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机构地区:[1]东北农业大学食品学院乳品科学教育部重点实验室,哈尔滨150030
出 处:《食品科技》2015年第5期2-9,共8页Food Science and Technology
基 金:教育部重点科技研究项目(20122325110017);教育部创新团队项目(IRT0959)
摘 要:从市售及实验室发酵的泡菜中分离筛选产葡聚糖的乳酸菌,获得一株葡聚糖产量为(5.24±0.14)g/L的菌株2-17,经生理生化以及16S r DNA序列同源性分析,鉴定该菌株为肠膜明串珠菌肠膜亚种。通过亚硝基胍和紫外复合诱变改善该菌株的葡聚糖产量,确定最佳复合诱变条件为:菌株在MRS培养基中培养9 h,经浓度为0.5 mg/m L亚硝基胍处理80 min,置于30 W紫外灯45 cm处照射30 s。经2轮复合诱变后,得到一突变菌株UN2-18,葡聚糖产量为(7.54±0.08)g/L,较出发菌株提高了43.89%。该突变株连续传10代后,葡聚糖产量仍维持在7.5 g/L。通过单因素试验,确定最优廉价培养基为2%豆粕(水解度10%)、10%蔗糖、2%K2HPO4,在此条件下葡聚糖产量为(34.4±0.07)g/L,较优化前提高了3.56倍。One lactic acid bacteria strain 2-17 with the glucan-producing capacity of(5.24±0.14) g/L was isolated from the commercial pickles and the pickles made in the laboratory. This strain was identifi ed as Leuconostoc mesenteroides subsp. mesenteroides by a series of physiological and biochemical tests and analysing the 16 SrDNA sequence. The glucan-producing capacity of the strain was improved by exposing the strain to nitrosoguanidine and UV irradiation successively, and the optimal mutagenic condition was determined as the following: the strain was first cultured in the MRS medium for 9h and then was exposed to 0.5 mg/m L nitrosoguanidine for 80 minutes followed by exposure to UV radiation(30 W) from distance of 45.0 cm for 30 s; then the culture was treated by the same nitrosoguanidine-UV complex mutation again. After that, one mutant UN2-18 with the glucan-producing capacity of(7.54±0.08) g/L was obtained and the glucan production of this mutant was 43.89% higher than that of its original strain. In addition, the strain obtained by continuous subculturing the mutant UN2-18 for 10 generations leveled out its glucan production by around 7.5 g/L. The optimal culture conditions of the cheap medium were determined for 2% soybean meal hydrolysised with degree of 10%, 10% sucrose and 2% K2HPO4. The glucan production of UN2-18 was(34.4±0.07) g/L, improving by 3.56 fold.
分 类 号:TS201.3[轻工技术与工程—食品科学]
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