Phytase from Citrobacter koseri PM-7: Cost-Effective Production Using Agro-Industrial Residues, Biochemical Characterization and Application in de-Phytinization

被引:4
|
作者
Tripathi, Preeti [1 ]
Garg, Silvi [1 ]
Panwar, Deepesh [1 ,2 ]
Kaira, Gaurav Singh [1 ,2 ]
Kumar, Rahul [1 ]
Kapoor, Mukesh [1 ,2 ]
机构
[1] CSIR, Cent Food Technol Res Inst, Dept Prot Chem & Technol, Mysuru 570020, India
[2] CSIR, CFTRI, Acad Sci & Innovat Res AcSIR, Mysuru, India
关键词
Citrobacter; Phytase; Agro-industrial residues; Fermentation; Biochemical characterization; Dephytinization; MOLD SPOROTRICHUM-THERMOPHILE; SOLID-STATE FERMENTATION; ACID-STABLE PHYTASE; BACILLUS SP CFR1601; BIOTECHNOLOGICAL APPLICATIONS; THERMOSTABLE PHYTASE; ASPERGILLUS-NIGER; PICHIA-PASTORIS; ENDO-MANNANASE; GENE CLONING;
D O I
10.1007/s12649-016-9662-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The study explored the potential of low-cost agro-industrial residues in the production of phytase from bacterial sources which was (1) active at high temperature and broad range of pH and, (2) can act as a supplement for animal feed in order to improve its nutritional efficiency. Optimization of various factors (incubation period, initial pH, inoculum age/size, and carbon/nitrogen source) under submerged fermentation resulted in 21.55-fold (0.431 U/ml) improvement in phytase (Phy-Ck) production from Citrobacter koseri PM-7 [isolated from the rhizosphere of black sesame (Sesamum indicum)]. Under solid state fermentation using wheat bran, 9.372 U/g dry substrate of Phy-Ck production was obtained after 120 h of incubation. Partially purified Phy-Ck exhibited maximum activity at pH 5 and was stable in a pH (3-6) range by retaining more than 40 % of its activity after 3 h of incubation. Phy-Ck was optimally active at 70 A degrees C. Ca2+ was found to marginally stimulate Phy-Ck while, moderate to complete inhibition of enzyme activity was observed in presence of Mn2+, Mg2+, Ni2+, Li2+, Hg2+, Cu2+, and EDTA. Thermal inactivation kinetics of Phy-Ck at 50-63 A degrees C in the presence of Ca2+ led up to 12.33-fold improvement in half-life (t(1/2)) and better values for thermodynamic parameters [deactivation energy (E-d), enthalpy (H) and entropy (S)]. The K (m) and V (max) values of Phy-Ck were 0.408 mM and 3.586 mu mol/ml/min, respectively. Phy-Ck displayed good tolerance (up to 98.5 % activity) towards proteolytic enzymes (pepsin, trypsin, and chymotrypsin). Phy-Ck was able to dephytinize agro-industrial residues with concomitant liberation of inorganic phosphate and soluble protein. The study demonstrated valorization of agro-residues for production of phytase useful for feed industry.
引用
收藏
页码:1105 / 1118
页数:14
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