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Photooxidative stress-inducible orange and pink water-soluble astaxanthin-binding proteins in eukaryotic microalga

机译:光氧基应激诱导橙色和粉红色水溶性虾青色蛋白结合蛋白在真核微藻中

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摘要

a Light microscope view of Oki-4N. Cells were grown under non-stressed (left) or 0.5 M NaCl with high light (w/HL) for 4 days (middle) conditions and were continued for 2 weeks (right). Scale bar = 10 µm. b Scanning electron micrographs of Oki-4N. Scale bar = 10 µm. c Colour of aqueous cell extracts obtained after ultracentrifugation at 100,000 × g for 3 h. A 1 g aliquot of wet cells (the cell pellet after harvesting by centrifugation was lightly dried with filter paper to remove excess liquid medium) was suspended in 10 mL of cell suspension buffer (50 mM Tris-HCl at pH 7.5), disrupted by French press, and then ultra-centrifuged. Pigment concentrations were measured as optical density (OD) at 480 nm. The data are representative of at least three independent experiments. d Elution profiles of aqueous cell extracts from the cells under non-stressed or 0.5 M NaCl w/HL conditions for 2 or 4 days were evaluated by gel-filtration column chromatography. Elution profiles were monitored by using an HPLC photodiode array detector. The colour of the elution peak is shown above each elution peak. The data are representative of at least three independent experiments.
机译:oki-4n光显微镜视图。细胞在非应激(左)或0.5M NaCl下生长4天(中间)条件,并持续2周(右)。秤条=10μm。 B扫描电子显微照片OKI-4N。秤条=10μm。在100,000×g以100,000×g以100,000×g以3小时后获得的C颜色的含水细胞提取物。 1g等分试样的湿细胞(通过离心收获后的电池沉淀用滤纸将过量液体介质用10ml细胞悬浮缓冲液(pH7.5的50mm Tris-HCl)悬浮在悬浮在10ml细胞悬浮缓冲液中,被法国破坏按压,然后超离心。用480nm的光密度(OD)测量颜料浓度。数据代表至少三个独立实验。通过凝胶过滤柱色谱法评估来自非应激或0.5M NaCl W / HL条件下的细胞的水细胞提取物的洗脱谱。通过凝胶过滤柱色谱法评价2或4天。通过使用HPLC光电二极管阵列检测器监测洗脱曲线。洗脱峰的颜色显示在每个洗脱峰上方。数据代表至少三个独立实验。

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