Jump to content

Sulfur-reducing bacteria

From Wikipedia, the free encyclopedia
On the left: Bioconstructions created by sulfur bacteria in a sulfurous cave at a depth of about 30 mt in Santa Cesarea Terme, Lecce, Italy. On the right: The same bioconstructions suspended in water. These structures are extremely fragile, and even a small air bubble emitted by a diver can disperse them in the water.

Sulfur-reducing bacteria are microorganisms able to reduce elemental sulfur (S0) to hydrogen sulfide (H2S).[1] These microbes use inorganic sulfur compounds as electron acceptors to sustain several activities such as respiration, conserving energy and growth, in absence of oxygen.[2] The final product of 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.[3] 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 H
2 as electron donor.[4] 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.[5] Only few taxa are true sulfur-reducing bacteria, using sulfur reduction as the only or main catabolic reaction.[6] 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.[2] 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.

Taxonomy

[edit]

Sulfur reducers are known to cover about 74 genera within the Bacteria domain.[2][7][8][9][10][1] Several types of sulfur-reducing bacteria have been discovered in different habitats like deep and shallow sea hydrothermal vents, freshwater, volcanic acidic hot springs and others.[11] Many sulfur reducers belong to the phylum Thermodesulfobacteriota (Desulfuromonas, Pelobacter, Desulfurella, Geobacter), the class Gammaproteobacteria, and the phylum Campylobacterota[12][13] according to GTDB classification. Other phyla that present sulfur-reducing bacteria are: Bacillota (Desulfitobacterium, Ammonifex, and Carboxydothermus), Aquificota (Desulfurobacterium and Aquifex), Synergistota (Dethiosulfovibrio), Deferribacterota (Geovibrio), Thermodesulfobacteriota, Spirochaetota, and Chrysiogenota.[1][2]

Table 1. Genera of sulfur-reducing bacteria (NCBI classification).[1][2][8][9][10][14]
Phylum Class Genus (74) (and species)
Aquificota Aquificia Aquifex (pyrophilus), Balnearium (lithotrophicum), Desulfurobacterium (crinifex, pacificum, thermolithotrophum),

Persephonella (guaimasensis, marina), Thermocrinis (ruber), Thermosulfidibacter (takaii),

Thermovibrio (ammonificans, guaymasensis, ruber)

Bacteroidota Bacteroidia Petrimonas (sulfuriphila)
Caldisericota Caldisericia Caldisericum (exile)
Calditrichota Calditrichae Caldithrix (abyssi)
Chrysiogenota Chrysiogenetes Desulfurispirillum (alkaliphilum)
Coprothermobacterota Coprothermobacteria Coprothermobacter (proteoliticus)
Deferribacterota Deferribacteres Deferribacter (desulfuricans), Geovibrio (thiophilus)
Deinococcota Deinococci Oceanithermus (desulfurans)
Bacillota Clostridia Ammonifex (degensii), Carboxydothermus (pertinax), Clostridium (thiosulfatireducens, tunisiense, sulfidigenes), Dethiobacter (alkaliphilus),

Desulfitibacter (alkalitolerans), Desulfitispora (alkaliphila), Desulfitobacterium (hafniense, chlororespirans, dehalogenans, metallireducens),

Desulfosporosinus (acididurans, acidiphilus, orientis, meridiei, auripigmenti), Desulfotomaculum (thermosubterraneus, salinum,

geothermicum, reducens, intricatum), Ercella (succinogenes), Halanaerobium (congolense), Halarsenatibacter (silvermanii),

Sporanaerobacter (acetigenes), Thermoanaerobacter (sulfurophilus)

Pseudomonadota Gammaproteobacteria Acidithiobacillus (ferrooxidans), Pseudomonas (mendocina), Shewanella (putrefaciens)
Thermodesulfobacteriota Desulfobacter (postgatei), Desulfobacterium, Desulfobotulus (alkaliphilus), Desulfobulbus (propionicus), Desulfomicrobium (baculatum),

Desulfomonile (tiedjei), Desulfonatronovibrio (thiodismutans), Desulfonatronum (thioautotrophicum), Desulfovermiculus (halophilus),

Desulfovibrio, Desulfurella, Desulfurivibrio (alkaliphilus), Desulfuromonas, Desulfuromusa, Geoalkalibacter (subterraneus), Geobacter,

Hippea (maritima), Pelobacter

Caldimicrobium (exile), Thermodesulfobacterium (geofontis)

Campylobacterota Caminibacter, Hydrogenimonas, Lebetimonas, Nautilia, Nitratiruptor, Sulfurimonas, Sulfurospirillum, Sulfurovum,

Thioreductor (incertae sedis), Wolinella (succinogenes)

Spirochaetota Spirochaetia Spirochaeta (perfilievii, smaragdinae)
Synergistota Synergistia Anaerobaculum (mobile, thermoterrenum), Dethiosulfovibrio (acidaminovorans, marinus, peptidovorans, russensis),

Thermanaerovibrio (acidaminovorans, velox), Thermovirga (lienii),

Thermotogota Thermotogae Fervidobacterium (changbaicum, islandicum, nodosum, riparium, ), Geotoga (petraea, subterranea), Marinitoga (camini, hydrogenitolerans, okinawensis, piezophila),

Mesotoga (infera, prima), Petrotoga (mexicana, miotherma, mobilis), Thermosipho (aficanus), Thermotoga (lettingae, maritima, naphthophila, neapolitana),

Table 2. Genera of sulfur-reducing bacteria (GTDB classification) [2][7][9][10][1]
Phylum Class Genus (74)
Aquificota Aquificia Aquifex, Persephonella, Thermocrinis
Thermodesulfobacteriota Balnearium, Desulfurobacterium, Thermovibrio
Desulfobacteria Desulfobacter, Desulfobacterium, Desulfobotulus
Desulfobulbia Desulfobulbus, Desulfurivibrio
Desulfovibrionia Desulfomicrobium, Desulfonatronovibrio, Desulfonatronum, Desulfovermiculus, Desulfovibrio,
Desulfuromonadia; Desulfuromonas, Desulfuromusa, Geoalkalibacter, Geobacter,

Pelobacter

Desulfomonilia Desulfomonile
Thermodesulfobacteria Caldimicrobium, Thermodesulfobacterium,
Thermosulfidibacteria Thermosulfidibacter
Bacteroidota Bacteroidia Petrimonas
Caldisericota Caldisericia Caldisericum
Calditrichota Calditrichia Caldithrix
Campylobacterota Campylobacteria Caminibacter, Hydrogenimonas, Lebetimonas,

Nautilia, Nitratiruptor, Sulfurimonas, Sulfurospirillum,

Sulfurovum, Wolinella

Desulfurellia Desulfurella, Hippea
Chrysiogenota Chrysiogenetes Desulfurispirillum
Coprothermobacterota Coprothermobacteria Coprothermobacter
Deferribacterota Deferribacteres Deferribacter, Geovibrio
Deinococcota Deinococci Oceanithermus
Bacillota_A Clostridia Clostridium, Sporanaerobacter
Thermoanaerobacteria Thermoanaerobacter
Bacillota_B Desulfitobacteria Desulfitobacterium, Desulfosporosinus
Desulfotomaculia Ammonifex, Carboxydothermus, Desulfotomaculum
Moorellia Desulfitibacter
Bacillota_D Dethiobacteria Dethiobacter
Bacillota_F Halanaerobia Halanaerobium, Halarsenatibacter
Pseudomonadota Gammaproteobacteria Acidithiobacillus, Pseudomonas, Shewanella
Spirochaetota Spirochaetia Sediminispirochaeta
Synergistota Synergistia Anaerobaculum, Dethiosulfovibrio, Thermanaerovibrio,
Thermotogota Thermotogae Fervidobacterium, Geotoga, Marinitoga, Mesotoga, Petrotoga, Thermosipho, Thermotoga
Unclassified (from NCBI) Desulfitispora (alkaliphila), Ercella (succinogenes), Thermovirga, Thioreductor

Metabolism

[edit]

Sulfur reduction metabolism is an ancient process, found in the deep branches of the phylogenetic tree.[15] Sulfur reduction uses elemental sulfur (S0) and generates hydrogen sulfide (H2S) as the main end product. This metabolism is largely present in extreme environments where, especially in recent years, many microorganisms have been isolated, bringing new and important data on the subject.[2]

Many sulfur-reducing bacteria are able to produce ATP through lithotrophic sulfur respiration, using zero-valence sulfur as electron acceptor, for instance the genera Wolinella, Ammonifex, Desulfuromonas and Desulfurobacterium. On the other side, there are obligate fermenters able to reduce elemental sulfur, for example Thermotoga, Thermosipho and Fervidobacterium. Among these fermenters there are species, such as Thermotoga maritina, that are not dependent on sulfur reduction, and utilize it as a supplementary electron sink.[10] Some researches[10][16][17] propose the hypothesis that polysulfide could be an intermediate of sulfur respiration, due to the conversion of elemental sulfur into polysulfide that occurs in sulfide solutions, performing this reaction:

[10]

Pseudomonadota

[edit]

The Pseudomonadota are a  major phylum of gram-negative bacteria. There is a wide range of metabolisms. Most members are facultative or obligately anaerobic, chemoautotrophs and heterotrophs. Many are able to move using flagella, others are nonmotile.[18] They are currently divided into several classes, referred to by Greek letters, based on rRNA sequences: Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, Zetaproteobacteria, etc.[8][19]

Class Gammaproteobacteria

[edit]

The Gammaproteobacteria class include several medically, ecologically and scientifically important groups of bacteria. They are major organisms in diverse marine ecosystems and even extreme environments. This class contains a huge variety of taxonomic and metabolic diversity, including aerobic and anaerobic species, chemolitoauthotrophic, chemoorganotrophic and phototrophic species and also free living, biofilms formers, commensal and symbionts.[20]

Acidithiobacillus spp.
[edit]

Acidithiobacillus are chemolithoautrophics, Gram-negative road-shaped bacteria, using energy from the oxidation of iron and sulfur containing minerals for growth. They are able to live at extremely low pH (pH 1–2) and fixes both carbon and nitrogen from the atmosphere. It solubilizes copper and other metals from rocks and plays an important role in nutrient and metal biogeochemical cycling in acid environments.[21] Acidithiobacillus ferrooxidans is abundant in natural environments associated with pyritic ore bodies, coal deposits, and their acidified drainages. It obtain energy by the oxidation of reduced sulfur compounds and it can also reduce ferric ion and elemental sulfur, thus promoting the recycling of iron and sulfur compounds under anaerobic conditions. It can also fix CO2 and nitrogen and be a primary producer of carbon and nitrogen in acidic environments.[22]

Shewanella spp.
[edit]

Shewanella are Gram-negative, motile bacilli. The first description of the species was provided in 1931, Shewanella putrefaciens, a non-fermentative bacilli with a single polar flagellum which grow well on conventional solid media. This species is pathogenic for humans, even if infections are rare and reported especially in the geographic area characterized by warm climates.[23]

Pseudomonas spp.
[edit]

Pseudomonas are Gram-negative chemoorganotrophic Gammaproteobacteria, straight or slightly curved rod-shaped. They are able to move thanks to one or several polar flagella; rarely nonmotile. Aerobic, having a strictly respiratory type of metabolism with oxygen as the terminal electron acceptor; in some cases, allowing growth anaerobically, nitrate can be used as an alternate electron acceptor. Almost all the species fail to grow under acid conditions (pH 4.5 or lower). Pseudomonas are widely distributed in nature. Some species are pathogenic for humans, animals, or plants.[24] Type species: Pseudomonas mendocina.

Phylum Thermodesulfobacteriota

[edit]

The Thermodesulfobacteriota phylum comprises several morphologically different bacterial groups, Gram-negative, non-sporeforming that exhibit either anaerobic or aerobic growth. They are ubiquitous in marine sediments and contains most of the known sulfur reducing bacteria (e.g. Desulfuromonas spp.). The aerobic representatives are able to digest other bacteria and several of these members are important constituents of the microflora in soil and waters.[25]

Desulfuromusa spp.

[edit]

Desulfuromusa genus includes bacteria obligately anaerobic that use sulfur as an electron acceptor and short-chain fatty acids, dicarboxylic acids, and amino acids, as electron donors that are oxidized completely to CO2. They are gram negative and complete oxidizer bacteria; their cells are motile and slightly curved or rod shaped. Three sulfur reducing species are known, Desulfromusa kysingii, Desulfuromusa bakii and Desulfuromusa succinoxidans.[26]

Desulfurella spp.

[edit]

Desulfurella are short rod-shaped, gram-negative cells, motile thanks to a single polar flagellum or nonmotile, non-sporeforming. Obligately anaerobic, moderate thermophilic, they generally occur in warm sediments and in thermally heated cyanobacterial or bacterial communities that are rich in organic compounds and elemental sulfur. Type species: Desulfurella acetivorans.[27]

Hippea spp.

[edit]

Hippea species are moderate thermophiles neutrophiles to moderate acidophiles, obligate anaerobes sulfur-reducing bacteria with gram-negative rod-shaped cells. They are able to grow lithotrophically with hydrogen and sulfur, and oxidize completely volatile fatty acids, fatty acids and alcohols. They inhabit submarine hot vents. The type species is Hippea maritima.[28]

Desulfuromonas spp.

[edit]

Desulfuromonas species are gram-negative, mesophilic, obligately anaerobic and complete oxidizers [1] sulfur-reducing bacteria. They are able to grow on acetate as sole organic substrate and reduce elemental sulfur or polysulfide to sulfide.[29] Currently known species of the genus Desulfuromonas are Desulfuromonas acetoxidans, Desulfuromonas acetexigens, the marine organism Desulfuromonas palmitates and Desulfuromonas thiophila.

  • Desulfiromonas thiophila is an obligate anaerobic bacteria, that uses sulfur as only electron acceptor. Multiplies by binary fission and cells are motile thanks to polar flagella. They live in anoxic mud of freshwater sulfur springs, at a temperature from 26 to 30 °C and pH 6.9 to 7.9.[30]

Geobacter spp.

[edit]

Geobacter species have a respiratory metabolism with Fe(III) serving as the common terminal electron acceptor in all species.

  • Geobacter sulfurreducens was isolated from a drainage ditch in Norman, Okla. It is rod-shaped, gram-negative, non-motile and non-spore forming. The optimum temperature range is 30 to 35°. About the metabolism, is strict anaerobic chemoorganotroph which oxidizes acetate with Fe(III), S, Co(III), fumarate, or malate as the electron acceptor. Hydrogen is also used as an electron donor for Fe(III) reduction, whereas other carboxylic acids, sugars, alcohols, amino acids, yeast extract, phenol, and benzoate are not. C-type cytochromes was found in cells.[31]

Pelobacter spp.

[edit]

Pelobacter is unique group of fermentative microorganisms belonging to the phylum Thermodesulfobacteriota. They consume fermentatively alcohols such as 2,3-butanediol, acetoin and ethanol, but not sugars, with acetate plus ethanol and/or hydrogen as the end products.[32]

  • Paleobacter carbinolcus, isolated from anoxic mud, it belongs to the family Desulfuromonadaceae. This bacterial species grow by fermentation,  syntrophic hydrogen/formate transfer, or electron transfer to sulfur from short-chain alcohols, hydrogen or formate but they don't oxidize acetate. There is no recent information about sugar fermentation or autotrophic growth. The sequencing analysis of genome demonstrated the expression of c-type cytochromes and the utilization of Fe (III) as a terminal acceptor with the indirect reduction of elemental sulfur that acts as a shuttle for electron transfer to Fe (III). Recent study thought that this electron transfer involves two periplasmic thioredoxins (Pcar_0426, Pcar_0427), an outer membrane protein (Pcar_0428), and a cytoplasmic oxidoreductase (Pcar_0429) encoded by the most highly upregulated genes.[32]

Thermodesulfobacteriota

[edit]

Thermodesulfobacteriota are Gram- negative, rod-shaped cells, occur singly, in pairs, or in chains in young cultures. Do not form spores. Usually nonmotile, but motility might be observed in some species. Thermophilic, strictly anaerobic, chemoheterotrophs.[33]

Phylum Campylobacterota

[edit]

The phylum Campylobacterota presents many sulfur-oxidizing known species, that have been recently recognized as able to reduce elemental sulfur, in some cases also preferring this pathway, coupled with hydrogen oxidation.[34] Here's a list of the species able to reduce elemental sulfur. The mechanism used to reduce sulfur is still unclear for some of these species.[9]

Table 3. Sulfur-reducing bacteria among Epsiloproteobacteria/Campylobacteriota[1][10][9]
Species
From Hydrothermal vents Caminibacter spp. (C. hydrogeniphilus, C. mediatlanticus, C. profundus)
Hydrogenimonas thermophila
Lebetimonas acidiphila
Nautilia spp. (N. abyssi, N. lithotrophica, N. nitratireducens, N. profundicola)
Nitratiruptor tergarcus
Sulfurimonas spp.
Sulfurospirillum sp. Am-N
Sulfurovum sp. NCB37-1
Thioreductor micantisoli
From cattle rumen Wolinella succinogenes

Wolinella

[edit]

Wolinella is a sulfur reducing genus of bacteria and incomplete oxidizer that cannot use acetate as an electron donor.[1] Publicly known is one species, Wolinella succinogenens.[35]

  • Wolinella succinogenens is a well known non-vent sulfur-reducing bacteria, found in cattle rumen, that utilizes a [Ni-fe] hydrogenase to oxidize hydrogen and a single periplasmatic polysulfide reductase (PsrABC) bounded to the inner membrane to reduce elemental sulfur.[10] PsrA is responsible for polysulfide reduction to H2S, at a molybdopterin active site, PsrB is an [FeS] electron transfer protein and PsrC is a quinone-containing membrane anchor.[36]

Sulfurospirillum

[edit]

Sulfurospirillum species are sulfur reducing bacteria and incomplete oxidizer that use either H
2 or formate as electron donor but not acetate.[1]

Sulfurovum

[edit]
  • Sulfurovum sp. NCB37-1 has been given the hypothesis in which a polysulfide reductase (PsrABC) is involved in its sulfur reduction.[9][37]

Sulfurimonas

[edit]

Sulfurimonas species were previously considered to be chemolithoautotrophic sulfur-oxidizing bacteria (SOB), and there were only genetic evidences supporting a possible sulfur-reducing metabolism, but now it has been shown that sulfur reduction also occurs in this genus. The mechanism and the enzymes involved in this process have also been deduced, using Sulfurimonas sp. NW10 as a representative. In particular the presence of both a cytoplasmic and a periplasmic polysulfide reductases has been detected, in order to reduce cyclooctasulfur, which is the most common form of elemental sulfur in vent environments.[9]

  • Sulfurimonas sp. NW10 shows an over-expression of the gene clusters ( and ) coding for the two reductases while reducing sulfur. These clusters were also found in other Sulfurimonas species isolated from hydrothermal vents, meaning that sulfur reduction is common in Sulfurimonas spp.[9]

Further genetic analysis revealed that the polysulfide reductases from Sulfurimonas sp.NW10 share less than 40% sequence similarity with the one from W. succinogenes. This means that through time there has been a significant genetic differentiation between the two bacteria, most likely due to their different environments. Furthermore, the cytoplasmic sulfur-reduction performed by Sulfurimonas sp. NW10 is nowadays considered unique, being the only example among all the mesophilic sulfur-reducing bacteria.[9] Before this discovery, only two hyperthermophilic bacteria were known to be able to do cytoplasmic sulfur-reduction, Aquifex aeolicus[38] and Thermovibrio ammonificans.[36]

Nautilia

[edit]

Nautilia species are anaerobic, neutrophile, thermophilic sulfur-reducing bacteria, first discovered and isolated from a polychaete worm inhabiting deep sea hydrothermal vents, Alvinella pompejana. They are very short, gram-negative, motile and rod-shaped cells with a single polar flagellum.[39] They grow chemolithoautotrophically on molecular hydrogen, elemental sulfur and CO2.[40] The use of sugars, peptides, organic acids or alcohols are not required in either the absence nor presence of sulfur. They rarely use sulfite and colloidal sulfur as electron acceptors. Sulfate, thiosulfate, nitrate, fumarate and ferric iron are not used. Four species have been found: Nautilia lithotrophica, Nautilia profundicola, Nautilia nitratireducens and Nautilia abyssi. The type species is Nautilia lithotrophica.[39]

  • Nautilia abyssi is a gram-negative sulfur-reducing bacterium that lives in anaerobic conditions at hydrothermal vents. It was first discovered living on a chimney at a depth of 2620 meters on the East Pacific Rise. It grows at temperatures between 33° and 65°C, and within a pH range of 5.0–8.0. Under optimal conditions (60°C, pH 6.0–6.5), the generation time is 120 minutes. Like other species in this genus, cells move by means of a single polar flagellum. For metabolism N. abyssi use H
    2     as an electron donor, elemental sulfur as an electron acceptor and CO2 as the carbon source.[41]

Caminibacter

[edit]
  • Caminibacter mediatlanticus was first isolated from a deep-sea hydrothermal vent on the Middle Atlantic Ridge.[42] It is a thermophilic chemolithoautotroph, H
    2    -oxidizing marine bacteria, that uses nitrate or elemental sulfur as electron acceptors, producing ammonia or hydrogen sulfide and it cannot use oxygen, thiosulfate, sulfite, selenate and arsenate. Its growth optimum is at 55 °C, and it seems to be inhibited by acetate, formate, lactate and peptone.[42]

Aquificota

[edit]

Aquificota phylum comprises rod-shaped, motile cells. Includes chemoorganotrophs and some of them are able to reduce elemental sulfur. Growth has been observed between pH 6.0 and 8.0.[43]

Aquifex

[edit]

Aquifex are rod-shaped, Gram-negative, nonsporulating cells with rounded ends. Wedge-shaped refractile areas in the cells are formed during growth. Type species: Aquifex pyrophilus.[43]

Desulfurobacterium

[edit]

Desulfurobacterium are rod-shaped, Gram-negative cells. Type species: Desulfurobacterium thermolithotrophum.[43]

Thermovibrio ammonificans

[edit]

Thermovibrio ammonificans[36] is a gram-negative sulfur reducing bacteria, found in deep sea hydrothermal vent chimney. It is a chemolithoautotroph that grows in the presence of H
2 and CO2, using nitrate or elemental sulfur as electron acceptors with concomitant formation of ammonium or hydrogen sulfide, respectively. Thiosulfate, sulfite and oxygen are not used as electron acceptors. Cells are short rods shape and motile thanks to polar flagellation. Their growth range temperature is from 60 °C to 80 °C and pH 5–7.[44]

Thermosulfidibacter spp.

[edit]

Thermosulfidibacter are gram-negative, anaerobic, thermophilic and neutrophilic bacteria. Strictly chemolithoautotrophic. The type species is Thermosulfidibacter takaii.

  • Thermosulfidibacter takaii are motile rods with a polar flagellum. Strictly anaerobic. Growth occurs at 55–78 °C (optimum, 70 °C), pH 5.0–7.5 (optimum, pH 5.5–6.0). They are sulfur-reducers.[45]

Bacillota

[edit]

Bacillota are mostly Gram-positive bacteria with some Gram-negative exceptions.[46]

Ammonifex

[edit]

These bacteria are Gram-negative, extremely thermophilic, strictly anaerobic, faculatative chemolithoautotrophic. Type species: Ammonifex degensii.[47][48]

Carboxydothermus

[edit]
  • Carboxydothermus pertinax differs from other members of his genus by its ability to grow chemolithoautotrophically with reduction of elemental sulfur or thiosulfate coupled to CO oxidation. The other electron acceptor is ferric citrate, amorphous iron (III) oxide, 9,10-anthraquinone 2,6-disulfonate. Hydrogen is used as energy source and CO2 as carbon source. Cells are rod-shaped with peritrichous flagella and grow at 65 °C temperature.[49]

Chrysiogenota

[edit]

Chrysiogenota are Gram-negative bacteria, motile thanks to a single polar flagellum, curved, rod-shaped cells. They are mesophilic, exhibiting anaerobic respiration in which arsenate serves as the electron acceptor. Strictly anaerobic, these bacteria are grown at 25–30 °C.[50]

Desulfurispirillum spp.

[edit]

Desulfurispirillum species are gram-negative, motile spirilla, obligately anaerobic with respiratory metabolism. Use elemental sulfur and nitrate as electron acceptors, and short-chain fatty acids and hydrogen as electron donors. Alkaliphilic and slightly halophilic.[51]

  • Desulfurispirillum alkaliphilum[51] is obligate anaerobic and heterotrophic bacteria, motile by single bipolar flagella. It uses elemental sulfur, polysulfide, nitrate and fumarate as electron acceptors. The final products are sulfide and ammonium. Utilizes short-chain fatty acids and H2 as electron donor and carbon as source. It is moderate alkaliphilic with a pH range for growth between 8.0 and 10.2 and an optimum at pH 9.0 and slightly halophilic with a salt range from 0.1 to 2.5 M Na+. Mesophilic with a maximum temperature for growth at 45 and an optimum at 35 °C.[51]

Spirochaetota

[edit]

Spirochaetes are free-living, gram-negative, helical-shaped and motile bacteria, often protist or animal-associated. They are obligate and facultative anaerobes.[52] Among this phylum, two species are recognized as sulfur-reducing bacteria, Spirochaeta perfilievii and Spirochaeta smaragdinae.

  • Spirochaeta perfilievii are gram-negative, helical bacteria. Their size range varies from 10 to 200 μm. The shortest cells are those grown in extremely anaerobic environments. They are mesophilic with a temperature range 4–32 °C (optimum at 28–30 °C). Grows at pH 6.5–8.5 (optimum pH 7.0–7.5). Obligate, moderate halophile. Under anaerobic conditions, sulfur and thiosulfate are reduced to sulfide.[53]
  • Spirochaeta smaragdinae are gram-negative, chemoorganotrophic, obligately anaerobic and halophilic bacteria. They are able to reduce sulfur to sulfide. Their temperature range is from 20 to 40 °C (optimum 37 °C), their pH range varies from 5.5 to 8.0 (optimum 7.0).[54]

Synergistota

[edit]

Dethiosulfovibrio spp.

[edit]

Dethiosulfovibrio are a gram negative sulfur reducing bacteria that was isolated from "Thiodendron", bacterial sulfur mats obtained from different saline environments. Cells are curved or fibroid-like rods and motile thanks to flagella located on the concave side of the cells. The temperature range is from 15° to 40 °C and at pH values between 5±5 and 8±0. About their metabolism, they ferments proteins, peptides, some organic acids and amino acids like serine, histidine, lysine, arginine, cysteine and threonine. Only in the presence of sulfur or thiosulfate can use alanine, glutamate, isoleucine, leucine and valine, moreover the presence of sulfur or thiosulfate increases the cell yield and the growth rate. They are obligately anaerobic and slightly halophilic. In the presence of fermentable substrates they are able to reduce elemental sulfur and thiosulfate but not sulfate or sulfite to sulfide. Growth did not occur with H
2 as electron donor and carbon dioxide or acetate as carbon sources in the presence of thiosulfate or elemental sulfur as electron acceptor. Unable to utilize carbohydrates, alcohols and some organic acids like acetate or succinate. Four species were found, Dethiosulfovibrio russensis, Dethiosulfovibrio marinus, Dethiosulfovibrio peptidovorans and Dethiosulfovibrio acidaminovorans.[55]

Thermanaerovibrio spp.

[edit]

Thermophilic and neutrophilic Gram-negative bacteria. Motile thanks to lateral flagella, located on the concave side of the cell. Non-spore-forming. Multiplication occurs by binary fission. Strictly anaerobic with chemo-organotrophic growth on fermentable substrates or lithoheterotrophic growth with molecular hydrogen and elemental sulfur, reducing the sulfur to H2S. Inhabits the granular methanogenic sludge and neutral hot springs. The type species is Thermanaerovibrio acidaminovorans.[56]

  • Thermanaerovibrio velox is gram-negative bacteria that was isolated from a thermophilic cyanobacterial mat from caldera Uzon, Kamchatka, Russia. The reproduction occurs by binary-fission and they do not form spore. Growth temperature goes from 45° to 70°, and pH range from 4 to 8.[56]

Thermotogota

[edit]

Thermotoga spp. are gram-negative, rod-shaped, non-spore forming, hyperthermophilic microorganisms, given their name by the presence of a sheathlike envelope called “toga”. They are strictly anaerobes and fermenters, catabolizing sugars or starch and producing lactate, acetate, CO2, and H
2 as products,[1] and can grow in a range temperature of 48–90 °C.[57] High levels of H
2 inhibit their growth, and they share many genetic similarities with Archaea, caused by horizontal gene transfer[58] They are also able to perform anaerobic respiration using H
2 as electron donor and usually Fe(III) as electron acceptor. Species belonging to the genus Thermotoga were found in terrestrial hot springs and marine hydrothermal vents. The species able to reduce sulfur do not show an alteration of growth yield and stoichiometry of organic products, and no ATP production occurs. Furthermore, toleration to H
2 increases during sulfur reduction, thus they produce H2S to overcome growth inhibition.[14] The genome of Thermotoga spp. is widely used as a model for studying adaptation to high temperatures, microbial evolution and biotechnological opportunities, such as biohydrogen production and biocatalysis.[59]

  • Thermotoga maritima is the type species for the genus Thermotoga, growth is observed between 55 °C and 90 °C, the optimum is at 80 °C. Each cell presents a unique sheath- like structure and monotrichous flagellum. It was firstly isolated from a geothermally heated, shallow marine sediment at Vulcano, in Italy.[60]
  • Thermotoga neapolitana is the second species isolated belonging to the genus Thermotoga. It was firstly found in a submarine thermal vent at Lucrino, near Naples, Italy, and has its optimum growth at 77 °C[61][62]

Ecology

[edit]

Sulfur-reducing bacteria are mostly mesophilic and thermophilic.[10] Growth has been observed between a temperature range 37-95 °C, however the optimum is different depending on the species (i.e. Thermotoga neapolitana optimum 77 °C, Nautilia lithotrophica optimum 53 °C).[61][39][62] They have been reported in many different environments, such as anoxic marine sediments, brackish and freshwater sediments, anoxic muds, bovine rumen, hot waters from solfataras and volcanic areas.[10] Many of these bacteria are found in hot vents, where elemental sulfur is an abundant sulfur species. This happens due to volcanic activities, in which hot vapours and elemental sulfur are released together through the fractures of Earth's crust.[63] The ability of using zero valence sulfur as both an electron donor or acceptor, allows Sulfurimonas spp. to spread widely among different habitats, from highly reducing to more oxidizing deep-sea environments.[9] In some communities found in hydrothermal vents, their proliferation is enhanced thanks to the reactions carried out by thermophilic photo- or chemoautotrophs, in which there is simultaneously production of elemental sulfur and organic matter, respectively electron acceptor and energy source for sulfur-reducing bacteria.[63] Sulfur reducers of hydrothermal vents can be free-living organisms, or endosymbionts of animals such as shrimps and tube worms.[41]

Symbiosis

[edit]

Thiodendron latens is a symbiotic association of aerotolerant spirochaetes and anaerobic sulfidogenes. The spirochaete species are the main structural and functional component of these mats and they may accumulate elemental sulfur in the intracellular space. This association of micro-organisms inhabits sulfide-rich habitats, where the chemical oxidation of sulfide by oxygen, manganese or ferric iron or by the activity of sulfide-oxidizing bacteria results in the formation of thiosulfate or elemental sulfur. The partly oxidized sulfur compounds can be either completely oxidized to sulfate by sulfur-oxidizing bacteria, if enough oxygen is present, or reduced to sulfide by sulfidogenic bacteria. In such places oxygen limitation is frequent, as indicated by micro-profile measurements from such habitats. This relationship may represent an effective shortcut in the sulfur cycle.[55]

Synthophy

[edit]

Desulfuromonas acetooxidans is able to grow in cocultures with green sulfur bacteria such as Chlorobium (vibrioforme and phaeovibroides). The electron donor for the sulfur-reducing bacterium is acetate, coupled with elemental sulfur reduction to sulfide. The green sulfur bacterium produces H
2 re-oxidizing the H2S previously produced, in presence of light. During these cocultures experiments no elemental sulfur appears in the medium because it is immediately reduced.[64]

Sulfur cycle

[edit]

The sulfur cycle is one of the major biogeochemical processes.[65] The majority of sulfur on Earth is present in sediments and rocks, but its quantity in the oceans represents the primary reservoir of sulfate of the entire biosphere. Human activities such as burning fossil fuels, also contribute to the cycle by entering a significant amount of sulfur dioxide in the atmosphere.[66] The earliest life forms on Earth were sustained by sulfur metabolism, and the enormous diversity of present microorganisms is still supported by the sulfur cycle.[66] It also interacts with numerous biogeochemical cycles of other elements such as carbon, oxygen, nitrogen and iron.[67][66] Sulfur has diverse oxidation states ranging from +6 to −2, which permit to sulfur compounds to be used as electron donors and electron acceptors in numerous microbial metabolisms, which transform organic and inorganic sulfur compounds, contributing to physical, biological and chemical components of the biosphere.[2][67]

The sulfur cycle follows several linked pathways.

Sulfate Reduction

The sulfur cycle

Under anaerobic conditions, sulfate is reduced to sulfide by sulfate reducing bacteria, such as Desulfovibrio and Desulfobacter.

SO2−4 + 4H2 → H2S + 2H2O + 2OH−

Sulfide Oxidation

Under aerobic conditions, sulfide is oxidized to sulfur and then sulfate by sulfur oxidizing bacteria, such as Thiobacillus, Beggiatoa and many others. Under anaerobic conditions, sulfide can be oxidized to sulfur and then sulfate by Purple and Green sulfur bacteria.

H2S → S0 → SO2−4

Sulfur Oxidation

Sulfur can also be oxidized to sulfuric acid by chemolithotrophic bacteria, such as Thiobacillus and Acidithiobacillus

S0 + 2O2 → H2SO4

Sulfur Reduction

Some bacteria are capable to reduce sulfur to sulfide enacting a sort of anaerobic respiration. This process can be carried out by both sulfate reducing bacteria and sulfur reducing bacteria. Although they thrive in the same habitats, sulfur reducing bacteria are incapable of sulfate reduction. Bacteria like Desulfuromonas acetoxidans are able to reduce sulfur at the cost of acetate. Some iron reducing bacteria reduce sulfur to generate ATP.[68]

S0 + H2 → H2S

These are the main inorganic processes involved in the sulfur cycle but organic compounds can contribute as well to the cycle. The most abundant in nature is dimethyl sulfide (CH3−S−CH3) produced by the degradation of dimethylsulfoniopropionate. Many other organic S compounds affect the global sulfur cycle, including methanethiol, dimethyl disulfide, and carbon disulfide.[66]

Uses

[edit]

Microorganisms that have sulfur-based metabolism represent a great opportunity for industrial processes, in particular the ones that execute sulfidogenesis (production of sulfide). For example, these type of bacteria can be used in to generate hydrogen sulfide in order to obtain the selective precipitation and recovery of heavy metals in metallurgical and mining industries.[2]

Flue gases treatment

[edit]

According to innovative Chinese research, the SCDD process used to desulfurize flue gases can be lowered in costs and environmental impact, using biological reduction of elemental sulfur to H2S, which represents the reducing agent in this process. The electron donors would be organics from wastewater, such as acetate and glucose. The SCDD process revisited in this way would take three steps at determinate conditions of pH, temperature and reagents concentration. The first in which biological sulfur reduction occurs, the second through which dissolved H2S in wastewaters is stripped into hydrogen sulfide gas, and the third consists in the treatment of flue gases, removing over 90% of SO2 and NO, according to this study. Furthermore, the 88% of the sulfur input would be recovered as octasulfur and then reutilized, representing both a chemical-saving and a profitable solution.[69]

Treatment of arsenic-contaminated waters

[edit]

Sulfur reducing bacteria are used to remove Arsenite from the arsenic-contaminated waters, like acid mine drainage (AMD), metallurgy industry effluents, soils, surface and ground waters. The sulfidogenic process driven by sulfur reducing bacteria (Desulfurella) take place under acid condition and produce sulfide with which arsenite precipitates. Microbial sulfur reduction also produces protons that lower the pH in arsenic-contaminated water and prevent the formation of thioarsenite by-production with sulfide.[70]

[70]

Treatment of mercury-contaminated waters

[edit]

Wastewater deriving from industries that work on chloralkali and battery production, contains high levels of mercury ions, threatening aquatic ecosystems.[71] Recent studies demonstrate that sulfidogenic process by sulfur reducing bacteria can be a good technology in the treatment of mercury-contaminate waters.[72]

References

[edit]
  1. ^ a b c d e f g h i j Madigan MT, Martinko JM, Bender KS, Buckley DH, Stahl DA (2014). Brock Biology of Microorganisms. Benjamin-Cummings Pub Co. pp. 448–449. ISBN 978-0321897398.
  2. ^ a b c d e f g h i Florentino AP, Weijma J, Stams AJ, Sánchez-Andrea I (2016). "Ecophysiology and Application of Acidophilic Sulfur-Reducing Microorganisms". In Rampelotto PH (ed.). Biotechnology of Extremophiles. Grand Challenges in Biology and Biotechnology. Vol. 1. Cham: Springer International Publishing. pp. 141–175. doi:10.1007/978-3-319-13521-2_5. ISBN 978-3-319-13521-2.
  3. ^ Rabus R, Hansen TA, Widdel F (2006). "Dissimilatory Sulfate- and Sulfur-Reducing Prokaryotes". In Dworkin M, Falkow S, Rosenberg E, Schleifer KH, Stackebrandt E (eds.). The Prokaryotes. New York, NY: Springer New York. pp. 659–768. doi:10.1007/0-387-30742-7_22. ISBN 978-0-387-25492-0.
  4. ^ Parker CT, Taylor D, Garrity GM (2003-01-01). Parker CT, Garrity GM (eds.). "Exemplar Abstract for Chlorobium vibrioforme Pelsh 1936 (Approved Lists 1980) and Prosthecochloris vibrioformis (Pelsh 1936) Imhoff 2003". The NamesforLife Abstracts. doi:10.1601/ex.789 (inactive 1 November 2024).{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  5. ^ Pfennig N, Biebl H (October 1976). "Desulfuromonas acetoxidans gen. nov. and sp. nov., a new anaerobic, sulfur-reducing, acetate-oxidizing bacterium". Archives of Microbiology. 110 (1): 3–12. doi:10.1007/BF00416962. PMID 1015937. S2CID 9330789.
  6. ^ Stetter KO, Zillig W (1985-01-01). Woese CR, Wolfe RS (eds.). Chapter 2: Thermoplasma and the Thermophilic Sulfur-Dependent Archaebacteria. Academic Press. pp. 85–170. doi:10.1016/b978-0-12-307208-5.50008-8. ISBN 978-0-12-307208-5. {{cite book}}: |work= ignored (help)
  7. ^ a b "GTDB – Tree". gtdb.ecogenomic.org. Retrieved 2020-12-11.
  8. ^ a b c "Home – Taxonomy – NCBI". www.ncbi.nlm.nih.gov. Retrieved 2020-12-11.
  9. ^ a b c d e f g h i j Wang S, Jiang L, Hu Q, Liu X, Yang S, Shao Z (September 2020). "Elemental sulfur reduction by a deep-sea hydrothermal vent Campylobacterium Sulfurimonas sp. NW10". Environmental Microbiology. 23 (2): 965–979. doi:10.1111/1462-2920.15247. PMID 32974951. S2CID 221917122.
  10. ^ a b c d e f g h i j Hedderich R, Klimmek O, Kröger A, Dirmeier R, Keller M, Stetter KO (1998-12-01). "Anaerobic respiration with elemental sulfur and with disulfides". FEMS Microbiology Reviews. 22 (5): 353–381. doi:10.1111/j.1574-6976.1998.tb00376.x. ISSN 1574-6976.
  11. ^ Munn CB (2011). Marine microbiology : ecology and applications (2nd ed.). New York: Garland Science. ISBN 978-0-8153-6517-4. OCLC 671701780.
  12. ^ Waite DW, Vanwonterghem I, Rinke C, Parks DH, Zhang Y, Takai K, et al. (2017). "Epsilonproteobacteria and Proposed Reclassification to Epsilonbacteraeota (phyl. nov.)". Frontiers in Microbiology. 8: 682. doi:10.3389/fmicb.2017.00682. PMC 5401914. PMID 28484436.
  13. ^ Waite DW, Vanwonterghem I, Rinke C, Parks DH, Zhang Y, Takai K, et al. (2018). "Epsilonproteobacteria and Proposed Reclassification to Epsilonbacteraeota (phyl. nov.)". Frontiers in Microbiology. 9: 772. doi:10.3389/fmicb.2018.00772. PMC 5915535. PMID 29720974.
  14. ^ a b Janssen PH, Morgan HW (September 1992). "Heterotrophic sulfur reduction by Thermotoga sp. strain FjSS3.B1". FEMS Microbiology Letters. 75 (2–3): 213–7. doi:10.1111/j.1574-6968.1992.tb05419.x. PMID 1398039.
  15. ^ Loka Bharathi PA (2008). "Sulfur Cycle". Encyclopedia of Ecology. Elsevier. pp. 3424–3431. doi:10.1016/b978-008045405-4.00761-8. ISBN 978-0-08-045405-4.
  16. ^ Schauder R, Müller E (1993-11-01). "Polysulfide as a possible substrate for sulfur-reducing bacteria". Archives of Microbiology. 160 (5): 377–382. doi:10.1007/BF00252224. ISSN 1432-072X. S2CID 25603061.
  17. ^ Zöphel A, Kennedy MC, Beinert H, Kroneck PM (February 1991). "Investigations on microbial sulfur respiration. Isolation, purification, and characterization of cellular components from Spirillum 5175". European Journal of Biochemistry. 195 (3): 849–56. doi:10.1111/j.1432-1033.1991.tb15774.x. PMID 1847872.
  18. ^ "Proteobacteria | Boundless Microbiology". courses.lumenlearning.com. Retrieved 2020-12-04.
  19. ^ Stackebrandt E, Murray RG, Trüper HG (1988). "Proteobacteria classis nov., a Name for the Phylogenetic Taxon That Includes the "Purple Bacteria and Their Relatives"". International Journal of Systematic and Evolutionary Microbiology. 38 (3): 321–325. doi:10.1099/00207713-38-3-321. ISSN 1466-5026.
  20. ^ Williams KP, Gillespie JJ, Sobral BW, Nordberg EK, Snyder EE, Shallom JM, Dickerman AW (May 2010). "Phylogeny of gammaproteobacteria". Journal of Bacteriology. 192 (9): 2305–14. doi:10.1128/JB.01480-09. PMC 2863478. PMID 20207755.
  21. ^ Zhan Y, Yang M, Zhang S, Zhao D, Duan J, Wang W, Yan L (March 2019). "Iron and sulfur oxidation pathways of Acidithiobacillus ferrooxidans". World Journal of Microbiology & Biotechnology. 35 (4): 60. doi:10.1007/s11274-019-2632-y. PMID 30919119. S2CID 85544603.
  22. ^ Valdés J, Pedroso I, Quatrini R, Dodson RJ, Tettelin H, Blake R, et al. (December 2008). "Acidithiobacillus ferrooxidans metabolism: from genome sequence to industrial applications". BMC Genomics. 9 (1): 597. doi:10.1186/1471-2164-9-597. PMC 2621215. PMID 19077236.
  23. ^ Holt HM, Gahrn-Hansen B, Bruun B (May 2005). "Shewanella algae and Shewanella putrefaciens: clinical and microbiological characteristics". Clinical Microbiology and Infection. 11 (5): 347–52. doi:10.1111/j.1469-0691.2005.01108.x. PMID 15819859.
  24. ^ Palleroni NJ (2015). "Pseudomonas". In Trujillo ME, Dedysh S, DeVos P, Hedlund B, Kämpfer P, Rainey FA, Whitman WB (eds.). Bergey's Manual of Systematics of Archaea and Bacteria. American Cancer Society. p. 1. doi:10.1002/9781118960608.gbm01210. ISBN 978-1-118-96060-8.
  25. ^ Garrity GM, Holt JG (2015-04-17). Trujillo ME, Dedysh S, DeVos P, Hedlund B, Kämpfer P, Rainey FA, Whitman WB (eds.). Bergey's Manual of Systematics of Archaea and Bacteria. Wiley. doi:10.1002/9781118960608. ISBN 978-1-118-96060-8.
  26. ^ Liesack W, Finster K (1994). "Phylogenetic Analysis of Five Strains of Gram-Negative, Obligately Anaerobic, Sulfur-Reducing Bacteria and Description of Desulfuromusa gen. nov., Including Desulfuromusa kysingii sp. nov., Desulfuromusa bakii sp. nov., and Desulfuromusa succinoxidans sp. nov". International Journal of Systematic Bacteriology. 44 (4): 753–758. doi:10.1099/00207713-44-4-753.
  27. ^ Rainey FA, Hollen B (2015). "Desulfurella". Desulfurella. American Cancer Society. pp. 1–4. doi:10.1002/9781118960608.gbm01037. ISBN 978-1-118-96060-8. {{cite book}}: |work= ignored (help)
  28. ^ Miroshnichenko ML, Rainey FA, Rhode M, Bonch-Osmolovskaya EA (July 1999). "Hippea maritima gen. nov., sp. nov., a new genus of thermophilic, sulfur-reducing bacterium from submarine hot vents". International Journal of Systematic Bacteriology. 49 Pt 3 (3): 1033–8. doi:10.1099/00207713-49-3-1033. PMID 10425760.
  29. ^ Finster K, Bak F, Pfennig N (1994-04-01). "Desulfuromonas acetexigens sp. nov., a dissimilatory sulfur-reducing eubacterium from anoxic freshwater sediments". Archives of Microbiology. 161 (4): 328–33 2. doi:10.1007/BF00303588. ISSN 1432-072X. S2CID 24380675.
  30. ^ Finster K, Coates JD, Liesack W, Pfennig N (July 1997). "Desulfuromonas thiophila sp. nov., a new obligately sulfur-reducing bacterium from anoxic freshwater sediment". International Journal of Systematic Bacteriology. 47 (3): 754–8. doi:10.1099/00207713-47-3-754. PMID 9226908.
  31. ^ Caccavo F, Lonergan DJ, Lovley DR, Davis M, Stolz JF, McInerney MJ (October 1994). "Geobacter sulfurreducens sp. nov., a hydrogen- and acetate-oxidizing dissimilatory metal-reducing microorganism". Applied and Environmental Microbiology. 60 (10): 3752–9. Bibcode:1994ApEnM..60.3752C. doi:10.1128/AEM.60.10.3752-3759.1994. PMC 201883. PMID 7527204.
  32. ^ a b Aklujkar M, Haveman SA, DiDonato R, Chertkov O, Han CS, Land ML, et al. (December 2012). "The genome of Pelobacter carbinolicus reveals surprising metabolic capabilities and physiological features". BMC Genomics. 13: 690. doi:10.1186/1471-2164-13-690. PMC 3543383. PMID 23227809.
  33. ^ Garrity GM, Holt JG, Hatchikian EC, Ollivier B, Garcia JL (2001). "Phylum BIII. Thermodesulfobacteria phy. Nov.". In Boone DR, Castenholz RW, Garrity GM (eds.). Bergey's Manual® of Systematic Bacteriology. New York, NY: Springer. pp. 389–393. doi:10.1007/978-0-387-21609-6_20. ISBN 978-0-387-21609-6. {{cite book}}: |work= ignored (help)
  34. ^ Sievert SM, Vetriani C (2012). "Chemoautotrophy at Deep-Sea Vents: Past, Present, and Future". Oceanography. 25 (1): 218–233. doi:10.5670/oceanog.2012.21. hdl:1912/5172. ISSN 1042-8275. JSTOR 24861161.
  35. ^ Wolin MJ, Wolin EA, Jacobs NJ (June 1961). "Cytochrome-producing anaerobic Vibrio succinogenes, sp. n". Journal of Bacteriology. 81 (6): 911–7. doi:10.1128/JB.81.6.911-917.1961. PMC 314759. PMID 13786398.
  36. ^ a b c Jelen B, Giovannelli D, Falkowski PG, Vetriani C (June 2018). "Elemental sulfur reduction in the deep-sea vent thermophile, Thermovibrio ammonificans". Environmental Microbiology. 20 (6): 2301–2316. doi:10.1111/1462-2920.14280. PMID 29799164. S2CID 44134055.
  37. ^ Yamamoto M, Nakagawa S, Shimamura S, Takai K, Horikoshi K (May 2010). "Molecular characterization of inorganic sulfur-compound metabolism in the deep-sea epsilonproteobacterium Sulfurovum sp. NBC37-1". Environmental Microbiology. 12 (5): 1144–53. doi:10.1111/j.1462-2920.2010.02155.x. PMID 20132283.
  38. ^ Guiral M, Tron P, Aubert C, Gloter A, Iobbi-Nivol C, Giudici-Orticoni MT (December 2005). "A membrane-bound multienzyme, hydrogen-oxidizing, and sulfur-reducing complex from the hyperthermophilic bacterium Aquifex aeolicus". The Journal of Biological Chemistry. 280 (51): 42004–15. doi:10.1074/jbc.M508034200. PMID 16236714. S2CID 21987444.
  39. ^ a b c Miroshnichenko ML, Kostrikina NA, L'Haridon S, Jeanthon C, Hippe H, Stackebrandt E, Bonch-Osmolovskaya EA (July 2002). "Nautilia lithotrophica gen. nov., sp. nov., a thermophilic sulfur-reducing epsilon-proteobacterium isolated from a deep-sea hydrothermal vent". International Journal of Systematic and Evolutionary Microbiology. 52 (Pt 4): 1299–1304. doi:10.1099/00207713-52-4-1299. PMID 12148643.
  40. ^ Smith JL, Campbell BJ, Hanson TE, Zhang CL, Cary SC (July 2008). "Nautilia profundicola sp. nov., a thermophilic, sulfur-reducing epsilonproteobacterium from deep-sea hydrothermal vents". International Journal of Systematic and Evolutionary Microbiology. 58 (Pt 7): 1598–602. doi:10.1099/ijs.0.65435-0. PMID 18599701. S2CID 12751566.
  41. ^ a b Alain K, Callac N, Guégan M, Lesongeur F, Crassous P, Cambon-Bonavita MA, et al. (June 2009). "Nautilia abyssi sp. nov., a thermophilic, chemolithoautotrophic, sulfur-reducing bacterium isolated from an East Pacific Rise hydrothermal vent" (PDF). International Journal of Systematic and Evolutionary Microbiology. 59 (Pt 6): 1310–5. doi:10.1099/ijs.0.005454-0. PMID 19502307. S2CID 39110522.
  42. ^ a b Voordeckers JW, Starovoytov V, Vetriani C (March 2005). "Caminibacter mediatlanticus sp. nov., a thermophilic, chemolithoautotrophic, nitrate-ammonifying bacterium isolated from a deep-sea hydrothermal vent on the Mid-Atlantic Ridge". International Journal of Systematic and Evolutionary Microbiology. 55 (Pt 2): 773–779. doi:10.1099/ijs.0.63430-0. PMID 15774661.
  43. ^ a b c Garrity GM, Holt JG, Castenholz RW, Pierson BK, Keppen OI, Gorlenko WM (2001). "Phylum BVI. Chloroflexi phy. Nov.". Bergey's Manual® of Systematic Bacteriology. New York, NY: Springer New York. pp. 427–446. doi:10.1007/978-0-387-21609-6_23. ISBN 978-1-4419-3159-7. {{cite book}}: |work= ignored (help)
  44. ^ Vetriani C, Speck MD, Ellor SV, Lutz RA, Starovoytov V (January 2004). "Thermovibrio ammonificans sp. nov., a thermophilic, chemolithotrophic, nitrate-ammonifying bacterium from deep-sea hydrothermal vents". International Journal of Systematic and Evolutionary Microbiology. 54 (Pt 1): 175–181. doi:10.1099/ijs.0.02781-0. PMID 14742477.
  45. ^ Nunoura T, Oida H, Miyazaki M, Suzuki Y (March 2008). "Thermosulfidibacter takaii gen. nov., sp. nov., a thermophilic, hydrogen-oxidizing, sulfur-reducing chemolithoautotroph isolated from a deep-sea hydrothermal field in the Southern Okinawa Trough". International Journal of Systematic and Evolutionary Microbiology. 58 (Pt 3): 659–65. doi:10.1099/ijs.0.65349-0. PMID 18319474.
  46. ^ Schleifer KH (2009). "Phylum XIII. Firmicutes Gibbons and Murray 1978, 5 (Firmacutes [sic] Gibbons and Murray 1978, 5)". In De Vos P, Garrity GM, Jones D, Krieg NR (eds.). Systematic Bacteriology. New York, NY: Springer. pp. 19–1317. doi:10.1007/978-0-387-68489-5_3. ISBN 978-0-387-68489-5. {{cite book}}: |work= ignored (help)
  47. ^ Huber R (2015). "Ammonifex". Bergey's Manual of Systematics of Archaea and Bacteria. American Cancer Society. pp. 1–4. doi:10.1002/9781118960608.gbm00744. ISBN 978-1-118-96060-8.
  48. ^ Huber R, Rossnagel P, Woese CR, Rachel R, Langworthy TA, Stetter KO (March 1996). "Formation of ammonium from nitrate during chemolithoautotrophic growth of the extremely thermophilic bacterium ammonifex degensii gen. nov. sp. nov". Systematic and Applied Microbiology. 19 (1): 40–9. doi:10.1016/S0723-2020(96)80007-5. PMID 11539844.
  49. ^ Yoneda Y, Yoshida T, Kawaichi S, Daifuku T, Takabe K, Sako Y (July 2012). "Carboxydothermus pertinax sp. nov., a thermophilic, hydrogenogenic, Fe(III)-reducing, sulfur-reducing carboxydotrophic bacterium from an acidic hot spring". International Journal of Systematic and Evolutionary Microbiology. 62 (Pt 7): 1692–1697. doi:10.1099/ijs.0.031583-0. PMID 21908679.
  50. ^ Garrity GM, Holt JG, Macy JM, Krafft T, Sly LI (2001). "Phylum BV. Chrysiogenetes phy. Nov.". In Boone DR, Castenholz RW, Garrity GM (eds.). Bergey's Manual® of Systematic Bacteriology. New York, NY: Springer. pp. 421–425. doi:10.1007/978-0-387-21609-6_22. ISBN 978-0-387-21609-6.
  51. ^ a b c Sorokin DY, Foti M, Tindall BJ, Muyzer G (March 2007). "Desulfurispirillum alkaliphilum gen. nov. sp. nov., a novel obligately anaerobic sulfur- and dissimilatory nitrate-reducing bacterium from a full-scale sulfide-removing bioreactor". Extremophiles. 11 (2): 363–70. doi:10.1007/s00792-006-0048-8. PMID 17242870. S2CID 20745693.
  52. ^ Olsen I, Paster B, Dewhirst FE (2000-02-01). "Taxonomy of spirochetes". Anaerobe. 6 (1): 39–57. doi:10.1006/anae.1999.0319. ISSN 1075-9964.
  53. ^ Dubinina G, Grabovich M, Leshcheva N, Rainey FA, Gavrish E (January 2011). "Spirochaeta perfilievii sp. nov., an oxygen-tolerant, sulfide-oxidizing, sulfur- and thiosulfate-reducing spirochaete isolated from a saline spring". International Journal of Systematic and Evolutionary Microbiology. 61 (Pt 1): 110–117. doi:10.1099/ijs.0.018333-0. PMID 20173011.
  54. ^ Magot M, Fardeau ML, Arnauld O, Lanau C, Ollivier B, Thomas P, Patel BK (October 1997). "Spirochaeta smaragdinae sp. nov., a new mesophilic strictly anaerobic spirochete from an oil field". FEMS Microbiology Letters. 155 (2): 185–91. doi:10.1111/j.1574-6968.1997.tb13876.x. PMID 9351200.
  55. ^ a b Surkov AV, Dubinina GA, Lysenko AM, Glöckner FO, Kuever J (March 2001). "Dethiosulfovibrio russensis sp. nov., Dethosulfovibrio marinus sp. nov. and Dethosulfovibrio acidaminovorans sp. nov., novel anaerobic, thiosulfate- and sulfur-reducing bacteria isolated from 'Thiodendron' sulfur mats in different saline environments". International Journal of Systematic and Evolutionary Microbiology. 51 (Pt 2): 327–37. doi:10.1099/00207713-51-2-327. PMID 11321077.
  56. ^ a b Zavarzina DG, Zhilina TN, Tourova TP, Kuznetsov BB, Kostrikina NA, Bonch-Osmolovskaya EA (May 2000). "Thermanaerovibrio velox sp. nov., a new anaerobic, thermophilic, organotrophic bacterium that reduces elemental sulfur, and emended description of the genus Thermanaerovibrio". International Journal of Systematic and Evolutionary Microbiology. 50 Pt 3 (3): 1287–1295. doi:10.1099/00207713-50-3-1287. PMID 10843074.
  57. ^ Huber R, Hannig M (2006). "Thermotogales". In Dworkin M, Falkow S, Rosenberg E, Schleifer KH (eds.). The Prokaryotes: Volume 7: Proteobacteria: Delta, Epsilon Subclass. New York, NY: Springer. pp. 899–922. doi:10.1007/0-387-30747-8_38. ISBN 978-0-387-30747-3.
  58. ^ Nelson KE, Clayton RA, Gill SR, Gwinn ML, Dodson RJ, Haft DH, et al. (May 1999). "Evidence for lateral gene transfer between Archaea and bacteria from genome sequence of Thermotoga maritima". Nature. 399 (6734): 323–9. Bibcode:1999Natur.399..323N. doi:10.1038/20601. PMID 10360571. S2CID 4420157.
  59. ^ Frock AD, Notey JS, Kelly RM (September 2010). "The genus Thermotoga: recent developments". Environmental Technology. 31 (10): 1169–81. doi:10.1080/09593330.2010.484076. PMC 3752655. PMID 20718299.
  60. ^ Huber R, Langworthy TA, König H, Thomm M, Woese CR, Sleytr UB, Stetter KO (1986-05-01). "Thermotoga maritima sp. nov. represents a new genus of unique extremely thermophilic eubacteria growing up to 90°C". Archives of Microbiology. 144 (4): 324–333. doi:10.1007/BF00409880. ISSN 1432-072X. S2CID 12709437.
  61. ^ a b Belkin S, Wirsen CO, Jannasch HW (June 1986). "A new sulfur-reducing, extremely thermophilic eubacterium from a submarine thermal vent". Applied and Environmental Microbiology. 51 (6): 1180–5. Bibcode:1986ApEnM..51.1180B. doi:10.1128/AEM.51.6.1180-1185.1986. PMC 239042. PMID 16347075.
  62. ^ a b Jannasch HW, Huber R, Belkin S, Stetter KO (1988-05-01). "Thermotoga neapolitana sp. nov. of the extremely thermophilic, eubacterial genus Thermotoga". Archives of Microbiology. 150 (1): 103–104. doi:10.1007/BF00409725. ISSN 1432-072X. S2CID 22417048.
  63. ^ a b Bonch-Osmolovskaya EA (1994-09-01). "Bacterial sulfur reduction in hot vents". FEMS Microbiology Reviews. 15 (1): 65–77. doi:10.1111/j.1574-6976.1994.tb00122.x. ISSN 0168-6445.
  64. ^ Warthmann R, Cypionka H, Pfennig N (1992-04-01). "Photoproduction of H
    2     from acetate by syntrophic cocultures of green sulfur bacteria and sulfur-reducing bacteria". Archives of Microbiology. 157 (4): 343–348. doi:10.1007/BF00248679. ISSN 1432-072X. S2CID 25411079.
  65. ^ Anantharaman K, Hausmann B, Jungbluth SP, Kantor RS, Lavy A, Warren LA, et al. (June 2018). "Expanded diversity of microbial groups that shape the dissimilatory sulfur cycle". The ISME Journal. 12 (7): 1715–1728. doi:10.1038/s41396-018-0078-0. PMC 6018805. PMID 29467397.
  66. ^ a b c d Brock TD, Martinko JM, Parker J (1994). Biology of microorganisms. Upper Saddle River: Prentice Hall. pp. 694–95. ISBN 1-4058-5345-X.
  67. ^ a b Canfield DE, Farquhar J (2012-03-30). "The Global Sulfur Cycle". In Knoll AH, Canfield DE, Konhauser KO (eds.). Fundamentals of Geobiology. Chichester, UK: John Wiley & Sons, Ltd. pp. 49–64. doi:10.1002/9781118280874.ch5. ISBN 978-1-118-28087-4.
  68. ^ Loka Bharathi PA (2008). "Sulfur Cycle". Encyclopedia of Ecology. Elsevier. pp. 3424–3431. doi:10.1016/b978-008045405-4.00761-8. ISBN 978-0-08-045405-4.
  69. ^ Sun J, Li L, Zhou G, Wang X, Zhang L, Liu Y, et al. (April 2018). "2 and NO and Sulfur Recovery from Flue Gas". Environmental Science & Technology. 52 (8): 4754–4762. doi:10.1021/acs.est.7b06551. PMID 29547691.
  70. ^ a b Sun J, Hong Y, Guo J, Yang J, Huang D, Lin Z, Jiang F (March 2019). "Arsenite removal without thioarsenite formation in a sulfidogenic system driven by sulfur reducing bacteria under acidic conditions". Water Research. 151: 362–370. Bibcode:2019WatRe.151..362S. doi:10.1016/j.watres.2018.12.027. PMID 30616048. S2CID 58657337.
  71. ^ Huang Y, Du JR, Zhang Y, Lawless D, Feng X (2015-11-01). "Removal of mercury (II) from wastewater by polyvinylamine-enhanced ultrafiltration". Separation and Purification Technology. 154: 1–10. doi:10.1016/j.seppur.2015.09.003. ISSN 1383-5866.
  72. ^ Wang JT, Zhang L, Kang Y, Chen G, Jiang F (April 2018). "Long-Term Feeding of Elemental Sulfur Alters Microbial Community Structure and Eliminates Mercury Methylation Potential in Sulfate-Reducing Bacteria Abundant Activated Sludge". Environmental Science & Technology. 52 (8): 4746–4753. Bibcode:2018EnST...52.4746W. doi:10.1021/acs.est.7b06399. PMID 29617126.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Sulfur-reducing_bacteria&oldid=1254977770"