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机构地区:[1]哈尔滨商业大学黑龙江省高校食品科学与工程重点实验室,黑龙江哈尔滨150076
出 处:《食品科学》2016年第7期123-127,共5页Food Science
基 金:黑龙江省科技厅应用技术项目(G013B203);黑龙江省自然科学基金项目(C201201);黑龙江省高校科技创新团队建设计划项目(2010td04)
摘 要:采用对硝基苯基-β-D-葡萄糖苷法,与黑曲霉相比较考察素食者肠道菌LJ-G1、LJ-Q2产β-葡萄糖苷酶能力,再经单因素、响应面试验对菌种的产酶条件进行优化。结果表明:LJ-G1、LJ-Q2菌株均能产β-葡萄糖苷酶,且LJ-Q2产酶能力高于LJ-G1,与黑曲霉相比较,在发酵时间短于64 h时LJ-G1、LJ-Q2产酶能力高于黑曲霉;LJ-Q2菌种的最优产酶条件为:培养基p H 8.0、培养温度38℃、培养时间38 h。在最优条件下进行验证实验,酶活力达到1.70 IU/m L。加入大豆异黄酮原料进行发酵培养,得到游离大豆异黄酮转化率为39.4%。The β-glucosidase-producing capacity of strains LJ-G1 and LJ-Q2 isolated from the feces of vegetarians was measured using 4-nitrophenol-β-D-glucoside(p NPG) as substrate and compared with that of Aspergillus niger. The fermentation conditions for β-glucosidase production by the selected strain were optimized using combination of single factor method and response surface methodology. The results showed that both intestinal strains were able to produce β-glucosidase, and LJ-Q2 had higher β-glucosidase-producing capacity than LJ-G1. LJ-G1 and LJ-Q2 had higher β-glucosidase-producing capacity than Aspergillus niger in 64 h of fermentation. The optimal fermentation conditions for β-glucosidase production were determined as follows: culture medium p H, 8.0; temperature, 38 ℃; and time, 38 h. The experimental value of β-glucosidase activity produced under the optimized conditions was 1.70 IU/m L. The fermentation process could convert 39.4% of soybean isoflavones into aglycones.
分 类 号:TS201.3[轻工技术与工程—食品科学]
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