Chemosynthesis Of Sulfur

Chemosynthesis Of Sulfur-21
Two distinct microbial mat morphotypes cover the floor of the sinkhole: one is white, irregularly shaped, and cohesive and the other is brown, non-cohesive, and sometimes associated with pink ‘fingers’ (Biddanda et al., 2006).

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Mats at both sites also contained Deltaproteobacteria with genes for dissimilatory sulfate reduction (sat, apr, and dsr) and hydrogen oxidation (Ni-Fe hydrogenases).

Overall, the microbial mats at the two sites held low-diversity microbial communities, displayed evidence of coupled sulfur cycling, and did not differ largely in their metabolic potentials, despite the environmental differences. Assessment of the stoichiometry and efficiency of CO2 fixation coupled to reduced sulfur oxidation.

In communities beneath the cyanobacterial mats chemosynthetic primary production is fueled by redox reactions of an active sulfur cycle driven by sulfur-oxidizing and sulfate-reducing bacteria (Nold et al., 2010; Voorhies et al., 2012).

The Isolated Sinkhole sits in the aphotic zone at a water depth of 93 m and covers an area of approximately 55 m × 40 m, as described in detail in Biddanda et al. Groundwater seeps into the sinkhole and is characterized by high chlorine, sulfate, phosphorus, particulate organic matter, and conductivity.

The Isolated Sinkhole community was dominated by novel members of the Beggiatoaceae that are phylogenetically intermediate between known freshwater and marine groups.

Several of these Beggiatoaceae had 16S r RNA genes that contained introns previously observed only in marine taxa. Although this marked the first known example of complex communities based on inorganic energy sources, the concept of chemosynthesis dates back far earlier, to Winogradsky’s studies of large sulfur bacteria (LSB) (Ackert, 2006). Chemosynthetic microbial communities have now been well studied in many marine and terrestrial environments. LSB thrive in marine seeps (Larkin et al., 1994; Joye et al., 2004; Jones et al., 2015), mud volcanoes (Girnth et al., 2011), deep-sea hydrothermal systems (Mc Kay et al., 2012), organic-rich sediments, terrestrial hydrothermal vents (Konkol et al., 2010) and sulfide springs (Caldwell et al., 1975; Nelson and Castenholz, 1981; Larkin et al., 1994; Teske, 2006; Chaudhary et al., 2009), sulfidic caves (Engel et al., 2001; Macalady et al., 2006) and phototrophic mats (Hinck et al., 2011). have been studied in some large lakes (Zemskaya et al., 2009), little is known about chemosynthetic communities or LSB in large freshwater lakes such as the Laurentian Great Lakes (Biddanda et al., 2006). doi: 10.1016/b978-1-4832-3211-9.50009-7 Cross Ref Full Text | Google Scholar Kearse, M., Moir, R., Wilson, A., Stones-Havas, S., Cheung, M., Sturrock, S., et al. Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. doi: 10.1093/bioinformatics/bts199 Pub Med Abstract | Cross Ref Full Text | Google Scholar Kinsman-Costello, L. In submerged sinkholes of Lake Huron, venting of low-oxygen, saline, sulfate-rich, sulfidic groundwater supports chemosynthetic microbial communities (Biddanda et al., 2006). The Alpena fountain was dominated by populations closely related to Thiothrix lacustris and an SM1 euryarchaeon known to live symbiotically with Thiothrix spp. The SM1 genomic bin contained evidence of H and nitrate as electron acceptors. doi: 10.3389/fmicb.2015.00484 Pub Med Abstract | Cross Ref Full Text | Google Scholar Konkol, N. We used a metagenomic approach to identify genes that underpin energy metabolisms, focusing on sulfur metabolism, hydrogen oxidation, aerobic respiration, denitrification, and carbon fixation. Pathways and microbiology of thiosulfate transformations and sulfate reduction in a marine sediment (Kattegat, Denmark). Our results indicate that these two communities are driven by similar suites of largely sulfur-based metabolic pathways held within different taxa at the two sites. doi: 10.1128/AEM.00647-10 Pub Med Abstract | Cross Ref Full Text | Google Scholar Jørgensen, B. For comparison, we also analyzed a white mat in an artesian fountain that is fed by groundwater similar to Isolated Sinkhole, but that sits in shallow water and is exposed to sunlight. De novo assembly and binning of metagenomic data from these two communities yielded near complete genomes and revealed representatives of two families of LSB. on an aquatic macrophyte in a hydrothermal vent flume in Sedge Bay, Yellowstone Lake, Wyoming.


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