Method for producing L-lactic acid through biomass fermentation
A biomass fermentation and biomass technology, applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problem of high production cost of lactic acid, and achieve the effect of reducing alkali consumption and wastewater discharge
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Embodiment 1
[0028] Weigh 1 kg of corncobs, crush them into particles of about 1 to 2 cm, add 0.5 kg of sodium hydroxide and 7.5 kg of water, cook at about 100° C. for 60 minutes, press filter to separate the cooking liquid and residue, and obtain alkali treatment waste liquid I and Alkaline Treatment of Corncob Residue II.
[0029] Prepare 2L simultaneous saccharification and fermentation medium in a 3L saccharification and fermentation tank: absolute dry alkali treatment corncob residue II 150g / L, yeast extract 5g / L, ammonium chloride 1g / L, MgSO 4 0.5g / L, pH natural. Add 20 mL of cellulose degrading enzyme with an enzyme activity of 150 FPIU / mL (cellulolytic enzyme Celluclast is Novozymes commercial enzyme, produced by Trichoderma reesei ATCC 26921), heat up to 50°C, stir at 200 rpm, and perform hydrolysis for 6 hours.
[0030] Pre-cultivation of Bacillus coagulans: Add Bacillus coagulans (DSM 23183) into 200 mL of seed medium, and cultivate for 18 hours at 180 rpm and 50° C. without ve...
Embodiment 2
[0035] Weigh 3kg of corn stalks, cut them into pieces of about 1-2cm, add NaOH solution with a concentration of 5% (w / w) according to the solid-liquid weight ratio of 1:10, cook at about 90°C for 120min, centrifuge at 3500rpm for 15min to solidify The liquid is separated to obtain the alkali-treated waste liquid I and the alkali-treated corn stalk residue II.
[0036] Prepare 3L simultaneous saccharification and fermentation medium in a 5L saccharification and fermentation tank: Alkali-treated corn stalk residue II 200g / L, yeast extract 7g / L, ammonium chloride 1.2g / L, MgSO 4 0.5g / L, pH natural. Add 20 mL of cellulose-degrading enzyme with an enzyme activity of 150 FPIU / mL (derived from Trichoderma koningeni), heat up to 50° C., stir at 200 rpm, and perform hydrolysis for 6 hours.
[0037] Pre-cultivation of Bacillus coagulans: Inoculate Bacillus coagulans (DSM 23183) into 300mL of fresh seed medium, and cultivate for 18h at 180rpm, 50°C without ventilation. Seed medium form...
Embodiment 3
[0042] Weigh 1kg of bagasse after sugar industry pressing, add NaOH with a concentration of 3% (w / w) according to the solid-liquid weight ratio of 1:10, cook at about 100°C for 60min, centrifuge at 3500rpm for 15min for solid-liquid separation, and obtain alkali treatment Waste liquid I and alkali-treated sugarcane residue II.
[0043] Prepare 2L simultaneous saccharification and fermentation medium in a 3L saccharification and fermentation tank: Alkali-treated bagasse 100g / L, corn steep liquor powder 5g / L, ammonium chloride 1g / L, MgSO 4 0.5g / L, pH natural. Add 13 mL of cellulose degrading enzyme with an enzyme activity of 150 FPIU / mL (the cellulose degrading enzyme Celluclast is a Novozymes commercial enzyme, produced by Trichoderma reesei ATCC 26921); the temperature is raised to 50° C., the stirring speed is 200 rpm, and the hydrolysis reaction is carried out for 3 hours.
[0044] Pre-cultivation of Bacillus coagulans: Inoculate Bacillus coagulans (DSM 23183) into 200 mL ...
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