From Wikipedia, the free encyclopedia
(Redirected from Sulphur metabolism)

Sulfur is metabolized by all organisms, from bacteria and archaea to plants and animals. Sulfur can have an oxidation state from -2 to +6 and is reduced or oxidized by a diverse range of organisms. [1] The element is present in proteins, sulfate esters of polysaccharides, steroids, phenols, and sulfur-containing coenzymes. [2]

Oxidation

Reduced sulfur compounds are oxidized by most organisms, including higher animals and higher plants. [2] Some organisms can conserve energy (i.e., produce ATP) from the oxidation of sulfur and it can serve as the sole energy source for some lithotrophic bacteria and archaea. [3] Sulfur oxidizers use enzymes such as Sulfide:quinone reductase, sulfur dioxygenase and sulfite oxidase to oxidize sulfur compounds to sulfate.

Sulfur-oxidizing microorganisms

Reduced sulfur compounds, such as hydrogen sulfide, elemental sulfur, sulfite, thiosulfate, and various polythionates (e.g., tetrathionate), are oxidized by chemotrophic, phototrophic, and mixotrophic bacteria for energy. [1] Some chemosynthetic archaea use hydrogen sulfide as an energy source for carbon fixation, producing sugars.

Chemotrophic sulfur-oxidizing bacteria

In order to have sufficient redox potential, microorganisms that use sulfur as an electron donor often use oxygen or nitrate as terminal electron acceptors. [4] Members of the chemotrophic Acidithiobacillus genus are able to oxidize a vast range of reduced sulfur compounds, but are restricted to acidic environments. [5] Chemotrophs that can produce sugars through chemosynthesis make up the base of some food chains. Food chains have formed in the absence of sunlight around hydrothermal vents, which emit hydrogen sulfide and carbon dioxide.

Phototrophic sulfur-oxidizing bacteria

Microbial sulfur cycle

Some bacteria use light energy to couple sulfur oxidation to carbon dioxide (CO2) fixation for growth. These fall into two general groups: green sulfur bacteria (GSB) and purple sulfur bacteria (PSB). [6] However, some Cyanobacteria are also able to use hydrogen sulfide as an electron donor during anoxygenic photosynthesis. [7] All PSB are part of the class Gammaproteobacteria and are found in two families: Chromatiaceae and Ectothiorhodospiraceae. Typically, sulfur globules accumulate intracellularly in Chromatiaceae and extracellularly in Ectothiorhodospiraceae, which is one distinguishing feature between these two groups of PSB. [8] GSB are found within the family Chlorobiaceae generally oxidize sulfide or elemental sulfur, but some members are able to utilize thiosulfate. [9]

Reduction

Sulfur reduction occurs in plants, fungi, and many bacteria. [10] Sulfate can serve as an electron acceptor in anaerobic respiration and can also be reduced for the formation of organic compounds. Sulfate-reducing bacteria reduce sulfate and other oxidized sulfur compounds, such as sulfite, thiosulfate, and elemental sulfur, to sulfide.

Dissimilatory sulfur reduction

Some microorganisms are capable of reducing sulfate and elemental sulfur for energy by coupling sulfur reduction with the oxidation of molecular hydrogen or organic compounds such as acetate in anaerobic respiration. [11] These processes typically produce hydrogen sulfide as a byproduct, which can go on to serve as an electron donor in sulfur oxidation. [11] Sulfate reduction by sulfate-reducing bacteria is dissimilatory; the purpose of reducing the sulfate is to produce energy, and the sulfide is excreted. Dissimilatory sulfate reduction use the enzymes ATP sulfurylase, APS reductase, and sulfite reductase. [12]

Assimilatory sulfur reduction

In assimilatory sulfate reduction the sulfate is assimilated, or incorporated into organic compounds such as cysteine, methionine, or iron-sulfur clusters and enzyme cofactors. [13] In bacteria, sulfate and thiosulfate are transported into the cell by sulfate permeases where it can then be reduced and incorporated into biomolecules. [14] In some organisms (e.g., gut flora, cyanobacteria, and yeast), [15] assimilatory sulfate reduction is a more complex process that makes use of the enzymes ATP sulfurylase, APS kinase, PAPS reductase, and sulfite reductase. [10]

Disproportionation

Sulfur can also serve as both an electron donor and electron acceptor by microorganisms is disproportionation reactions. For example, Acidianus ambivalens uses sulfur oxygenase reductase (SOR) to convert elemental sulfur to sulfate, thiosulfate, and hydrogen sulfide through disproportionation. [16] Elemental sulfur disproportionation is restricted to environments where the concentration of the sulfide products are kept low, which typically happens in the presence of scavenging minerals that contain iron or manganese. [17] Disproportionation of thiosulfate often occurs in anoxic layers of marine and freshwater sediments. [18] [19]

Use by plants and animals

Plants take up sulfate in their roots and reduce it to sulfide (see Sulfur assimilation). However, some Brassica species are able to assimilate atmospheric sources of sulfur in the absence of other sources. [20] Plants reduce APS directly to sulfite (using APS reductase) without phosphorylating APS to PAPS. From the sulfide they form the amino acids cysteine and methionine, sulfolipids, and other sulfur compounds. Animals obtain sulfur from cysteine and methionine in the protein that they consume.

Sulfur is the third most abundant mineral element in the body. [21] The amino acids cysteine and methionine are used by the body to make glutathione. Excess cysteine and methionine are oxidized to sulfate by sulfite oxidase, eliminated in the urine, or stored as glutathione (which can serve as a store for sulfur). [21] The lack of sulfite oxidase, known as sulfite oxidase deficiency, causes physical deformities, mental retardation, and death.

See also

References

  1. ^ a b Loka Bharathi, P. A. (2008-01-01), "Sulfur Cycle", in Fath, Brian (ed.), Encyclopedia of Ecology (Second Edition), Oxford: Elsevier, pp. 192–199, doi: 10.1016/b978-0-444-63768-0.00761-7, ISBN  978-0-444-64130-4, retrieved 2023-02-12
  2. ^ a b Schiff JA (1979). "Pathways of assimilatory sulphate reduction in plants and microorganisms". In CIBA Foundation Symposium (ed.). Sulphur in Biology. John Wiley & Sons. pp. 49–50. ISBN  9780470718230.
  3. ^ Friedrich, Cornelius G. (1997-01-01), Poole, R. K. (ed.), "Physiology and Genetics of Sulfur-oxidizing Bacteria", Advances in Microbial Physiology, vol. 39, Academic Press, pp. 235–289, retrieved 2023-02-13
  4. ^ Wasmund, Kenneth; Mußmann, Marc; Loy, Alexander (August 2017). "The life sulfuric: microbial ecology of sulfur cycling in marine sediments: Microbial sulfur cycling in marine sediments". Environmental Microbiology Reports. 9 (4): 323–344. doi: 10.1111/1758-2229.12538. PMC  5573963. PMID  28419734.
  5. ^ Pronk JT, Meulenberg R, Hazeu W, Bos P, Kuenen JG (1990). "Oxidation of reduced inorganic sulphur compounds by acidophilic thiobacilli". FEMS Microbiology Letters. 75 (2–3): 293–306. doi: 10.1111/j.1574-6968.1990.tb04103.x.
  6. ^ Dahl, Christiane; Friedrich, Cornelius G. (2008). Microbial sulfur metabolism. Berlin: Springer. ISBN  978-3-540-72682-1. OCLC  213092503.
  7. ^ Cohen, Yehuda; Jørgensen, Bo Barker; Revsbech, Niels Peter; Poplawski, Ricardo (1986). "Adaptation to Hydrogen Sulfide of Oxygenic and Anoxygenic Photosynthesis among Cyanobacteria". Applied and Environmental Microbiology. 51 (2): 398–407. doi: 10.1128/aem.51.2.398-407.1986. ISSN  0099-2240. PMC  238881. PMID  16346996.
  8. ^ Frigaard, Niels-Ulrik; Dahl, Christiane (2008-01-01), Poole, Robert K. (ed.), Sulfur Metabolism in Phototrophic Sulfur Bacteria, Advances in Microbial Physiology, vol. 54, Academic Press, pp. 103–200, doi: 10.1016/s0065-2911(08)00002-7, ISBN  9780123743237, PMID  18929068, retrieved 2023-02-12
  9. ^ Sakurai, Hidehiro; Ogawa, Takuro; Shiga, Michiko; Inoue, Kazuhito (2010-06-01). "Inorganic sulfur oxidizing system in green sulfur bacteria". Photosynthesis Research. 104 (2): 163–176. doi: 10.1007/s11120-010-9531-2. ISSN  1573-5079. PMID  20143161. S2CID  1091791.
  10. ^ a b " Pathway: sulfate reduction I (assimilatory)." MetaCyc.
  11. ^ a b Rabus, Ralf; Hansen, Theo A.; Widdel, Friedrich (2006), Dworkin, Martin; Falkow, Stanley; Rosenberg, Eugene; Schleifer, Karl-Heinz (eds.), "Dissimilatory Sulfate- and Sulfur-Reducing Prokaryotes", 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, retrieved 2023-02-13
  12. ^ " Pathway: sulfate reduction IV (dissimilatory)." MetaCyc.
  13. ^ Moran, Mary Ann; Durham, Bryndan P. (2019). "Sulfur metabolites in the pelagic ocean". Nature Reviews Microbiology. 17 (11): 665–678. doi: 10.1038/s41579-019-0250-1. ISSN  1740-1534. PMID  31485034. S2CID  201834195.
  14. ^ Aguilar-Barajas, Esther; Díaz-Pérez, César; Ramírez-Díaz, Martha I.; Riveros-Rosas, Héctor; Cervantes, Carlos (2011-08-01). "Bacterial transport of sulfate, molybdate, and related oxyanions". BioMetals. 24 (4): 687–707. doi: 10.1007/s10534-011-9421-x. ISSN  1572-8773. PMID  21301930. S2CID  1935648.
  15. ^ " Pathway: sulfate reduction II (assimilatory)." MetaCyc.
  16. ^ Janosch, Claudia; Remonsellez, Francisco; Sand, Wolfgang; Vera, Mario (2015-10-21). "Sulfur Oxygenase Reductase (Sor) in the Moderately Thermoacidophilic Leaching Bacteria: Studies in Sulfobacillus thermosulfidooxidans and Acidithiobacillus caldus". Microorganisms. 3 (4): 707–724. doi: 10.3390/microorganisms3040707. ISSN  2076-2607. PMC  5023260. PMID  27682113.
  17. ^ Fike, David A.; Bradley, Alexander S.; Rose, Catherine V. (2015-05-30). "Rethinking the Ancient Sulfur Cycle". Annual Review of Earth and Planetary Sciences. 43 (1): 593–622. doi: 10.1146/annurev-earth-060313-054802. ISSN  0084-6597.
  18. ^ Jørgensen, Bo Barker (1990). "The sulfur cycle of freshwater sediments: Role of thiosulfate". Limnology and Oceanography. 35 (6): 1329–1342. doi: 10.4319/lo.1990.35.6.1329.
  19. ^ Jørgensen, Bo Barker (1990-07-13). "A Thiosulfate Shunt in the Sulfur Cycle of Marine Sediments". Science. 249 (4965): 152–154. doi: 10.1126/science.249.4965.152. ISSN  0036-8075. PMID  17836966. S2CID  220093825.
  20. ^ Aghajanzadeh, Tahereh; Hawkesford, Malcolm J.; De Kok, Luit J. (2016-04-01). "Atmospheric H
    2
    S
    and SO
    2
    as sulfur sources for Brassica juncea and Brassica rapa: Regulation of sulfur uptake and assimilation"
    . Environmental and Experimental Botany. 124: 1–10. doi: 10.1016/j.envexpbot.2015.12.001. ISSN  0098-8472.
  21. ^ a b Nimni ME, Han B, Cordoba F (2007). "Are we getting enough sulfur in our diet?". Nutrition & Metabolism (Lond). 4 (1): 24. doi: 10.1186/1743-7075-4-24. ISSN  1743-7075. PMC  2198910. PMID  17986345.
From Wikipedia, the free encyclopedia
(Redirected from Sulphur metabolism)

Sulfur is metabolized by all organisms, from bacteria and archaea to plants and animals. Sulfur can have an oxidation state from -2 to +6 and is reduced or oxidized by a diverse range of organisms. [1] The element is present in proteins, sulfate esters of polysaccharides, steroids, phenols, and sulfur-containing coenzymes. [2]

Oxidation

Reduced sulfur compounds are oxidized by most organisms, including higher animals and higher plants. [2] Some organisms can conserve energy (i.e., produce ATP) from the oxidation of sulfur and it can serve as the sole energy source for some lithotrophic bacteria and archaea. [3] Sulfur oxidizers use enzymes such as Sulfide:quinone reductase, sulfur dioxygenase and sulfite oxidase to oxidize sulfur compounds to sulfate.

Sulfur-oxidizing microorganisms

Reduced sulfur compounds, such as hydrogen sulfide, elemental sulfur, sulfite, thiosulfate, and various polythionates (e.g., tetrathionate), are oxidized by chemotrophic, phototrophic, and mixotrophic bacteria for energy. [1] Some chemosynthetic archaea use hydrogen sulfide as an energy source for carbon fixation, producing sugars.

Chemotrophic sulfur-oxidizing bacteria

In order to have sufficient redox potential, microorganisms that use sulfur as an electron donor often use oxygen or nitrate as terminal electron acceptors. [4] Members of the chemotrophic Acidithiobacillus genus are able to oxidize a vast range of reduced sulfur compounds, but are restricted to acidic environments. [5] Chemotrophs that can produce sugars through chemosynthesis make up the base of some food chains. Food chains have formed in the absence of sunlight around hydrothermal vents, which emit hydrogen sulfide and carbon dioxide.

Phototrophic sulfur-oxidizing bacteria

Microbial sulfur cycle

Some bacteria use light energy to couple sulfur oxidation to carbon dioxide (CO2) fixation for growth. These fall into two general groups: green sulfur bacteria (GSB) and purple sulfur bacteria (PSB). [6] However, some Cyanobacteria are also able to use hydrogen sulfide as an electron donor during anoxygenic photosynthesis. [7] All PSB are part of the class Gammaproteobacteria and are found in two families: Chromatiaceae and Ectothiorhodospiraceae. Typically, sulfur globules accumulate intracellularly in Chromatiaceae and extracellularly in Ectothiorhodospiraceae, which is one distinguishing feature between these two groups of PSB. [8] GSB are found within the family Chlorobiaceae generally oxidize sulfide or elemental sulfur, but some members are able to utilize thiosulfate. [9]

Reduction

Sulfur reduction occurs in plants, fungi, and many bacteria. [10] Sulfate can serve as an electron acceptor in anaerobic respiration and can also be reduced for the formation of organic compounds. Sulfate-reducing bacteria reduce sulfate and other oxidized sulfur compounds, such as sulfite, thiosulfate, and elemental sulfur, to sulfide.

Dissimilatory sulfur reduction

Some microorganisms are capable of reducing sulfate and elemental sulfur for energy by coupling sulfur reduction with the oxidation of molecular hydrogen or organic compounds such as acetate in anaerobic respiration. [11] These processes typically produce hydrogen sulfide as a byproduct, which can go on to serve as an electron donor in sulfur oxidation. [11] Sulfate reduction by sulfate-reducing bacteria is dissimilatory; the purpose of reducing the sulfate is to produce energy, and the sulfide is excreted. Dissimilatory sulfate reduction use the enzymes ATP sulfurylase, APS reductase, and sulfite reductase. [12]

Assimilatory sulfur reduction

In assimilatory sulfate reduction the sulfate is assimilated, or incorporated into organic compounds such as cysteine, methionine, or iron-sulfur clusters and enzyme cofactors. [13] In bacteria, sulfate and thiosulfate are transported into the cell by sulfate permeases where it can then be reduced and incorporated into biomolecules. [14] In some organisms (e.g., gut flora, cyanobacteria, and yeast), [15] assimilatory sulfate reduction is a more complex process that makes use of the enzymes ATP sulfurylase, APS kinase, PAPS reductase, and sulfite reductase. [10]

Disproportionation

Sulfur can also serve as both an electron donor and electron acceptor by microorganisms is disproportionation reactions. For example, Acidianus ambivalens uses sulfur oxygenase reductase (SOR) to convert elemental sulfur to sulfate, thiosulfate, and hydrogen sulfide through disproportionation. [16] Elemental sulfur disproportionation is restricted to environments where the concentration of the sulfide products are kept low, which typically happens in the presence of scavenging minerals that contain iron or manganese. [17] Disproportionation of thiosulfate often occurs in anoxic layers of marine and freshwater sediments. [18] [19]

Use by plants and animals

Plants take up sulfate in their roots and reduce it to sulfide (see Sulfur assimilation). However, some Brassica species are able to assimilate atmospheric sources of sulfur in the absence of other sources. [20] Plants reduce APS directly to sulfite (using APS reductase) without phosphorylating APS to PAPS. From the sulfide they form the amino acids cysteine and methionine, sulfolipids, and other sulfur compounds. Animals obtain sulfur from cysteine and methionine in the protein that they consume.

Sulfur is the third most abundant mineral element in the body. [21] The amino acids cysteine and methionine are used by the body to make glutathione. Excess cysteine and methionine are oxidized to sulfate by sulfite oxidase, eliminated in the urine, or stored as glutathione (which can serve as a store for sulfur). [21] The lack of sulfite oxidase, known as sulfite oxidase deficiency, causes physical deformities, mental retardation, and death.

See also

References

  1. ^ a b Loka Bharathi, P. A. (2008-01-01), "Sulfur Cycle", in Fath, Brian (ed.), Encyclopedia of Ecology (Second Edition), Oxford: Elsevier, pp. 192–199, doi: 10.1016/b978-0-444-63768-0.00761-7, ISBN  978-0-444-64130-4, retrieved 2023-02-12
  2. ^ a b Schiff JA (1979). "Pathways of assimilatory sulphate reduction in plants and microorganisms". In CIBA Foundation Symposium (ed.). Sulphur in Biology. John Wiley & Sons. pp. 49–50. ISBN  9780470718230.
  3. ^ Friedrich, Cornelius G. (1997-01-01), Poole, R. K. (ed.), "Physiology and Genetics of Sulfur-oxidizing Bacteria", Advances in Microbial Physiology, vol. 39, Academic Press, pp. 235–289, retrieved 2023-02-13
  4. ^ Wasmund, Kenneth; Mußmann, Marc; Loy, Alexander (August 2017). "The life sulfuric: microbial ecology of sulfur cycling in marine sediments: Microbial sulfur cycling in marine sediments". Environmental Microbiology Reports. 9 (4): 323–344. doi: 10.1111/1758-2229.12538. PMC  5573963. PMID  28419734.
  5. ^ Pronk JT, Meulenberg R, Hazeu W, Bos P, Kuenen JG (1990). "Oxidation of reduced inorganic sulphur compounds by acidophilic thiobacilli". FEMS Microbiology Letters. 75 (2–3): 293–306. doi: 10.1111/j.1574-6968.1990.tb04103.x.
  6. ^ Dahl, Christiane; Friedrich, Cornelius G. (2008). Microbial sulfur metabolism. Berlin: Springer. ISBN  978-3-540-72682-1. OCLC  213092503.
  7. ^ Cohen, Yehuda; Jørgensen, Bo Barker; Revsbech, Niels Peter; Poplawski, Ricardo (1986). "Adaptation to Hydrogen Sulfide of Oxygenic and Anoxygenic Photosynthesis among Cyanobacteria". Applied and Environmental Microbiology. 51 (2): 398–407. doi: 10.1128/aem.51.2.398-407.1986. ISSN  0099-2240. PMC  238881. PMID  16346996.
  8. ^ Frigaard, Niels-Ulrik; Dahl, Christiane (2008-01-01), Poole, Robert K. (ed.), Sulfur Metabolism in Phototrophic Sulfur Bacteria, Advances in Microbial Physiology, vol. 54, Academic Press, pp. 103–200, doi: 10.1016/s0065-2911(08)00002-7, ISBN  9780123743237, PMID  18929068, retrieved 2023-02-12
  9. ^ Sakurai, Hidehiro; Ogawa, Takuro; Shiga, Michiko; Inoue, Kazuhito (2010-06-01). "Inorganic sulfur oxidizing system in green sulfur bacteria". Photosynthesis Research. 104 (2): 163–176. doi: 10.1007/s11120-010-9531-2. ISSN  1573-5079. PMID  20143161. S2CID  1091791.
  10. ^ a b " Pathway: sulfate reduction I (assimilatory)." MetaCyc.
  11. ^ a b Rabus, Ralf; Hansen, Theo A.; Widdel, Friedrich (2006), Dworkin, Martin; Falkow, Stanley; Rosenberg, Eugene; Schleifer, Karl-Heinz (eds.), "Dissimilatory Sulfate- and Sulfur-Reducing Prokaryotes", 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, retrieved 2023-02-13
  12. ^ " Pathway: sulfate reduction IV (dissimilatory)." MetaCyc.
  13. ^ Moran, Mary Ann; Durham, Bryndan P. (2019). "Sulfur metabolites in the pelagic ocean". Nature Reviews Microbiology. 17 (11): 665–678. doi: 10.1038/s41579-019-0250-1. ISSN  1740-1534. PMID  31485034. S2CID  201834195.
  14. ^ Aguilar-Barajas, Esther; Díaz-Pérez, César; Ramírez-Díaz, Martha I.; Riveros-Rosas, Héctor; Cervantes, Carlos (2011-08-01). "Bacterial transport of sulfate, molybdate, and related oxyanions". BioMetals. 24 (4): 687–707. doi: 10.1007/s10534-011-9421-x. ISSN  1572-8773. PMID  21301930. S2CID  1935648.
  15. ^ " Pathway: sulfate reduction II (assimilatory)." MetaCyc.
  16. ^ Janosch, Claudia; Remonsellez, Francisco; Sand, Wolfgang; Vera, Mario (2015-10-21). "Sulfur Oxygenase Reductase (Sor) in the Moderately Thermoacidophilic Leaching Bacteria: Studies in Sulfobacillus thermosulfidooxidans and Acidithiobacillus caldus". Microorganisms. 3 (4): 707–724. doi: 10.3390/microorganisms3040707. ISSN  2076-2607. PMC  5023260. PMID  27682113.
  17. ^ Fike, David A.; Bradley, Alexander S.; Rose, Catherine V. (2015-05-30). "Rethinking the Ancient Sulfur Cycle". Annual Review of Earth and Planetary Sciences. 43 (1): 593–622. doi: 10.1146/annurev-earth-060313-054802. ISSN  0084-6597.
  18. ^ Jørgensen, Bo Barker (1990). "The sulfur cycle of freshwater sediments: Role of thiosulfate". Limnology and Oceanography. 35 (6): 1329–1342. doi: 10.4319/lo.1990.35.6.1329.
  19. ^ Jørgensen, Bo Barker (1990-07-13). "A Thiosulfate Shunt in the Sulfur Cycle of Marine Sediments". Science. 249 (4965): 152–154. doi: 10.1126/science.249.4965.152. ISSN  0036-8075. PMID  17836966. S2CID  220093825.
  20. ^ Aghajanzadeh, Tahereh; Hawkesford, Malcolm J.; De Kok, Luit J. (2016-04-01). "Atmospheric H
    2
    S
    and SO
    2
    as sulfur sources for Brassica juncea and Brassica rapa: Regulation of sulfur uptake and assimilation"
    . Environmental and Experimental Botany. 124: 1–10. doi: 10.1016/j.envexpbot.2015.12.001. ISSN  0098-8472.
  21. ^ a b Nimni ME, Han B, Cordoba F (2007). "Are we getting enough sulfur in our diet?". Nutrition & Metabolism (Lond). 4 (1): 24. doi: 10.1186/1743-7075-4-24. ISSN  1743-7075. PMC  2198910. PMID  17986345.

Videos

Youtube | Vimeo | Bing

Websites

Google | Yahoo | Bing

Encyclopedia

Google | Yahoo | Bing

Facebook