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Flv3B 黄素铁氧还蛋白过表达增强固氮蓝藻 Nostoc PCC 7120 的光生物制氢。

Overproduction of the Flv3B flavodiiron, enhances the photobiological hydrogen production by the nitrogen-fixing cyanobacterium Nostoc PCC 7120.

机构信息

Aix Marseille Univ, CNRS, LCB, Laboratoire de Chimie Bactérienne, Marseille, France.

Aix Marseille Univ, CNRS, BIP, Laboratoire de Bioénergétique et Ingénierie des Protéines, Marseille, France.

出版信息

Microb Cell Fact. 2020 Mar 10;19(1):65. doi: 10.1186/s12934-020-01320-5.

Abstract

BACKGROUND

The ability of some photosynthetic microorganisms, particularly cyanobacteria and microalgae, to produce hydrogen (H) is a promising alternative for renewable, clean-energy production. However, the most recent, related studies point out that much improvement is needed for sustainable cyanobacterial-based H production to become economically viable. In this study, we investigated the impact of induced O-consumption on H photoproduction yields in the heterocyte-forming, N-fixing cyanobacterium Nostoc PCC7120.

RESULTS

The flv3B gene, encoding a flavodiiron protein naturally expressed in Nostoc heterocytes, was overexpressed. Under aerobic and phototrophic growth conditions, the recombinant strain displayed a significantly higher H production than the wild type. Nitrogenase activity assays indicated that flv3B overexpression did not enhance the nitrogen fixation rates. Interestingly, the transcription of the hox genes, encoding the NiFe Hox hydrogenase, was significantly elevated, as shown by the quantitative RT-PCR analyses.

CONCLUSION

We conclude that the overproduced Flv3B protein might have enhanced O-consumption, thus creating conditions inducing hox genes and facilitating H production. The present study clearly demonstrates the potential to use metabolic engineered cyanobacteria for photosynthesis driven H production.

摘要

背景

一些光合微生物,特别是蓝细菌和微藻,具有生产氢气(H)的能力,这是可再生清洁能源生产的一种很有前途的替代方案。然而,最近的相关研究指出,为了使可持续的基于蓝细菌的 H 生产具有经济可行性,还需要进行大量改进。在这项研究中,我们研究了诱导的 O 消耗对异形胞形成、固氮蓝细菌 Nostoc PCC7120 中 H 光生产产量的影响。

结果

过表达编码天然存在于 Nostoc 异形胞中的黄素铁蛋白的 flv3B 基因。在需氧和光合生长条件下,重组菌株的 H 产量明显高于野生型。固氮酶活性测定表明,flv3B 的过表达并没有提高固氮速率。有趣的是,如定量 RT-PCR 分析所示,编码 NiFe Hox 氢化酶的 hox 基因的转录显著升高。

结论

我们得出结论,过表达的 Flv3B 蛋白可能增强了 O 消耗,从而创造了诱导 hox 基因和促进 H 生产的条件。本研究清楚地表明,利用代谢工程化的蓝细菌进行光合作用驱动的 H 生产具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a28/7063810/3183df4a9913/12934_2020_1320_Fig1_HTML.jpg

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