Fructo-oligosaccharides production by an Aspergillus aculeatus commercial enzyme preparation with fructosyltransferase activity covalently immobilized on Fe3O4-chitosan-magnetic nanoparticles

被引:55
作者
de Oliveira, Rodrigo Lira [1 ]
da Silva, Marcos Fellipe [2 ]
da Silva, Suzana Pedroza [2 ]
Vaz de Araujo, Ana Claudia [3 ]
Fernandes Lima Cavalcanti, Jorge Vinicius [4 ]
Converti, Attilio [5 ]
Porto, Tatiana Souza [2 ]
机构
[1] Fed Rural Univ Pernambuco UFRPE, Northeast Biotechnol Network RENORBIO, BR-52171900 Recife, PE, Brazil
[2] Fed Rural Univ Pernambuco UFRPE, Acad Unit Garanhuns UAG, Av Bom Pastor, BR-55296901 Garanhuns, PE, Brazil
[3] Fed Rural Univ Pernambuco UFRPE, Acad Unit Cabo de St Agostinho UACSA, Rua Cento & Sessenta & Tres 300, BR-54518430 Cabo De St Agostinho, PE, Brazil
[4] Fed Univ Pernambuco UFPE, Dept Chem Engn, Av Prof Moraes Rego,1235,Cidade Univ, BR-50670901 Recife, PE, Brazil
[5] Genoa Univ, Dept Civil Chem & Environm Engn, Pole Chem Engn, Via Opera Pia 15, I-16145 Genoa, Italy
关键词
Fructo-oligosacchandes; Fructosylrransferase; Magnetic nanoparticles; ULTRA SP-L; BETA-FRUCTOFURANOSIDASE; SUPERPARAMAGNETIC NANOPARTICLES; ALPHA-GLUCOSIDASE; FRUCTOOLIGOSACCHARIDES; PURIFICATION; STABILITY; PECTINASE;
D O I
10.1016/j.ijbiomac.2020.02.152
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
Pectinex Ultra SP-L, a commercial enzyme preparation with fructosyltransferase activity, was successfully immobilized by covalent binding to Fe3O4-chitosan-magnetic nanoparticles. Immobilization carried out according to a 2(3)-full factorial design where glutaraldehyde concentration, activation time and time of contact between enzyme and support were selected as the independent variables and immobilization yield as the response. The highest immobilization yield (94.84%) was obtained using 3.0% (v/v) glutaraldehyde and activation and contact times of 180 and 30 min, respectively. The immobilized biocatalyst, which showed for both hydrolytic and transfructosylating activities optimum pH and temperature of 7.0 and 60 respectively, retained 70 and 86% of them after 6 cycles of reuse. A kinetic/thermodynamic study focused on thermal inactivation of the immobilized construct indicated high thermostability at temperatures commonly used for fructo-oligosaccharides (FOS) production. Maximum FOS concentration obtained in lab-scale experiments was 101.56 g L-1,with predominant presence of 1-kestose in the reaction mixture. The results obtained in this study suggest that the immobilized-enzyme preparation may be effectively exploited for FOS production and easily recovered from the reaction mixture by action of a magnetic field. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:922 / 929
页数:8
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