Evaluation of Strategies to Produce Highly Porous Cross-Linked Aggregates of Porcine Pancreas Lipase with Magnetic Properties

被引:45
作者
Guimaraes, Jose Renato [1 ]
Giordano, Raquel de Lima Camargo [1 ]
Fernandez-Lafuente, Roberto [2 ]
Tardioli, Paulo Waldir [1 ]
机构
[1] Univ Fed Sao Carlos, Dept Chem Engn, Grad Program Chem Engn, Rod Washington Luis,Km 235,SP-310, BR-13565905 Sao Carlos, SP, Brazil
[2] CSIC, ICP, Dept Biocatalisis, Campus UAM CSIC Madrid, Madrid 28049, Spain
来源
MOLECULES | 2018年 / 23卷 / 11期
基金
巴西圣保罗研究基金会;
关键词
silica magnetic nanoparticles; bovine serum albumin; soy protein; starch; protein surface modifiers; BOVINE SERUM-ALBUMIN; ENZYME IMMOBILIZATION; INDUSTRIAL APPLICATIONS; INTERFACIAL ADSORPTION; MICROBIAL LIPASES; SOY PROTEIN; OPEN FORM; CLEAS; PURIFICATION; HYDROLYSIS;
D O I
10.3390/molecules23112993
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
The preparation of highly porous magnetic crosslinked aggregates (pm-CLEA) of porcine pancreas lipase (PPL) is reported. Some strategies to improve the volumetric activity of the immobilized biocatalyst were evaluated, such as treatment of PPL with enzyme surface-modifying agents (polyethyleneimine or dodecyl aldehyde), co-aggregation with protein co-feeders (bovine serum albumin and/or soy protein), use of silica magnetic nanoparticles functionalized with amino groups (SMNPs) as separation aid, and starch as pore-making agent. The combination of enzyme surface modification with dodecyl aldehyde, co-aggregation with SMNPs and soy protein, in the presence of 0.8% starch (followed by hydrolysis of the starch with -amylase), yielded CLEAs expressing high activity (immobilization yield around 100% and recovered activity around 80%), high effectiveness factor (approximately 65% of the equivalent free enzyme activity) and high stability at 40 degrees C and pH 8.0, i.e., PPL CLEAs co-aggregated with SMNPs/bovine serum albumin or SMNPs/soy protein retained 80% and 50% activity after 10 h incubation, respectively, while free PPL was fully inactivated after 2 h. Besides, highly porous magnetic CLEAs co-aggregated with soy protein and magnetic nanoparticles (pm-SP-CLEAs) showed good performance and reusability in the hydrolysis of tributyrin for five 4h-batches.
引用
收藏
页数:21
相关论文
共 76 条
  • [1] Immobilisation and application of lipases in organic media
    Adlercreutz, Patrick
    [J]. CHEMICAL SOCIETY REVIEWS, 2013, 42 (15) : 6406 - 6436
  • [2] A review on enzymatic synthesis of aromatic esters used as flavor ingredients for food, cosmetics and pharmaceuticals industries
    Amanda Gomes Almeida, S. A.
    de Meneses, Alessandra Cristina
    Hermes de Araujo, Pedro Henrique
    de Oliveira, Debora
    [J]. TRENDS IN FOOD SCIENCE & TECHNOLOGY, 2017, 69 : 95 - 105
  • [3] Maltose Production Using Starch from Cassava Bagasse Catalyzed by Cross-Linked β-Amylase Aggregates
    Araujo-Silva, Rafael
    Oliveira Mafra, Agnes Cristina
    Rojas, Mayerlenis Jimenez
    Kopp, Willian
    Giordano, Roberto de Campos
    Fernandez-Lafuente, Roberto
    Tardioli, Paulo Waldir
    [J]. CATALYSTS, 2018, 8 (04)
  • [4] Magnetic gold nanoparticles in SERS-based sandwich immunoassay for antigen detection by well oriented antibodies
    Baniukevic, Julija
    Boyaci, Ismail Hakki
    Bozkurt, Akif Goktug
    Tamer, Ugur
    Ramanavicius, Arunas
    Ramanaviciene, Almira
    [J]. BIOSENSORS & BIOELECTRONICS, 2013, 43 : 281 - 288
  • [5] Heterofunctional Supports in Enzyme Immobilization: From Traditional Immobilization Protocols to Opportunities in Tuning Enzyme Properties
    Barbosa, Oveimar
    Torres, Rodrigo
    Ortiz, Claudia
    Berenguer-Murcia, Angel
    Rodrigues, Rafael C.
    Fernandez-Lafuente, Roberto
    [J]. BIOMACROMOLECULES, 2013, 14 (08) : 2433 - 2462
  • [6] Bastida A, 1998, BIOTECHNOL BIOENG, V58, P486, DOI 10.1002/(SICI)1097-0290(19980605)58:5<486::AID-BIT4>3.0.CO
  • [7] 2-9
  • [8] Beisson F, 2000, EUR J LIPID SCI TECH, V102, P133, DOI 10.1002/(SICI)1438-9312(200002)102:2<133::AID-EJLT133>3.3.CO
  • [9] 2-O
  • [10] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3