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Exploration of potential jarosite biomineralization mechanism based on extracellular polymer substances of Purpureocillium lilacinum Y3

机译:基于紫红素含紫外素含量的细胞外聚合物物质的潜在钾状生物碳化机理的探讨

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In the present study, the mechanism of jarosite biosynthesis mediated by extracellular polymer substances (EPSs) of Purpureocillium lilacinum strain Y3 at gene level was investigated. Yellow-ocher jarosite minerals covered mycelia pellets entirely within 72h, corresponding to a reduction of Fe3+ of 70.9% in the biomineralization process induced by P. lilacinum Y3. The maximum biomass accumulation reached to 12.9 g/L in pure culture, 2.8 g/L with only 0.02M Fe3+ addition, and 6.4 g/L with both 0.02M Fe3+ and 0.1M K( )(+)addition, respectively, indicating that jarosite biosynthesis largely alleviated the inhibition of Fe3+ to the fungal strain. Thereafter, the analysis of EPSs compositions suggested that protein content was affected more evidently than polysaccharides in the biomineralization system. Furthermore, real time quantitative PCR assays revealed that signal transduction genes and abundance of membrane transporters were activated quickly in responding to the stimulation of Fe3+ and fungus-mineral interactions. Then, the expression of adhesive proteins and extracellular proteins was highly up-regulated to facilitate the formation of jarosite minerals on the cell surface. Finally, X-ray photoelectron spectroscopy analysis supported that amine, carboxyl, phosphate groups present on the mycelia provided Fe3+ and K+ binding sites for biosynthesis of jarosite.
机译:在本研究中,研究了通过在基因水平下丙二氟胞菌菌株Y3的细胞外聚合物物质(EPS)介导的jARISE生物合成的机制。黄色赭石罐装矿物完全在72h内完全覆盖了菌丝颗粒,对应于由P.Lilacinum Y3诱导的生物矿化过程中减少的Fe3 + 70.9%。在纯培养物中达到12.9g / L的最大生物质积累,2.8克/升,仅0.02m FE3 +加入,0.02m FE3 +和0.1MK()(+)添加,表明JARY生物合成在很大程度上缓解了Fe3 +对真菌菌株的抑制作用。此后,对EPS组合物的分析表明,蛋白质含量比生物矿化体系中的多糖更明显地受到影响。此外,实时定量PCR测定揭示了在响应Fe3 +和真菌 - 矿物相互作用的刺激时快速激活信号转导基因和膜转运蛋白的丰度。然后,高度调节粘合剂蛋白和细胞外蛋白的表达,以促进细胞表面上的joro矿物质的形成。最后,X射线光电子能谱分析支持该胺,羧基,菌丝体上存在的磷酸盐基团提供摩西二氧化碳的生物合成的Fe3 +和K +结合位点。

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