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改变轨道:筛选电子转移蛋白以支持氢气生产。

Changing the tracks: screening for electron transfer proteins to support hydrogen production.

机构信息

Faculty of Biology and Biotechnology, Photobiotechnology, Ruhr-University Bochum, Universitätsstraße 150, 44801, Bochum, Germany.

出版信息

J Biol Inorg Chem. 2022 Oct;27(7):631-640. doi: 10.1007/s00775-022-01956-1. Epub 2022 Aug 29.

Abstract

Ferredoxins are essential electron transferring proteins in organisms. Twelve plant-type ferredoxins in the green alga Chlamydomonas reinhardtii determine the fate of electrons, generated in multiple metabolic processes. The two hydrogenases HydA1 and HydA2 of. C. reinhardtii compete for electrons from the photosynthetic ferredoxin PetF, which is the first stromal mediator of the high-energy electrons derived from the absorption of light energy at the photosystems. While being involved in many chloroplast-located metabolic pathways, PetF shows the highest affinity for ferredoxin-NADP oxidoreductase (FNR), not for the hydrogenases. Aiming to identify other potential electron donors for the hydrogenases, we screened as yet uncharacterized ferredoxins Fdx7, 8, 10 and 11 for their capability to reduce the hydrogenases. Comparing the performance of the Fdx in presence and absence of competitor FNR, we show that Fdx7 has a higher affinity for HydA1 than for FNR. Additionally, we show that synthetic FeS-cluster-binding maquettes, which can be reduced by NADPH alone, can also be used to reduce the hydrogenases. Our findings pave the way for the creation of tailored electron donors to redirect electrons to enzymes of interest.

摘要

铁氧还蛋白是生物中重要的电子传递蛋白。绿藻莱茵衣藻中的 12 种植物型铁氧还蛋白决定了在多个代谢过程中产生的电子的命运。莱茵衣藻的两种氢化酶 HydA1 和 HydA2 竞争来自光合铁氧还蛋白 PetF 的电子,PetF 是来自光合作用系统吸收光能的高能电子的第一个基质中介体。虽然参与了许多叶绿体定位的代谢途径,但 PetF 对铁氧还蛋白-NADP 氧化还原酶 (FNR) 的亲和力最高,而不是对氢化酶。为了确定氢化酶的其他潜在电子供体,我们筛选了尚未表征的铁氧还蛋白 Fdx7、8、10 和 11,以确定它们还原氢化酶的能力。比较 Fdx 在有和没有竞争 FNR 的情况下的性能,我们表明 Fdx7 对 HydA1 的亲和力高于对 FNR 的亲和力。此外,我们还表明,仅由 NADPH 还原的合成 FeS 簇结合模型也可用于还原氢化酶。我们的发现为创建定制的电子供体以将电子重定向到感兴趣的酶铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c54e/9569306/8012344a4416/775_2022_1956_Fig1_HTML.jpg

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