Chemotroph

Chemotrophs are organisms that obtain energy by the oxidation of electron donors in their environments. These molecules can be organic (chemoorganotrophs) or inorganic (chemolithotrophs). The chemotroph designation is in contrast to phototrophs, which utilize solar energy. Chemotrophs can be either autotrophic or heterotrophic.

• Chemoautotrophs (or chemotrophic autotroph), (Gr: Chemo (χημία) = chemical, auto (αὐτός) = self, troph (τροφιά) = nourishment) in addition to deriving energy from chemical reactions, synthesize all necessary organic compounds from carbon dioxide. Chemoautotrophs use inorganic energy sources, such as hydrogen sulfide, elemental sulfur, ferrous iron, molecular hydrogen, and ammonia. Most are bacteria or archaea that live in hostile environments such as deep sea vents and are the primary producers in such ecosystems. Evolutionary scientists believe that the first organisms to inhabit Earth were chemoautotrophs that produced oxygen as a by-product and later evolved into both aerobic, animal-like organisms and photosynthetic, plant-like organisms. Chemoautotrophs generally fall into several groups: methanogens, halophiles, sulfur oxidizers and reducers, nitrifiers, anammox bacteria, and thermoacidophiles. Chemolithotrophic growth could be dramatically fast, such as Thiomicrospira crunogena with a doubling time around one hour.^[1]
• Chemoheterotrophs (or chemotrophic heterotrophs) (Gr: Chemo (χημία) = chemical, hetero (ἕτερος) = (an)other, troph (τροφιά) = nourishment) are unable to fix carbon and form their own organic compounds. Chemoheterotrophs can be chemolithoheterotrophs, utilizing inorganic energy sources such as sulfur or chemoorganoheterotrophs, utilizing organic energy sources such as carbohydrates, lipids, and proteins.^[2][3][4][5]

Iron and manganese oxidizing bacteria

In the deep oceans, iron oxidizing bacteria derive their energy needs by oxidizing iron(II) to iron(III). The extra electron obtained from this reaction powers the cells, replacing or augmenting traditional phototrophism.

• In general, iron oxidizing bacteria can exist only in areas with high iron concentrations, such as new lava beds or areas of hydrothermal activity (where there is dissolved Fe). Most of the ocean is devoid of iron, due to both the oxidative effect of dissolved oxygen in the water and the tendency of prokaryotes to take up the iron.
• Lava beds supply bacteria with iron straight from the Earth's mantle, but only newly formed igneous rocks have high enough levels of unoxidized iron. In addition, because oxygen is necessary for the reaction, these bacteria are much more common in the upper ocean, where oxygen is more abundant.
• What is still unknown, though, is how exactly iron bacteria extract the iron out of the rock. It is accepted that some mechanism exists that eats away at the rock, perhaps through specialized enzymes or compounds that bring more FeO to the surface. It has been long debated about how much of the weathering of the rock is due to biotic components and how much can be attributed to abiotic components.
• Hydrothermal vents also release large quantities of dissolved iron into the deep ocean, allowing bacteria to survive. In addition, the high thermal gradient around vent systems means a wide variety of bacteria can coexist, each with its own specialized temperature niche.
• Regardless of the catalytic method used, chemoautotrophic bacteria provide a significant but frequently overlooked food source for deep sea ecosystems - which otherwise receive limited sunlight and organic nutrients.

Manganese oxidizing bacteria also make use of igneous lava rocks in much the same way - by oxidizing Mn²⁺ into Mn⁴⁺. Manganese is much rarer than iron in oceanic crust, but is much easier for bacteria to extract from the igneous glass. In addition, each manganese oxidation yields around twice the energy as an iron oxidation due to the gain of twice the number of electrons. Much still remains unknown about manganese oxidizing bacteria because they have not been cultured and documented to any great extent.

Flowchart

• Autotroph
  • Chemoautotroph
  • Photoautotroph
• Heterotroph
  • Chemoheterotroph
  • Photoheterotroph

See also

• Primary nutritional groups
• Chemosynthesis

Notes

1. ^ The Carbon-Concentrating Mechanism of the Hydrothermal Vent Chemolithoautotroph Thiomicrospira crunogena J Bacteriol. 2005 August; 187(16): 5761–5766
2. ^ Davis, Mackenzie Leo, et al. (2004). Principles of environmental engineering and science. 清华大学出版社. p. 133. ISBN 9787302097242. http://books.google.com/books?id=e0OsNiQthNQC&pg=PA133&dq=chemoheterotroph&lr=&cd=41#v=onepage&q=&f=false. 
3. ^ Lengeler, Joseph W.; Drews, Gerhart; Schlegel, Hans Günter (1999). Biology of the Prokaryotes. Georg Thieme Verlag. p. 238. ISBN 9783131084118. http://books.google.com/books?id=MiwpFtTdmjQC&pg=PA238&dq=chemolithoheterotroph+sulfur+bacteria&cd=6#v=onepage&q=chemolithoheterotroph%20sulfur%20bacteria&f=false. 
4. ^ Dworkin, Martin (2006). The Prokaryotes: Ecophysiology and biochemistry (3rd ed.). Springer. p. 989. ISBN 9780387254920. http://books.google.com/books?id=uleTr2jKzJMC&pg=PA989&dq=chemolithoheterotroph+sulfur+bacteria&cd=3#v=onepage&q=chemolithoheterotroph%20sulfur%20bacteria&f=false. 
5. ^ Bergey, David Hendricks; Holt, John G. (1994). Bergey's manual of determinative bacteriology (9th ed.). Lippincott Williams & Wilkins. p. 427. ISBN 9780683006032. http://books.google.com/books?id=jtMLzaa5ONcC&pg=PA427&dq=chemolithotrophic+sulfur+bacteria&cd=1#v=onepage&q=chemolithotrophic%20sulfur%20bacteria&f=false. 

References

1. Katrina Edwards. Microbiology of a Sediment Pond and the Underlying Young, Cold, Hydrologically Active Ridge Flank. Woods Hole Oceanographic Institution.

2. Coupled Photochemical and Enzymatic Mn(II) Oxidation Pathways of a Planktonic Roseobacter-Like Bacterium Colleen M. Hansel and Chris A. Francis* Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305-2115 Received 28 September 2005/ Accepted 17 February 2006