生态系统中细菌生物修复的遗传适应性和机理认识。

IF 3.5 4区 生物学 Q2 MICROBIOLOGY
Yamini Vinayagam, Vijayarangan Devi Rajeswari
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引用次数: 0

摘要

金属污染对生态系统和人类健康构成重大威胁,需要有效的修复策略。生物修复利用细菌中独特的抗金属基因,为重金属污染提供了一种经济高效的解决方案。Cad、Chr、Cop 等基因为改善生态系统的解毒功能提供了途径。通过多种技术,基因工程使细菌基因组更有能力提高金属解毒能力;然而,关于新的抗金属基因的本质,仍有一些问题没有得到解答。本文探讨了细菌对有毒金属解毒的复杂过程,包括生物吸附、生物累积、生物沉淀和生物浸出。文章还探讨了参与分解有毒金属的重要基因、蛋白质、信号机制和细菌生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Adaptations and Mechanistic Insights Into Bacterial Bioremediation in Ecosystems

Metal pollution poses significant threats to the ecosystem and human health, demanding effective remediation strategies. Bioremediation, which leverages the unique metal-resistant genes found in bacteria, offers a cost-effective and efficient solution to heavy metal contamination. Genes such as Cad, Chr, Cop, and others provide pathways to improve the detoxification of the ecosystem. Through multiple techniques, genetic engineering makes bacterial genomes more capable of improving metal detoxification; nonetheless, there are still unanswered questions regarding the nature of new metal-resistant genes. This article examines bacteria's complex processes to detoxify toxic metals, including biosorption, bioaccumulation, bio-precipitation, and bioleaching. It also explores essential genes, proteins, signaling mechanisms, and bacterial biomarkers involved in breaking toxic metals.

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来源期刊
Journal of Basic Microbiology
Journal of Basic Microbiology 生物-微生物学
CiteScore
6.10
自引率
0.00%
发文量
134
审稿时长
1.8 months
期刊介绍: The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions. Papers published deal with: microbial interactions (pathogenic, mutualistic, environmental), ecology, physiology, genetics and cell biology/development, new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications) novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).
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