Abstract

The lipophilic electron-transport cofactor rhodoquinone (RQ) facilitates anaerobic metabolism in a variety of bacteria and selected eukaryotic organisms in hypoxic environments. We have shown that an intact rquA gene in Rhodospirillum rubrum is required for RQ production and efficient growth of the bacterium under anoxic conditions. While the explicit details of RQ biosynthesis have yet to be fully delineated, ubiquinone (Q) is a required precursor to RQ in R. rubrum, and the RquA gene product is homologous to a class I methyltransferase. In order to identify any additional requirements for RQ biosynthesis or factors influencing RQ production in R. rubrum, we performed transcriptome analysis to identify differentially expressed genes in anoxic, illuminated R. rubrum cultures, compared with those aerobically grown in the dark. To further select target genes, we employed a bioinformatics approach to assess the likelihood that a given differentially expressed gene under anoxic conditions may also have a direct role in RQ production or regulation of its levels in vivo. Having thus compiled a list of candidate genes, nine were chosen for further study by generation of knockout strains. RQ and Q levels were quantified using liquid chromatography-mass spectrometry, and rquA gene expression was measured using the real-time quantitative polymerase chain reaction. In one case, Q and RQ levels were decreased relative to wild type; in another case, the opposite effect was observed. These results comport with the crucial roles of rquA and Q in RQ biosynthesis, and reveal the existence of potential modulators of RQ levels in R. rubrum.

Highlights

  • Bacteria and simple eukaryotic organisms that have adapted to anoxic or hypoxic conditions for all or part of their life-cycle employ a variety of metabolic strategies to cope with such environments [1,2]

  • Of the 806 genes upregulated during anaerobic growth, 51 genes were found to be members of orthologous gene clusters shared with R. ferrireducens, but not with R. sphaeroides (S1 Table)

  • To search for additional genes that may be involved in RQ biosynthesis in R. rubrum, we used a candidate gene approach

Read more

Summary

Introduction

Bacteria and simple eukaryotic organisms that have adapted to anoxic or hypoxic conditions for all or part of their life-cycle employ a variety of metabolic strategies to cope with such environments [1,2]. One such strategy relies upon fumarate (E0 = +30 mV) as an electron acceptor in a reversal of the succinate dehydrogenase (SDH) reaction of the citric acid cycle that comprises a fundamental component of aerobic metabolism. The subunit composition of Complex II is altered in favor of fumarate reduction; in this case, RQ is employed as the low potential electron carrier, and it becomes the predominant mitochondrial quinone component [5]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call