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
  • [1] CARRIER MEMBRANE AS A STATIONARY PHASE FOR AFFINITY-CHROMATOGRAPHY AND KINETIC-STUDIES OF MEMBRANE-BOUND ENZYMES
    ABOUREBYEH, H
    KORBER, F
    SCHUBERTREHBERG, K
    REUSCH, J
    JOSIC, D
    [J]. JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1991, 566 (02): : 341 - 350
  • [2] New Generation Polymeric Nanospheres for Catalase Immobilization
    Akgol, Sinan
    Ozturk, Nevra
    Denizli, Adil
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2009, 114 (02) : 962 - 970
  • [3] Potential applications of enzymes immobilized on/in nano materials: A review
    Ansari, Shakeel Ahmed
    Husain, Qayyum
    [J]. BIOTECHNOLOGY ADVANCES, 2012, 30 (03) : 512 - 523
  • [4] Co-immobilization of D-hydantoinase and D-carboamylase on Chitin: Application to the Synthesis of p-hydroxyphenylglycine
    Aranaz, I
    Ramos, V
    De La Escalera, S
    Heras, A
    [J]. BIOCATALYSIS AND BIOTRANSFORMATION, 2003, 21 (06) : 349 - 356
  • [5] ORGANIZATION OF CITRIC-ACID CYCLE ENZYMES INTO A MULTIENZYME CLUSTER
    BARNES, SJ
    WEITZMAN, PDJ
    [J]. FEBS LETTERS, 1986, 201 (02): : 267 - 270
  • [6] Tailored porous materials
    Barton, TJ
    Bull, LM
    Klemperer, WG
    Loy, DA
    McEnaney, B
    Misono, M
    Monson, PA
    Pez, G
    Scherer, GW
    Vartuli, JC
    Yaghi, OM
    [J]. CHEMISTRY OF MATERIALS, 1999, 11 (10) : 2633 - 2656
  • [7] Different mechanisms of protein immobilization on glutaraldehyde activated supports:: Effect of support activation and immobilization conditions
    Betancor, Lorena
    Lopez-Gallego, Fernando
    Hidalgo, Aurelio
    Alonso-Morales, Noelia
    Dellamora-Ortiz Cesar Mateo, Gisela
    Fernandez-Lafuente, Roberto
    Guisan, Jose M.
    [J]. ENZYME AND MICROBIAL TECHNOLOGY, 2006, 39 (04) : 877 - 882
  • [8] Advances in enzyme immobilisation
    Brady, Dean
    Jordaan, Justin
    [J]. BIOTECHNOLOGY LETTERS, 2009, 31 (11) : 1639 - 1650
  • [9] Protein multilayer formation on colloids through a stepwise self-assembly technique
    Caruso, F
    Möhwald, H
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (25) : 6039 - 6046
  • [10] Chen FH, 2005, ACS SYM SER, V900, P107