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Causes of Shear Sensitivity of the Toxic Dinoflagellate Protoceratium reticulatum

机译:网状有毒鞭毛原毛虫剪切敏感性的原因

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摘要

Dinoflagellates have proven extremely difficult to culture because they are inhibited by low-level shear forces. Specific growth rate of the toxic dinoflagellate Protoceratium reticulatum was greatly decreased compared with static control culture by intermittent exposure to a turbulent hydrodynamic environment with a bulk average shear rate that was as low as 0.3 s~(-1) . Hydrodynamic forces appeared to induce the production of reactive oxygen species (ROS) within the cells and this caused peroxidation of cellular lipids and ultimately cell damage. Exposure to damaging levels of shear rate correlated with the elevated level of lipoperoxides in the cells,but ROS levels measured directly by flow cytometry did not correlate with shear induced cell damage. This was apparently because the measured level of ROS could not distinguish between the ROS that are normally generated by photosynthesis and the additional ROS produced as a consequence of hydrodynamic shear forces. Continuously subjecting the cells to a bulk average shear rate value of about 0.3 s~(-1) for 24-h caused an elevation in the levels of chlorophyll a,peridinin and dinoxanthin,as the cells apparently attempted to counter the damaging effects of shear fields by producing pigments that are potential antioxidants. In static culture,limitation of carbon dioxide produced a small but measureable increase in ROS. The addition of ascorbic acid (0.1 mM) to the culture medium resulted in a significant protective effect on lipid peroxidation,allowing cells to grow under damaging levels of shear rates. This confirmed the use of antioxidant additives as an efficient strategy to counter the damaging effects of turbulence in photobioreactors where shear sensitive dinoflagellates are cultivated.
机译:事实证明,鞭毛藻很难培养,因为它们受到低水平的剪切力的抑制。与静态对照培养相比,有毒的鞭毛藻原毛网菌的特定生长速率与静态对照培养相比大大降低,这是因为间歇性地将其暴露于湍流的流体动力学环境中,其体均剪切速率低至0.3 s〜(-1)。流体动力似乎诱导了细胞内活性氧(ROS)的产生,这引起了细胞脂质的过氧化作用并最终导致了细胞损伤。暴露于剪切速率的破坏水平与细胞中脂过氧化物的升高水平相关,但是直接通过流式细胞术测量的ROS水平与剪切诱导的细胞损伤无关。显然这是因为所测量的ROS水平无法区分通常由光合作用产生的ROS和由于水动力剪切力而产生的其他ROS。连续使细胞经受约0.3 s〜(-1)的体积平均剪切速率值24小时,导致叶绿素a,peridinin和dinoxanthin的水平升高,因为细胞显然试图抵消剪切的破坏作用。通过生产作为潜在抗氧化剂的颜料来实现这一领域。在静态培养中,二氧化碳的限制会使ROS产生少量但可测量的增加。向培养基中添加抗坏血酸(0.1 mM)对脂质过氧化具有明显的保护作用,使细胞能够在破坏性剪切速率下生长。这证实了抗氧化剂添加剂的使用作为一种有效的策略,以应对湍流在培养剪切敏感的鞭毛藻的光生物反应器中的破坏作用。

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