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首页> 外文期刊>Scientific reports. >Biosynthesis of organic photosensitizer Zn-porphyrin by diphtheria toxin repressor (DtxR)-mediated global upregulation of engineered heme biosynthesis pathway in Corynebacterium glutamicum
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Biosynthesis of organic photosensitizer Zn-porphyrin by diphtheria toxin repressor (DtxR)-mediated global upregulation of engineered heme biosynthesis pathway in Corynebacterium glutamicum

机译:白喉毒素阻遏物(DtxR)介导的谷氨酸棒状杆菌血红素生物合成途径的整体上调生物合成有机光敏剂锌卟啉

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Zn-porphyrin is a promising organic photosensitizer in various fields including solar cells, interface and biomedical research, but the biosynthesis study has been limited, probably due to the difficulty of understanding complex biosynthesis pathways. In this study, we developed a Corynebacterium glutamicum platform strain for the biosynthesis of Zn-coproporphyrin III (Zn-CP III), in which the heme biosynthesis pathway was efficiently upregulated. The pathway was activated and reinforced by strong promoter-induced expression of hemAM (encoding mutated glutamyl-tRNA reductase) and hemL (encoding glutamate-1-semialdehyde aminotransferase) genes. This engineered strain produced 33.54?±?3.44?mg/l of Zn-CP III, while the control strain produced none. For efficient global regulation of the complex pathway, the dtxR gene encoding the transcriptional regulator diphtheria toxin repressor (DtxR) was first overexpressed in C. glutamicum with hemAM and hemL genes, and its combinatorial expression was improved by using effective genetic tools. This engineered strain biosynthesized 68.31?±?2.15?mg/l of Zn-CP III. Finally, fed-batch fermentation allowed for the production of 132.09?mg/l of Zn-CP III. This titer represents the highest in bacterial production of Zn-CP III reported to date, to our knowledge. This study demonstrates that engineered C. glutamicum can be a robust biotechnological model for the production of photosensitizer Zn-porphyrin.
机译:锌卟啉是在太阳能电池,界面和生物医学研究等各个领域中很有前途的有机光敏剂,但是生物合成研究受到限制,这可能是由于难以理解复杂的生物合成途径所致。在这项研究中,我们开发了谷氨酸棒杆菌平台菌株用于锌-卟啉III(Zn-CP III)的生物合成,其中血红素的生物合成途径被有效地上调。 hemAM(编码突变的谷氨酰胺-tRNA还原酶)和hemL(编码谷氨酸-1-半醛氨基转移酶)基因的强烈启动子诱导表达激活并加强了该途径。该工程菌株产生33.54±±3.44μmg/ l的Zn-CP III,而对照菌株则不产生。为了有效地进行复杂途径的整体调控,首先使用hemAM和hemL基因在谷氨酸棒杆菌中过表达编码转录调节白喉毒素阻遏物(DtxR)的dtxR基因,并使用有效的遗传工具改善其组合表达。该工程菌株生物合成了68.31?±?2.15?mg / l的Zn-CP III。最后,分批补料发酵可以生产132.09?mg / l的Zn-CP III。据我们所知,该滴度代表了迄今为止所报告的Zn-CP III细菌生产中的最高水平。这项研究表明,工程谷氨酸棒杆菌可以成为生产光敏剂锌卟啉的强大生物技术模型。

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