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黑曲霉线粒体细胞色素 c 在氯化钙胁迫下还原孔雀石绿的可能作用。

A possible role of Aspergillus niger mitochondrial cytochrome c in malachite green reduction under calcium chloride stress.

机构信息

Microbiology Department, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, 3 Ahmad El Zomor St., Nasr City, Cairo, 11371, Egypt,

出版信息

Cell Biochem Biophys. 2013;67(3):1291-9. doi: 10.1007/s12013-013-9661-1.

Abstract

In previous work, decolorization of malachite green (MG) was studied in Aspergillus niger in the presence and absence of calcium chloride stress. Decolorization took place within 24 h, and a signal transduction process that initiated MG decolorization was suggested to be involved. In the present study, further investigation of the relationship between calcium chloride stress and enhanced MG biodegradation was conducted at the sub-cellular level. MG-NADH reductase activity, a key enzyme in MG decolorization, was produced as decolorization commenced, and enzyme activity increased threefold upon exposure to calcium chloride. Inhibitors of cytochrome p450, Ca(2+) channel activity as well as activity of the signaling protein phosphoinositide 3-kinase were tested. All three activities were inhibited to different extents resulting in reduced MG decolorization. Spectral analysis of the mitochondrial fraction showed a heme signal at 405 nm and A405/A280 ratio that is characteristic of the porphoryin ring of cytochromes. There were no peaks detected for cytochromes a or b, but a shoulder appearing at 550 nm was observed, which suggested that cytochrome c is involved; the absorbance for cytochrome c doubled after calcium chloride stress supporting this idea. MG decolorization took place via a series of demethylation steps, and cytotoxicity analysis revealed a decrease in the toxicity associated with generation of leucomalachite green.

摘要

在之前的工作中,我们研究了黑曲霉在氯化钙胁迫存在和不存在的情况下对孔雀石绿(MG)的脱色作用。24 小时内完成了脱色,并且提出了一种涉及启动 MG 脱色的信号转导过程。在本研究中,我们在亚细胞水平上进一步研究了氯化钙胁迫与增强 MG 生物降解之间的关系。MG-NADH 还原酶活性是 MG 脱色的关键酶,在脱色开始时产生,并且在暴露于氯化钙时酶活性增加了三倍。测试了细胞色素 p450 的抑制剂、Ca(2+)通道活性以及信号蛋白磷酸肌醇 3-激酶的活性。所有三种活性都受到不同程度的抑制,导致 MG 脱色减少。线粒体部分的光谱分析显示出在 405nm 处的血红素信号和 A405/A280 比值,这是细胞色素的卟啉环的特征。没有检测到细胞色素 a 或 b 的峰,但观察到 550nm 处出现一个肩峰,表明细胞色素 c 参与其中;氯化钙胁迫后细胞色素 c 的吸光度增加了一倍,支持了这一观点。MG 脱色通过一系列去甲基化步骤进行,细胞毒性分析显示与生成无色孔雀石绿相关的毒性降低。

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