Preparation method of oxygen consumption protective layer on chlorella cell surface
A cell surface, chlorella technology, applied in the biological field, achieves good biocompatibility, promotes continuous hydrogen production, and is easy to operate
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specific Embodiment approach 1
[0016] Specific embodiment one: the preparation method of a kind of chlorella cell surface oxygen-consuming protective layer of this embodiment is specifically carried out according to the following steps:
[0017] 1. Cultivation of Chlorella pyrenoidosa cells: Select Chlorella pyrenoidosa as a biological template, and use TAP medium to cultivate in a light incubator with a temperature of 25-30°C under continuous light of 1200-4800LUX. When pyrenoid pellets Coating is carried out when the number of algae cells reaches the logarithmic growth phase to obtain Chlorella pyrenoidosa cells in the logarithmic growth phase;
[0018] 2. First use a NaCl solution with a concentration of 0.01 to 0.06mol / L to clean the logarithmic phase of the growth of Chlorella pyrenoidosa cells, and then use deionized water to clean the growth of the logarithmic phase of the Chlorella pyrenoidosa cells, Collect the cells by centrifugation, add the collected cells to the Tris buffer solution to obtain t...
specific Embodiment approach 2
[0022] Embodiment 2: This embodiment differs from Embodiment 1 in that: the OD value of the cell culture buffer in Step 2 is 2.0. Others are the same as in the first embodiment.
specific Embodiment approach 3
[0023] Embodiment 3: This embodiment differs from Embodiment 1 or Embodiment 2 in that the mass ratio of dopamine in step 2 to the cell culture buffer is 1 mg:0.375 mL. Others are the same as in the first or second embodiment.
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