Characterization of ferredoxins from the thermophilic, acetogenic bacterium Thermoanaerobacter kivui

Author:

Katsyv Alexander1ORCID,Essig Melanie1,Bedendi Giada2,Sahin Selmihan2,Milton Ross D.2,Müller Volker1ORCID

Affiliation:

1. Department of Molecular Microbiology & Bioenergetics, Institute of Molecular Biosciences Johann Wolfgang Goethe University Frankfurt am Main Germany

2. Department of Inorganic and Analytical Chemistry University of Geneva Geneva Switzerland

Abstract

A major electron carrier involved in energy and carbon metabolism in the acetogenic model organism Thermoanaerobacter kivui is ferredoxin, an iron–sulfur‐containing, electron‐transferring protein. Here, we show that the genome of T. kivui encodes four putative ferredoxin‐like proteins (TKV_c09620, TKV_c16450, TKV_c10420 and TKV_c19530). All four genes were cloned, a His‐tag encoding sequence was added and the proteins were produced from a plasmid in T. kivui. The purified proteins had an absorption peak at 430 nm typical for ferredoxins. The determined iron–sulfur content is consistent with the presence of two predicted [4Fe4S] clusters in TKV_c09620 and TKV_c19530 or one predicted [4Fe4S] cluster in TKV_c16450 and TKV_c10420 respectively. The reduction potential (Em) for TKV_c09620, TKV_c16450, TKV_c10420 and TKV_c19530 was determined to be −386 ± 4 mV, −386 ± 2 mV, −559 ± 10 mV and −557 ± 3 mV, respectively. TKV_c09620 and TKV_c16450 served as electron carriers for different oxidoreductases from T. kivui. Deletion of the ferredoxin genes led to only a slight reduction of growth on pyruvate or autotrophically on H2 + CO2. Transcriptional analysis revealed that TKV_c09620 was upregulated in a ΔTKV_c16450 mutant and vice versa TKV_c16450 in a ΔTKV_c09620 mutant, indicating that TKV_c09620 and TKV_c16450 can replace each other. In sum, our data are consistent with the hypothesis that TKV_c09620 and TKV_c16450 are ferredoxins involved in autotrophic and heterotrophic metabolism of T. kivui.

Funder

Bundesministerium für Bildung und Forschung

Deutsche Forschungsgemeinschaft

H2020 Marie Skłodowska-Curie Actions

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

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