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中国精品科技期刊2020

一株琼胶降解菌的筛选、鉴定及粗酶学性质

刘兴凯, 朱丹, 周薪, 房玲, 郭爽, 郭瑞, 程凡升

刘兴凯, 朱丹, 周薪, 房玲, 郭爽, 郭瑞, 程凡升. 一株琼胶降解菌的筛选、鉴定及粗酶学性质[J]. 食品工业科技, 2017, (19): 100-104. DOI: 10.13386/j.issn1002-0306.2017.19.019
引用本文: 刘兴凯, 朱丹, 周薪, 房玲, 郭爽, 郭瑞, 程凡升. 一株琼胶降解菌的筛选、鉴定及粗酶学性质[J]. 食品工业科技, 2017, (19): 100-104. DOI: 10.13386/j.issn1002-0306.2017.19.019
LIU Xing-kai, ZHU Dan, ZHOU Xin, FANG Ling, GUO Shuang, GUO Rui, CHENG Fan-sheng. Isolation, identification and enzymology properties of an agarase-producing strain[J]. Science and Technology of Food Industry, 2017, (19): 100-104. DOI: 10.13386/j.issn1002-0306.2017.19.019
Citation: LIU Xing-kai, ZHU Dan, ZHOU Xin, FANG Ling, GUO Shuang, GUO Rui, CHENG Fan-sheng. Isolation, identification and enzymology properties of an agarase-producing strain[J]. Science and Technology of Food Industry, 2017, (19): 100-104. DOI: 10.13386/j.issn1002-0306.2017.19.019

一株琼胶降解菌的筛选、鉴定及粗酶学性质

基金项目: 

国家自然科学基金项目(31301438,31501331); 山东省优秀中青年科学家奖励基金(BS2013SW034); 校高层次人才启动基金(1113321); 青岛农业大学应用型人才培养特色名校建设工程大学生科技创新项目;

详细信息
    作者简介:

    刘兴凯 (1994-) , 男, 本科, 研究方向:食品生物技术, E-mail:1176738058@qq.com。;

  • 中图分类号: TS201.3

Isolation, identification and enzymology properties of an agarase-producing strain

  • 摘要: 本研究通过初筛、复筛从青岛近海沉积物中分离出一株具有琼胶酶活性的菌株,该菌的最佳发酵时间为26 h,对该菌培养基进行卢戈氏碘液染色后菌落周围出现明显透明圈,镜检观察菌株的革兰氏染色结果表明,该菌为革兰氏阴性菌。经过鉴定,该菌株为不动杆菌(Acinetobacter sp.),命名为Acinetobacter sp.LXK,对该菌的粗酶学特性进行初步研究,结果显示,该酶的最适反应温度为40℃,最适底物浓度为0.5%,最适反应体系p H为8.0,K+和Ca2+对酶解反应有促进作用,Fe2+、Mn2+和Ba2+对酶解反应有不同程度的抑制作用。 
    Abstract: An agar-decomposing strain was isolated from Qingdao offshore deposits. The optimal fermentation time was 26 h, transparent zones appeared after staining with lugol 's iodine. The bacteria was gram-negative and classified in the genus Acinetobacter, named as Acinetobacter sp.LXK.By studying the primary properties of agarase and study showed that: the optimal p H and temperature for enzymolysis were p H8.0 and 40 ℃ respectively, the optimum concentration of substrate was 0.5%, the enzyme was activate by K+, Ca2 +and inhabited by Fe (2+), Mn2+), Ba2+).
  • [1]

    Fu X T, Kim S M.Agarase:Review of Major Sources, Categories, Purification Method, Enzyme Characteristics and Applications[J].Marine Drugs, 2010, 8 (1) :200-218.

    [2] 欧昌荣, 汤海青, 管斌.琼胶酶生产菌的筛选、鉴定及其酶学性质的初步研究[J].食品科学, 2005 (6) :86-90.
    [3]

    Temuujin U, Chi W J, Chang Y K, et al.Identification and Biochemical Characterization of Sco3487 from Streptomyces coelicolor A3 (2) , an Exo-and Endo-Type-Agarase-Producing Neoagarobiose[J].Journal of Bacteriology, 2011, 194 (1) :142-149.

    [4] 王祥红, 贾仁洁, 张超, 等.产琼胶酶海洋细菌的分离、鉴定及其分解琼胶实验[J].生物学通报, 2011, 46 (5) :50-51.
    [5] 梅建凤, 李莎, 茅鹤婷, 等.一株产琼胶酶海洋细菌的分离与鉴定[J].海洋科学, 2014 (2) :71-75.
    [6] 刘丽莉, 祖国仁.新型产琼胶酶海洋细菌的筛选和鉴定[J].湖北农业科学, 2014, 53 (20) :4831-4834.
    [7]

    Fu X T, Lin H, Kim S M.Purification and characterization of a novelβ-agarase, Aga A34, from Agarivorans albus YKW-34[J].Applied Microbiology and Biotechnology, 2008, 78 (2) :265-273.

    [8]

    Mehdi H, Giti E.Investigation of alkane biodegradation using the microtiter plate method and correlation between biofilm formation, biosurfactant production and crude oil biodegradation[J].International Biodeterioration&Biodegradation, 2008, 62 (2) :170-178.

    [9]

    Chi W, Park D Y, Seo Y B, et al.Cloning, expression, and biochemical characterization of a novel GH16β-agarase Aga G1from Alteromonas sp.GNUM-1[J].Applied Microbiology and Biotechnology, 2014, 98 (10) :4545-4555.

    [10] 马芮萍, 朱艳冰, 倪辉, 等.一株产琼胶酶细菌的分离、鉴定及其琼胶酶基本性质[J].微生物学报, 2014, 54 (5) :543-551.
    [11]

    Long M, Yu Z, Xu X.A Novelβ-Agarase with High p H Stability from Marine Agarivorans sp.LQ48[J].Marine Biotechnology, 2010, 12 (1) :62-69.

    [12] 徐丽, 刘江涛, 蔡俊鹏.一株琼胶酶高产菌株的筛选鉴定及产酶条件的优化[J].现代食品科技, 2006, 22 (4) :19-22.
    [13]

    Liu N, Mao X, Yang M, et al.Gene cloning, expression and characterisation of a newβ-agarase, Ag WH50C, producing neoagarobiose from Agarivorans gilvus WH0801[J].World Journal of Microbiology and Biotechnology, 2014, 30 (6) :1691-1698.

    [14] 卢斌, 柯才焕, 杨明, 等.一株高产琼胶酶菌株MA-B22的分子鉴定与产酶条件优化[J].水产学报, 2009, 33 (6) :1037-1043.
    [15]

    Oh C, Nikapitiya C, Lee Y, et al.Cloning, purification and biochemical characterization of beta agarase from the marine bacterium Pseudoalteromonas sp.AG4[J].Journal of Industrial Microbiology&Biotechnology, 2010, 37 (5) :483-494.

    [16]

    Lakshmikanth M, Manohar S, Souche Y, et al.Extracellularβ-agarase LSL-1 producing neoagarobiose from a newly isolated agar-liquefying soil bacterium, Acinetobacter sp., AG LSL-1[J].World Journal of Microbiology and Biotechnology, 2006, 22 (10) :1087-1094.

    [17] 蔡俊鹏, 刘江涛.产琼胶酶菌株的筛选及其胞内外酶活的测定[J].天然产物研究与开发, 2005, 17 (6) :730-732.
    [18] 郭彦岑, 尹群健, 卓书辉, 等.琼胶酶高产细菌的分离及鉴定[J].西北师范大学学报:自然科学版, 2012, 48 (6) :76-81.
    [19] 马悦欣, 安军, 刘双连, 等.仿刺参消化道内产琼胶酶菌株的选育及培养条件优化[J].大连水产学院学报, 2007, 22 (2) :86-91.
    [20] 杜宗军, 赵苑, 李美菊, 等.青岛近海琼胶降解细菌的筛选和多样性分析[J].中国海洋大学学报:自然科学版, 2007 (2) :277-282.
    [21] 褚艳, 于文功, 韩峰.琼胶酶高产海洋假单胞菌CY24的筛选及培养条件优化[J].中国海洋药物, 2003 (5) :1-4.
    [22] 牟宗娟, 李贵阳, 茅云翔, 等.4株琼胶降解菌的分离、鉴定及产酶条件分析[J].海洋科学, 2013 (4) :13-20.
    [23] 刘振华, 周晨妍, 王燕, 等.一株产琼胶酶细菌的鉴定和发酵条件优化[J].基因组学与应用生物学, 2016 (4) :892-900.
    [24] 杜宗军, 王鹏, 李筠, 等.两株琼胶酶高产细菌的筛选和鉴定[J].海洋科学, 2002, 26 (3) :1-4.
    [25] 陈虹, 张建芬, 柯薇.一株琼胶酶产生菌的分离及产酶培养基优化[J].食品科技, 2014 (4) :10-14.
    [26] 时岩玲, 于文功, 路新枝.海洋紫色杆菌β-琼胶酶的分离纯化及性质[J].武汉大学学报:理学版, 2008, 54 (4) :497-502.
    [27] 肖琼, 肖安风, 姚德恒, 等.琼胶酶水解工艺条件的优化及产物分析[J].中国食品学报, 2015, 15 (12) :99-106.
    [28] 张千, 曾润颖.厦门沿岸海域杂色鲍中产琼胶酶菌株的筛选及其酶学性质的研究[J].台湾海峡, 2011, 30 (2) :216-222.
    [29] 赵蕊, 倪辉, 洪清林, 等.海洋细菌JMUAZ5琼胶酶的酶学性质及酶解产物的抗氧化活性[J].中国食品学报, 2016, 16 (1) :61-68.
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出版历程
  • 收稿日期:  2017-02-20

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