Comparative evaluation of neutral protease production by Aspergillus oryzae in submerged and solid-state fermentation

被引:260
作者
Sandhya, C
Sumantha, A
Szakacs, G
Pandey, A [1 ]
机构
[1] CSIR, Reg Res Lab, Div Biotechnol, Trivandrum 695019, Kerala, India
[2] Tech Univ Budapest, Dept Agr & Chem Engn, Budapest, Hungary
关键词
neutral protease; submerged fermentation; solid-state fermentation; Aspergillus oryzae; agro-industrial residues;
D O I
10.1016/j.procbio.2004.12.001
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
A comparative study was carried out on the production of neutral protease using agro-industrial residues as substrate in solid-state fermentation (SSF) and submerged fermentation (SmF). Seven fungal cultures, viz. three strains of Aspergillus oryzae and four strains belonging to Penicillium sp, P. funiculosum, P. funiculosum, P. pinophilum, P. aculeatum were evaluated using a plate assay for enzyme production, which showed a strain of A. oryzae NRRL 1808 as the most useful culture. Several agro-industrial residues (wheat bran, rice husk, rice bran, spent brewing grain, coconut oil cake, palm kernel cake, sesame oil cake, jackfruit seed powder and olive oil cake) were screened for neutral protease production in SmF and SSF. In both systems, wheat bran was the best substrate. Best results in SSF were obtained in a medium having an initial moisture content of 43.6%, when inoculated with 1 ml of spore suspension (8 x 10(8) spores) and incubated at 30 degrees C for 72 h (31.2 U enzyme per gram of fermented substrate - U/gds). SmF medium (pH 7.5) containing 2% (w/v) wheat bran, when inoculated with 3 ml of spore suspension and incubated at 30 degrees C and 180 rpm for 72 h gave maximum enzyme yield of 8.7 U/gds. A comparative evaluation of protease yield by the two fermentation systems showed 3.5-fold more enzyme production in SSF, clearly demonstrating the superiority of SSF over SmF. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2689 / 2694
页数:6
相关论文
共 43 条
[1]  
ADESH K, 2002, INDIAN J MICROBIOL, V42, P233
[2]  
AGARWAL D, 2003, PROCESS BIOCHEM, P1
[3]   Xylanase production by thermophilic Bacillus licheniformis A99 in solid-state fermentation [J].
Archana, A ;
Satyanarayana, T .
ENZYME AND MICROBIAL TECHNOLOGY, 1997, 21 (01) :12-17
[4]  
BIJESEBEKE R, 2002, FEMS YEAST RES, V2, P245
[5]   PRODUCTION OF EXOCELLULAR PROTEOLYTIC-ENZYMES BY VARIOUS SPECIES OF PENICILLIUM [J].
CHRZANOWSKA, J ;
KOLACZKOWSKA, M ;
POLANOWSKI, A .
ENZYME AND MICROBIAL TECHNOLOGY, 1993, 15 (02) :140-143
[6]   PRODUCTION AND DEGRADATION OF ALKALINE PROTEASE IN BATCH CULTURES OF BACILLUS-SUBTILIS ATCC-14416 [J].
CHU, IM ;
LEE, C ;
LI, TS .
ENZYME AND MICROBIAL TECHNOLOGY, 1992, 14 (09) :755-761
[7]   Production and partial characterization of thermophilic proteases from Streptomyces sp isolated from Brazilian cerrado soil [J].
De Azeredo, LAI ;
Freire, DMG ;
Soares, RMA ;
Leite, SGF ;
Coelho, RRR .
ENZYME AND MICROBIAL TECHNOLOGY, 2004, 34 (3-4) :354-358
[8]  
Ellaiah P., 2002, Indian Journal of Microbiology, V42, P173
[9]   REGULATION OF THE SECRETION OF RHIZOPUS-OLIGOSPORUS EXTRACELLULAR CARBOXYL PROTEINASE [J].
FARLEY, PC ;
IKASARI, L .
JOURNAL OF GENERAL MICROBIOLOGY, 1992, 138 :2539-2544
[10]   Comparative study of protease production in solid substrate fermentation versus submerged fermentation [J].
George, S ;
Raju, V ;
Subramanian, TV ;
Jayaraman, K .
BIOPROCESS ENGINEERING, 1997, 16 (06) :381-382