Utilization of palm kernel cake for production of β-mannanase by Aspergillus niger FTCC 5003 in solid substrate fermentation using an aerated column bioreactor

被引:29
作者
Abdeshahian, Peyman [1 ]
Samat, Noraini [2 ]
Hamid, Aidil Abdul [1 ]
Yusoff, Wan Mohtar Wan [1 ]
机构
[1] Univ Kebangsaan Malaysia, Fac Sci & Technol, Sch Biosci & Biotechnol, Bangi 43600, Selangor, Malaysia
[2] MARDI Headquarters, Malaysian Agr Res & Dev Inst, Livestock Res Ctr, Kuala Lumpur 50774, Malaysia
关键词
Palm kernel cake; beta-Mannanase; Aspergillus niger; Solid substrate fermentation; Column bioreactor; STATE FERMENTATION; MULTIENZYME PRODUCTION; DEGRADING ENZYMES; OPTIMIZATION; PURIFICATION; INDUSTRY;
D O I
10.1007/s10295-009-0658-0
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
The production of beta-mannanase from palm kernel cake (PKC) as a substrate in solid substrate fermentation (SSF) was studied using a laboratory column bioreactor. The simultaneous effects of three independent variables, namely incubation temperature, initial moisture content of substrate and airflow rate, on beta-mannanase production were evaluated by response surface methodology (RSM) on the basis of a central composite face-centered (CCF) design. Eighteen trials were conducted in which Aspergillus niger FTCC 5003 was cultivated on PKC in an aerated column bioreactor for seven days under SSF process. The highest level of beta-mannanase (2117.89 U/g) was obtained when SSF process was performed at incubation temperature, initial moisture level and aeration rate of 32.5A degrees C, 60% and 0.5 l/min, respectively. Statistical analysis revealed that the quadratic terms of incubation temperature and initial moisture content had significant effects on the production of beta-mannanase (P < 0.01). A similar analysis also demonstrated that the linear effect of initial moisture level and an interaction effect between the initial moisture content and aeration rate significantly influenced the production of beta-mannanase (P < 0.01). The statistical model suggested that the optimal conditions for attaining the highest level of beta-mannanase were incubation temperature of 32A degrees C, initial moisture level of 59% and aeration rate of 0.5 l/min. A beta-mannanase yield of 2231.26 U/g was obtained when SSF process was carried out under the optimal conditions described above.
引用
收藏
页码:103 / 109
页数:7
相关论文
共 34 条
[1]   Softwood hemicellulose-degrading enzymes from Aspergillus niger:: Purification and properties of a β-mannanase [J].
Ademark, P ;
Varga, A ;
Medve, J ;
Harjunpää, V ;
Drakenberg, T ;
Tjerneld, F ;
Stålbrand, H .
JOURNAL OF BIOTECHNOLOGY, 1998, 63 (03) :199-210
[2]   EXTRACELLULAR MANNANASES AND GALACTANASES FROM SELECTED FUNGI [J].
ARAUJO, A ;
WARD, OP .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1990, 6 (03) :171-178
[3]  
AWALUDIN R, 2001, PALM OIL DEV, V34, P7
[4]   Carbohydrolase production by the ericoid mycorrhizal fungus Hymenoscyphus ericae under solid-state fermentation conditions [J].
Burke, RM ;
Cairney, JWG .
MYCOLOGICAL RESEARCH, 1997, 101 :1135-1139
[5]  
CHOI MH, 2005, 2 INT C CHEM BIOPR E
[6]  
DURAND A, 1988, J BIOTECHNOL, V8, P59, DOI [10.1016/0168-1656(88)90068-5, 10.1016/S0168-1656(00)00402-8]
[7]   NONSTARCH POLYSACCHARIDES FROM SUNFLOWER (HELIANTHUS-ANNUUS) MEAL AND PALM-KERNEL (ELAEIS-GUINEENSIS) MEAL INVESTIGATION OF THE STRUCTURE OF MAJOR POLYSACCHARIDES [J].
DUSTERHOFT, EM ;
POSTHUMUS, MA ;
VORAGEN, AGJ .
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 1992, 59 (02) :151-160
[8]   Production and characterization of cellulolytic enzymes from the thermoacidophilic fungal Aspergillus terreus M11 under solid-state cultivation of corn stover [J].
Gao, Jianmin ;
Weng, Haibo ;
Zhu, Daheng ;
Yuan, Mingxue ;
Guan, Fangxia ;
Xi, Yu .
BIORESOURCE TECHNOLOGY, 2008, 99 (16) :7623-7629
[9]   Endo-β-1,4-D-mannanase is efficiently produced by Sclerotium (Athelia) rolfsii under derepressed conditions [J].
Grosswindhager, C ;
Sachslehner, A ;
Nidetzky, B ;
Haltrich, D .
JOURNAL OF BIOTECHNOLOGY, 1999, 67 (2-3) :189-203
[10]  
Haaland PerryD., 1989, EXPT DESIGN BIOTECHN