TY - GEN
T1 - Effect of temperature and mixing speed on immobilization of crude enzyme from Aspergillus Niger on chitosan for hydrolyzing cellulose
AU - Hamzah, Afan
AU - Gek Ela Kumala, P.
AU - Ramadhani, Dwi
AU - Maziyah, Nurul
AU - Rahmah, Laila Nur
AU - Soeprijanto,
AU - Widjaja, Arief
N1 - Publisher Copyright:
© 2017 Author(s).
PY - 2017/5/24
Y1 - 2017/5/24
N2 - Conversion of cellulose into reducing sugar through enzymatic hydrolysis has advantageous because it produces greater product yield, higher selectivity, require less energy, more moderate operating conditions and environment friendly. However, the nature of the enzyme that is difficult to separate and its expensive price become an obstacle. These obstacles can be overcome by immobilizing the enzyme on chitosan material so that the enzyme can be reused. Chitosan is chosen because it is cheap, inert, hydrophilic, and biocompatible. In this research, we use covalent attachment and combination between covalent attachment and cross-linking method for immobilizing crude enzyme. This research was focusing in study of Effect of temperature and mixing speed on Immobilization Enzyme From Aspergillus Niger on Chitosan For Hydrolyzing both soluble (Carboxymethylcellulose) and insoluble Cellulose (coconut husk). This Research was carried out by three main step. First, coconut husk was pre-treated mechanically and chemically, Second, Crude enzyme from Aspergillus Niger strain was immobilized on chitosan in various immobilization condition. At last, the pre-treated coconut husk and Carboxymetylcellulose (CMC) were hydrolyzed by immobilized cellulose on chitosan for reducing sugar production. The result revealed that the most reducing sugar produced by immobilized enzyme on chitosan+GDA with immobilization condition at 30 °C and 125 rpm. Enzyme immobilized on chitosan cross-linked with GDA produced more reducing sugar from preteated coconut husk than enzyme immobilized on chitosan.
AB - Conversion of cellulose into reducing sugar through enzymatic hydrolysis has advantageous because it produces greater product yield, higher selectivity, require less energy, more moderate operating conditions and environment friendly. However, the nature of the enzyme that is difficult to separate and its expensive price become an obstacle. These obstacles can be overcome by immobilizing the enzyme on chitosan material so that the enzyme can be reused. Chitosan is chosen because it is cheap, inert, hydrophilic, and biocompatible. In this research, we use covalent attachment and combination between covalent attachment and cross-linking method for immobilizing crude enzyme. This research was focusing in study of Effect of temperature and mixing speed on Immobilization Enzyme From Aspergillus Niger on Chitosan For Hydrolyzing both soluble (Carboxymethylcellulose) and insoluble Cellulose (coconut husk). This Research was carried out by three main step. First, coconut husk was pre-treated mechanically and chemically, Second, Crude enzyme from Aspergillus Niger strain was immobilized on chitosan in various immobilization condition. At last, the pre-treated coconut husk and Carboxymetylcellulose (CMC) were hydrolyzed by immobilized cellulose on chitosan for reducing sugar production. The result revealed that the most reducing sugar produced by immobilized enzyme on chitosan+GDA with immobilization condition at 30 °C and 125 rpm. Enzyme immobilized on chitosan cross-linked with GDA produced more reducing sugar from preteated coconut husk than enzyme immobilized on chitosan.
UR - http://www.scopus.com/inward/record.url?scp=85020421984&partnerID=8YFLogxK
U2 - 10.1063/1.4982266
DO - 10.1063/1.4982266
M3 - Conference contribution
AN - SCOPUS:85020421984
T3 - AIP Conference Proceedings
BT - International Seminar on Fundamental and Application of Chemical Engineering 2016, ISFAChE 2016
A2 - Widiyastuti, null
A2 - Taufany, Fadlilatul
A2 - Nurkhamidah, Siti
PB - American Institute of Physics Inc.
T2 - 3rd International Seminar on Fundamental and Application of Chemical Engineering 2016, ISFAChE 2016
Y2 - 1 November 2016 through 2 November 2016
ER -