Purple sulfur bacteria
The purple sulfur bacteria (PSB) are part of a group of Proteobacteria capable of photosynthesis, collectively referred to as purple bacteria. They are anaerobic or microaerophilic, and are often found in stratified water environments including hot springs, stagnant water bodies, as well as microbial mats in intertidal zones. Unlike plants, algae, and cyanobacteria; though they use water as their reducing agent, they do not produce oxygen. Instead, they can use sulfur in the form of sulfide, or thiosulfate (as well, some species can use H2, Fe2+, or NO2−) as the electron donor in their photosynthetic pathways. The sulfur is oxidized to produce granules of elemental sulfur. This, in turn, may be oxidized to form sulfuric acid.
|Purple sulfur bacteria|
The purple sulfur bacteria are divided into two families, the Chromatiaceae and the Ectothiorhodospiraceae, which produce internal and external sulfur granules respectively, and show differences in the structure of their internal membranes. They make up part of the order Chromatiales, included in the gamma subdivision of the Proteobacteria. The genus Halothiobacillus is also included in the Chromatiales, in its own family, but it is not photosynthetic.
Purple sulfur bacteria are generally found in illuminated anoxic zones of lakes and other aquatic habitats where hydrogen sulfide accumulates and also in "sulfur springs" where geochemically or biologically produced hydrogen sulfide can trigger the formation of blooms of purple sulfur bacteria. Anoxic conditions are required for photosynthesis; these bacteria cannot thrive in oxygenated environments.
The most favorable lakes for the development of purple sulfur bacteria are meromictic (permanently stratified) lakes. Meromictic lakes stratify because they have denser (usually saline) water in the bottom and less dense (usually fresh water) nearer the surface. Growth of purple sulfur bacteria is also supported by the layering in holomictic lakes. These lakes are thermally stratified; in the spring and summer time, water at the surface is warmed making it less dense than underlying colder water which provides a stable enough stratification for purple sulfur bacteria growth. If sufficient sulfate is present to support sulfate reduction, the sulfide, produced in the sediments, diffuses upward into the anoxic bottom waters, where purple sulfur bacteria can form dense cell masses, called blooms, usually in association with green phototrophic bacteria.
Purple sulfur bacteria can also be found and are a prominent component in intertidal microbial mats. Mats, such as the Sippewissett Microbial Mat, have dynamic environments due to the flow of tides and incoming fresh water leading to similarly stratified environments as meromictic lakes. Purple sulfur bacteria growth is enabled as sulfur is supplied from the death and decomposition of microorganisms located above them within these intertidal pools. The stratification and sulfur source allows the PSB to grow in these intertidal pools where the mats occur. The PSB can help stabilize these microbial mat environment sediments through the secretion of extracellular polymeric substances that can bind the sediments in the pools.
Purple sulfur bacteria are able to affect their environment by contributing to nutrient cycling, and by using their metabolism to alter their surroundings. They are able to play a significant role in primary production suggesting that these organisms affect the carbon cycle through carbon fixation. Purple sulfur bacteria also contribute to the phosphorus cycle in their habitat. Through upwelling of these organisms, phosphorus, a limiting nutrient in the oxic layer of lakes, is recycled and provided to heterotrophic bacteria for use. This indicates that although purple sulfur bacteria are found in the anoxic layer of their habitat, they are able to promote the growth of many heterotrophic organisms by supplying inorganic nutrients to the above oxic layer. Another form of recycling of inorganic nutrients and dissolved organic matter by purple sulfur bacteria is through the food chain; they act as a source of food to other organisms.
Some purple sulfur bacteria have evolved to optimize their environmental conditions for their own growth. For example, in the South Andros Black Hole in the Bahamas, purple sulfur bacteria adopted a new characteristic in which they are able to use their metabolism to radiate heat energy into their surroundings. Due to the inefficiency of their carotenoids, or light-harvesting centres, the organisms are able to release excess light energy as heat energy. This adaptation allows them to compete more effectively within their environment. By raising the temperature of the surrounding water, they create an ecological niche which supports their own growth, while also allowing them to outcompete other non-thermotolerant organisms.
Growth in meromictic lakesEdit
Meromictic lakes are permanently stratified lakes produced by a gradient of saline concentrations. The highly salinated bottom layer is separated from the top layer of fresh water by the chemocline, where the salinity changes drastically. Due to the large difference in density, the upper and lower layers do not mix, resulting in an anoxic environment below the chemocline. This anoxic environment with light and sufficient sulfide availability is ideal for purple sulfur bacteria.
A study done at the Mahoney Lake suggested that purple sulfur bacteria contributes to the recycling of the inorganic nutrient, phosphorous. The upwelling of purple sulfur bacteria into the top layer of water creates a source of bound phosphorous, and phosphatase activity releases these phosphorous into the water. The soluble phosphorous is then incorporated into heterotrophic bacteria for use in developmental processes. In this way, purple sulfur bacteria participates in the phosphorous cycle and minimizes nutrient loss.
Purple sulfur bacteria make conjugated pigments called carotenoids that function in the light harvesting complex. When these organisms die and sink, some pigment molecules are preserved in modified form in the sediments. One carotenoid molecule produced, okenone, is diagenetically altered to the biomarker okenane. The discovery of okenane in marine sediments implies the presence of purple sulfur bacteria during the time of burial. So far, okenane has only been identified in one sedimentary outcrop from Northern Australia dating to 1640 million years ago. The authors of the study concluded that, based on the presence of purple sulfur bacteria's biomarker, the Paleoproterozoic ocean must have been anoxic and sulfidic at depth. This finding provides evidence for the Canfield Ocean hypothesis.
Purple sulfur bacteria can contribute to a reduction of environmentally harmful organic compounds and odour emission in manure wastewater lagoons where they are known to grow. Harmful compounds such as Methane, a greenhouse gas, and Hydrogen sulfide, a pungent, toxic compound, can be found in wastewater lagoons. PSB can help lower the concentration of both, and others.
Harmful organic carbon containing compounds can be removed through photoassimilation, the uptake of carbon by organisms through photosynthesis. When PSB in the lagoons perform photosynthesis they can utilize the carbon from harmful compounds, such as methane, as their carbon source. This removes methane, a greenhouse gas, from the lagoon and reduces the lagoons atmospheric pollution affect.
H2S can act as a sulfur source for PSB during these same photosynthetic processes that remove the organic compounds. The use of H2S as a reducing agent by PSB removes it from the lagoon and leads to a reduction of odour and toxicity in the lagoons.
- Boden R (2017). "Reclassification of Halothiobacillus hydrothermalis and Halothiobacillus halophilus to Guyparkeria gen. nov. in the Thioalkalibacteraceae fam. nov., with emended descriptions of the genus Halothiobacillus and family Halothiobacillaceae". International Journal of Systematic and Evolutionary Microbiology. 67: 3919–3928. doi:10.1099/ijsem.0.002222. PMID 28884673. Retrieved 9 December 2017.
- "Wenzhouxiangella". www.uniprot.org.
- Parker, Charles Thomas; Garrity, George M (2015). "Nomenclature Abstract for Wenzhouxiangellaceae Wang et al. 2015". The NamesforLife Abstracts. doi:10.1601/nm.27206.
- Proctor, Lita M (1997). "Nitrogen-fixing, photosynthetic, anaerobic bacteria associated with pelagic copepods" (PDF). Aquatic Microbial Ecology. 12: 105–113. doi:10.3354/ame012105.
- Van Germerden, Hans; Mas, Jordi (1995). Anoxygenic photosynthetic bacteria. Dordrecht: Kluwer Academic Publishers. pp. 50–57. ISBN 0-306-47954-0. Retrieved 6 October 2017.
- (Hubas, Cedric, et al. ""Proliferation of Purple Sulphur Bacteria at the Sediment Surface Affects Intertidal Mat Diversity and Functionality: E82329." PLOS One, vol. 8, no. 12, 2013.)
- Stal LJ (2010) https://ac.els-cdn.com/S0925857409000160/1-s2.0-S0925857409000160-main.pdf?_tid=2a3d5a5e-cd79-11e7-aa3b-00000aacb35f&acdnat=1511130774_f1d9f08b3f0de5ea6f90b0d1427800bb Microphytobenthos as a biogeomorphological force in intertidal sediment stabilization. Ecol Eng 36: 236–245. doi:10.1016/ j.ecoleng.2008.12.032.
- Storelli, Nicola; Peduzzi, Sandro; Saad, Maged; Frigaard, Niels-Ulrik; Perret, Xavier; Tonolla, Mauro (May 2013). "CO2 assimilation in the chemocline of Lake Cadagno is dominated by a few types of phototrophic purple sulfur bacteria". FEMS Microbiology Ecology. 84 (2): 421–432. doi:10.1111/1574-6941.12074. Retrieved 16 November 2017.
- Overmann, Jorg (1997). Advances in microbial ecology (PDF). Boston, MA: Springer US. pp. 252–258, 278, 279. ISBN 978-1-4757-9074-0. Retrieved 6 October 2017.
- Herbert, Rodney; Gall, Andrew; Maoka, Takashi; Cogdell, Richard; Robert, Bruno; Takaichi, Shinichi; Schwabe, Stephanie (Feb 2008). "Phototrophic purple sulfur bacteria as heat engines in the South Andros Black Hole". Photosynthesis Research. 95 (2–3): 261–268. doi:10.1007/s11120-007-9246-1.
- Overmann, Jorg; Beatty, J. Thomas; Hall, Ken J. (27 June 1996). "Purple Sulfur Bacteria Control the Growth of Aerobic Heterotrophic Bacterioplankton in a Meromictic Salt Lake" (PDF). American Society for Microbiology. 62: 3251–8. PMC . PMID 16535399. Retrieved 26 September 2017.
- Rogozin, D. Yu; Zykov, V. V.; Tarnovskii, M. O. (1 January 2016). "Dynamics of purple sulfur bacteria in a meromictic saline Lake Shunet (Khakassia, Siberia) in 2007–2013". Microbiology. 85: 93–101. doi:10.1134/S0026261716010100.
- Brocks, Jochen J.; Schaeffer, Philippe (2008-03-01). "Okenane, a biomarker for purple sulfur bacteria (Chromatiaceae), and other new carotenoid derivatives from the 1640 Ma Barney Creek Formation". Geochimica et Cosmochimica Acta. 72 (5): 1396–1414. Bibcode:2008GeCoA..72.1396B. doi:10.1016/j.gca.2007.12.006.
- McGarvey, JA, et al. http://onlinelibrary.wiley.com/doi/10.1111/j.1472-765X.2009.02683.x/epdf "Induction of Purple Sulfur Bacterial Growth in Dairy Wastewater Lagoons by Circulation." Letters in Applied Microbiology, vol. 49, no. 4, 2009, pp. 427-433.
- “Photoassimilation | Definition of photoassimilation in English by Oxford Dictionaries.” https://en.oxforddictionaries.com/definition/photoassimilation Oxford Dictionaries | English, Oxford Dictionaries, en.oxforddictionaries.com/definition/photoassimilation.
- Leytem, AB, et al. https://ac.els-cdn.com/S0022030217305799/1-s2.0-S0022030217305799-main.pdf?_tid=a8cdccc8-cd79-11e7-8cad-00000aab0f6c&acdnat=1511130986_0d85d5d96ffb65e1ca976c83f8706f90 "Methane Emissions from Dairy Lagoons in the Western United States."Journal of Dairy Science, vol. 100, no. 8, 2017, pp. 6785-6803.
- “Hydrogen sulfide.” http://www.npi.gov.au/resource/hydrogen-sulfide National Pollutant Inventory, Australian Government Department of Environment and Energy, www.npi.gov.au/resource/hydrogen-sulfide.
- Caumette, P (1993). "Ecology and physiology of phototrophic bacteria and sulfate-reducing bacteria in marine salterns" (PDF). Experientia. 49: 473–481. doi:10.1007/BF01955148. Retrieved 11 February 2018.
- Dungan, RS; Leytem, AB (2015). "Detection "of Purple Sulfur Bacteria in Purple and Non-Purple Dairy Wastewaters". Journal of Environmental Quality. 44 (5): 1550–1555. doi:10.2134/jeq2015.03.0128.