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利用假脱硫弧菌(一种硫酸盐还原菌)实现硫化铈的可持续合成。

Harnessing Pseudodesulfovibrio sp., a sulfate-reducing bacterium for the sustainable synthesis of cerium sulfide.

作者信息

Shete Sonal, Kapse Neelam, Dhakephalkar Prashant K

机构信息

Bioenergy Group, MACS-Agharkar Research Institute, Gopal Ganesh Agarkar Road, Pune, 411004, Maharashtra, India.

Department of Microbiology, Savitribai Phule Pune University, Ganeshkhind Rd., Aundh, Pune, 411007, Maharashtra, India.

出版信息

World J Microbiol Biotechnol. 2025 Jul 5;41(7):251. doi: 10.1007/s11274-025-04462-z.

Abstract

The present study investigates a novel sulfate-reducing bacterium, Pseudodesulfovibrio sp. MCM B-508, isolated from produced water, for its ability to produce cerium sulfide, an industrially valuable rare earth colorant. The study demonstrates a microbial route for pigment synthesis by cloning and expressing dissimilatory sulfite reductase (dsrAB) genes from this bacterium in Escherichia coli. The enzyme dissimilatory sulfite reductase shared a maximum of 94.09% homology with published dissimilatory sulfite reductase sequences from the GenBank database, highlighting its novelty. Using molecular engineering techniques, including chaperone co-expression with the pGro7 vector, the sulfate conversion efficiency was significantly enhanced to 71.23%, overcoming limitations in sulfate-reducing bacterial processes. The research successfully converted cerium sulfate to the desired gamma-form cerium sulfide (CeS) through a recombinant E. coli strain, achieving a more efficient and eco-friendly production method compared to conventional chemical synthesis approaches. X-ray diffraction analysis confirmed the formation of the targeted pigment, with major peaks at 25.3 and 32.8° 2θ, demonstrating the potential for an industrially viable, sustainable pigment production process.

摘要

本研究调查了一种从采出水中分离出的新型硫酸盐还原菌——假脱硫弧菌属(Pseudodesulfovibrio sp.)MCM B - 508,研究其生产硫化铈的能力,硫化铈是一种具有工业价值的稀土着色剂。该研究通过在大肠杆菌中克隆和表达来自这种细菌的异化亚硫酸盐还原酶(dsrAB)基因,展示了一条色素合成的微生物途径。这种异化亚硫酸盐还原酶与GenBank数据库中已发表的异化亚硫酸盐还原酶序列的同源性最高为94.09%,突出了其新颖性。使用分子工程技术,包括与pGro7载体共表达伴侣蛋白,硫酸盐转化效率显著提高到71.23%,克服了硫酸盐还原细菌过程中的局限性。该研究通过重组大肠杆菌菌株成功地将硫酸铈转化为所需的γ型硫化铈(CeS),与传统化学合成方法相比,实现了一种更高效、更环保的生产方法。X射线衍射分析证实了目标色素的形成,在2θ为25.3和32.8°处有主要峰,证明了具有工业可行性、可持续的色素生产工艺的潜力。

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