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基于逆向代谢工程对VK-2-3辅酶Q10改善机制的分析

Analysis of the improved mechanism of VK-2-3 coenzyme Q10 by reverse metabolic engineering.

作者信息

Zhang Long, Wang Le-Yi, Han Yi-Jun, Liu Yan-Xin, Li Yong-Li, Hu Jian-Hua, Tian Zhi-Jie, Liu Zhan-Ying

机构信息

Inner Mongolia Energy Conservation and Emission Reduction Engineering Technology Research Center for Fermentation Industry, Hohhot, China.

Engineering Research Center of Inner Mongolia for Green Manufacturing in Biofermentation Industry, Hohhot, China.

出版信息

Front Microbiol. 2024 Jul 4;15:1410505. doi: 10.3389/fmicb.2024.1410505. eCollection 2024.

Abstract

Coenzyme Q10 (CoQ10) is an essential medicinal ingredient. In this study, we obtained a high-yielding mutant strain of CoQ10, VK-2-3, by subjecting V-0 (V-0) to a C heavy ion beam and high-voltage prick electric field treatment. To investigate the mutation mechanism, the complete genomes of VK-2-3 and V-0 were sequenced. Collinearity analysis revealed that the nicotinamide adenine dinucleotide-dependent dehydrogenase (NAD) gene underwent rearrangement in the VK-2-3 genome. The NAD gene was overexpressed and silenced in V-0, and this construct was named RS.NAD and RS.ΔNAD. The results showed that the titers of CoQ10 in the RS.NAD and RS.ΔNAD increased and decreased by 16.00 and 33.92%, respectively, compared to those in V-0, and these differences were significant. Our results revealed the mechanism by which the VK-2-3 CoQ10 yield increases through reverse metabolic engineering, providing insights for genetic breeding and mechanistic analysis.

摘要

辅酶Q10(CoQ10)是一种重要的药用成分。在本研究中,我们通过对V-0进行碳重离子束和高压针刺电场处理,获得了一株辅酶Q10高产突变株VK-2-3。为了研究突变机制,我们对VK-2-3和V-0的全基因组进行了测序。共线性分析表明,烟酰胺腺嘌呤二核苷酸依赖性脱氢酶(NAD)基因在VK-2-3基因组中发生了重排。NAD基因在V-0中过表达和沉默,该构建体分别命名为RS.NAD和RS.ΔNAD。结果表明,与V-0相比,RS.NAD和RS.ΔNAD中辅酶Q10的产量分别增加和减少了16.00%和33.92%,且这些差异具有显著性。我们的研究结果揭示了VK-2-3辅酶Q10产量通过逆向代谢工程提高的机制,为遗传育种和机制分析提供了思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6255/11254814/9b0c312fe97a/fmicb-15-1410505-g001.jpg

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