海洋热藓糖酵解途径在缺氧和缺氧环境下的适应性

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Raja Lakhal, Manaf AlMatar, Tahani Alkalaf
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引用次数: 0

摘要

背景:热菌门由五个科组成:Fervidobacteriaceae、Thermatogaceae、Kosmotogaceae、Petrotogaceae和Mesoaciditogaceae;一类:热生菌;和四目:海藻目、岩藻目、中酸藻目。方法:共13属。热生物种的物理和代谢特征反映了它们从极端高温中分离出来。Thermotogae成员具有广泛的代谢能力,因此在许多不同部门具有潜在用途的有价值的化学品池。结果:基于核磁共振分析,我们的研究结果表明,海苔在缺氧情况下使用EM途径代谢90%的葡萄糖,ED途径代谢10%的葡萄糖。另一方面,当暴露于延长的氧化应激时,海苔继续同时使用EM和ED糖酵解途径;然而,ED途径的贡献从10%下降到5%左右。结论:与EM途径相比,ED途径具有更强的抑制转录本,这些转录本编码其独特的酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adaptability of Thermotoga Maritima's Glycolysis Pathway in Both Oxic and Anoxic Environments.

Background: The phylum Thermotogae is composed of five families: Fervidobacteriaceae, Thermatogaceae, Kosmotogaceae, Petrotogaceae, and Mesoaciditogaceae; one class: Thermotogae; and four orders: Kosmotogales, Petrotogales, and Mesoaciditogales.

Method: There are thirteen genera in all. The physical and metabolic characteristics of the Thermotogae species reflect the extreme heat from which they were separated. Thermotogae members have a broad spectrum of metabolic capacities, resulting in a pool of valuable chemicals with potential uses in many different sectors.

Result: Based on NMR analysis, our findings demonstrate that T. maritima uses the EM route to metabolize 90% of glucose in anoxia and the ED pathway for 10%. On the other hand, T. maritima continues to employ the EM and ED glycolysis routes concurrently when exposed to extended oxidative stress; however, the ED pathway's contribution drops from 10% to around 5%.

Conclusion: Compared to the EM route, the ED pathway has more strongly repressed transcripts that encode its unique enzymes.

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来源期刊
CiteScore
3.10
自引率
5.60%
发文量
327
审稿时长
7.5 months
期刊介绍: Combinatorial Chemistry & High Throughput Screening (CCHTS) publishes full length original research articles and reviews/mini-reviews dealing with various topics related to chemical biology (High Throughput Screening, Combinatorial Chemistry, Chemoinformatics, Laboratory Automation and Compound management) in advancing drug discovery research. Original research articles and reviews in the following areas are of special interest to the readers of this journal: Target identification and validation Assay design, development, miniaturization and comparison High throughput/high content/in silico screening and associated technologies Label-free detection technologies and applications Stem cell technologies Biomarkers ADMET/PK/PD methodologies and screening Probe discovery and development, hit to lead optimization Combinatorial chemistry (e.g. small molecules, peptide, nucleic acid or phage display libraries) Chemical library design and chemical diversity Chemo/bio-informatics, data mining Compound management Pharmacognosy Natural Products Research (Chemistry, Biology and Pharmacology of Natural Products) Natural Product Analytical Studies Bipharmaceutical studies of Natural products Drug repurposing Data management and statistical analysis Laboratory automation, robotics, microfluidics, signal detection technologies Current & Future Institutional Research Profile Technology transfer, legal and licensing issues Patents.
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