖质量计),在50℃、p H值5.6条件下,水解8 h制备木二糖,木二糖的酶解得率为13.8%。双水相水解体系对木聚糖酶回收率为66.4%,对木二糖回收率为87.2%;采用凝胶层析纯化方法,以葡聚糖凝胶LH-20为分离介质,脱气超纯水为洗脱剂,在柱温35℃、洗脱溶剂流速0.1 m L/min、上样量0.3 m L条件下,分离纯化木二糖,木二糖纯度为98.5%。Xylobiose was prepared by xylanase hydrolysis of birchwood xylan in the PEG6000 / sodium citrate aqueous two-phase system( ATPS). The optimized conditions for enzymatic hydrolysis in ATPS were birchwood xylan 10 g / L,xylanase 20 IU / g( calculated by the mass of xylan),50 ℃ and p H 5. 6. The enzymatic hydrolysis yield of xylobiose was 13. 8% for 8h. The recoveries of xylanase and xylobiose were 66. 4% and 87. 2%,respectively. Then,purification of xylobiose was carried out on Sephadex LH-20 with using degassed high purified water as eluent. The optimized conditions for purification of xylobiose were column temperature 35 ℃,0. 1 m L / min and sample volume 0. 3 m L. After purification,the purity of xylobiose was improved to98. 5% under the optimized conditions.
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