This article needs additional citations for verification. (September 2010) (Learn how and when to remove this template message)
Primary nutritional groups are groups of organisms, divided in relation to the nutrition mode according to the sources of energy and carbon, needed for living, growth and reproduction. The sources of energy can be light and organic or inorganic compounds; the sources of carbon can be of organic or inorganic origin. 
The terms aerobic respiration, anaerobic respiration and fermentation do not refer to primary nutritional groups, but simply reflect the different use of possible electron acceptors in particular organisms, such as O2 in aerobic respiration, or nitrate (NO3−), sulfate (SO42−) or fumarate in anaerobic respiration, or various metabolic intermediates in fermentation. Because all ATP-generating steps in fermentation involve modifications of metabolic intermediates instead of the use of an electron transport chain fermentation is often referred to as substrate-level phosphorylation.
Primary sources of energy
Some bacteria can alternate phototrophy and chemotrophy, depending on availability of light.
Primary sources of reducing equivalents
The electrons from reducing equivalents (electron donors) are needed by both phototrophs and chemotrophs, to keep running reduction-oxidation reactions that transfer energy in the anabolic processes of ATP synthesis (in heterotrophs) or biosynthesis (in autotrophs). The electron donors are taken up from the environment.
Organotrophic organisms are often also heterotrophic, using organic compounds as sources of electrons and carbon at the same time. Similarly, lithotrophic organisms are often also autotrophic, using inorganic sources of electrons and CO2 as inorganic carbon source.
Some lithotrophic bacteria can utilize diverse sources of electrons, depending on availability of possible donors.
For example, plants use water as electron donor to biosynthesis, being lithotrophs. Animals use organic compounds as electron donors to synthesize ATP, being organotrophs (plants also do it, but this is not taken into account). Both use oxygen in respiration as electron acceptor, but this character is not used to define them as lithotrophs.
Primary sources of carbon
Energy and carbon
|Electron donor||organic compound||organo-|
|Carbon source||organic compound||hetero-|
A chemoorganoheterotrophic organism is one that requires organic substrates to get its carbon for growth and development, and that produces its energy from the oxidation and reduction (redox) of an organic compound. This group of organisms may be further subdivided according to what kind of organic substrate and compound they use. Decomposers are examples of Chemoorganoheterotrophs which obtain carbon and electron reactions from dead organic matter. Herbivores and carnivores are examples of organisms that obtain carbon and electron reactions from living organic matter.
Chemoorganotrophs are organisms which oxidize the chemical bonds in organic compounds as their energy source. Chemoorganotrophs also attain the carbon molecules that they need for cellular function from these organic compounds. The organic compounds that they oxidize include sugars (i.e. glucose), fats and proteins.
All animals are chemoheterotrophs (meaning they oxidize chemical compounds as a source of energy and carbon), as are fungi, protozoa, and some bacteria. The important differentiation amongst this group is that chemoorganotrophs oxidize only organic compounds while chemolithotrophs instead use inorganic compounds as a source of energy.
Primary metabolism table
|Sun Light |
|Photoorganoheterotroph||Some bacteria (Rhodobacter)|
|Carbon dioxide |
|Photolithoheterotroph||Purple non-sulfur bacteria and Green non-sulfur bacteria|
|Carbon dioxide |
|Photolithoautotroph||Some bacteria (blue green algae), some eukaryotes (eukaryotic algae, land plants). Photosynthesis.|
|Chemoorganoheterotroph||Predatory, parasitic, and saprophytic prokaryotes. Some eukaryotes (heterotrophic protists, fungi, animals)|
|Carbon dioxide |
|Chemoorganoautotroph||Some archaea (anaerobic methanotrophic archaea). Chemosynthesis.|
|Chemolithoheterotroph||Some bacteria (Oceanithermus profundus)|
|Carbon dioxide |
|Chemolithoautotroph||Some bacteria (Nitrobacter), some archaea (Methanobacteria). Chemosynthesis.|
- Some authors use -hydro- when the source is water.
Some, usually unicellular, organisms can switch between different metabolic modes, for example between photoautotrophy, photoheterotrophy, and chemoheterotrophy in Chroococcales  Such mixotrophic organisms may dominate their habitat, due to their capability to use more resources than either photoautotrophic or organoheterotrophic organisms. 
All sorts of combinations may exist in nature. For example, most cyanobacteria are photoautotrophic, since they use light as an energy source, water as electron donor, and CO2 as a carbon source. Fungi are chemoorganotrophic since they use organic carbon as both an electron donor and carbon source. Eukaryotes are generally easy to categorise. All animals are heterotrophic, as are fungi. Plants are generally photoautotrophic. Some eukaryotic microorganisms, however, are not limited to just one nutritional mode. For example, some algae live photoautotrophically in the light, but shift to chemoorganotrophy in the dark. Even higher plants retained their ability to respire heterotrophically on the starch at night which had been synthesised phototrophically during the day.
Prokaryotes show a great diversity of nutritional categories. For example, purple sulfur bacteria and cyanobacteria are generally photoautotrophic whereas purple non-sulfur bacteria are photoorganotrophic. Some bacteria are limited to only one nutritional group, whereas others are facultative and switch from one mode to the other, depending on the nutrient sources available.
Notes and references
- Brock Biology of Microorganisms Definitions of metabolic strategies to obtain carbon and energy
- Kenneth Todar (2009). "Todar's Online Textbook of Bacteriology". Nutrition and Growth of Bacteria. Retrieved 2014-04-19.
- Kelly, DP; Julie Mason; Ann Wood. Energy Metabolism in Chemolithotrophs. Springer. pp. 186–187.
- 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, .
- Andrews, J. H. 1991. Comparative Ecology of Microorganisms and Macroorganisms. Springer Verlag, Berlin, p. 68, .
- Yafremava LS, Wielgos M, Thomas S, Nasir A, Wang M, Mittenthal JE, Caetano-Anollés G: A general framework of persistence strategies for biological systems helps explain domains of life. Front Genet 2013; 4:16; p.8, 
- Margulis, Lynn; McKhann, Heather I.; Olendzenski, Lorraine, eds. Illustrated Glossary of Protoctista: Vocabulary of the Algae, Apicomplexa, Ciliates, Foraminifera, Microspora, Water Molds, Slime Molds, and the Other Protoctists. Jones & Bartlett Learning, 1993, p. xxv, link.
- Y. Kellermann, Gunter Wegener, Marcus Elvert, Marcos Yukio Yoshinaga, Yu-Shih Lin, Thomas Holler, Xavier Prieto Mollar, Katrin Knittel, and Kai-Uwe Hinrichs. Autotrophy as a predominant mode of carbon fixation in anaerobic methane-oxidizing microbial communities. PNAS 2012, vol. 109 no. 47.
- M. L. Miroshnichenko et al., Oceanithermus profundus gen. nov., sp. nov., a thermophilic, microaerophilic, facultatively chemolithoheterotrophic bacterium from a deep-sea hydrothermal vent
- R. Rippka Photoheterotrophy and chemoheterotrophy among unicellular blue-green algae Archives of Microbiology; Volume 87, Number 1 / March, 1972; doi:10.1007/BF00424781
- Alexander Eiler Evidence for the Ubiquity of Mixotrophic Bacteria in the Upper Ocean: Implications and consequences Appl Environ Microbiol. 2006 December; 72(12): 7431–7437; doi:10.1128/AEM.01559-06.