Mariprofundus ferrooxydans

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Mariprofundus ferrooxydans
Mariprofundus ferrooxydans PV-1 stalks TEM image.tif
Scientific classification
Domain:
Phylum:
Class:
Order:
Mariprofundales

Hördt et al. 2020 [1]
Family:
Mariprofundaceae

Hördt et al. 2020 [1]
Genus:
Mariprofundus

Emerson et al. 2010 [2]
Species:
M. ferrooxydans
Binomial name
Mariprofundus ferrooxydans
Emerson et al. 2010 [2]
Synonyms [3]
  • "Mariprofundales" Makita et al. 2017
  • "Mariprofundales" Emerson et al. 2007

Mariprofundus ferrooxydans is a neutrophilic, chemolithotrophic, Gram-negative bacterium which can grow by oxidising ferrous to ferric iron. [2] It is one of the few members of the class Zetaproteobacteria in the phylum Pseudomonadota. It is typically found in iron-rich deep sea environments, particularly at hydrothermal vents. [4] M. ferrooxydans characteristically produces stalks of solid iron oxyhydroxides that form into iron mats. [2] Genes that have been proposed to catalyze Fe(II) oxidation in M. ferrooxydans are similar to those involved in known metal redox pathways, and thus it serves as a good candidate for a model iron oxidizing organism. [4]

Contents

Discovery

Yellow iron oxide-covered lava rock on the flank of Lo`ihi Loihiflank.jpg
Yellow iron oxide-covered lava rock on the flank of Lōʻihi

The bacterium was isolated from iron-rich microbial mats associated with hydrothermal vents at a submarine volcano, Lōʻihi Seamount, near Hawaii, and has only 85.3% 16S similarity to its nearest cultivated species Methylophaga marina . It has a doubling time at 23 °C of 12 hours and a curved rod (about 0.5×2–5 µm) morphology. [2]

Etymology

Despite being validly published, [3] the etymology of the generic epithet is grammatically incorrect, being a concatenation of the Latin neutral mare -is (the sea) with the Latin masculine adjective profundus (deep) intended to mean a deep-sea organism (the neuter of profundus is profundum). [3] The specific epithet is ferrum (Latin noun), iron and oxus (Greek adjective), acid or sour, and in combined words indicating oxygen. (N.L. v. oxydare, to make acid, to oxidize; N.L. part. adj. ferrooxydans, iron-oxidizing.) [3]

Physiology

M. ferrooxydans lives in microoxic conditions and uses Fe(II) as an electron donor and oxidizes it to Fe(III) as its main energy acquiring pathway, using oxygen as the electron acceptor and CO2 as its carbon source. [4] [5] It is a chemolithotroph that requires marine salts and has not been shown to grow heterotrophically. [2] Biotic iron oxidation is in competition with abiotic iron oxidation, so M. ferrooxydans thrives in environments with high concentrations of Fe(II) but low concentrations of oxygen, where biotic oxidation of iron is able to compete with abiotic oxidation. [2] Having high concentrations of Fe(II) in the environment is critical since iron oxidation is a low energy-yielding process, and high amounts of iron must be oxidized to yield an adequate amount of energy. [6] The proposed model of iron oxidation in M. ferrooxydans involves oxidation of Fe(II) by an outer membrane iron oxidase, funneling the electron through an electron transport chain made up of cytochromes; oxygen is used as the terminal electron acceptor and then reverse electron transport is used to make NADH. [4]

Lifestyle

M. ferrooxydans cells are Gram-negative curved rods that cycle through two life stages: they have a free-living stage where they are motile, and a second stage where they are oxidizing iron and forming solid iron oxides/ [4] The fibrous twisted stalks of iron oxyhydroxides extruded by M. ferrooxydans are found in iron mats and are predicted to consist of an organic matrix which allows the iron oxide structure to form in a manner characteristic of M. ferrooxydans. [4] [2] This organism is also motile and chemotactic, which enables it to move towards appropriate concentrations of oxygen even in the heterogeneous and rapidly changing environment of hydrothermal vents; the organism can rapidly detect and respond to changing oxygen concentrations to allow aerotaxis towards appropriate levels of oxygen. [4] Motility allows M. ferrooxydans to remain in microoxic conditions despite the amount of mixing occurring in its environment, and remain where it can out-compete abiotic iron oxidation to acquire enough energy to survive. [4]

Genome

M. ferrooxydans is capable of fixing CO2 using RuBisCo genes encoded in its genome; it has multiple different RuBisCo genes which suggests that the organism has adapted to fix CO2 across a broader spectrum of concentrations of oxygen and carbon dioxide. [4] This organism has never been observed to grow heterotrophically, yet its genome encodes for a sugar phosphotransferase system, typically used as a carbohydrate transporter, which is specific for fructose and mannose. [4] Carbohydrate transport is thus encoded in its genome, but it is unknown if they can be used as a carbon source or if they are used for forming the carbohydrate scaffolding matrix of the twisted stalks formed by the organism. [4]

Role in corrosion

M. ferrooxydans, along with other FeOB, have been implicated in the corrosion of Q235 steel; they are able to form a biofilm on the surface of the steel and cause pitting in the surface of the steel. [5] The main products of Q235 steel corrosion caused by M. ferrooxydans are iron oxides such as FeOOH and Fe2O3, and this organism also causes acidification of the environment around the attachment site, which allows the pitting to occur. [5]

See also

Related Research Articles

Rust Type of iron oxide

Rust is an iron oxide, a usually reddish-brown oxide formed by the reaction of iron and oxygen in the catalytic presence of water or air moisture. Rust consists of hydrous iron(III) oxides (Fe2O3·nH2O) and iron(III) oxide-hydroxide (FeO(OH), Fe(OH)3), and is typically associated with the corrosion of refined iron.

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 or chemical compounds; the sources of carbon can be of organic or inorganic origin.

In chemistry, a reducing agent is an element or compound in a redox chemical reaction that loses or "donates" an electron to an electron recipient. In other words, a reducer is any substance that reduces another substance. The oxidation state, which describes the degree of loss of electrons, of the reducer increases while that of the oxidizer decreases; this is expressed by saying that reducers "undergo oxidation" and "are oxidized" while oxidizers "undergo reduction" and "are reduced". Thus, reducing agents "reduce" oxidizers by reducing (decreasing) their oxidation state while oxidizing agents "oxidize" reducers by increasing their oxidation state.

Iron oxide Class of chemical compounds composed of iron and oxygen

Iron oxides are chemical compounds composed of iron and oxygen. There are sixteen known iron oxides and oxyhydroxides, the best known of which is rust, a form of iron(III) oxide.

Chemosynthesis Biological process building organic matter using inorganic compounds as the energy source

In biochemistry, chemosynthesis is the biological conversion of one or more carbon-containing molecules and nutrients into organic matter using the oxidation of inorganic compounds or ferrous ions as a source of energy, rather than sunlight, as in photosynthesis. Chemoautotrophs, organisms that obtain carbon from carbon dioxide through chemosynthesis, are phylogenetically diverse. Groups that include conspicuous or biogeochemically-important taxa include the sulfur-oxidizing Gammaproteobacteria, the Campylobacterota, the Aquificota, the methanogenic archaea, and the neutrophilic iron-oxidizing bacteria.

Acidithiobacillus is a genus of the Acidithiobacillia in the "Pseudomonadota". The genus includes acidophilic organisms capable of iron and/or sulfur oxidation. Like all "Pseudomonadota", Acidithiobacillus spp. are Gram-negative. They are also important generators of acid mine drainage, which is a major environmental problem around the world in mining.

Sulfate-reducing microorganism Microorganisms which "breathe" sulfates

Sulfate-reducing microorganisms (SRM) or sulfate-reducing prokaryotes (SRP) are a group composed of sulfate-reducing bacteria (SRB) and sulfate-reducing archaea (SRA), both of which can perform anaerobic respiration utilizing sulfate (SO2−
4
) as terminal electron acceptor, reducing it to hydrogen sulfide (H2S). Therefore, these sulfidogenic microorganisms "breathe" sulfate rather than molecular oxygen (O2), which is the terminal electron acceptor reduced to water (H2O) in aerobic respiration.

Iron cycle

The iron cycle (Fe) is the biogeochemical cycle of iron through the atmosphere, hydrosphere, biosphere and lithosphere. While Fe is highly abundant in the Earth's crust, it is less common in oxygenated surface waters. Iron is a key micronutrient in primary productivity, and a limiting nutrient in the Southern ocean, eastern equatorial Pacific, and the subarctic Pacific referred to as High-Nutrient, Low-Chlorophyll (HNLC) regions of the ocean.

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 use solar energy. Chemotrophs can be either autotrophic or heterotrophic. Chemotrophs can be found on ocean floors where sunlight cannot reach. Or above ground, such as the case with iron bacteria.

Pitting corrosion Form of insidious localized corrosion in which a pit develops at the anode site

Pitting corrosion, or pitting, is a form of extremely localized corrosion that leads to the random creation of small holes in metal. The driving power for pitting corrosion is the depassivation of a small area, which becomes anodic while an unknown but potentially vast area becomes cathodic, leading to very localized galvanic corrosion. The corrosion penetrates the mass of the metal, with a limited diffusion of ions.

Iron-oxidizing bacteria

Iron-oxidizing bacteria are chemotrophic bacteria that derive energy by oxidizing dissolved ferrous iron. They are known to grow and proliferate in waters containing iron concentrations as low as 0.1 mg/L. However, at least 0.3 ppm of dissolved oxygen is needed to carry out the oxidation.

Lithotrophs are a diverse group of organisms using an inorganic substrate to obtain reducing equivalents for use in biosynthesis or energy conservation via aerobic or anaerobic respiration. While lithotrophs in the broader sense include photolithotrophs like plants, chemolithotrophs are exclusively microorganisms; no known macrofauna possesses the ability to use inorganic compounds as electron 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. Chemolithotrophs belong to the domains Bacteria and Archaea. The term "lithotroph" was created from the Greek terms 'lithos' (rock) and 'troph' (consumer), meaning "eaters of rock". Many but not all lithoautotrophs are extremophiles.

<i>Beggiatoa</i> Genus of bacteria

Beggiatoa is a genus of Gammaproteobacteria belonging the order Thiotrichales, in the Pseudomonadota phylum. This genus was one of the first bacteria discovered by Ukrainian botanist Sergei Winogradsky. During his research in Anton de Bary’s laboratory of botany in 1887, he found that Beggiatoa oxidized hydrogen sulfide (H2S) as energy source, forming intracellular sulfur droplets, oxygen is the terminal electron acceptor and CO2 is used as carbon source. Winogradsky named it in honor of the Italian doctor and botanist Francesco Secondo Beggiato (1806 - 1883), from Venice. Winogradsky referred to this form of metabolism as "inorgoxidation" (oxidation of inorganic compounds), today called chemolithotrophy. These organisms live in sulfur-rich environments such as soil, both marine and freshwater, in the deep sea hydrothermal vents and in polluted marine environments. The finding represented the first discovery of lithotrophy. Two species of Beggiatoa have been formally described: the type species Beggiatoa alba and Beggiatoa leptomitoformis, the latter of which was only published in 2017. This colorless and filamentous bacterium, sometimes in association with other sulfur bacteria (for example the genus Thiothrix), can be arranged in biofilm visible at naked eye formed by very long white filamentous mate, the white color is due to the stored sulfur. Species of Beggiatoa have cells up to 200 µ in diameter and they are one of the largest prokaryotes on Earth.

Microbial metabolism is the means by which a microbe obtains the energy and nutrients it needs to live and reproduce. Microbes use many different types of metabolic strategies and species can often be differentiated from each other based on metabolic characteristics. The specific metabolic properties of a microbe are the major factors in determining that microbe's ecological niche, and often allow for that microbe to be useful in industrial processes or responsible for biogeochemical cycles.

Hydrogen oxidizing bacteria are a group of facultative autotrophs that can use hydrogen as an electron donor.

Acidophiles in acid mine drainage

The outflow of acidic liquids and other pollutants from mines is often catalysed by acid-loving microorganisms; these are the acidophiles in acid mine drainage.

Zetaproteobacteria Class of bacteria

The class Zetaproteobacteria is the sixth and most recently described class of the Pseudomonadota. Zetaproteobacteria can also refer to the group of organisms assigned to this class. The Zetaproteobacteria were originally represented by a single described species, Mariprofundus ferrooxydans, which is an iron-oxidizing neutrophilic chemolithoautotroph originally isolated from Loihi Seamount in 1996 (post-eruption). Molecular cloning techniques focusing on the small subunit ribosomal RNA gene have also been used to identify a more diverse majority of the Zetaproteobacteria that have as yet been unculturable.

Sulfurimonas is a bacterial genus within the class of Campylobacterota, known for reducing nitrate, oxidizing both sulfur and hydrogen, and containing Group IV hydrogenases. This genus consists of four species: Sulfurimonas autorophica, Sulfurimonas denitrificans, Sulfurimonas gotlandica, and Sulfurimonas paralvinellae. The genus' name is derived from "sulfur" in Latin and "monas" from Greek, together meaning a “sulfur-oxidizing rod”. The size of the bacteria varies between about 1.5-2.5 μm in length and 0.5-1.0 μm in width. Members of the genus Sulfurimonas are found in a variety of different environments which include deep sea-vents, marine sediments, and terrestrial habitats. Their ability to survive in extreme conditions is attributed to multiple copies of one enzyme. Phylogenetic analysis suggests that members of the genus Sulfurimonas have limited dispersal ability and its speciation was affected by geographical isolation rather than hydrothermal composition. Deep ocean currents affect the dispersal of Sulfurimonas spp., influencing its speciation. As shown in the MLSA report of deep-sea hydrothermal vents Campylobacterota, Sulfurimonas has a higher dispersal capability compared with deep sea hydrothermal vent thermophiles, indicating allopatric speciation.

Microbial oxidation of sulfur

Microbial oxidation of sulfur is the oxidation of sulfur by microorganisms to build their structural components. The oxidation of inorganic compounds is the strategy primarily used by chemolithotrophic microorganisms to obtain energy to survive, grow and reproduce. Some inorganic forms of reduced sulfur, mainly sulfide (H2S/HS) and elemental sulfur (S0), can be oxidized by chemolithotrophic sulfur-oxidizing prokaryotes, usually coupled to the reduction of energy-rich oxygen (O2) or nitrate (NO3). Anaerobic sulfur oxidizers include photolithoautotrophs that obtain their energy from sunlight, hydrogen from sulfide, and carbon from carbon dioxide (CO2).

Hydrothermal vent microbial communities Unicellular organisms that live and reproduce in a chemically distinct area around Hydrothermal vents

The hydrothermal vent microbial community includes all unicellular organisms that live and reproduce in a chemically distinct area around hydrothermal vents. These include organisms in the microbial mat, free floating cells, or bacteria in an endosymbiotic relationship with animals. Chemolithoautotrophic bacteria derive nutrients and energy from the geological activity at Hydrothermal vents to fix carbon into organic forms. Viruses are also a part of the hydrothermal vent microbial community and their influence on the microbial ecology in these ecosystems is a burgeoning field of research.

References

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