Gomaa Ola M, Selim Nabila S, Wee Josephine, Linz John E
Microbiology Department, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Cairo, Egypt.
Radiation Physics Department, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Cairo, Egypt.
Fungal Genet Biol. 2017 Aug;105:1-7. doi: 10.1016/j.fgb.2017.05.003. Epub 2017 May 24.
Aspergillus niger was previously demonstrated to decolorize the commercial dye malachite green (MG) and this process was enhanced under calcium chloride (CaCl) treatment. Previous data also suggested that the decolorization process is related to mitochondrial cytochrome c. In the current work, we analyzed in depth the specific relationship between CaCl treatment and MG decolorization. Gene expression analysis (RNA Seq) using Next Generation Sequencing (NGS) revealed up-regulation of 28 genes that are directly or indirectly associated with stress response functions as early as 30min of CaCl treatment; these data further strengthen our previous findings that CaCl treatment induces a stress response in A. niger which enhances the ability to decolorize MG. A significant increase in fluorescence observed by MitoTracker dye suggests that CaCl treatment also increased mitochondrial membrane potential. Isolated mitochondrial membrane protein fractions obtained from A. niger grown under standard growth conditions decolorized MG in the presence of NADH and decolorization was enhanced in samples isolated from CaCl-treated A. niger cultures. Treatment of whole mitochondrial fraction with KCN which inhibits electron transport by cytochrome c oxidase and Triton-X 100 which disrupts mitochondrial membrane integrity suggests that cyanide sensitive cytochrome c oxidase activity is a key biochemical step in MG decolorization. This suggestion was confirmed by the addition of palladium α-lipoic acid complex (PLAC) which resulted in an initial increase in decolorization. Although the role of cytochrome c and cytochrome c oxidase was confirmed at the biochemical level, changes in levels of transcripts encoding these enzymes after CaCl treatment were not found to be statistically significant in RNA Seq analysis. These data suggest that the regulation of cytochrome c enzymes occur predominantly at the post-transcriptional level under CaCl stress. Thus, using global transcriptomics and biochemical approaches, our study provides a molecular association between fungal mitochondrial electron transfer systems and MG decolorization.
先前已证明黑曲霉能够使商业染料孔雀石绿(MG)脱色,并且在氯化钙(CaCl)处理下该过程得到增强。先前的数据还表明,脱色过程与线粒体细胞色素c有关。在当前的工作中,我们深入分析了CaCl处理与MG脱色之间的具体关系。使用下一代测序(NGS)进行的基因表达分析(RNA测序)显示,早在CaCl处理30分钟后,就有28个与应激反应功能直接或间接相关的基因上调;这些数据进一步强化了我们之前的发现,即CaCl处理会在黑曲霉中诱导应激反应,从而增强其使MG脱色的能力。用MitoTracker染料观察到的荧光显著增加表明,CaCl处理也增加了线粒体膜电位。从在标准生长条件下生长的黑曲霉中获得的分离线粒体膜蛋白组分在有NADH存在的情况下使MG脱色,并且从CaCl处理的黑曲霉培养物中分离的样品中脱色增强。用抑制细胞色素c氧化酶电子传递的KCN和破坏线粒体膜完整性的Triton-X 100处理整个线粒体组分表明,氰化物敏感的细胞色素c氧化酶活性是MG脱色的关键生化步骤。添加钯α-硫辛酸复合物(PLAC)导致脱色最初增加,这证实了这一推测。尽管在生化水平上证实了细胞色素c和细胞色素c氧化酶的作用,但在RNA测序分析中未发现CaCl处理后编码这些酶的转录本水平变化具有统计学意义。这些数据表明,在CaCl胁迫下,细胞色素c酶的调节主要发生在转录后水平。因此,通过全局转录组学和生化方法,我们的研究提供了真菌线粒体电子传递系统与MG脱色之间的分子关联。