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在恶臭假单胞菌 TS44 中,谷胱甘肽还原酶 GorA 对于硒(0)-纳米粒子的生物合成以及谷胱甘肽对于 CdSe 量子点形成的重要性。

The essentialness of glutathione reductase GorA for biosynthesis of Se(0)-nanoparticles and GSH for CdSe quantum dot formation in Pseudomonas stutzeri TS44.

机构信息

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan 430070, PR China.

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan 430070, PR China.

出版信息

J Hazard Mater. 2019 Mar 15;366:301-310. doi: 10.1016/j.jhazmat.2018.11.092. Epub 2018 Nov 23.

Abstract

Pseudomonas stutzeri TS44 was able to aerobically reduce Se(IV) into SeNPs and transform Se(IV)/Cd(II) mixture into CdSe-QDs. The SeNPs and CdSe-QDs were systematically characterized by surface feature analyses, and the molecular mechanisms of SeNPs and CdSe-QD formation in P. stutzeri TS44 were characterized in detail. In vivo, under 2.5 mmol/L Se(IV) exposure, GorA was essential for catalyzing of Se(IV) reduction rate decreased by 67% when the glutathione reductase gene gorA was disrupted, but it was not decreased in the glutathione synthesis rate-limiting gene gshA mutated strain compared to the wild type. The complemented strains restored the phenotypes. While under low amount of Se(IV) (0.5 mmol/L), GSH played an important role for Se(IV) reduction. In vitro, GorA catalyzed Se(IV) reduction with NADPH as the electron donor (Vmax of 3.947 ± 0.1061 μmol/min/mg protein under pH 7.0 and 28℃). In addition, CdSe-QDs were successfully synthesized by a one-step method in which Se(IV) and Cd(II) were added to bacterial culture simultaneously. GSH rather than GorA is necessary for CdSe-QD formation in vivo and in vitro. In conclusion, the results provide new findings showing that GorA functions as a selenite reductase under high amount Se(IV) and GSH is essential for bacterial CdSe-QD synthesis.

摘要

恶臭假单胞菌 TS44 能够在需氧条件下将 Se(IV)还原为硒纳米颗粒,并将 Se(IV)/Cd(II)混合物转化为 CdSe-QDs。通过表面特征分析对 SeNPs 和 CdSe-QDs 进行了系统表征,并详细研究了恶臭假单胞菌 TS44 中硒纳米颗粒和 CdSe-QD 形成的分子机制。在体内,当暴露于 2.5mmol/L Se(IV)时,GorA 对于催化 Se(IV)还原是必需的,当谷胱甘肽还原酶基因 gorA 被破坏时,Se(IV)还原速率降低了 67%,而谷胱甘肽合成限速基因 gshA 突变株的还原速率并没有降低,与野生型相比。互补菌株恢复了表型。而在低浓度 Se(IV)(0.5mmol/L)下,GSH 对于 Se(IV)还原起着重要作用。在体外,GorA 以 NADPH 作为电子供体催化 Se(IV)还原(在 pH 7.0 和 28℃下,Vmax 为 3.947±0.1061μmol/min/mg 蛋白)。此外,通过一步法成功合成了 CdSe-QDs,同时向细菌培养物中添加 Se(IV)和 Cd(II)。GSH 而不是 GorA 是体内和体外 CdSe-QD 形成所必需的。总之,这些结果提供了新的发现,表明 GorA 在高浓度 Se(IV)下作为亚硒酸盐还原酶发挥作用,而 GSH 是细菌合成 CdSe-QD 的必要条件。

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