Method for extracting natural carotenoid from neurospora crassa and spores thereof
A technology of Neurospora brassica and carotene, applied in natural dyes, chemical instruments and methods, azo dyes, etc., can solve the problems of carotenoid loss, conidia wall thickness, etc., achieve short wall breaking time, Effects in a short time and mild conditions
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Embodiment 1
[0015] The solid-state culture of Neurospora stouti was dried at 45-60°C and then pulverized. The coarse powder was passed through a 40-mesh sieve. The coarse powder of the culture was broken by a 0.8mol / L hydrochloric acid solution at room temperature for 1-5min. The acid solution was added in an amount of 0.5~2L / kg culture, washed with water after wall breaking, squeezed filtration or suction filtration under reduced pressure, repeated washing and filtration twice until neutral, the obtained filter residue was leached with acetone for 5~10min, and the material-liquid ratio was 5~ The 10L / kg filter residue is leached twice, the extracts are combined, and the extracts are evaporated under reduced pressure at 45-50°C to recover the solvent to obtain the crude carotenoid extract. The extraction rate of pigment can reach more than 98%.
Embodiment 2
[0017] The spores of Neurospora stout were dried at 45-60°C and then broken by a 0.8mol / L hydrochloric acid solution at room temperature for 1-3min. The acid solution was added in an amount of 1.0-3.0L / kg of the spores. After the wall was broken, washed with water and squeezed Filtration or suction filtration under reduced pressure, repeat the water washing and filtration operations twice until neutral, the obtained filter residue is leached with acetone for 5-8min, the material-to-liquid ratio is 35-50L / kg filter residue, leached twice, combined the extract, the extract The carotenoid crude extract is obtained after the solvent is recovered by evaporation under reduced pressure at 45-50°C. The extraction rate of pigment can reach more than 96%.
Embodiment 3
[0019] After the liquid culture of Neurospora stouti was washed with water and filtered, the obtained mycelium was broken by a 1.0mol / L hydrochloric acid solution at room temperature for 5-10min, and the acid solution was added in an amount of 1.0-2.0L / kg of mycelium, and the wall was broken. After finishing, washing with water, extrusion filtration or vacuum suction filtration, repeating the washing and filtration operations twice until neutral, the obtained filter residue is leached with ethyl acetate for 8-10min, the material-to-liquid ratio is 15-25L / kg filter residue, leaching two Second, the extracts were combined, and the extracts were evaporated under reduced pressure at 45-50°C to recover the solvent to obtain the crude carotenoid extract. The extraction rate of pigment can reach more than 95%.
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