Abstract

Microbial life in exposed terrestrial surface layers in continental Antarctica is faced with extreme environmental conditions, including scarcity of organic matter. Bacteria in these exposed settings can therefore be expected to use alternative energy sources such as solar energy, abundant during the austral summer. Using Illumina MiSeq sequencing, we assessed the diversity and abundance of four conserved protein encoding genes involved in different key steps of light-harvesting pathways dependent on (bacterio)chlorophyll (pufM, bchL/chlL, and bchX genes) and rhodopsins (actinorhodopsin genes), in exposed soils from the Sør Rondane Mountains, East Antarctica. Analysis of pufM genes, encoding a subunit of the type 2 photochemical reaction center found in anoxygenic phototrophic bacteria, revealed a broad diversity, dominated by Roseobacter- and Loktanella-like sequences. The bchL and chlL, involved in (bacterio)chlorophyll synthesis, on the other hand, showed a high relative abundance of either cyanobacterial or green algal trebouxiophyceael chlL reads, depending on the sample, while most bchX sequences belonged mostly to previously unidentified phylotypes. Rhodopsin-containing phototrophic bacteria could not be detected in the samples. Our results, while suggesting that Cyanobacteria and green algae are the main phototrophic groups, show that light-harvesting bacteria are nevertheless very diverse in microbial communities in Antarctic soils.

Highlights

  • Antarctica is nearly completely covered by ice, with only ∼0.32% of its surface ice-free

  • Some species capable of aerobic anoxygenic phototrophy have been found in the Gemmatimonadetes, Acidobacteria, and Chloroflexi

  • For BchL/ChlL and BchX, the sequences grouped in 207 operational ChlL/BchL unit (OLU) and 48 operational BchX unit (OXU), respectively

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Summary

Introduction

Antarctica is nearly completely covered by ice, with only ∼0.32% of its surface ice-free. Later on (at least ∼2.4 Giga annum ago), oxygenic chlorophylldependent phototrophy, using H2O, arose in Cyanobacteria and played a key role in oxygenating the Earth’s atmosphere (Butterfield, 2015; Cardona, 2016) Under these new atmospheric conditions, many of the anaerobic anoxygenic phototrophic bacteria may have disappeared from the oxygenated habitats, some groups adapted and embarked on an aerobic lifestyle (Koblížek, 2015). These aerobic anoxygenic phototrophic bacteria (AAP) were first reported in 1978 (Harashima et al, 1978) and are defined as aerobic species that synthesize bacteriochlorophyll and use light energy as an auxiliary energy source for their mostly heterotrophic metabolism (Feng et al, 2011a; Koblížek, 2015) They do not contain carbon fixation enzymes (Yurkov and Csotonyi, 2009). These two puf genes are frequently used and convenient markers to study the diversity of anoxygenic phototrophic bacteria (Koh et al, 2011; Ritchie and Johnson, 2012; Koblížek, 2015)

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