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2.23: Halobacterium

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    Halobacterium is one of several organisms that can color high salt environments red, like the hypersaline pools in Owens Lake, California. Halobacterium is significant not just for its tolerance of extreme salinity but also because it is a member of the Archaea and because it has some peculiar metabolic abilities.

    This astronaut photograph highlights the mostly dry bed of Owens Lake, located in the Owens River Valley between the Inyo Mountains and the Sierra Nevada. Shallow groundwater, springs, and seeps support minor wetlands and a central brine pool. Two bright red areas along the margins of the brine pool indicate the presence of halophilic (salt-loving) organisms known as archaeans. Gray and white materials within the lake bed are exposed sediments and salt crusts. The nearby towns of Olancha and Lone Pine are marked by the presence of green vegetation, indicating a more constant availability of water.
    Owens Lake viewed from an orbiting satellite. The red color in the center is caused by the presence of Halobacteria.


    Halobacterium is an oxymoron, because it is not a bacterium, it is an archaeon, a member of the Archaea, a group of prokaryotes that in 1977 was distinguishedfrom the rest of prokaryotes (organisms lacking cellular organelles) by virtue of a suite of characteristics, in particular the sequence of bases in the 16s ribosome(actually the sequences of bases in DNA that codes for the RNA of the 16s ribosome). Thus most workers now describe two groups of prokaryotes, Archaea and Eubacteria. Although initially thought to be representative of the most ancient forms of life (hence the name Archaea) workers now believe that the Archaea were derived from Eubacteria. Based on metabolic pathways and genes, it appears that and that eukaryotes and Archaea are more closely related than eukaryotes and Eubacteria.


    Cells are rod-shaped and roughly 2-5 um in length with a single lipid bilayer membrane surrounded by a glycoprotein cell wall. Archaea cell membranes are made of phospholipids that are distinct from those found in bacteria and eukaryotes. Halobacterium cells are flagellated and capable of moving towards a source of light, especially light in the in the yellow-green, around 560 nm, which is where its photosynthetic pigment (bacteriorhodopsin, see below) has peak absorbance.

    Cells of Halobacterium, image taken by a high-powered microscope. The individual cells in this image are about 5 microns long (scale is only approximate)

    Sex and reproduction

    Like all prokaryotes, Halobacteria are not sexual but they are capable of exchanging genetic material by other means. They reproduce by cell division but, like all Archaeons do not produce endospores.

    Matter and energy

    Halobacteriaare photoheterotrophs. Like other heterotrophs they need to eat (i.e. assimilate) organic compounds to provide themselves with material to grow, but they also use light energy to generate ATP. In contrast, photosynthetic organisms are autotrophic: they make food (carbohydrates) and then 'eat' some of it to make ATP and use the rest as building material. Regular heterotrophs 'eat' both to acquire material for growth and to obtain energy, usually via cellular respiration.. If Halobacteria are deprived of light they need to eat more because they will behave like a 'normal' heterotroph, using the food they eat both to make themselves bigger and also to provide for their energetic needs.

    The pigment that interacts with light is bacteriorhodopsin, a form of rhodopsin, the same pigment that our eyes use to see. In both instances light causes a conformational change in the protein. In our eyes this causes a nerve impulse to be transmitted; in Halobacterium it causes protons to accumulate on one side of a membrane, allowing ATP to be synthesized. Halobacterium also possesses a second protein pigment, halorhodopsin, that can use light energy to pump chloride ions into the cell, increasing the solute concentration and preventing excessive water loss.

    Bacteriorhodopsin is a membrane-spanning protein that can acquire protons in the cytosol, change conformation due to the absorption of light and release protons on the outside of the membrane. Protons then flow into the cell, down their electrochemical gradient, in a process that is associated with ATP formation.


    Halobacterium is a classic example of an 'extremophile' , an organism that exists under extreme conditions, such as high temperature, high salinity, high acidity. Halobacterium can live, and indeed requires, salt concentrations far exceeding the tolerance levels of most other organisms. They can even survive in saturated brine solutions. Because of this they can actually be 'fossilized' in salt deposits and stay alive for thousands, perhaps millions of years. Tolerance of extreme conditions probably means reduced competition in such habitats.

    Although many archaeons are extremophiles, not all are; and there certainly are extremophiles that are not archaeons (one you should be aware of is the bacterium, Thermus aquaticus). Another non-archaeon that lives in high salt conditions is the unicellular green algae Dunaliella salina which can produce large quantities of the pigment beta-carotene and at one time was once thought to be the source of red coloration in hypersaline lakes. Most workers now believe that archaeons like Halobacterium are what make the lakes red, but that Dunaliella may be responsible in making flamingos pink, a result of their consumption of brine shrimp that have feasted on the beta-carotene loaded Dunaliella.

    This page titled 2.23: Halobacterium is shared under a CC BY-NC 4.0 license and was authored, remixed, and/or curated by George M. Briggs (Milne Library) via source content that was edited to the style and standards of the LibreTexts platform; a detailed edit history is available upon request.

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