Biology subjects

Johnston, D. T.

Publications and source records attributed to Johnston, D. T..

3 recordsLinked to original sources

bioRxiv2021

Expanded Genomic Sampling of the DesulfobulbalesReveals Distribution and Evolution of Sulfur Metabolisms

The reconstruction of modern and paleo-sulfur cycling relies on understanding the long-term relative contribution of its main actors; these include microbial sulfate reduction (MSR) and microbial sulfur disproportionation (MSD). However, a unifying theory is lacking for how MSR and MSD, with the same enzyme machinery and intimately linked evolutionary histories, perform two drastically different metabolisms. Here, we aim at shedding some light on the distribution, diversity, and evolutionary histories of MSR and MSD, with a focus on the Desulfobulbales as a test case. The Desulfobulbales is a diverse and widespread order of bacteria in the Desulfobacterota (formerly Deltaproteobacteria) phylum primarily composed of sulfate reducing bacteria. Recent culture- and sequence-based approaches have revealed an expanded diversity of organisms and metabolisms within this clade, including the presence of obligate and facultative sulfur disproportionators. Here, we present draft genomes of previously unsequenced species of Desulfobulbales, substantially expanding the available genomic diversity of this clade. We leverage this expanded genomic sampling to perform phylogenetic analyses, revealing an evolutionary history defined by vertical inheritance of sulfur metabolism genes with numerous convergent instances of transition from sulfate reduction to sulfur disproportionation.

microbiology↗

bioRxiv2021

Inter-domain Horizontal Gene Transfer of Nickel-binding Superoxide Dismutase

The ability of aerobic microorganisms to regulate internal and external concentrations of the reactive oxygen species (ROS) superoxide directly influences the health and viability of cells. Superoxide dismutases (SODs) are the primary regulatory enzymes that are used by microorganisms to degrade superoxide. SOD is not one, but three separate, non-homologous enzymes that perform the same function. Thus, the evolutionary history of genes encoding for different SOD enzymes is one of convergent evolution, which reflects environmental selection brought about by an oxygenated atmosphere, changes in metal availability, and opportunistic horizontal gene transfer (HGT). In this study we examine the phylogenetic history of the protein sequence encoding for the nickel-binding metalloform of the SOD enzyme (SodN). A comparison of organismal and SodN protein phylogenetic trees reveals several instances of HGT, including multiple inter-domain transfers of the sodN gene from the bacterial domain to the archaeal domain. Nearly half of the archaeal members with sodN live in the photic zone of the marine water column. The sodN gene is widespread and characterized by apparent vertical gene transfer in some sediment-associated lineages within the Actinobacteriota (Actinobacteria) and Chloroflexota (Chloroflexi) phyla, suggesting the ancestral sodN likely originated in one of these clades before expanding its taxonomic and biogeographic distribution to additional microbial groups in the surface ocean in response to decreasing iron availability. In addition to decreasing iron quotas, nickel-binding SOD has the added benefit of withstanding high reactant and product ROS concentrations without damaging the enzyme, making it particularly well suited for the modern surface ocean.

evolutionary biology↗

bioRxiv2020

Mud, microbes, and macrofauna: seasonal dynamics of the iron biogeochemical cycle in an intertidal mudflat

Microorganisms and burrowing animals exert a pronounced impact on the cycling of redox sensitive metals in coastal sediments. Sedimentary metal cycling is likely controlled by seasonal processes including changes in temperature, animal feeding behavior due to food availability, and availability of organic matter in sediments. We hypothesized that the iron biogeochemical cycle and associated sedimentary microbial community will respond to seasonal changes in a bioturbated intertidal mudflat. In this study, we monitored the spatiotemporal dynamics of porewater and highly reactive solid phase iron with the corresponding prokaryotic and eukaryotic sedimentary microbial communities over one annual cycle from November 2015 to November 2016. Continuous and seasonally variable pools of both porewater Fe(II) and highly reactive iron (FeHR) were observed throughout the season with significant increases of Fe(II) and FeHR in response to increased sediment temperature in summer months. Maximum concentrations of Fe(II) and FeHR were predominantly confined to the upper 5 cm of sediment throughout the season. Iron-oxidizing and -reducing microorganisms were present and stable throughout the season, and exhibited strong depth-dependent stratification likely due to availability of Fe(II) and FeHR pools, respectively. Otherwise, the community was dominated by Deltaproteobacteria, which are involved in sulfur and potentially iron cycling, as well as Gammaproteobacteria and Bacteroidetes. The microbial community was relatively stable throughout the seasonal cycle, but showed strong separation with depth, probably driven by changes in oxygen availability and organic matter. The relative abundance of diatoms revealed a noticeable seasonal signature, which we attribute to spring and fall blooms recorded in the sediments. Macro-, meio, and microfauna were detected throughout the season with some seasonal variations that may influence sedimentary iron transformations by active microbial grazing. The seasonal dynamics of the sedimentary iron cycle are controlled by numerous, interdependent processes, with macrobiota-microbiota relationships and depth stratification comprising primary components. Deciphering these processes in natural ecosystems is essential to understand how they might respond to future environmental perturbations, such as anthropogenic nutrient release to coastal systems.

microbiology↗