Abstract

Sterols are essential components of eukaryotic cells whose biosynthesis and function has been studied extensively. Sterols are also recognized as the diagenetic precursors of steranes preserved in sedimentary rocks where they can function as geological proxies for eukaryotic organisms and/or aerobic metabolisms and environments. However, production of these lipids is not restricted to the eukaryotic domain as a few bacterial species also synthesize sterols. Phylogenomic studies have identified genes encoding homologs of sterol biosynthesis proteins in the genomes of several additional species, indicating that sterol production may be more widespread in the bacterial domain than previously thought. Although the occurrence of sterol synthesis genes in a genome indicates the potential for sterol production, it provides neither conclusive evidence of sterol synthesis nor information about the composition and abundance of basic and modified sterols that are actually being produced. Here, we coupled bioinformatics with lipid analyses to investigate the scope of bacterial sterol production. We identified oxidosqualene cyclase (Osc), which catalyzes the initial cyclization of oxidosqualene to the basic sterol structure, in 34 bacterial genomes from five phyla (Bacteroidetes, Cyanobacteria, Planctomycetes, Proteobacteria, and Verrucomicrobia) and in 176 metagenomes. Our data indicate that bacterial sterol synthesis likely occurs in diverse organisms and environments and also provides evidence that there are as yet uncultured groups of bacterial sterol producers. Phylogenetic analysis of bacterial and eukaryotic Osc sequences confirmed a complex evolutionary history of sterol synthesis in this domain. Finally, we characterized the lipids produced by Osc-containing bacteria and found that we could generally predict the ability to synthesize sterols. However, predicting the final modified sterol based on our current knowledge of sterol synthesis was difficult. Some bacteria produced demethylated and saturated sterol products even though they lacked homologs of the eukaryotic proteins required for these modifications emphasizing that several aspects of bacterial sterol synthesis are still completely unknown.

Highlights

  • Sterols are tetracyclic triterpenoid lipids that are required by all eukaryotes for critical cellular functions including maintaining membrane fluidity, phagocytosis, stress tolerance, and cell signaling (Bloch, 1991; Swan and Watson, 1998; Castoreno et al, 2005; Xu et al, 2005; Riobo, 2012)

  • Sterol biosynthesis is primarily viewed as a eukaryotic feature that is rarely observed in the bacterial domain

  • Our phylogenetic analysis of one of the key proteins involved in sterol biosynthesis, the oxidosqualene cyclase (Osc), demonstrates that the evolutionary history of this pathway in the bacterial domain is complex

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Summary

Introduction

Sterols are tetracyclic triterpenoid lipids that are required by all eukaryotes for critical cellular functions including maintaining membrane fluidity, phagocytosis, stress tolerance, and cell signaling (Bloch, 1991; Swan and Watson, 1998; Castoreno et al, 2005; Xu et al, 2005; Riobo, 2012). Sterane signatures in the rock record date as far back as 1.6 billion years (Brocks et al, 2005) and, based on their distribution in modern eukaryotes, are utilized as biomarkers for the existence of specific eukaryotic organisms at the time of deposition (Peters et al, 2007a,b). Because eukaryotes are the predominant extant producers of sterols and because they require sterols for growth, the use of steranes as biomarkers for eukaryotes seems robust. Sterol production has been observed in a few bacterial species raising the question as to whether bacterial sterol production is significant for the interpretation of sterane signatures (Volkman, 2003, 2005)

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