H2 production under stress: [FeFe]-hydrogenases reveal strong stability in high pressure environments

被引:0
|
作者
Edenharter, Kristina [1 ]
Jaworek, Michel W. [2 ]
Engelbrecht, Vera [1 ]
Winter, Roland [2 ]
Happe, Thomas [1 ]
机构
[1] Ruhr Univ Bochum, Fac Biol & Biotechnol, Photobiotechnol, D-44801 Bochum, Germany
[2] TU Dortmund Univ, Dept Chem & Chem Biol, Phys Chem Biophys Chem 1, Otto Hahn Str 4a, D-44227 Dortmund, Germany
关键词
Enzymatic reactions; High pressure; Hydrogenases; ACTIVE-SITE; INFRARED-SPECTROSCOPY; HYDROGENASE; ACTIVATION; PROTEINS;
D O I
10.1016/j.bpc.2024.107217
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydrogenases are a diverse group of metalloenzymes that catalyze the conversion of H2 into protons and electrons and the reverse reaction. A subgroup is formed by the [FeFe]-hydrogenases, which are the most efficient enzymes of microbes for catalytic H2 conversion. We have determined the stability and activity of two [FeFe]-hydrogenases under high temperature and pressure conditions employing FTIR spectroscopy and the high-pressure stopped-flow methodology in combination with fast UV/Vis detection. Our data show high temperature stability and an increase in activity up to the unfolding temperatures of the enzymes. Remarkably, both enzymes reveal a very high pressure stability of their structure, even up to pressures of several kbars. Their high pressure-stability enables high enzymatic activity up to 2 kbar, which largely exceeds the pressure limit encountered by organisms in the deep sea and sub-seafloor on Earth.
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页数:6
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