Desulfobacter hydrogenophilus | |
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Species: | D. hydrogenophilus |
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Desulfobacter hydrogenophilus Widdell, 1987 | |
Desulfobacter hydrogenophilus is a strictly anaerobic sulfate-reducing bacterium. [1] It was isolated and characterized in 1987 by Friedrich Widdel of the University of Konstanz (Germany). Like most sulfate-reducing bacteria (SRB), D. hydrogenophilus is capable of completely oxidizing organic compounds (specifically acetate, pyruvate and ethanol) to CO2, and therefore plays a key role in biomineralization in anaerobic marine environments. [2] However, unlike many SRB, D. hydrogenophilus is a facultative lithoautotroph, and can grow using H2 as an electron donor and CO2 as a carbon source. [1] D. hydrogenophilus is also unique because it is psychrophilic (and has been shown to grow at temperatures as low as 0 °C or 32 °F). It is also diazotrophic, or capable of fixing nitrogen. [1]
Cells are elongated-oval shaped, and 1–1.3 by 2–3 μm in size. They are non-motile, gram-negative, and non-sporulating. [1]
D. hydrogenophilus is the only described species of Desulfobacter that can grow chemolithoautotrophically. [3] Using H2 as an electron donor and CO2 as a carbon source, D. hydrogenophilus reduces sulfate, SO42− (and also sulfite, SO32−, and thiosulfate, S2O32−) to sulfide, S2−. [1] However, D. hydrogenophilus is a facultative lithoautotroph, and may also use acetate, pyruvate, or ethanol as both an electron donor and carbon source. [1] A modified tricarboxylic acid (TCA) cycle is employed for acetate metabolism and autotrophic growth. [4] When D. hydrogenophilus is grown with either H2 or acetate, doubling time is less than 30 hours, but when grown with pyruvate or ethanol, doubling time is over 30 hours. The shortest doubling time observed on acetate was 18 hours. [1]
Butyrate cannot be used as an electron donor, and neither elemental sulfur, S0, nor nitrate, NO3−, can be used as electron acceptors. [1] Fermentative growth has not been observed. [1]
Diazotrophic growth was observed in D. hydrogenophilus. [1] Other Desulfobacter strains have also exhibited diazotrophic growth, but D. hydrogenophilus has exhibited the fastest diazotrophic growth rates of all the strains. D. hydrogenophilus’ doubling time with N2 as the nitrogen source was 36 hours, whereas other strains grew with a doubling time of 50 hours or more. [1]
The strain AcRS1, which was isolated for the enrichment culture used to describe the species in 1986, was taken from Rio di San Giacomo in Venice, Italy. [1]
D. hydrogenophilus is most commonly found in anoxic brackish or marine sediments, but has also been found in anoxic freshwater sediments and in activated sludge. [3]
D. hydrogenophilus is ecologically unique in that it has a wide temperature and pH range. Unlike any other species in its genus, D. hydrogenophilus is psychrophilic, or capable of growth and reproduction at cold temperatures. [1] Slow growth on acetate with a doubling time of 5 weeks still occurred at 0 °C in an ice water bath. [1] Its optimum growth temperature is 29–32 °C (84–90 °F), but growth occurs at temperatures of 0–35 °C (32–95 °F). [1] Optimum pH is 6.6–7.0, but growth occurs at pH values of 5.5–7.6. [1]
Guanine and cytosine were found to make up 44.6% of D. hydrogenophilus DNA sequences. [1]
The fatty acid methyl esters (FAME) detected in D. hydrogenophilus consist of a wide variety of structures, including normal, branched and unsaturated FAME 14 to 19 carbon atoms long, with a greater variety of FAME when grown with acetate. [4] Cis-9,10-methylenehexadecanoic acid and 10-methylhexadecanoic acid have been considered biomarkers for D. hydrogenophilus. However, the relative amount of these fatty acids decreases substantially at cold temperatures. This has led to the concern about their reliability as biomarkers in cold environments, and has prompted further research in this area. [5]
The δ13C values of individual fatty acids can be useful for interpreting carbon utilization by D. hydrogenophilus in natural environments. [4] Fatty acid δ13C values were more depleted relative to biomass under heterotrophic (−13.3‰) than under autotrophic (−11.8‰) growth conditions. [4]
The green sulfur bacteria (Chlorobiaceae) are a family of obligately anaerobic photoautotrophic bacteria. Together with the non-photosynthetic Ignavibacteriaceae, they form the phylum Chlorobi.
Carbon fixation or сarbon assimilation is the process by which inorganic carbon is converted to organic compounds by living organisms. The compounds are then used to store energy and as structure for other biomolecules. The most prominent example of carbon fixation is photosynthesis; another form known as chemosynthesis can take place in the absence of sunlight.
Purple bacteria or purple photosynthetic bacteria are Gram-negative proteobacteria that are phototrophic, capable of producing their own food via photosynthesis. They are pigmented with bacteriochlorophyll a or b, together with various carotenoids, which give them colours ranging between purple, red, brown, and orange. They may be divided into two groups – purple sulfur bacteria and purple non-sulfur bacteria (Rhodospirillaceae). Purple bacteria are anoxygenic phototrophs widely spread in nature, but especially in aquatic environments, where there are anoxic conditions that favor the synthesis of their pigments.
Acidogenesis is the second stage in the four stages of anaerobic digestion:
Sulfur-reducing bacteria are microorganisms able to reduce elemental sulfur (S0) to hydrogen sulfide (H2S). These microbes use inorganic sulfur compounds as electron acceptors to sustain several activities such as respiration, conserving energy and growth, in absence of oxygen. The final product or these processes, sulfide, has a considerable influence on the chemistry of the environment and, in addition, is used as electron donor for a large variety of microbial metabolisms. Several types of bacteria and many non-methanogenic archaea can reduce sulfur.Microbial sulfur reduction was already shown in early studies, which highlighted the first proof of S0 reduction in a vibrioid bacterium from mud, with sulfur as electron acceptor and H2 as electron donor. The first pure cultured species of sulfur-reducing bacteria, Desulfuromonas acetoxidans, was discovered in 1976 and described by Pfennig Norbert and Biebel Hanno as an anaerobic sulfur-reducing and acetate-oxidizing bacterium, not able to reduce sulfate. Only few taxa are true sulfur-reducing bacteria, using sulfur reduction as the only or main catabolic reaction. Normally, they couple this reaction with the oxidation of acetate, succinate or other organic compounds.In general, sulfate-reducing bacteria, are able to use both sulfate and elemental sulfur as electron acceptors. Thanks to its abundancy and thermodynamic stability, sulfate is the most studied electron acceptor for anaerobic respiration that involves sulfur compounds. Elemental sulfur, however, is very abundant and important, especially in deep-sea hydrothermal vents, hot springs and other extreme environments, making its isolation more difficult. Some bacteria – such as Proteus, Campylobacter, Pseudomonas and Salmonella – have the ability to reduce sulfur, but can also use oxygen and other terminal electron acceptors.
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.
Beggiatoa is a genus of Gammaproteobacteria belonging the order Thiotrichales, in the Proteobacteria phylum. This genus was one of the first bacteria discovered by Russian 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. 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.
Mixed acid fermentation is the biological process by which a six-carbon sugar e.g. glucose is converted into a complex and variable mixture of acids. It is an anaerobic fermentation reaction that is common in bacteria. It is characteristic for members of the Enterobacteriaceae, a large family of Gram-negative bacteria that includes E. coli.
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.
In biology, syntrophy, synthrophy, or cross-feeding is the phenomenon of one species living off of the metabolic products of another species. In this type of biological interaction, the growth of one partner depends on the nutrients, growth factors, or substrates provided by the other partner. Jan Dolfing describes syntrophy as "the critical interdependency between producer and consumer". This term for nutritional interdependence is often used in microbiology to describe this symbiotic relationship between bacterial species. Morris et al. have described the process as "obligately mutualistic metabolism".
Fermentation is a metabolic process that produces chemical changes in organic substrates through the action of enzymes. In biochemistry, it is narrowly defined as the extraction of energy from carbohydrates in the absence of oxygen. In food production, it may more broadly refer to any process in which the activity of microorganisms brings about a desirable change to a foodstuff or beverage. The science of fermentation is known as zymology.
Desulfococcus oleovorans Strain Hxd3 was isolated from the saline water phase of an oil-water separator from a northern German oil field. Hxd3 is a delta-proteobacterium capable of utilizing C12-C20 alkanes as growth substrates. Hxd3 activates alkanes via carboxylation at C3, with subsequent elimination of the terminal and subterminal carbons, yielding a fatty acid that is one carbon shorter than the parent alkane. Hxd3 is the only pure culture that is known to carboxylate aliphatic hydrocarbons.
Hydrogen oxidizing bacteria are a group of facultative autotrophs that can use hydrogen as an electron donor.
Sulfurimonas is a bacterial genus within the class of Epsilonproteobacteria, 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 Epsilonproteobacteria, Sulfurimonas has a higher dispersal capability compared with deep sea hydrothermal vent thermophiles, indicating allopatric speciation.
Desulfobulbus propionicus is a Gram-negative, anaerobic chemoorganotroph. Three separate strains have been identified: 1pr3T, 2pr4, and 3pr10. It is also the first pure culture example of successful disproportionation of elemental sulfur to sulfate and sulfide. Desulfobulbus propionicus has the potential to produce free energy and chemical products.
Rhodoferax is a genus of Betaproteobacteria belonging to the purple nonsulfur bacteriarophic. Originally, Rhodoferax species were included in the genus Rhodocyclus as the Rhodocyclus gelatinous-like group. The genus Rhodoferax was first proposed in 1991 to accommodate the taxonomic and phylogenetic discrepancies arising from its inclusion in the genus Rhodocyclus. Rhodoferax currently comprises four described species: R. fermentans, R. antarcticus, R. ferrireducens, and R. saidenbachensis. R. ferrireducens, lacks the typical phototrophic character common to two other Rhodoferax species. This difference has led researchers to propose the creation of a new genus, Albidoferax, to accommodate this divergent species. The genus name was later corrected to Albidiferax. Based on geno- and phenotypical characteristics, A. ferrireducens was reclassified in the genus Rhodoferax in 2014. R. saidenbachensis, a second non-phototrophic species of the genus Rhodoferax was described by Kaden et al. in 2014.
Syntrophococcus sucromutans is a Gram-negative strictly anaerobic chemoorganotrophic Firmicute. These bacteria can be found forming small chains in the habitat where it was first isolated, the rumen of cows. It is the type strain of genus Syntrophococcus and it has an uncommon one-carbon metabolic pathway, forming acetate from formate as a product of sugar oxidation.
Desulfobacter latus is a sulfate-reducing bacteria, with type strain AcRS2.
Desulfobacter curvatus is a sulfate-reducing bacteria, with type strain AcRM3.
Thiosocius is a genus of bacteria that lives in symbiosis with the giant shipworm Kuphus polythalamius. It contains a single species, Thiosocius teredinicola, which was isolated from the gills of the shipworm. The specific name derives from the Latin terms teredo (shipworm) and incola (dweller).