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Optimisation of Growth of Raphidocelis subcapitata Immobilised for Biofuel Production: Influence of Alginate and CaCl 2 Concentrations on Growth

机译:固定化用于生物燃料生产的水生楠竹生长的优化:藻酸盐和CaCl 2浓度对生长的影响

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The growth of the green microalga Raphidocelis subcapitata in sodium alginate beads was studied. The beads were generated by the extrusion technique, which was followed by gelling in a Ca 2+ solution. The alginate concentrations studied were 1%, 1.5% and 2% ( w / v ), while the concentrations of CaCl 2 were 0.2%, 0.5% and 1% ( w / v ). The growth monitoring of the cells in the beads was performed by dissolving the gel in a sodium phosphate buffer and reading the optical density at 685 nm using a spectrophotometer. The results clearly showed that alginate and divalent Ca 2+ ions do not contribute directly to the growth of microalgae but play a decisive role in preserving the integrity of the beads and protecting them from shrinkage. Furthermore, they have an important role in the transfer of nutrients, light and CO 2 in the beads. The highest growth (3.92 × 10 6 ± 0.39 cells/bead) was obtained with the concentrations of alginate being 1.5% and CaCl 2 being 0.2%. However, the beads began to shrink and this resulted in the cells being released into the culture medium after the 8th day. Of all the combinations studied, the combination of 2% alginate and 1% CaCl 2 was the best because it ensured the stability of the beads during the 10 days of culture and resulted in a low concentration of free cells detected in the culture medium. These concentrations were determined as the optimal conditions for the immobilization of microalgae and will be used in the following work.
机译:研究了藻酸钠钠微珠中绿色微藻角叉菜的生长。通过挤出技术产生珠子,随后在Ca 2+溶液中胶凝。研究的藻酸盐浓度为1%,1.5%和2%(w / v),而CaCl 2的浓度为0.2%,0.5%和1%(w / v)。通过将凝胶溶解在磷酸钠缓冲液中并使用分光光度计读取685 nm的光密度来进行珠中细胞的生长监测。结果清楚地表明,藻酸盐和二价Ca 2+离子并不能直接促进微藻的生长,但在保持微珠的完整性和防止微珠收缩方面起着决定性的作用。此外,它们在珠粒中养分,光和CO 2的转移中也具有重要作用。海藻酸盐的浓度为1.5%,CaCl 2的浓度为0.2%,生长最快(3.92×10 6±0.39个细胞/珠)。但是,珠子开始收缩,这导致细胞在第8天后释放到培养基中。在所有研究的组合中,2%海藻酸盐和1%CaCl 2的组合是最好的,因为它确保了培养10天期间珠子的稳定性,并导致在培养基中检测到低浓度的游离细胞。这些浓度被确定为固定微藻的最佳条件,并将在以下工作中使用。

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