A halophile (from the Greek word for 'salt-loving') is an extremophile that thrives in high salt concentrations. In chemical terms, halophile refers to a Lewis acidic species that has some ability to extract halides from other chemical species.
While most halophiles are classified into the domain Archaea, there are also bacterial halophiles and some eukaryotic species, such as the alga Dunaliella salina and fungus Wallemia ichthyophaga. Some well-known species give off a red color from carotenoid compounds, notably bacteriorhodopsin.
Halophiles can be found in water bodies with salt concentration more than five times greater than that of the ocean, such as the Great Salt Lake in Utah, Owens Lake in California, the Lake Urmia in Iran, the Dead Sea, and in evaporation ponds. They are theorized to be a possible analogues for modeling extremophiles that might live in the salty subsurface water ocean of Jupiter's Europa and similar moons.[1]
Classification
editHalophiles are categorized by the extent of their halotolerance: slight, moderate, or extreme. Slight halophiles prefer 0.3 to 0.8 M (1.7 to 4.8%—seawater is 0.6 M or 3.5%), moderate halophiles 0.8 to 3.4 M (4.7 to 20%), and extreme halophiles 3.4 to 5.1 M (20 to 30%) salt content.[2] Halophiles require sodium chloride (salt) for growth, in contrast to halotolerant organisms, which do not require salt but can grow under saline conditions.
Lifestyle
editHigh salinity represents an extreme environment in which relatively few organisms have been able to adapt and survive. Most halophilic and all halotolerant organisms expend energy to exclude salt from their cytoplasm to avoid protein aggregation ('salting out'). To survive the high salinities, halophiles employ two differing strategies to prevent desiccation through osmotic movement of water out of their cytoplasm. Both strategies work by increasing the internal osmolarity of the cell. The first strategy is employed by some archaea, the majority of halophilic bacteria, yeasts, algae, and fungi; the organism accumulates organic compounds in the cytoplasm—osmoprotectants which are known as compatible solutes. These can be either synthesised or accumulated from the environment.[3] The most common compatible solutes are neutral or zwitterionic, and include amino acids, sugars, polyols, betaines, and ectoines, as well as derivatives of some of these compounds.
The second, more radical adaptation involves selectively absorbing potassium (K ) ions into the cytoplasm. This adaptation is restricted to the extremely halophilic archaeal family Halobacteriaceae, the moderately halophilic bacterial order Halanaerobiales, and the extremely halophilic bacterium Salinibacter ruber. The presence of this adaptation in three distinct evolutionary lineages suggests convergent evolution of this strategy, it being unlikely to be an ancient characteristic retained in only scattered groups or passed on through massive lateral gene transfer.[3] The primary reason for this is the entire intracellular machinery (enzymes, structural proteins, etc.) must be adapted to high salt levels, whereas in the compatible solute adaptation, little or no adjustment is required to intracellular macromolecules; in fact, the compatible solutes often act as more general stress protectants, as well as just osmoprotectants.[3]
Of particular note are the extreme halophiles or haloarchaea (often known as halobacteria), a group of archaea, which require at least a 2 M salt concentration and are usually found in saturated solutions (about 36% w/v salts). These are the primary inhabitants of salt lakes, inland seas, and evaporating ponds of seawater, such as the deep salterns, where they tint the water column and sediments bright colors. These species most likely perish if they are exposed to anything other than a very high-concentration, salt-conditioned environment. These prokaryotes require salt for growth. The high concentration of sodium chloride in their environment limits the availability of oxygen for respiration. Their cellular machinery is adapted to high salt concentrations by having charged amino acids on their surfaces, allowing the retention of water molecules around these components. They are heterotrophs that normally respire by aerobic means. Most halophiles are unable to survive outside their high-salt native environments. Many halophiles are so fragile that when they are placed in distilled water, they immediately lyse from the change in osmotic conditions.
Halophiles use a variety of energy sources and can be aerobic or anaerobic; anaerobic halophiles include phototrophic, fermentative, sulfate-reducing, homoacetogenic, and methanogenic species.[2][4]
The Haloarchaea, and particularly the family Halobacteriaceae, are members of the domain Archaea, and comprise the majority of the prokaryotic population in hypersaline environments.[5] Currently, 15 recognised genera are in the family.[6] The domain Bacteria (mainly Salinibacter ruber) can comprise up to 25% of the prokaryotic community, but is more commonly a much lower percentage of the overall population.[7] At times, the alga Dunaliella salina can also proliferate in this environment.[8]
A comparatively wide range of taxa has been isolated from saltern crystalliser ponds, including members of these genera: Haloferax, Halogeometricum, Halococcus, Haloterrigena, Halorubrum, Haloarcula, and Halobacterium.[5] However, the viable counts in these cultivation studies have been small when compared to total counts, and the numerical significance of these isolates has been unclear. Only recently has it become possible to determine the identities and relative abundances of organisms in natural populations, typically using PCR-based strategies that target 16S small subunit ribosomal ribonucleic acid (16S rRNA) genes. While comparatively few studies of this type have been performed, results from these suggest that some of the most readily isolated and studied genera may not in fact be significant in the in situ community. This is seen in cases such as the genus Haloarcula, which is estimated to make up less than 0.1% of the in situ community,[9] but commonly appears in isolation studies.
Genomic and proteomic signature
editThe comparative genomic and proteomic analysis showed distinct molecular signatures exist for the environmental adaptation of halophiles. At the protein level, the halophilic species are characterized by low hydrophobicity, an overrepresentation of acidic residues, underrepresentation of Cys, lower propensities for helix formation, and higher propensities for coil structure. The core of these proteins is less hydrophobic, such as DHFR, that was found to have narrower β-strands.[10] In one study, the net charges (at pH 7.4) of the ribosomal proteins (r-proteins) that comprise the S10-spc cluster were observed to have an inverse relationship with the halophilicity/halotolerance levels in both bacteria and archaea.[11] At the DNA level, the halophiles exhibit distinct dinucleotide and codon usage.[12]
Examples
editHalobacteriaceae is a family that includes a large part of halophilic archaea.[13] The genus Halobacterium under it has a high tolerance for elevated levels of salinity. Some species of halobacteria have acidic proteins that resist the denaturing effects of salts. Halococcus is another genus of the family Halobacteriaceae.
Some hypersaline lakes are habitat to numerous families of halophiles. For example, the Makgadikgadi Pans in Botswana form a vast, seasonal, high-salinity water body that manifests halophilic species within the diatom genus Nitzschia in the family Bacillariaceae, as well as species within the genus Lovenula in the family Diaptomidae.[14] Owens Lake in California also contains a large population of the halophilic bacterium Halobacterium halobium.
Wallemia ichthyophaga is a basidiomycetous fungus, which requires at least 1.5 M sodium chloride for in vitro growth, and it thrives even in media saturated with salt.[15] Obligate requirement for salt is an exception in fungi. Even species that can tolerate salt concentrations close to saturation (for example Hortaea werneckii) in almost all cases grow well in standard microbiological media without the addition of salt.[16]
The fermentation of salty foods (such as soy sauce, Chinese fermented beans, salted cod, salted anchovies, sauerkraut, etc.) often involves halophiles as either essential ingredients or accidental contaminants. One example is Chromohalobacter beijerinckii, found in salted beans preserved in brine and in salted herring. Tetragenococcus halophilus is found in salted anchovies and soy sauce.
Artemia is a ubiquitous genus of small halophilic crustaceans living in salt lakes (such as Great Salt Lake) and solar salterns that can exist in water approaching the precipitation point of NaCl (340 g/L)[17][18] and can withstand strong osmotic shocks due to its mitigating strategies for fluctuating salinity levels, such as its unique larval salt gland and osmoregulatory capacity.
North Ronaldsay sheep are a breed of sheep originating from Orkney, Scotland. They have limited access to freshwater sources on the island and their only food source is seaweed. They have adapted to handle salt concentrations that would kill other breeds of sheep.[19]
See also
editReferences
edit- ^ Marion, Giles M.; Fritsen, Christian H.; Eicken, Hajo; Payne, Meredith C. (2003-12-01). "The search for life on Europa: Limiting environmental factors, potential habitats, and Earth analogues". Astrobiology. 3 (4): 785–811. Bibcode:2003AsBio...3..785M. doi:10.1089/153110703322736105. ISSN 1531-1074. PMID 14987483.
- ^ a b Ollivier B, Caumette P, Garcia JL, Mah RA (March 1994). "Anaerobic bacteria from hypersaline environments". Microbiological Reviews. 58 (1): 27–38. doi:10.1128/MMBR.58.1.27-38.1994. PMC 372951. PMID 8177169.
- ^ a b c Santos H, da Costa MS (2002). "Compatible solutes of organisms that live in hot saline environments". Environmental Microbiology. 4 (9): 501–509. doi:10.1046/j.1462-2920.2002.00335.x. hdl:10316/8134. PMID 12220406.
- ^ Oren A (January 2002). "Diversity of halophilic microorganisms: environments, phylogeny, physiology, and applications". Journal of Industrial Microbiology & Biotechnology. 28 (1): 56–63. doi:10.1038/sj/jim/7000176. PMID 11938472. S2CID 24223243.
- ^ a b Oren, Aharon (2002). "Molecular ecology of extremely halophilic Archaea and Bacteria". FEMS Microbiology Ecology. 39 (1): 1–7. doi:10.1111/j.1574-6941.2002.tb00900.x. ISSN 0168-6496. PMID 19709178.
- ^ Gutierrez MC, Kamekura M, Holmes ML, Dyall-Smith ML, Ventosa A (December 2002). "Taxonomic characterization of Haloferax sp. (" H. alicantei") strain Aa 2.2: description of Haloferax lucentensis sp. nov". Extremophiles. 6 (6): 479–83. doi:10.1007/s00792-002-0282-7. PMID 12486456. S2CID 24337996.
- ^ Antón J, Rosselló-Mora R, Rodríguez-Valera F, Amann R (July 2000). "Extremely halophilic bacteria in crystallizer ponds from solar salterns". Applied and Environmental Microbiology. 66 (7): 3052–3057. doi:10.1128/aem.66.7.3052-3057.2000. PMC 92110. PMID 10877805.
- ^ Casamayor EO, Massana R, Benlloch S, Øvreås L, Díez B, Goddard VJ, Gasol JM, Joint I, Rodríguez-Valera F, Pedrós-Alió C (2002). "Changes in archaeal, bacterial and eukaryal assemblages along a salinity gradient by comparison of genetic fingerprinting methods in a multipond solar saltern". Environmental Microbiology. 4 (6): 338–348. doi:10.1046/j.1462-2920.2002.00297.x. PMID 12071979.
- ^ Antón J, Llobet-Brossa E, Rodríguez-Valera F, Amann R (December 1999). "Fluorescence in situ hybridization analysis of the prokaryotic community inhabiting crystallizer ponds". Environmental Microbiology. 1 (6): 517–23. doi:10.1046/j.1462-2920.1999.00065.x. PMID 11207773.
- ^ Kastritis PL, Papandreou NC, Hamodrakas SJ (October 2007). "Haloadaptation: Insights from comparative modeling studies of halophilic archaeal DHFRs". International Journal of Biological Macromolecules. 41 (4): 447–453. doi:10.1016/j.ijbiomac.2007.06.005. PMID 17675150.
- ^ Tirumalai MR, Anane-Bediakoh D, Rajesh S, Fox GE (December 2021). "Net Charges of the Ribosomal Proteins of the S10 and spc Clusters of Halophiles Are Inversely Related to the Degree of Halotolerance". Microbiol Spectr. 9 (3): e0178221. doi:10.1128/spectrum.01782-21. PMC 8672879. PMID 34908470.
- ^ Paul S, Bag SK, Das S, Harvill ET, Dutta C (April 2008). "Molecular signature of hypersaline adaptation: insights from genome and proteome composition of halophilic prokaryotes". Genome Biology. 9 (4): R70. doi:10.1186/gb-2008-9-4-r70. PMC 2643941. PMID 18397532.
- ^ Oren, Aharon (September 2014). "Taxonomy of halophilic Archaea: Current status and future challenges". Extremophiles. 18 (5): 825–834. doi:10.1007/s00792-014-0654-9. PMID 25102811. S2CID 5395569.
- ^ Hogan, C. Michael (5 December 2008). Burnham, A. (ed.). "Makgadikgadi – ancient settlement in Botswana". The Megalithic Portal. — website hosts a collection of fossil and archeological find-site profiles.
- ^ Zalar P, Sybren de Hoog G, Schroers HJ, Frank JM, Gunde-Cimerman N (May 2005). "Taxonomy and phylogeny of the xerophilic genus Wallemia (Wallemiomycetes and Wallemiales, cl. et ord. nov.)". Antonie van Leeuwenhoek. 87 (4): 311–28. doi:10.1007/s10482-004-6783-x. PMID 15928984. S2CID 4821447.
- ^ Gostincar C, Grube M, de Hoog S, Zalar P, Gunde-Cimerman N (January 2010). "Extremotolerance in fungi: evolution on the edge". FEMS Microbiology Ecology. 71 (1): 2–11. doi:10.1111/j.1574-6941.2009.00794.x. PMID 19878320.
- ^ Gajardo GM, Beardmore JA (2012). "The brine shrimp artemia: adapted to critical life conditions". Frontiers in Physiology. 3: 185. doi:10.3389/fphys.2012.00185. PMC 3381296. PMID 22737126.
- ^ de Vos S, Van Stappen G, Vuylsteke M, Rombauts S, Bossier P (2018). "Identification of salt stress response genes using the Artemia transcriptome". Aquaculture. 500: 305–314. doi:10.1016/j.aquaculture.2018.09.067. S2CID 92842322.
- ^ Mirkena T, Duguma G, Haile A, Tibbo M, Okeyo AM, Wurzinger M, Sölkner J (2010). "Genetics of adaptation in domestic farm animals: A review". Livestock Science. 132 (1–3): 3. doi:10.1016/j.livsci.2010.05.003.
Further reading
edit- Weinisch L, Kühner S, Roth R, Grimm M, Roth T, Netz DJ, et al. (January 2018). Sourjik V (ed.). "Identification of osmoadaptive strategies in the halophile, heterotrophic ciliate Schmidingerothrix salinarum". PLOS Biology. 16 (1): e2003892. doi:10.1371/journal.pbio.2003892. PMC 5794333. PMID 29357351.
- Yin J, Fu XZ, Wu Q, Chen JC, Chen GQ (November 2014). "Development of an enhanced chromosomal expression system based on porin synthesis operon for halophile Halomonas sp". Applied Microbiology and Biotechnology. 98 (21): 8987–97. doi:10.1007/s00253-014-5959-1. PMID 25070598. S2CID 1773197.
- Zaretsky M, Roine E, Eichler J (2018-09-07). "Halorubrum sp. PV6". Frontiers in Microbiology. 9: 2133. doi:10.3389/fmicb.2018.02133. PMC 6137143. PMID 30245679.
- Batista-García RA, Balcázar-López E, Miranda-Miranda E, Sánchez-Reyes A, Cuervo-Soto L, Aceves-Zamudio D, et al. (2014-08-27). Mormile MR (ed.). "Characterization of lignocellulolytic activities from a moderate halophile strain of Aspergillus caesiellus isolated from a sugarcane bagasse fermentation". PLOS ONE. 9 (8): e105893. Bibcode:2014PLoSO...9j5893B. doi:10.1371/journal.pone.0105893. PMC 4146556. PMID 25162614.
- Chua MJ, Campen RL, Wahl L, Grzymski JJ, Mikucki JA (March 2018). "Genomic and physiological characterization and description of Marinobacter gelidimuriae sp. nov., a psychrophilic, moderate halophile from Blood Falls, an antarctic subglacial brine". FEMS Microbiology Ecology. 94 (3). doi:10.1093/femsec/fiy021. PMID 29444218.
- González-Martínez S, Galindo-Sánchez C, López-Landavery E, Paniagua-Chávez C, Portillo-López A (September 2019). "Aspergillus loretoensis, a single isolate from marine sediment of Loreto Bay, Baja California Sur, México resulting as a new obligate halophile species". Extremophiles. 23 (5): 557–568. doi:10.1007/s00792-019-01107-6. PMID 31227903. S2CID 195246075.
- Laye VJ, DasSarma S (April 2018). "An Antarctic Extreme Halophile and Its Polyextremophilic Enzyme: Effects of Perchlorate Salts". Astrobiology. 18 (4): 412–418. Bibcode:2018AsBio..18..412L. doi:10.1089/ast.2017.1766. PMC 5910040. PMID 29189043.
- Ongagna-Yhombi SY, McDonald ND, Boyd EF (January 2015). Pettinari MJ (ed.). "Deciphering the role of multiple betaine-carnitine-choline transporters in the Halophile Vibrio parahaemolyticus". Applied and Environmental Microbiology. 81 (1): 351–63. doi:10.1128/AEM.02402-14. PMC 4272712. PMID 25344241.
- Solovchenko AE, Selivanova EA, Chekanov KA, Sidorov RA, Nemtseva NV, Lobakova ES (November 2015). "Induction of Secondary Carotenogenesis in New Halophile Microalgae from the Genus Dunaliella (Chlorophyceae)". Biochemistry. Biokhimiia. 80 (11): 1508–13. doi:10.1134/S0006297915110139. PMID 26615443. S2CID 9259513.
- Strillinger E, Grötzinger SW, Allers T, Eppinger J, Weuster-Botz D (February 2016). "Production of halophilic proteins using Haloferax volcanii H1895 in a stirred-tank bioreactor". Applied Microbiology and Biotechnology. 100 (3): 1183–1195. doi:10.1007/s00253-015-7007-1. hdl:10754/579494. PMID 26428236. S2CID 15001309.
- Tao P, Li H, Yu Y, Gu J, Liu Y (August 2016). "Ectoine and 5-hydroxyectoine accumulation in the halophile Virgibacillus halodenitrificans PDB-F2 in response to salt stress". Applied Microbiology and Biotechnology. 100 (15): 6779–6789. doi:10.1007/s00253-016-7549-x. PMID 27106915. S2CID 14058059.
- Van-Thuoc D, Huu-Phong T, Minh-Khuong D, Hatti-Kaul R (March 2015). "Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) production by a moderate halophile Yangia sp. ND199 using glycerol as a carbon source". Applied Biochemistry and Biotechnology. 175 (6): 3120–32. doi:10.1007/s12010-015-1479-4. PMID 25600362. S2CID 30712412.