• EI
  • Scopus
  • 中国科技期刊卓越行动计划项目资助期刊
  • 北大核心期刊
  • DOAJ
  • EBSCO
  • 中国核心学术期刊RCCSE A+
  • 中国精品科技期刊
  • JST China
  • FSTA
  • 中国农林核心期刊
  • 中国科技核心期刊CSTPCD
  • CA
  • WJCI
  • 食品科学与工程领域高质量科技期刊分级目录第一方阵T1
中国精品科技期刊2020

枯草芽孢杆菌ZH-Zj016产亮氨酸氨肽酶的发酵控制研究

枯草芽孢杆菌ZH-Zj016产亮氨酸氨肽酶的发酵控制研究[J]. 食品工业科技, 2013, (08): 192-195. DOI: 10.13386/j.issn1002-0306.2013.08.037
引用本文: 枯草芽孢杆菌ZH-Zj016产亮氨酸氨肽酶的发酵控制研究[J]. 食品工业科技, 2013, (08): 192-195. DOI: 10.13386/j.issn1002-0306.2013.08.037
Study on fermentation control study for leucine aminopeptidase production by Bacillus subtilis ZH-Zj016[J]. Science and Technology of Food Industry, 2013, (08): 192-195. DOI: 10.13386/j.issn1002-0306.2013.08.037
Citation: Study on fermentation control study for leucine aminopeptidase production by Bacillus subtilis ZH-Zj016[J]. Science and Technology of Food Industry, 2013, (08): 192-195. DOI: 10.13386/j.issn1002-0306.2013.08.037

枯草芽孢杆菌ZH-Zj016产亮氨酸氨肽酶的发酵控制研究

基金项目: 

“十二五”国家863课题资助计划项目(2011AA100905);

详细信息
  • 中图分类号: TQ925

Study on fermentation control study for leucine aminopeptidase production by Bacillus subtilis ZH-Zj016

  • 摘要: 一种通过原生质体转化技术所获得的可产亮氨酸氨肽酶的枯草芽孢杆菌工程菌ZH-Zj016,在对其发酵条件单因素初步优化的基础上,通过控制最低溶氧、两阶段变温培养、细胞通透性调节等,获得15L自控式发酵罐最适发酵条件:初始pH8.0,装液量8.0L,发酵温度(15h前39℃,15h后37℃),培养时间28h,接种量7‰(V/V),搅拌转速为250500r/min,罐压控制在0.060.08MPa,通气量1.2vvm,溶氧和搅拌转速相偶联,最低溶氧维持在40%,在此条件下,酶活可达138U/mL,与该菌摇瓶优化条件下相当,是原野生菌15L发酵罐平均水平(6.5U/mL)的21倍。 
    Abstract: A leucine aminopeptidase producing strain Bacillus subtilis ZH-Zj016 was obtained by protoplast transformation technology. Fermentation conditions of the strain were firstly optimized through single factor experiments. Then a series of fermentation control strategies, such as the minimum dissolved oxygen control, temperature-shift culture and cell permeability regulation, were performed and the optimal fermentation conditions for 15L fermenter was confirmed as follows:medium volume of 8L, initial pH8.0, 7‰ of inoculum volume, agitation rate of 250500r/min pressure at 0.060.08MPa, 40% dissolved oxygen (DO) upholding (The DO and agitation rate were coupled) , ventilation volume of 1.2vvm, culture temperature at 39℃ within 15h and to 37℃ thereafter. After fermentation for 28h, leucine aminopeptidase activity produced by the strain reached 138U/mL, which was 21 times of the original strain.
  • [1]

    Jia H, Nishikawa Y, Luo Y, et al.Characterization of a leucine aminopeptidase from Toxoplasma gondii[J].Mol Biochem Parasit, 2010, 170 (1) :1-6.

    [2]

    Narayanan SS, Ramanujan A, Krishna S, et al.Purification and biochemical characterization of methionine aminopeptidase (MetAP) from Mycobacterium smegmatis mc2155[J].Appl Biochem Biotech, 2008, 151 (2/3) :512-521.

    [3]

    Matsushita-Morita M, Furukawa I, Suzuki S, et al.Characterization of recombinant prolyl aminopeptidase from Aspergillus oryzae[J].J Appl Microbiol, 2010, 109 (1) :156-165.

    [4] 赵国华, 陈宗道.蛋白质水解物苦味研究[J].粮食与油脂, 2000 (1) :28-30.
    [5]

    Shen Y, Wang F, Lan D, et al.Biochemical properties and potential applications of recombinant leucine aminopeptidase from Bacillus kaustophilus CCRC11223[J].Int J Mol Sci, 2011, 12 (11) :7609-7625.

    [6]

    Wickstrom M, Larsson R, Nygren P, et al.Aminopeptidase N (CD13) as a target for cancer chemotherapy[J].Cancer Sci, 2011, 102 (3) :501-508.

    [7]

    Zhang SC, Martin E, Shimada M, et al.Aminopeptidase substrate preference affects HIV epitope presentation and predicts immune escape patterns in HIV-infected individuals[J].J Immunol, 2012, 188 (12) :5924-5934.

    [8]

    Waditee-Sirisattha R, Hattori A, Shibato J, et al.Role of the Arabidopsis leucine aminopeptidase2[J].Plant Signal Behav, 2011, 6 (10) :1581-1583.

    [9] 高应东, 王书奎.亮氨酸氨肽酶的种类及临床应用[J].国际检验医学杂志, 2010, 12:1408-1410.
    [10]

    Matsui M, Fowler JH, Walling LL.Leucine aminopeptidases:diversity in structure and function[J].Biol Chem, 2006, 387 (12) :1535-1544.

    [11]

    Rao MB, Tanksale AM, Ghatge MS, et al.Molecular and biotechnological aspects of microbial proteases[J].Microbiol Mol Biol Rev, 1998, 62 (3) :597-635.

    [12]

    Terenius L, Sandin J, Sakurada T.Nociceptin/orphanin FQ metabolism and bioactive metabolites[J].Peptides, 2000 (21) , 7:919-922.

    [13]

    Goldberg AL, Cascio P, Saric T, et al.The importance of the proteasome and subsequent proteolytic steps in the generation of antigenic peptides[J].Mol Immunol, 2002, 39 (3/4) :147-164.

    [14]

    Toldra F, Aristoy AC, Flores M.Contribution of muscle aminopeptidases to flavor development in dry-cured ham[J].Food Res Int, 2000, 33 (3/4) :181-185.

    [15] 须瑛敏.氨肽酶脱苦效果的研究[J].食品与药品, 2007, 11:36-39.
    [16] 魏亚娟, 田亚平, 须瑛敏.枯草芽孢杆菌脱苦氨肽酶在水解大豆分离蛋白中的应用研究[J].食品工业科技, 2008, 4:149-151.
    [17] 吕广林, 田亚平.氨肽酶与中性蛋白酶协同水解大豆分离蛋白的研究[J].食品与生物技术学报, 2011 (1) :101-105.
    [18]

    Wang F, Ning Z, Lan D, et al.Biochemical properties of recombinant leucine aminopeptidase II from Bacillus stearothermophilus and potential applications in the hydrolysis of Chinese anchovy (Engraulis japonicus) proteins[J].J Agric Food Chem, 2012, 60 (1) :165-172.

    [19]

    Carroll RK, Robison TM, Rivera FE, et al.Identification of an intracellular M17family leucine aminopeptidase that is required for virulence in Staphylococcus aureus[J].Microbes Infect, 2012 (14) , 11:989-999.

    [20]

    Maggioli G, Acosta D, Silveira F, et al.The recombinant gut-associated M17leucine aminopeptidase in combination with different adjuvants confers a high level of protection against Fasciola hepatica infection in sheep[J].Vaccine, 2011, 29:9057-9063.

    [21] 张霞, 高雅楠, 侯敏, 等.亮氨酸氨肽酶在日本血吸虫感染中的抗体应答特征[J].中国血吸虫病防治杂志, 2011 (2) :163-167.
    [22] 张龙翔, 张庭芳, 李令媛.生化实验方法和技术[M].北京:高等教育出版社, 2001.
计量
  • 文章访问数:  112
  • HTML全文浏览量:  15
  • PDF下载量:  135
  • 被引次数: 0
出版历程
  • 收稿日期:  2012-11-06

目录

    /

    返回文章
    返回