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Utilization of pyrolytic substrate by microalga Chlamydomonas reinhardtii: cell membrane property change as a response of the substrate toxicity

机译:微藻莱茵衣藻对热解底物的利用:细胞膜性质变化作为底物毒性的反应

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摘要

Acetic acid derived from fast pyrolysis of lignocellulosic biomass is a promising substrate for microalgae fermentation for producing lipid-rich biomass. However, crude pyrolytic acetic acid solution contains various toxic compounds inhibiting algal growth. It was hypothesized that such an inhibition was mainly due to the cell membrane damage. In this work, the cell membrane property of algal cells was evaluated at various conditions to elucidate the mechanisms of inhibition caused by the pyrolytic substrate solution. It was found that acetic acid itself served a carbon source for boosting algal cell growth but also caused cell membrane leakage. The acetic acid concentration for highest cell density was 4 g/L. Over-liming treatment of crude pyrolytic acetic acid increased the algal growth with a concurrent reduction of cell membrane leakage. Directed evolution of algal strain enhanced cell membrane integrity and thus increased its tolerance to the toxicity of the crude substrate. Statistical analysis shows that there was a significant correlation between the cell growth performance and the cell membrane integrity (leakage) but not membrane fluidity. The addition of cyto-protectants such as Pluronic F68 and Pluronic F127 enhanced the cell membrane integrity and thus, resulted in enhanced cell growth. The transmission electron microscopy (TEM) of algal cells visually confirmed the cell membrane damage as the mechanism of the pyrolytic substrate inhibition. Collectively, this work indicates that the cell membrane is one major reason for the toxicity of pyrolytic acetic acid when being used for algal culture. To better use this pyrolytic substrate, cell membrane of the microorganism needs to be strengthened through either strain improvement or addition of membrane protectant reagents.
机译:来自木质纤维素生物质快速热解的乙酸是微藻发酵生产富含脂质的生物质的有希望的底物。但是,粗制的热解乙酸溶液含有多种抑制藻类生长的有毒化合物。假设这种抑制主要是由于细胞膜损伤。在这项工作中,在各种条件下评估藻类细胞的细胞膜特性,以阐明由热解底物溶液引起的抑制机制。发现乙酸本身充当碳源以促进藻类细胞生长,但也引起细胞膜泄漏。最高细胞密度的乙酸浓度为4 g / L。粗解热乙酸的超石灰处理增加了藻类的生长,同时减少了细胞膜的泄漏。藻类菌株的定向进化增强了细胞膜的完整性,因此增加了其对粗底物毒性的耐受性。统计分析表明,细胞生长性能和细胞膜完整性(渗漏)之间存在显着相关性,而膜流动性则不存在显着相关性。添加细胞保护剂(如Pluronic F68和Pluronic F127)可增强细胞膜的完整性,从而增强细胞的生长。藻类细胞的透射电子显微镜(TEM)在视觉上证实了细胞膜损伤是热解底物抑制的机制。总的来说,这项工作表明细胞膜是用于藻类培养时热解乙酸毒性的主要原因之一。为了更好地利用这种热解底物,需要通过菌株改良或添加膜保护剂来增强微生物的细胞膜。

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