Optimization of the immobilization of sweet potato amylase using glutaraldehyde-agarose support. Characterization of the immobilized enzyme

被引:50
|
作者
Tavano, Olga Luisa [1 ]
Fernandez-Lafuente, Roberto [2 ]
Goulart, Antonio Jose [3 ]
Monti, Rubens [3 ]
机构
[1] Univ Fed Triangulo Mineiro, ICS, Dept Nutr, BR-38025360 Uberaba, MG, Brazil
[2] CSIC, ICP, Dept Biocatalysis, Canto Blanco 28049, Madrid Zc, Spain
[3] UNESP Sao Paulo State Univ, Fac Pharmaceut Sci, Dept Food Nutr, BR-14840000 Araraquara, SP, Brazil
关键词
Beta-amylase; Immobilization; Sweet potato; Agarose; Glutaraldehyde; BETA-AMYLASE; ACTIVATED SUPPORTS; PROTEIN IMMOBILIZATION; GLYOXYL-AGAROSE; ALPHA-AMYLASE; STABILIZATION; STABILITY; STARCH; PERFORMANCE;
D O I
10.1016/j.procbio.2013.05.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A simplified procedure for the preparation of immobilized beta-amylase using non-purified extract from fresh sweet potato tubers is established in this paper, using differently activated agarose supports. Beta-amylase glutaraldehyde derivative was the preparation with best features, presenting improved temperature and pH stability and activity. The possibility of reusing the amylase was also shown, when this immobilized enzyme was fully active for five cycles of use. However, immobilization decreased enzyme activity to around 15%. This seems to be mainly due to diffusion limitations of the starch inside the pores of the biocatalyst particles. A fifteen-fold increase in the Km was noticed, while the decrease of Vmax was only 30% (10.1 U mg(-1) protein and 7.03 U mg(-1) protein for free and immobilized preparations, respectively). (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1054 / 1058
页数:5
相关论文
共 15 条
  • [1] OPTIMIZATION OF GLUTARALDEHYDE ACTIVATION OF A SUPPORT FOR ENZYME IMMOBILIZATION
    MONSAN, P
    JOURNAL OF MOLECULAR CATALYSIS, 1978, 3 (05): : 371 - 384
  • [2] THIOLATION AND REVERSIBLE IMMOBILIZATION OF SWEET-POTATO BETA-AMYLASE ON THIOLSULFONATE-AGAROSE
    BRENA, BM
    OVSEJEVI, K
    LUNA, B
    BATISTAVIERA, F
    JOURNAL OF MOLECULAR CATALYSIS, 1993, 84 (03): : 381 - 390
  • [3] Magnetic immobilization and characterization of α-amylase as nanobiocatalyst for hydrolysis of sweet potato starch
    Baskar, G.
    Banu, N. Afrin
    Leuca, G. Helan
    Gayathri, V.
    Jeyashree, N.
    BIOCHEMICAL ENGINEERING JOURNAL, 2015, 102 : 18 - 23
  • [4] Preparation and characterization of sugilite glass from basalt for α-amylase immobilization, statistical optimization of the immobilization process and description of free and immobilized enzyme
    Abdel-Hameed, Salwa A. M.
    Ahmed, Samia A.
    Mostafa, Faten A.
    Almasarawi, Ola. N.
    Wahab, Walaa A. Abdel
    HELIYON, 2022, 8 (07)
  • [5] Covalent immobilization of xylanase on glutaraldehyde activated alginate beads using response surface methodology: Characterization of immobilized enzyme
    Pal, Ajay
    Khanum, Farhath
    PROCESS BIOCHEMISTRY, 2011, 46 (06) : 1315 - 1322
  • [6] Glutaraldehyde modification of lipases immobilized on octyl agarose beads: Roles of the support enzyme loading and chemical amination of the enzyme on the final enzyme features
    Abellanas-Perez, Pedro
    Carballares, Diego
    Fernandez-Lafuente, Roberto
    Rocha-Martin, Javier
    INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2023, 248
  • [8] Cellulase entrapment into alginate-PEG beads cross-linked with glutaraldehyde: Optimization of the immobilization conditions and kinetic characterization of the immobilized enzyme
    Zhu, Tao
    Zhao, Fangyuan
    Zhang, Yuqing
    Ye, Yanxin
    Chen, Yanyan
    Li, Bingbing
    Liu, Junhong
    Liu, Yaqiong
    BIOCATALYSIS AND BIOTRANSFORMATION, 2024, 42 (06) : 807 - 816
  • [9] Sweet potato acid phosphatase immobilized on glutaraldehyde-activated aminopropyl controlled-pore glass: Activation, repeated use and enzyme fatigue
    Yamato, S
    Kawakami, N
    Shimada, K
    Ono, M
    Idei, N
    Itoh, Y
    Tachikawa, E
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2004, 27 (02) : 210 - 215
  • [10] Efficient Immobilization of Porcine Pancreatic α-Amylase on Amino-Functionalized Magnetite Nanoparticles: Characterization and Stability Evaluation of the Immobilized Enzyme
    M. Akhond
    Kh. Pashangeh
    H. R. Karbalaei-Heidari
    G. Absalan
    Applied Biochemistry and Biotechnology, 2016, 180 : 954 - 968