Deyu Li, Rui Jiang, Jun Li, Zhen Liu, Yasmeen Zamir Ahmed, Qiankun Zhao, Yongxin Song, Mengqi Li
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引用次数: 0
Abstract
The viability detection of microalgae with the electrokinetic (EK) technique shows vast applications in the biology and maritime industry. However, due to the slight variations in the EK properties between alive and dead microalgae cells, the accuracy and practicability of this technique is limited. In this paper, the light illumination pretreatment was conducted to modify the EK velocity of microalgae for enhancing the EK difference. The effects of the illumination time and light color on the EK velocities of Chlorella vulgaris and Isochrysis galbana were systematically measured, and the EK differences between alive and dead cells were calculated and compared. The results indicate that under light illumination, the photosynthesis of the alive cells leads to the amplification of the zeta potential, leading toward increase in the EK difference along with the illumination time. By using light with different color spectra to treat the microalgae, it was found that the EK difference changes with the light color according to the following order: white light > red light > blue light > green light. The difference in EK potential with exposure to white light treatment surpasses over 10-fold in comparison to those without such treatment. The light pretreatment technique, as illustrated in this study, offers an advantageous strategy to enhance the EK difference between living and dead cells, proving beneficial in the field of microalgae biotechnology.
利用电动动力学(EK)技术检测微藻的活力在生物和海事领域有着广泛的应用。然而,由于活的和死的微藻细胞之间的 EK 特性存在细微差别,该技术的准确性和实用性受到了限制。本文通过光照预处理来改变微藻的 EK 速度,以增强 EK 差异。系统测量了光照时间和光色对绿球藻(Chlorella vulgaris)和矶藻(Isochrysis galbana)EK速度的影响,并计算和比较了活细胞和死细胞的EK差异。结果表明,在光照下,活细胞的光合作用会导致zeta电位的放大,从而导致EK差随着光照时间的延长而增大。通过使用不同颜色光谱的光处理微藻,发现 EK 电位差随光色的变化顺序如下:白光 > 红光 > 蓝光 > 绿光。与未经过白光处理的微藻相比,经过白光处理的微藻的电位差超过 10 倍。如本研究所示,光预处理技术为增强活细胞和死细胞之间的电位差提供了一种有利的策略,在微藻生物技术领域证明是有益的。
期刊介绍:
ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.).
Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences.
Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases.
Papers describing the application of standard electrophoretic methods will not be considered.
Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics:
• Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry
• Single cell and subcellular analysis
• Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS)
• Nanoscale/nanopore DNA sequencing (next generation sequencing)
• Micro- and nanoscale sample preparation
• Nanoparticles and cells analyses by dielectrophoresis
• Separation-based analysis using nanoparticles, nanotubes and nanowires.