Optimized bioprocess for production of fructofuranosidase by recombinant Aspergillus niger

被引:54
作者
Driouch, Habib [1 ]
Roth, Andreas [2 ]
Dersch, Petra [2 ,3 ]
Wittmann, Christoph [1 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Biochem Engn, D-38106 Braunschweig, Germany
[2] Tech Univ Carolo Wilhelmina Braunschweig, Inst Microbiol, D-38106 Braunschweig, Germany
[3] Helmholtz Ctr Infect Res, Braunschweig, Germany
关键词
Morphology engineering; Central composite design; Fed-batch; Enzyme; GFP; BETA-FRUCTOFURANOSIDASE; MICROBIAL-PRODUCTION; ENZYME; FRUCTOOLIGOSACCHARIDES; PURIFICATION; SUBSTRATE;
D O I
10.1007/s00253-010-2661-9
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
A comprehensive approach of bioprocess design at various levels was used to optimize microbial production of extracellular fructofuranosidase, important as biocatalyst to derive fructooligosaccharides with broad application in food or pharmaceutical industry. For production, the recombinant strain Aspergillus niger SKAn1015 was used, which expresses the fructofuranosidase encoding gene suc1 under control of a strong constitutive promoter. In a first screening towards an optimized medium, glucose, nitrate, Fe2+, and Mn2+ were identified as beneficial for production. A minimal medium with optimized concentration of these key nutrients, obtained by central composite design experiments and quadratic modelling, provided a threefold increased fructofuranosidase activity in the culture supernatant (400 U/mL) as compared to the originally described medium. Utilizing the optimized medium, the process was then transferred from shake flask into a fed-batch-operated bioreactor. Hereby, the intended addition of talc microparticles allowed engineering the morphology of A. niger into a highly active mycelial form, which strongly boosted production. Fructofuranosidase production was highly specific as confirmed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis. The secreted enzyme activity of 2,800 U/mL, corresponding to about 3 g/L of fructofuranosidase, achieved by the microparticle-enhanced fed-batch process, is tenfold higher than that of any other process reported so far, so that the presented bioprocess strategy appears as a milestone towards future industrial fructofuranosidase production.
引用
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页码:2011 / 2024
页数:14
相关论文
共 29 条
[1]  
BABU SI, 2008, RES MICROBIOL, V3, P114
[2]   Optimization of media for β-fructofuranosidase production by Aspergillus niger in submerged and solid state fermentation [J].
Balasubramaniem, AK ;
Nagarajan, KV ;
Paramasamy, G .
PROCESS BIOCHEMISTRY, 2001, 36 (12) :1241-1247
[3]   Production of beta-fructofuranosidase by Aspergillus japonicus [J].
Chen, WC ;
Liu, CH .
ENZYME AND MICROBIAL TECHNOLOGY, 1996, 18 (02) :153-160
[4]   Production of fructooligosaccharides by the mycelia of Aspergillus japonicus immobilized in calcium alginate [J].
Cruz, R ;
Cruz, VD ;
Belini, MZ ;
Belote, JG ;
Vieira, CR .
BIORESOURCE TECHNOLOGY, 1998, 65 (1-2) :139-143
[5]   Effect of substrate feeding on production of fructosyltransferase by Penicillium purpurogenum [J].
Dhake, A. B. ;
Patil, M. B. .
BRAZILIAN JOURNAL OF MICROBIOLOGY, 2007, 38 (02) :194-199
[6]   Morphology Engineering of Aspergillus niger for Improved Enzyme Production [J].
Driouch, Habib ;
Sommer, Becky ;
Wittmann, Christoph .
BIOTECHNOLOGY AND BIOENGINEERING, 2010, 105 (06) :1058-1068
[7]   Production of fructooligosaccharides by β-fructofuranosidase from Aspergillus sp 27H [J].
Fernández, RC ;
Maresma, BG ;
Juárez, A ;
Martínez, J .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2004, 79 (03) :268-272
[8]   Screening of β-fructofuranosidase-producing microorganisms and effect of pH and temperature on enzymatic rate [J].
Fernandez, Ruben Cuervo ;
Ottoni, Cristiane Angelica ;
da Silva, Elda Sabino ;
Saito Matsubara, Rosa Mitiko ;
Carter, Jose Marcio ;
Magossi, Luis Roberto ;
Alves Wada, Maria Alice ;
Rodrigues, Maria Filomena de Andrade ;
Maresma, Beatriz Guilarte ;
Maiorano, Alfredo Eduardo .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 75 (01) :87-93
[9]   Glucoamylase::green fluorescent protein fusions to monitor protein secretion in Aspergillus niger [J].
Gordon, CL ;
Khalaj, V ;
Ram, AFJ ;
Archer, DB ;
Brookman, JL ;
Trinci, APJ ;
Jeenes, DJ ;
Doonan, JH ;
Wells, B ;
Punt, PJ ;
van den Hondel, CAMJJ ;
Robson, GD .
MICROBIOLOGY-UK, 2000, 146 :415-426
[10]   Production of β-fructofuranosidases by Aspergillus niveus using agroindustrial residues as carbon sources: Characterization of an intracellular enzyme accumulated in the presence of glucose [J].
Guimaraes, Luis Henrique S. ;
Somera, Alexandre Favarin ;
Terenzi, Hector Francisco ;
Teixeira de Moraes Polizeli, Maria de Lourdes ;
Jorge, Joao Atilio .
PROCESS BIOCHEMISTRY, 2009, 44 (02) :237-241