Food-grade aspergillus niger strain and application of strain in zearalenone degradation
A technology of zearalenone and Aspergillus niger, which is applied in the field of Aspergillus niger, can solve the problems of nutrient composition destruction, time-consuming and labor-consuming, loss of animal feed nutrients, etc., and achieve the effect of reducing the content
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Embodiment 1
[0018] Embodiment 1: the screening method of Aspergillus niger in sauce unstrained spirits
[0019] The non-toxin-producing filamentous fungi in the fermented sauce were qualitatively isolated from the fermented sauce with β-cyclodextrin-containing PDA medium, and then the toxin-producing ability of the isolated strains was quantitatively analyzed by ELISA method, and finally Screen out non-toxigenic molds. Re-screen the toxin-producing bacteria that can inhibit Aspergillus flavus, and screen out the strains that can prevent and control mycotoxins.
[0020] Through the observation of colony characteristics and individual morphology, the 18S rDNA of the strain was compared with the GenBank database ( http: / / blast.ncbi.nlm.nih.gov / Blast.cgi ) and found that its homology with Aspergillus niger was 100%. Combined with the morphological characteristics and molecular biological identification of the strain, it can be determined that the strain is Aspergillus niger. This strain w...
Embodiment 2
[0021] Embodiment 2: Degradation of Zearalenone by Aspergillus niger
[0022] The isolated strain FS-Z1 was inoculated into 60ml of sterile PDB medium at a 2% inoculum size, cultured on a shaker at 28°C and 150rpm for 5 days. Add zearalenone to the fermentation broth to make the final concentration reach 2ppm, use sterile PDB culture fluid plus zearalenone as a blank control, and after culturing for 48 hours, draw 2ml of liquid from two groups of samples and add 4ml of trichloro Methane, extracted 3 times, dried with nitrogen, then redissolved with 1ml of mobile phase [acetonitrile: water = 50:50 (v / v)], passed through a 0.22μm organic filter membrane and carried out by high performance liquid chromatography (HPLC) detection.
[0023] The chromatographic detection conditions are: chromatographic column: C18 column 6mm×150mm×5um; mobile phase: acetonitrile:water=50:50; detection temperature: 25°C; flow rate: 1ml / min; detection wavelength: excitation wavelength: 274nm; emission...
Embodiment 3
[0025] Embodiment 3: Aspergillus niger FS-Z1 is to the control of the corn steep liquor of zearalenone toxin pollution
[0026] The isolated strain FS-Z1 was inoculated into 60ml of sterile PDB medium at a 2% inoculum size, cultured on a shaker at 28°C and 150rpm for 5 days. Filter the mycelium of Aspergillus niger with four layers of sterile gauze to obtain the fermentation liquid of Aspergillus niger. Mix the fermented liquid with corn steep liquor [1:1 (v / v)] and shake evenly, mix the sterile PDB medium with equal volume of corn steep liquor as a blank control, culture at 28°C and 150rpm for 48h, filter through glass fiber filter paper Filter 1 to 2 times until the filtrate is clear, extract zearalenone in the sample according to the above method, and detect the content of residual zearalenone toxin by high performance liquid chromatography.
[0027] Measured by high-performance liquid chromatography, it was found that the concentration of zearalenone in 0h corn steep liqu...
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