Active substance for inducing autolysis of microalgae cells and method for producing the same
A technology of microalgae cells and active substances, which is applied in the field of active substances that induce self-lysis of microalgae cells, and can solve the problems of consumption of microalgae cells, recycling of unfavorable products, and large energy
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Embodiment 1
[0066] Example 1. Confirmation of the Volatile Properties of Active Substances Inducing Microalgae Cell Autolysis
[0067] 1. Treatment of the culture solution of Bacillus thuringiensis ITRI-G1 (preservation number DSM29807, German Culture Collection of Microorganisms, Leibniz Research Institute DSMZ, Inhoffenstr.7B, D-38124Braunschweig)
[0068] (1) Cultivation of Bacillus thuringiensis ITRI-G1
[0069] Cultivate Bacillus thuringiensis ITRI-G1 with the culture medium and culture conditions shown below
[0070] Culture medium: 2g / L peptone + 0.2g / L yeast extract
[0071] Culture conditions: Culture at 28°C for 2 days at a shaking rate of 150rpm
[0072] After the cultivation of Bacillus thuringiensis ITRI-G1 was completed, 300 mL of the culture solution was taken to carry out the vacuum distillation procedure. Collect residual liquid (non-volatile part) at different distillation times, and collect all distillate when distilling 2 hours, the condition of underpressure distil...
Embodiment 2
[0081] Example 2, the cell-breaking test of chlorella by inducing the active substance of microalgae cell autolysis
[0082] 1. Preparation of active substances that induce self-lysis of microalgal cells
[0083] (1) Cultivation of Bacillus thuringiensis ITRI-G1
[0084] Cultivate Bacillus thuringiensis ITRI-G1 with the culture medium and culture conditions shown below
[0085] Culture medium: 2g / L peptone + 0.2g / L yeast extract
[0086] Culture conditions: Culture at 28°C for 2 days at a shaking rate of 150rpm
[0087] (2) Separation and purification of active substances that induce autolysis of microalgal cells
[0088] After the cultivation of Bacillus thuringiensis ITRI-G1 was completed, 300 mL of the culture solution was taken for separation and purification by vacuum distillation, and 100 mL of the distilled solution was obtained. The conditions for vacuum distillation are as follows:
[0089] Distillation temperature: 50°C
[0090] Pressure: 110hPa
[0091] Time:...
Embodiment 3
[0096] Example 3, the active substance that induces the autolysis of microalgae cells has a cell-breaking effect on different microalgae
[0097] 1. Preparation of active substances that induce self-lysis of microalgal cells
[0098] (1) Cultivation of Bacillus thuringiensis ITRI-G1 and Bacillus thuringiensis BCRC 14683 (purchased from Taiwan Food Industry Development Institute Biological Resource Preservation and Research Center)
[0099] Bacillus thuringiensis ITRI-G1 and Bacillus thuringiensis BCRC 14683 were respectively cultured in the culture medium and culture conditions shown below
[0100] Culture medium: 2g / L peptone + 0.2g / L yeast extract
[0101] Culture conditions: Culture at 28°C for 2 days at a shaking rate of 150rpm
[0102] (2) Separation and purification of active substances that induce autolysis of microalgal cells
[0103] After the cultivation of Bacillus thuringiensis ITRI-G1 or Bacillus thuringiensis BCRC 14683 was completed, 300 mL of the culture sol...
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