Materials-Based Strategies for Multi-Enzyme Immobilization and Co-Localization: A Review

被引:216
作者
Jia, Feng [1 ]
Narasimhan, Balaji [1 ]
Mallapragada, Surya [1 ]
机构
[1] Iowa State Univ, Dept Chem & Biol Engn, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
enzymes; co-localization; immobilization; PHOSPHOLIPID POLYMER NANOPARTICLES; ENZYME IMMOBILIZATION; MESOPOROUS SILICA; ALPHA-CHYMOTRYPSIN; CROSS-LINKING; ELECTROCHEMICAL BIOSENSORS; MAGNETIC NANOPARTICLES; PROTEIN IMMOBILIZATION; GOLD NANOPARTICLES; AU NANOPARTICLES;
D O I
10.1002/bit.25136
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Immobilized enzymes as biocatalysts have great potential both scientifically and industrially because of their technological and economic importance. Their highly efficient catalytic mechanisms and reusability have made them excellent candidates for green and sustainable applications. Previous studies have primarily focused on single enzyme immobilization. However, there are many situations where a single enzyme cannot completely catalyze reactions and multiple enzymes working together in a cascade are needed. It is very challenging to efficiently drive the multi-step reaction toward the desired direction, which is especially true when reactive intermediates are present. Nature overcomes this limitation through the use of multi-enzyme complexes (MECs) to promote the overall catalytic efficiency, which has inspired researchers to synthesize artificial MECs to controllably enhance the production of the desired compounds in multi-step reaction cascades in vitro. The most common approaches to synthesize artificial MECs are to use genetic engineering techniques to create fusion proteins or to co-localize multiple enzymes on suitable carriers. This review focuses on the latter with a particular emphasis on materials-based approaches to enzyme co-localization, which builds on techniques developed for single enzyme immobilization. The attachment techniques used in single enzyme immobilization are also effective in multiple enzyme co-localization, which has a direct impact on the overall enzyme orientation and activity. For carrier-based strategies, the platforms developed for single enzyme immobilization are also appropriate for attaching and co-localizing multiple enzymes. However, the involvement of multiple components in co-localization brings many challenges. The properties of different enzymes makes co-localization complicated when selecting attachment techniques and platforms to preserve enzymatic activity, because the structure and function of each component enzyme needs to be taken into consideration to preserve the overall enzyme activity. In addition, the relative position of the multiple enzymes in a confined space plays a significant role in the interactions between different enzymes, This review focuses on the potential of materials-based approaches for multiple enzyme co-localization for the design of sustainable multi-enzyme biocatalysts. A critical analysis of the attachment techniques and carriers platforms that have been used in enzyme immobilization and multienzyme co-localization in vitro is provided. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:209 / 222
页数:14
相关论文
共 116 条
  • [11] Latex particles with thermo-flocculation and magnetic properties for immobilization of α-chymotrypsin
    Chen, JP
    Su, DR
    [J]. BIOTECHNOLOGY PROGRESS, 2001, 17 (02) : 369 - 375
  • [12] Catalase-coupled gold nanoparticles: Comparison between the carbodiimide and biotin-streptavidin methods
    Chirra, Hariharasudhan D.
    Sexton, Travis
    Biswal, Dipti
    Hersh, Louis B.
    Hilt, J. Zach
    [J]. ACTA BIOMATERIALIA, 2011, 7 (07) : 2865 - 2872
  • [13] Micropatterning of biomolecules on glass surfaces modified with various functional groups using photoactivatable biotin
    Choi, HJ
    Kim, NH
    Chung, BH
    Seong, GH
    [J]. ANALYTICAL BIOCHEMISTRY, 2005, 347 (01) : 60 - 66
  • [14] UAF1 Is a Subunit of Multiple Deubiquitinating Enzyme Complexes
    Cohn, Martin A.
    Kee, Younghoon
    Haas, Wilhelm
    Gygi, Steven P.
    D'Andrea, Alan D.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (08) : 5343 - 5351
  • [15] Engineering the spatial organization of metabolic enzymes: mimicking nature's synergy
    Conrado, Robert J.
    Varner, Jeffrey D.
    DeLisa, Matthew P.
    [J]. CURRENT OPINION IN BIOTECHNOLOGY, 2008, 19 (05) : 492 - 499
  • [16] Novel multienzyme oxidative biocatalyst for lignin bioprocessing
    Crestini, Claudia
    Melone, Federica
    Saladino, Raffaele
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2011, 19 (16) : 5071 - 5078
  • [17] Preparation and characterization of combi-CLEAs catalyzing multiple non-cascade reactions
    Dalal, Sohel
    Kapoor, Manah
    Gupta, Munishwar N.
    [J]. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2007, 44 (3-4) : 128 - 132
  • [18] Adsorption of poly(ethylene glycol)-modified ribonuclease A to a poly(lactide-co-glycolide) surface
    Daly, SM
    Przybycien, TM
    Tilton, RD
    [J]. BIOTECHNOLOGY AND BIOENGINEERING, 2005, 90 (07) : 856 - 868
  • [19] ENZYME IMMOBILIZATION IN NANOPARTICLES PRODUCED BY INVERSE MICROEMULSION POLYMERIZATION
    DAUBRESSE, C
    GRANDFILS, C
    JEROME, R
    TEYSSIE, P
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1994, 168 (01) : 222 - 229
  • [20] Enzyme immobilization in MCM-41 molecular sieve
    Diaz, JF
    Balkus, KJ
    [J]. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 1996, 2 (2-3) : 115 - 126