Abstract

To exchange electrons with extracellular substrates, some microorganisms employ extracellular electron transfer (EET) pathways that physically connect extracellular redox reactions to intracellular metabolic activity. These pathways are made of redox and structural proteins that work cooperatively to transfer electrons between extracellular substrates and the cytoplasmic membrane. Crucial to the bacterial and archaeal EET pathways are the quinol oxidases and/or quinone reductases in the cytoplasmic membrane where they recycle the quinone/quinol pool in the cytoplasmic membrane during EET reaction. Up to date, three different families of quinol oxidases and/or quinone reductases involved in bacterial EET have been discovered. They are the CymA, CbcL/MtrH/MtoC, and ImcH families of quinol oxidases and/or quinone reductases that are all multiheme c-type cytochromes (c-Cyts). To investigate to what extent they are distributed among microorganisms, we search the bacterial as well as archaeal genomes for the homologs of these c-Cyts. Search results reveal that the homologs of these c-Cyts are only found in the Domain Bacteria. Moreover, the CymA homologs are only found in the phylum of Proteobacteria and most of them are in the Shewanella genus. In addition to Shewanella sp., CymA homologs are also found in other Fe(III)-reducing bacteria, such as of Vibrio parahaemolyticus. In contrast to CymA, CbcL/MtrH/MtoC, and ImcH homologs are much more widespread. CbcL/MtrH/MtoC homologs are found in 15 phyla, while ImcH homologs are found in 12 phyla. Furthermore, the heme-binding motifs of CbcL/MtrH/MtoC and ImcH homologs vary greatly, ranging from 3 to 23 and 6 to 10 heme-binding motifs for CbcL/MtrH/MtoC and ImcH homologs, respectively. Moreover, CymA and CbcL/MtrH/MtoC homologs are found in both Fe(III)-reducing and Fe(II)-oxidizing bacteria, suggesting that these families of c-Cyts catalyze both quinol-oxidizing and quinone-reducing reactions. ImcH homologs are only found in the Fe(III)-reducing bacteria, implying that they are only the quinol oxidases. Finally, some bacteria have the homologs of two different families of c-Cyts, which may improve the bacterial capability to exchange electrons with extracellular substrates.

Highlights

  • Many microorganisms can exchange electrons between the redox proteins in the cytoplasmic or inner membrane and extracellular substrates, such as metal ions associated with minerals, humic substances and electrodes, and microbial cells of the same or difference species

  • Sixty-three percent of identified CymA homologs were found in the genus of Shewanella and the rest were found in 11 bacterial genera and 2 bacteria that were not classified at the genus level, which were all in the phylum of Proteobacteria (Table 1 and Supplementary Table S1)

  • Compared to the CymA homologs that are found only one phylum, CbcL/MtoC/MtrH homologs were much more widespread and were identified in 15 bacterial phyla that included 33 genera and the bacteria whose classification could not be assigned to the genus level

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Summary

Introduction

Many microorganisms can exchange electrons between the redox proteins in the cytoplasmic or inner membrane and extracellular substrates, such as metal ions associated with minerals, humic substances and electrodes, and microbial cells of the same or difference species. Given that they are found in both metal-reducing and metal-oxidizing bacteria, CbcL/MtoC/MtrH homologs are most likely involved in both quinol oxidation as well as quinone reduction. Different from that from the homologs of CymA and CbcL/MtoC/MtrH, distribution of ImcH homologs in different bacteria has been searched.

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