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串联寡聚表达金属硫蛋白增强大肠杆菌对重金属的耐受性和生物积累。

Tandem oligomeric expression of metallothionein enhance heavy metal tolerance and bioaccumulation in Escherichia coli.

机构信息

School of Life Science, Shanxi University, Taiyuan, 030006, PR China.

School of Life Science, Shanxi University, Taiyuan, 030006, PR China.

出版信息

Ecotoxicol Environ Saf. 2019 Oct 15;181:301-307. doi: 10.1016/j.ecoenv.2019.06.022. Epub 2019 Jun 13.

Abstract

Metallothioneins (MTs) are a family of low molecular weight, cysteine-rich, metal-binding proteins, which play important roles in metal homeostasis and heavy metal detoxification. In our previous study, a novel full length MT cDNA was successfully cloned from the freshwater crab (Sinopotamon henanense). In the present study, tandem repeats of two and three copies of the crab MT gene were integrated by overlap extension PCR (SOE-PCR) and expressed in Escherichia coli. The SUMO fusion expression system was adopted to increase the stability and solubility of the recombinant MT proteins. The recombinant proteins were purified and their metal-binding abilities were further analyzed by the ultraviolet absorption spectral scan. Furthermore, the metal tolerance and bioaccumulation of E. coli cells expressing oligomeric MTs were determined. Results showed that the recombinant plasmids pET28a-SUMO-2MT and pET28a-SUMO-3MT were successfully constructed. SDS-PAGE analysis showed that the SUMO-2MT and SUMO-3MT were expressed mainly in the soluble forms. Oligomeric MTs expression significantly enhanced Cu, Cd or Zn tolerance and accumulation in E. coli in the order: SUMO-3MT˃SUMO-2MT˃SUMO-MT˃control. Cells harboring pET28a-SUMO -3MT exhibited the highest Cu, Cd or Zn bioaccumulation at 5.8-fold, 3.1-fold or 6.7-fold higher than that of the control cells. Our research could lay a foundation for large-scale preparation of MTs and provide a scientific basis for bioremediation of heavy metal pollution by oligomeric MTs.

摘要

金属硫蛋白(MTs)是一类富含半胱氨酸、分子量较小、能与金属结合的蛋白质,在金属离子稳态和重金属解毒中发挥重要作用。在我们之前的研究中,成功地从淡水蟹(Sinopotamon henanense)中克隆出一种新型全长 MT cDNA。在本研究中,通过重叠延伸 PCR(SOE-PCR)将蟹 MT 基因的两个和三个拷贝串联重复序列整合,并在大肠杆菌中表达。采用 SUMO 融合表达系统提高重组 MT 蛋白的稳定性和可溶性。纯化重组蛋白,并通过紫外吸收光谱扫描进一步分析其金属结合能力。此外,还测定了表达寡聚 MT 的大肠杆菌细胞的金属耐受性和生物积累能力。结果表明,成功构建了重组质粒 pET28a-SUMO-2MT 和 pET28a-SUMO-3MT。SDS-PAGE 分析表明,SUMO-2MT 和 SUMO-3MT 主要以可溶性形式表达。寡聚 MT 的表达显著增强了大肠杆菌对 Cu、Cd 或 Zn 的耐受性和积累能力,顺序为:SUMO-3MT>SUMO-2MT>SUMO-MT>对照。携带 pET28a-SUMO-3MT 的细胞在 Cu、Cd 或 Zn 的生物积累量上分别比对照细胞高 5.8 倍、3.1 倍和 6.7 倍。我们的研究为 MTs 的大规模制备奠定了基础,并为寡聚 MTs 生物修复重金属污染提供了科学依据。

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