Lithotrophs are a diverse group of organisms using inorganic substrate (usually of mineral origin) to obtain reducing equivalents for use in biosynthesis (e.g., carbon dioxide fixation) or energy conservation (i.e., ATP production) via aerobic or anaerobic respiration. Known chemolithotrophs are exclusively microorganisms; no known macrofauna possesses the ability to use inorganic compounds as energy sources. Macrofauna and lithotrophs can form symbiotic relationships, in which case the lithotrophs are called "prokaryotic symbionts". An example of this is chemolithotrophic bacteria in giant tube worms or plastids, which are organelles within plant cells that may have evolved from photolithotrophic cyanobacteria-like organisms. Lithotrophs belong to either the domain Bacteria or the domain Archaea. The term "lithotroph" was created from the Greek terms 'lithos' (rock) and 'troph' (consumer), meaning "eaters of rock". Many lithoautotrophs are extremophiles, but this is not universally so.
A chemolithotroph (named after the process of chemolithotropy) is able to use inorganic reduced compounds as a source of energy. This process is accomplished through oxidation and ATP synthesis. The majority of chemolithotrophs are able to fix carbon dioxide (CO2) through the Calvin cycle, a metabolic pathway in which carbon enters as CO2 and leaves as glucose. This group of organisms includes sulfur oxidizers, nitrifying bacteria, iron oxidizers, and hydrogen oxidizers.
The term "chemolithotrophy" refers to a cell’s acquisition of energy from the oxidation of inorganic compounds, also known as electron donors. This form of metabolism is believed to occur only in prokaryotes and was first characterized by microbiologist Sergei Winogradsky.
Habitat of chemolithotrophsEdit
The survival of these bacteria is dependent on the physiochemical conditions of their environment. Although they are sensitive to certain factors such as quality of inorganic substrate, they are able to thrive under some of the most inhospitable conditions in the world, such as temperatures above 110 degrees Celsius and below 2 pH. The most important requirement for chemolithotropic life is an abundant source of rich inorganic compounds. These compounds are crucial for chemolithotrophs because they provide a suitable energy source/electron donor from which the microorganisms can fix CO2 and produce the energy they need to survive. Since chemosynthesis can take place in the absence of sunlight, these organisms are found mostly around hydrothermal vents and other locations rich in inorganic substrate.
The energy obtained from inorganic oxidation varies depending on the substrate and the reaction. For example, the oxidation of hydrogen sulfide to elemental sulfur produces far less energy (50.1 kcal/mol or 210.4 kJ/mol) than the oxidation of elemental sulfur to sulfate (149.8 kcal/mol or 629.2 kJ/mol). The majority of lithotrophs fix carbon dioxide through the Calvin cycle, an energetically expensive process. For some substrates, such as ferrous iron, the cells must cull through large amounts of inorganic substrate to secure just a small amount of energy. This makes their metabolic process inefficient in many places and hinders them from thriving.
Overview of the Metabolic ProcessEdit
There is a fairly large variation in the types of inorganic substrates that these microorganisms can use to produce energy. Sulfur is one of many inorganic substrates that can be utilized in different reduced forms depending on the specific biochemical process that a lithotroph uses. The chemolithotrophs that are best documented are aerobic respirers, meaning that they use oxygen in their metabolic process. The high electronegativity of oxygen and resulting large energy gains makes it ideal for use as a Terminal Electron Acceptor (TEA). The list of these microorganisms that employ anaerobic respiration though is growing. At the heart of this metabolic process is an electron transport system that is similar to that of chemoorganotrophs. The major difference between these two microorganisms is that chemolithotrophs directly provide electrons to the electron transport chain, while chemoorganotrophs must generate their own cellular reducing power by oxidizing reduced organic compounds. Chemolithotrophs bypass this by obtaining their reducing power directly from the inorganic substrate or by the reverse electron transport reaction. Certain specialized chemolithotrophic bacteria utilize different derivatives of the Sox system; a central pathway specific to sulfur oxidation. This ancient and unique pathway illustrates the power that chemolithotrophs have evolved to utilize from inorganic substrates, such as sulfur.
In chemolithotrophs, the compounds - the electron donors - are oxidized in the cell, and the electrons are channeled into respiratory chains, ultimately producing ATP. The electron acceptor can be oxygen (in aerobic bacteria), but a variety of other electron acceptors, organic and inorganic, are also used by various species. Aerobic bacteria such as the nitrifying bacteria, Nitrobacter, utilize oxygen to oxidize nitrite to nitrate. Some lithotrophs produce organic compounds from carbon dioxide in a process called chemosynthesis, much as plants do in photosynthesis. Plants use energy from sunlight to drive carbon dioxide fixation, since both water and carbon dioxide are low in energy. By contrast, the hydrogen compounds used in chemosynthesis are high in energy, so chemosynthesis can take place in the absence of sunlight (e.g., around a hydrothermal vent). Ecosystems establish in and around hydrothermal vents as the abundance of inorganic substances, namely hydrogen, are constantly being supplied via magma in pockets below the sea floor. Other lithotrophs are able to directly utilize inorganic substances, e.g., iron, hydrogen sulfide, elemental sulfur, or thiosulfate, for some or all of their energy needs.
Here are a few examples of chemolithotrophic pathways, any of which may use oxygen, sulfur or other molecules as electron acceptors:
Photolithotrophs obtain energy from light and therefore use inorganic electron donors only to fuel biosynthetic reactions (e. g., carbon dioxide fixation in lithoautotrophs).
Lithoheterotrophs versus lithoautotrophsEdit
Lithotrophic bacteria cannot use, of course, their inorganic energy source as a carbon source for the synthesis of their cells. They choose one of three options:
- Lithoheterotrophs do not have the possibility to fix carbon dioxide and must consume additional organic compounds in order to break them apart and use their carbon. Only a few bacteria are fully heterolithotrophic.
- Lithoautotrophs are able to use carbon dioxide from the air as carbon source, the same way plants do.
- Mixotrophs will take up and use organic material to complement their carbon dioxide fixation source (mix between autotrophy and heterotrophy). Many lithotrophs are recognised as mixotrophic in regard of their C-metabolism.
Chemolithotrophs versus photolithotrophsEdit
In addition to this division, lithotrophs differ in the initial energy source which initiates ATP production:
- Chemolithotrophs use the above-mentioned inorganic compounds for aerobic or anaerobic respiration. The energy produced by the oxidation of these compounds is enough for ATP production. Some of the electrons derived from the inorganic donors also need to be channeled into biosynthesis. Mostly, additional energy has to be invested to transform these reducing equivalents to the forms and redox potentials needed (mostly NADH or NADPH), which occurs by reverse electron transfer reactions.
- Photolithotrophs use light as energy source. These bacteria are photosynthetic; photolithotrophic bacteria are found in the purple bacteria (e. g., Chromatiaceae), green bacteria (Chlorobiaceae and Chloroflexi) and Cyanobacteria. Purple and green bacteria oxidize sulfide, sulfur, sulfite, iron or hydrogen. Cyanobacteria extract reducing equivalents from water, i.e., they oxidise water to oxygen. The electrons obtained from the electron donors are not used for ATP production (as long as there is light); they are used in biosynthetic reactions. Some photolithotrophs shift over to chemolithotrophic metabolism in the dark.
Lithotrophs participate in many geological processes, such as the formation of soil and the biogeochemical cycling of carbon, nitrogen, and other elements. Lithotrophs also associate with the modern-day issue of acid mine drainage. Lithotrophs may be present in a variety of environments, including deep terrestrial subsurfaces, soils, mines, and in endolith communities.
A primary example of lithotrophs that contribute to soil formation is Cyanobacteria. This group of bacteria are nitrogen-fixing photolithotrophs that are capable of using energy from sunlight and inorganic nutrients from rocks as reductants. This capability allows for their growth and development on native, oligotrophic rocks and aids in the subsequent deposition of their organic matter (nutrients) for other organisms to colonize. Colonization can initiate the process of organic compound decomposition: a primary factor for soil genesis. Such a mechanism has been attributed as part of the early evolutionary processes that helped shape the biological Earth.
Biogeochemical cycling of elements is an essential component of lithotrophs within microbial environments. For example, in the carbon cycle, there are certain bacteria classified as photolithoautotrophs that generate organic carbon from atmospheric carbon dioxide. Certain chemolithoautotrophic bacteria can also produce organic carbon, some even in the absence of light. Similar to plants, these microbes provide a usable form of energy for organisms to consume. On the contrary, there are lithotrophs that have the ability to ferment, implying their ability to convert organic carbon into another usable form. Another example is the cycling of nitrogen. Many lithotrophic bacteria play a role in reducing inorganic nitrogen (nitrogen gas) to organic nitrogen (ammonium) in a process called nitrogen fixation. Likewise, there are many lithotrophic bacteria that also convert ammonium into nitrogen gas in a process called denitrification. Carbon and nitrogen are important nutrients, essential for metabolic processes, and can sometimes be the limiting factor that affects organismal growth and development. Thus, lithotrophs are key players in both providing and removing these important resource.
Acid Mine DrainageEdit
Lithotrophic microbes are responsible for the phenomenon known as acid mine drainage. Typically occurring in mining areas, this process concerns the active metabolism of energy-rich pyrites and other reduced sulfur components to sulfate. One example is the acidophilic bacterial genus, A. ferrooxidans, that utilize iron(II) sulfide (FeS2) and oxygen (O2) to generate sulfuric acid. The acidic product of these specific lithotrophs has the potential to drain from the mining area via water run-off and enter the environment.
Acid mine drainage drastically alters the acidity (pH values of 2 - 3) and chemistry of groundwater and streams, and may endanger plant and animal populations downstream of mining areas. Activities similar to acid mine drainage, but on a much lower scale, are also found in natural conditions such as the rocky beds of glaciers, in soil and talus, on stone monuments and buildings and in the deep subsurface.
It has been suggested that biominerals could be important indicators of extraterrestrial life and thus could play an important role in the search for past or present life on the planet Mars. Furthermore, organic components (biosignatures) that are often associated with biominerals are believed to play crucial roles in both pre-biotic and biotic reactions.
On January 24, 2014, NASA reported that current studies by the Curiosity and Opportunity rovers on Mars will now be searching for evidence of ancient life, including a biosphere based on autotrophic, chemotrophic and/or chemolithoautotrophic microorganisms, as well as ancient water, including fluvio-lacustrine environments (plains related to ancient rivers or lakes) that may have been habitable. The search for evidence of habitability, taphonomy (related to fossils), and organic carbon on the planet Mars is now a primary NASA objective.
- Zwolinski, Michele D. "Lithotroph Archived 2013-08-24 at the Wayback Machine." Weber State University. p. 1-2.
- Lwoff, A., C.B. van Niel, P.J. Ryan, and E.L. Tatum (1946). Nomenclature of nutritional types of microorganisms. Cold Spring Harbor Symposia on Quantitative Biology (5th edn.), Vol. XI, The Biological Laboratory, Cold Spring Harbor, NY, pp. 302–303, .
- Chang, Kenneth (September 12, 2016). "Visions of Life on Mars in Earth's Depths". New York Times. Retrieved 2016-09-12.
- Kuenen, G. (2009). "Oxidation of Inorganic Compounds by Chemolithotrophs". In Lengeler, J.; Drews, G.; Schlegel, H. (eds.). Biology of the Prokaryotes. John Wiley & Sons. p. 242. ISBN 9781444313307.
- Kuenen, G. (2009). "Oxidation of Inorganic Compounds by Chemolithotrophs". In Lengeler, J.; Drews, G.; Schlegel, H. (eds.). Biology of the Prokaryotes. John Wiley & Sons. p. 243. ISBN 9781444313307.
- "Archived copy" (PDF). Archived from the original (PDF) on 2013-08-26. Retrieved 2013-05-15.CS1 maint: Archived copy as title (link)
- Ogunseitan, Oladele (2008). Microbial Diversity: Form and Function in Prokaryotes. John Wiley & Sons. p. 169. ISBN 9781405144483.
- Lengeler, Joseph W; Drews, Gerhart; Schlegel, Hans G (2009-07-10). Biology of the Prokaryotes. ISBN 9781444313307.
- Ghosh, W; Dam, B (2009). "Biochemistry and molecular biology of lithotrophic sulfur oxidation by taxonomically and ecologically diverse bacteria and archaea". National Centre for Biotechnology Information. 33 (6): 999–1043. doi:10.1111/j.1574-6976.2009.00187.x. PMID 19645821.
- Paustian, Timothy. "Lithotrophic Bacteria - Rock Eaters". Lecturer. University of Wisconsin-Madison. Retrieved 6 October 2017.
- "Archived copy". Archived from the original on 2013-05-04. Retrieved 2013-05-15.CS1 maint: Archived copy as title (link)
- Alberts, Bruce; Johnson, Alexander; Lewis, Julian; Morgan, David; Raff, Martin; Roberts, Keith; Walter, Peter (Nov 20, 2014). Molecular Biology of the Cell (Sixth ed.). Garland Science. pp. 11–12.
- Jorge G. Ibanez; Margarita Hernandez-Esparza; Carmen Doria-Serrano; Mono Mohan Singh (2007). Environmental Chemistry: Fundamentals. Springer. p. 156. ISBN 978-0-387-26061-7.
- Kuenen, G. (2009). "Oxidation of Inorganic Compounds by Chemolithotrophs". In Lengeler, J.; Drews, G.; Schlegel, H. (eds.). Biology of the Prokaryotes. John Wiley & Sons. p. 249. ISBN 9781444313307.
- Lengeler, Joseph W.; Drews, Gerhart; Schlegel, Hans Günter (1999). Biology of the Prokaryotes. Georg Thieme Verlag. p. 249. ISBN 978-3-13-108411-8.
- Reddy, K. Ramesh; DeLaune, Ronald D. (2008). Biogeochemistry of Wetlands: Science and Applications. CRC Press. p. 466. ISBN 978-1-56670-678-0.
- Canfield, Donald E.; Kristensen, Erik; Thamdrup, Bo (2005). Aquatic Geomicrobiology. Elsevier. p. 285. ISBN 978-0-12-026147-5.
- Meruane G, Vargas T (2003). "Bacterial oxidation of ferrous iron by Acidithiobacillus ferrooxidans in the pH range 2.5–7.0" (PDF). Hydrometallurgy. 71 (1): 149–58. doi:10.1016/S0304-386X(03)00151-8.
- Zwolinski, Michele D. "Lithotroph Archived 2013-08-24 at the Wayback Machine." Weber State University. p. 7.
- "Nitrifying bacteria." PowerShow. p. 12.
- Libert M, Esnault L, Jullien M, Bildstein O (2010). "Molecular hydrogen: an energy source for bacterial activity in nuclear waste disposal" (PDF). Physics and Chemistry of the Earth. Archived from the original (PDF) on 2014-07-27.
- Kartal B, Kuypers MM, Lavik G, Schalk J, Op den Camp HJ, Jetten MS, Strous M (2007). "Anammox bacteria disguised as denitrifiers: nitrate reduction to dinitrogen gas via nitrite and ammonium". Environmental Microbiology. 9 (3): 635–42. doi:10.1111/j.1462-2920.2006.01183.x. PMID 17298364.
- Zwolinski, Michele D. "Lithotroph Archived 2013-08-24 at the Wayback Machine." Weber State University. p. 3.
- Evans, J. Heritage; E. G. V.; Killington, R. A. (1999). Microbiology in action (Repr ed.). Cambridge [u.a.]: Cambridge Univ. Press. ISBN 9780521621113.
- eds, François Buscot, Ajit Varma (2005). Microorganisms in soils roles in genesis and functions. Soil Biology. 3. Berlin: Springer. doi:10.1007/b137872. ISBN 978-3-540-26609-9.
- Paul, Eldor A. (2014-11-14). Soil Microbiology, Ecology and Biochemistry. Academic Press, 2014. p. 598. ISBN 9780123914118.
- Steele, Andrew; Beaty, David, eds. (September 26, 2006). "Final report of the MEPAG Astrobiology Field Laboratory Science Steering Group (AFL-SSG)". The Astrobiology Field Laboratory (.doc). U.S.A.: Mars Exploration Program Analysis Group (MEPAG) - NASA. p. 72.
- Grotzinger, John P. (January 24, 2014). "Introduction to Special Issue - Habitability, Taphonomy, and the Search for Organic Carbon on Mars". Science. 343 (6169): 386–387. doi:10.1126/science.1249944. PMID 24458635.
- Various (January 24, 2014). "Special Issue - Table of Contents - Exploring Martian Habitability". Science. 343 (6169): 345–452. Retrieved 2014-01-24.CS1 maint: Uses authors parameter (link)
- Various (January 24, 2014). "Special Collection - Curiosity - Exploring Martian Habitability". Science. Retrieved 2014-01-24.CS1 maint: Uses authors parameter (link)
- Grotzinger, J.P. et al. (January 24, 2014). "A Habitable Fluvio-Lacustrine Environment at Yellowknife Bay, Gale Crater, Mars". Science. 343 (6169): 1242777. CiteSeerX 10.1.1.455.3973. doi:10.1126/science.1242777. PMID 24324272.CS1 maint: Uses authors parameter (link)