裂解酶过表达大肠杆菌捕获有机汞及其细胞内放射测定法评价*

Y. Morimoto, K. Takamiya
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引用次数: 1

摘要

在大肠杆菌中过表达的有机汞裂解酶(MerB)捕获并分解了有机汞化合物,并通过中子辐射的放射性分析进行了检测。当细菌在24至72小时内生长时,转基因大肠杆菌从培养液中捕获大量汞,回收率约为80%。由于经过修饰的大肠杆菌没有汞代谢的附加基因,细菌可以通过MerB酶将汞紧紧地固定在细胞中,而不会将其释放到培养基中。在后期,72小时后,细菌的回收率较低;它可能受到细菌生长过程中未被分解的汞化合物的影响。添加MerB产生试剂(IPTG)不会改变细菌的回收能力。汞原子的定量值是通过反应堆中子从滤纸上的干燥细胞或溶液中发射的γ射线来估计的,滤纸可用于对含有汞原子的细菌进行无损检测。在这种方法中,从污染溶液中有效回收有毒汞的系统已经存档,而不会破坏样本,即所谓的细胞内分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Organomercury Captured by Lyase Overexpressed Escherichia coli and Its Evaluation by In-Cell Radiometry*
Organomercury lyase (MerB) overexpressed in Escherichia coli captured and decomposed organomercury compounds, and it has been detected by radioactive analysis with neutron irradiation. Genetically modified E. coli captures a lot of mercury from a cultivation solution with about 80% recovery, when the bacteria are growing during 24 to 72 hours. Since the modified E. coli has no additive gene for mercury metabolism, the bacteria could hold mercury tightly by the MerB enzyme in their cell and do not release them into medium. In the later, 72 hours after, bacteria have less recovery ratio; it may be affected by undecompsed mercury compounds in bacteria growth. The recovery ability of the bacteria would not be changed by addition of the MerB producing reagent (IPTG). A quantitative value of mercury atom is estimated by an emission of γ-ray by reactor neutron from a dried cell or solution on a filter paper, which is available for nondestructive testing of bacteria holding mercury atoms. In this method an efficient recovery system of toxic mercury from a polluted solution has been archived without destruction of samples, so called in-cell analysis.
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