Characterization of a mycelial fructosyltransferase from Aspergillus tamarii NKRC 1229 for efficient synthesis of fructooligosaccharides

被引:25
作者
Choukade, Ritumbhara [1 ]
Kango, Naveen [1 ]
机构
[1] Dr Hari Singh Gour Vishwavidyalaya, Dept Microbiol, Enzyme Technol & Mol Catalysis Lab, Sagar 470003, Madhya Pradesh, India
关键词
Fructooligosaccharides (FOS); Fructosyltransferase (FTase); Prebiotics; Zymography; Aspergillus; Bio-Gel P2; BETA-FRUCTOFURANOSIDASE; ENZYMATIC-SYNTHESIS; FRUCTO-OLIGOSACCHARIDES; HETEROLOGOUS EXPRESSION; INFRARED-SPECTROSCOPY; IMMOBILIZED CELLS; SUCROSE; ENZYMES; PURIFICATION; PENICILLIUM;
D O I
10.1016/j.foodchem.2019.02.025
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An efficient system for biotransformation of sucrose to fructooligosaccharides (FOS) was obtained using Aspergillus tamarii NKRC 1229 mycelial fructosyltransferase (m-FTase). Zymographic analysis confirmed mycelial localization of the FTase (36 U/g) and lyophilized fungal pellets were used for bioconversion. m-FTase had molecular weight similar to 75 kDa with optimum activity at pH 7.0 and 20 degrees C. FOS production after parametric optimization (sucrose-50% w/v, m-FTase dose - 4.5% w/v, inoculum age - 48 h and incubation time-24 h) reached 325 g/L (55% yield) with 14% residual sucrose, 25% glucose and 6% fructose. FTase activity was enhanced after pre-treatment with organic solvents and SDS. FOS was purified in a single step using gel filtration matrix, Bio-Gel P2. FOS was characterized using Diffusion ordered spectroscopy-Nuclear Magnetic Resonance (H-1 DOSY-NMR) and Fourier-transform infrared spectroscopy (FTIR). Continuous generation of FOS was achieved using recyclable mycelia upto 10 consecutive cycles.
引用
收藏
页码:434 / 440
页数:7
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