葛根纤维低聚糖的酶解制备及其对乳酸菌的体外促生长作用
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摘要
葛根富含淀粉、异黄酮和膳食纤维,其中的淀粉和异黄酮已得到较好利用,而大量膳食纤维作为垃圾丢弃。本研究采用β-葡聚糖酶酶解葛根膳食纤维制备纤维低聚糖;并以葛根纤维低聚糖为碳源,探讨其对肠道益生菌的体外促生长作用。采用Box-Benhnken中心组合试验设计优化得到葛根纤维低聚糖酶解制备工艺:酶用量5U/g,pH5.8,酶解时间3.0hr,温度48℃;此优化条件下,酶解产物中葡萄糖质量浓度最低,为0.49mg/mL,纤维低聚糖质量浓度可达到2.07mg/mL,其中纤维二糖1.36mg/mL,纤维三糖为0.71mg/mL。以葛根纤维低聚糖完全取代乳酸菌基础培养基中的碳源,培养24hr后,保加利亚乳杆菌、嗜热链球菌及青春双歧杆菌活菌数分别比基础培养基提高123%,124%and 146%。
Radix Puerariae is richedin isoflavonoids,starch and dietary fiber.Itis mainly used for production of starch and isoflavonoids nowadays.But plenty of dietary fiberwasignored.In the present work,cellooligosaccharides were prepared from Radix Puerariae dietary fiber by β-glucanase.By using Radix Puerariae cellooligosaccharidesas carbon source substitute in microbiological culture media,its growth-promoting effects on lactic acid bacteria in Vitro were also investigated.The preparing conditionsof Radix Puerariae cellooligosaccharides were optimized by Box-Benhnken design:β-glucanaseaddtion 5U/g,enzymolysis pH5.8,enzymolysis time 3.0 hr,enzymolysis temperature 48 ℃.Under these conditions,the glucose concentration in hydrolysatewas 0.49mg/mL,while the cellooligosaccharideconcentration was 2.07mg/mL,in which,cellobiose was1.36mg/mL,cellotriose was 0.71mg/mL.When carbon sourcein microbiological culture media was totally substituted by Radix Puerariae cellooligosaccharides,the number of Bulgaria Lactobacillus,Thermophilic streptococcus and Bifidobacterium adolescentis were increased by 123%,124%and 146%respectively 24 hr later.
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