Optimization of medium composition and culture conditions for agarase production by Agarivorans albus YKW-34

被引:26
作者
Fu, Xiao Ting [1 ,2 ]
Lin, Hong [2 ]
Kim, Sang Moo [1 ]
机构
[1] Kangnung Wonju Natl Univ, Fac Marine Biosci & Technol, Kangnung 210702, South Korea
[2] Ocean Univ China, Coll Food Sci & Engn, Qingdao 266003, Peoples R China
关键词
Agarase; Agarivorans albus; Enzyme production; Optimization; Plackett-Burman design; Central composite design; RESPONSE-SURFACE METHODOLOGY; BETA-AGARASE; EXTRACELLULAR AGARASE; MARINE BACTERIUM; ALGINATE LYASE; PURIFICATION; SP; NEOAGAROBIOSE;
D O I
10.1016/j.procbio.2009.06.012
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
Effect of medium composition and culture conditions on agarase production by Agarivorans albus YKW-34 was investigated in shake flasks. The most suitable carbon source, nitrogen source, and culture temperature were agar, yeast extract, and 25 degrees C, respectively, for agarase production by one-factor-at-a-time design. The nutritional components of the medium and culture conditions were analyzed by Plackett-Burman design. Among the nine factors studied, agar, yeast extract, and initial pH had significant effects on agarase production (p < 0.05). The optimum levels of these key variables were further determined using a central composite design. The highest agarase production was obtained in the medium consisting of 0.23% agar and 0.27% yeast extract at initial pH 7.81. The whole optimization strategy enhanced the agarase production from 0.23 U/ml to 0.87 U/ml. The economic medium composition and culture condition as well as the dominant occupation of agarase with high activity in culture fluid enlighten the potential application of A. albus YKW-34 for the production of agarase. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1158 / 1163
页数:6
相关论文
共 28 条
[1]   PURIFICATION AND CHARACTERIZATION OF A NOVEL BETA-AGARASE FROM VIBRIO SP AP-2 [J].
AOKI, T ;
ARAKI, T ;
KITAMIKADO, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 187 (02) :461-465
[2]  
Araki T, 1998, J MAR BIOTECHNOL, V6, P193
[3]  
Araki T, 1998, J MAR BIOTECHNOL, V6, P260
[4]   Production of multiple xylanolytic and cellulolytic enzymes by thermophilic fungus Myceliophthora sp IMI 387099 [J].
Badhan, A. K. ;
Chadha, B. S. ;
Kaur, Jatinder ;
Saini, H. S. ;
Bhat, M. K. .
BIORESOURCE TECHNOLOGY, 2007, 98 (03) :504-510
[5]   Modeling and optimization I: Usability of response surface methodology [J].
Bas, Deniz ;
Boyaci, Ismail H. .
JOURNAL OF FOOD ENGINEERING, 2007, 78 (03) :836-845
[6]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[7]   AN EXTRACELLULAR AGARASE FROM A CYTOPHAGA SPECIES [J].
DUCKWORT.M ;
TURVEY, JR .
BIOCHEMICAL JOURNAL, 1969, 113 (01) :139-&
[8]   Purification and characterization of a novel β-agarase, AgaA34, from Agarivorans albus YKW-34 [J].
Fu, Xiao Ting ;
Lin, Hong ;
Kim, Sang Moo .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2008, 78 (02) :265-273
[9]   Purification and characterization of a Na+/K+ dependent alginate lyase from turban shell gut Vibrio sp. YKW-34 [J].
Fu, Xiao Ting ;
Lin, Hong ;
Kim, Sang Moo .
ENZYME AND MICROBIAL TECHNOLOGY, 2007, 41 (6-7) :828-834
[10]   Gene Cloning, Expression, and Characterization of a β-Agarase, AgaB34, from Agarivorans albus YKW-34 [J].
Fu, Xiao Ting ;
Pan, Cheol-Ho ;
Lin, Hong ;
Kim, Sang Moo .
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, 2009, 19 (03) :257-264