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中国精品科技期刊2020
严芬, 连燕萍, 杨光, 王培松, 吴晨烁, 陈宁辛. 高产褐藻胶裂解酶菌株的筛选及发酵条件优化[J]. 食品工业科技, 2015, (22): 287-292. DOI: 10.13386/j.issn1002-0306.2015.22.051
引用本文: 严芬, 连燕萍, 杨光, 王培松, 吴晨烁, 陈宁辛. 高产褐藻胶裂解酶菌株的筛选及发酵条件优化[J]. 食品工业科技, 2015, (22): 287-292. DOI: 10.13386/j.issn1002-0306.2015.22.051
YAN Fen, LIAN Yan-ping, YANG Guang, WANG Pei-song, WU Chen-shuo, CHEN Ning-xin. Screening of alginate lyase-producing strains and optimization of fermentation conditions[J]. Science and Technology of Food Industry, 2015, (22): 287-292. DOI: 10.13386/j.issn1002-0306.2015.22.051
Citation: YAN Fen, LIAN Yan-ping, YANG Guang, WANG Pei-song, WU Chen-shuo, CHEN Ning-xin. Screening of alginate lyase-producing strains and optimization of fermentation conditions[J]. Science and Technology of Food Industry, 2015, (22): 287-292. DOI: 10.13386/j.issn1002-0306.2015.22.051

高产褐藻胶裂解酶菌株的筛选及发酵条件优化

Screening of alginate lyase-producing strains and optimization of fermentation conditions

  • 摘要: 采用透明圈初筛方法得到一株产褐藻胶裂解酶菌株B1,通过形态观察和16S r DNA序列分析鉴定该菌株为假交替单胞菌属(Pseudoalteromonas sp.)。通过单因素实验对菌株B1产酶条件进行优化,最佳培养基组成为:褐藻酸钠1%,氯化铵0.2%,Na Cl 3%,KH2PO40.02%,Mg SO40.01%,Ca Cl2·2H2O 0.1%,初始p H5.5。最佳的培养条件:装液量75 m L,培养温度30℃,摇床转速180 r/min,培养22 h。在该条件下,褐藻胶裂解酶最高酶活力提高到71.94 U/m L,提高了72.11%。 

     

    Abstract: A bacterial alginate lyase-producing strain B1 was screened with transparent circle method,It was identified as Pseudoalteromonas sp. according to its morphological observation and 16 S r DNA sequence analysis to identified strain B1.And by single-factor method to optimize its enzyme production conditions,the optimal medium component were,sodium alginate 1%,NH4 Cl 0.2%,Na Cl 3%,KH2PO40.02%,Mg SO40.01%,Ca Cl2·2H2O 0.1%,initial p H5.5,the optimal culture conditions were as follows :75 m L medium in 250 m L Erlenmeyer flask,Cultured at 30 ℃,shaking speed of 180 r/min,for 22 h. Under the optimal culture conditions,the highest enzyme activity of alginate lyase was up to 71.94 U/m L,improving 72.11%.

     

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