Patent Application
20160222367
The present disclosure relates to an enzyme composition. More specifically, the present disclosure relates to a process for the synthesis of an enzyme composition from Aspergillus niger NCIM 563 (MTCC 5213), isolated from soil and its mutant strains A. niger MCC0013 and MCC0014.
Phytase has low activity under submerged fermentation conditions. The inventors have published that the organism Aspergillus niger can produce mutant strains and that both isolate and mutants produce phytase enzyme (Bhaysar el al., Appl Microbiol Biotechnol., 2013, 97(2), 673-9. Hence, the mutants of Aspergillus niger NCIM 563 overproducing phytase under such conditions have direct commercial potential.
Mutant strains show higher activity of phytase than earlier reports. New more efficient strains generated using combination of UV and Chemical mutagenesis.
The main object of the present disclosure is to provide a process for the synthesis of an enzyme composition from Aspergillus niger NCIM 563, isolated from soil and its mutant strains Aspergillus niger MCC0013 and MCC0014.
In an aspect of the present disclosure, there is provided a process for the production of multienzyme system using fermentation, said process comprising: (a) growing Aspergillus niger on a medium having sucrose at a concentration of about 1% and yeast extract at a concentration of about 0.2% and at a temperature in the range of 25-35 deg C. and pH in the range of 5-6 for a period in the range of 48-120 hours under shaking condition having angular speed in the range of 200-250 rpm in order to obtain an inoculum; (b) adding the inoculum, obtained in step (a), to the fermentation medium at the concentration in the range of 10-25 percent (v/v) followed by fermenting for a period in the range of 48-120 hours under shaking condition having angular speed in the range of 200-250 rpm for a period in the range of 48-120 hours in order to obtain the fermentation culture; wherein said fermentation medium has the following composition:
and, (c) centrifuging the fermentation culture, obtained in step (b), followed by separation of culture fluid from pellets using filter paper (Whatman no.1) to obtain the said multienzyme system in form of culture fluids.
In an embodiment of the present disclosure, there is provided a process for the production of multienzyme system using fermentation, said process comprising: (a) growing Aspergillus niger on a medium having sucrose at a concentration of about 1% and yeast extract at a concentration of about 0.2% and at a temperature in the range of 25-35 deg C. and pH in the range of 5-6 for a period in the range of 48-120 hours under shaking condition having angular speed in the range of 200-250 rpm in order to obtain an inoculum; (b) adding the inoculum, obtained in step (a), to the fermentation medium at the concentration in the range of 10-25 percent(v/v) followed by fermenting for a period in the range of 48-120 hours under shaking condition having angular speed in the range of 200-250 rpm for a period in the range of 48-120 hours in order to obtain the fermentation culture; wherein said fermentation medium has the following composition:
and, (c) centrifuging the fermentation culture, obtained in step (b), followed by separation of culture fluid from pellets using filter paper (Whatman no.1) to obtain the said multienzyme system in form of culture fluids.
In an embodiment of the present disclosure, there is provided an enzyme composition from Aspergillus niger NCIM 563 Aspergillus niger NCIM 563: NCIM NRS-2 (1953). Putman strain 3, isolated from soil and its mutant strains. A. niger MCC0013 and MCC0014.
In an embodiment of the present disclosure, there is provided an enzyme composition comprising CMCase, xylanase, acid phosphatase, amylase, phytase, β-glucosidase, pectinase and α-galactosidase.
In an embodiment of the present disclosure, there is provided an isolated fungal strain Aspergillus niger NCIM 563 deposited with Microbial Type Culture Collection and Gene Bank (MTCC) having accession number MTCC 5213.
In an embodiment, the present disclosure, there is provided a process for the synthesis of an enzyme composition comprising CMCase, xylanase, acid phosphatase, amylase, Phytase, β-glucosidase, pectinase and α-galactosidase from A. niger NCIM 563, isolated from soil and its mutant strains A. niger MCC0013 and MCC0014, said process being a submerged fermentation process comprising the steps of:
In an embodiment, the present disclosure, there is provided an enzyme composition obtained from Aspergillus niger NCIM 563, said composition comprising:
In another embodiment of the present disclosure, there is provided an enzyme composition obtained from Aspergillus niger mutant NCIM MCC0014, said composition comprising:
In yet another embodiment, the present invention provides an enzyme composition obtained from Aspergillus niger mutant NCIM MCC0014, said composition comprising:
The following examples are given by way of illustration of the present invention and therefore should not be construed to limit the scope of the present invention.
Phytic acid sodium salt was purchased from Sigma Chemical Company (St. Louis, Mo., USA). All other chemicals used were of analytical grade. Rice bran was purchased from the local market.
Microorganism, culture media, and enzyme production
Aspergillus niger MTCC 5213, used in the present disclosure, was maintained on Potato Dextrose Agar (PDA) slant and stored at 4° C. Spores for inoculation were obtained by culturing the strain at 30° C. on a PDA slant for 7 days, followed by washing with 10 ml sterile saline containing 0.01% Tween 80.
The basal fermentation medium according to Bhaysar et al. 2008 contained rice bran, glucose, NaNO3, MgSO4.7H2O, KCl, and FeSO4.7H2O. The fermentation medium for optimization via statistical design of experiments included additional components, namely, MnSO4, dextrin, and Tween 80 at various concentrations as required by the experimental design.
The fermentation medium pH 5.5 before sterilization (100 ml in 250 ml Erlenmeyer flask) was sterilized by autoclaving at 121 ° C. for 15 min. On cooling the fermentation medium was inoculated with desired spore suspension and the incubation time adjusted as per the experimental design. Flasks were incubated at 30° C. at 200 rpm and samples removed after every 24 h. Enzyme production was expressed as enzyme activity U/ml.
After fermentation, the mycelium was separated by filtration followed by centrifugation at 10,000×g for 30 min and the clear supernatant was collected. Solid ammonium sulphate was added to the supernatant to 95% saturation with constant stirring. The precipitate was collected by centrifugation at 15,000×g for 20 min and dissolved in minimum volume of 100 mM Glycine-HCl buffer, pH 2.5 and the salt was removed by passing through Sephadex G-25 column. Active fractions were concentrated through YM-30 membrane (Millipore) and used for enzyme activity measurement.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2641/DEL/2013 | Sep 2013 | IN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IN2014/000583 | 9/5/2014 | WO | 00 |
