Method for rapid identification of microalgae on single cell level
A single-cell, microalgae technology, used in material excitation analysis, Raman scattering, etc., to avoid errors and reduce sample requirements
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[0024] 1) Four strains of Chlamydonomas reinhardtii mutants CC124, CC4324, CC4333 and CC4334 were purchased from Chlamydomonas Resource Center: http: / / chlamycollection.org / strains / .
[0025] 2) Chlamydomonas reinhardtii was inoculated into TAP (Tris acetate phosphate) liquid medium with or without nitrogen (3 biological replicates), 150 μmol photons m -2 the s -1 Light, 25 ° C, aeration and stirring culture. Samples were taken when culturing to 0h, 12h, 24h, 48h, 72h and 96h. Among them, TAP liquid medium with nitrogen or nitrogen deficiency, TAP (Tris acetate phosphate) medium:
[0026] NH 4 Cl (7.48mM), MgSO 4 (406 μM), CaCl 2 (340μM), K 2 HPO 4 (540μM), KH 2 PO 4 (463μM), 20mM Tris, 17.4mM acetate, H 3 BO 3 (184μM), ZnSO 4 (76.5μM),MnCl 2 (25.5μM), FeSO 4 (17.9 μM), CoCl 2 (6.77μM),(NH4) 6 Mo 7 o 24 (0.88μM), CuSO 4 (6.29μM), and Na 2 EDTA (148μM)
[0027] 3) Take the algae liquid of different culture time in step 2), take 1mL of the algae liquid for ea...
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