Stereocaulon ramulosum

Last updated

Snow lichen
Lichen Stereocaulon Devils Hole.jpg
Barrington Tops National Park, Australia
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Lecanoromycetes
Order: Lecanorales
Family: Stereocaulaceae
Genus: Stereocaulon
Species:
S. ramulosum
Binomial name
Stereocaulon ramulosum
Synonyms
  • Lichen ramulosus Sw.

Stereocaulon ramulosum, commonly known as snow lichen, is a terricolous fruticose lichen belonging to the family Stereocaulaceae. [1] It has cosmopolitan distribution. In the Australasian region, it is common in eastern Australia, New Zealand and has also been recorded at Lord Howe Island and Macquarie Island. [2]

Its habitat is often cooler, moist areas with a high level of cloud cover. It may be found on rocky ground or as an epiphyte on tree branches. Stereocaulon ramulosum was the first lichen known to contain an amylose polysaccharide. [3] [4]

This species is unusual, as the fungal component is associated with two different chlorophyll forming species; usually there is only one. The more significant one is a green alga which gives the lichen its characteristic colour. The second is a cyanobacteria which is found in the cephalodia, a wart-like structure. Three different kingdoms are represented in this single life form; Fungi, Protista and Eubacteria. [5]

The generic name Stereocaulon is derived from ancient Greek stereós and Latin caulis, referring to the hard stem of the central part of the lichen. [6] The specific epithet ramulosum is derived from the Latin ramulose, and means "having many small branches". [7]

Phytochemistry

The characteristic secondary metabolite of S. ramulosum is atranorin, a depside. During the extraction phase, atranorin suffer an alcoholysis reaction, producing methyl/ethyl haemmatomate and methyl ß-orcinol carboxylate. Has been identified in New Zealand and in east central Africa, perlatolic acid, anziaic acid and methyl haemmatomate. [8] Methyl haemmatomate has in-vitro antifungical activity. [9] Huneck in Chiloe, Chile, identify atranorin, perlatolic acid and lobaric acid. [10] Also, in Pongo, Bolivia, Vila et al. aislate the polyol galactitol and 1,3,7-trimethylguanine, an unusual alkaloid. [11] [ clarification needed ]

Carbohydrates have been found.[ clarification needed ]. A linear (1→3) linked ß-D-glucan, [3] and β-GalCer-lich, a new immune stimulant carbohydrate. [12]

Related Research Articles

<span class="mw-page-title-main">Hemicellulose</span> Class of plant cell wall polysaccharides

A hemicellulose is one of a number of heteropolymers, such as arabinoxylans, present along with cellulose in almost all terrestrial plant cell walls. Cellulose is crystalline, strong, and resistant to hydrolysis. Hemicelluloses are branched, shorter in length than cellulose, and also show a propensity to crystallize. They can be hydrolyzed by dilute acid or base as well as a myriad of hemicellulase enzymes.

A glucan is a polysaccharide derived from D-glucose, linked by glycosidic bonds. Glucans are noted in two forms: alpha glucans and beta glucans. Many beta-glucans are medically important. They represent a drug target for antifungal medications of the echinocandin class.

<span class="mw-page-title-main">Beta-glucan</span> Class of chemical compounds

Beta-glucans, β-glucans comprise a group of β-D-glucose polysaccharides (glucans) naturally occurring in the cell walls of cereals, bacteria, and fungi, with significantly differing physicochemical properties dependent on source. Typically, β-glucans form a linear backbone with 1–3 β-glycosidic bonds but vary with respect to molecular mass, solubility, viscosity, branching structure, and gelation properties, causing diverse physiological effects in animals.

<span class="mw-page-title-main">Echinocandin</span> Group of chemical compounds

Echinocandins are a class of antifungal drugs that inhibit the synthesis of β-glucan in the fungal cell wall via noncompetitive inhibition of the enzyme 1,3-β glucan synthase. The class has been termed the "penicillin of antifungals," along with the related papulacandins, as their mechanism of action resembles that of penicillin in bacteria. β-glucans are carbohydrate polymers that are cross-linked with other fungal cell wall components, the fungal equivalent to bacterial peptidoglycan. Caspofungin, micafungin, and anidulafungin are semisynthetic echinocandin derivatives with limited clinical use due to their solubility, antifungal spectrum, and pharmacokinetic properties.

<span class="mw-page-title-main">CLEC7A</span> Protein-coding gene in humans

C-type lectin domain family 7 member A or Dectin-1 is a protein that in humans is encoded by the CLEC7A gene. CLEC7A is a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded glycoprotein is a small type II membrane receptor with an extracellular C-type lectin-like domain fold and a cytoplasmic domain with a partial immunoreceptor tyrosine-based activation motif. It functions as a pattern-recognition receptor for a variety of β-1,3-linked and β-1,6-linked glucans from fungi and plants, and in this way plays a role in innate immune response. Expression is found on myeloid dendritic cells, monocytes, macrophages and B cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region.

Oligosaccharides and polysaccharides are an important class of polymeric carbohydrates found in virtually all living entities. Their structural features make their nomenclature challenging and their roles in living systems make their nomenclature important.

<i>Punctelia</i> Genus of foliose lichens

Punctelia is a genus of foliose lichens belonging to the large family Parmeliaceae. The genus, which contains about 50 species, was segregated from genus Parmelia in 1982. Characteristics that define Punctelia include the presence of hook-like to thread-like conidia, simple rhizines, and point-like pseudocyphellae. It is this last feature that is alluded to in the vernacular names speckled shield lichens or speckleback lichens.

Arabinoxylan is a hemicellulose found in both the primary and secondary cell walls of plants, including woods and cereal grains, consisting of copolymers of two pentose sugars: arabinose and xylose.

Fungal isolates have been researched for decades. Because fungi often exist in thin mycelial monolayers, with no protective shell, immune system, and limited mobility, they have developed the ability to synthesize a variety of unusual compounds for survival. Researchers have discovered fungal isolates with anticancer, antimicrobial, immunomodulatory, and other bio-active properties. The first statins, β-Lactam antibiotics, as well as a few important antifungals, were discovered in fungi.

<span class="mw-page-title-main">Oat beta-glucan</span>

Oat β-glucans are water-soluble β-glucans derived from the endosperm of oat kernels known for their dietary contribution as components of soluble fiber. Due to their property to lower serum total cholesterol and low-density lipoprotein cholesterol, and potentially reduce the risk of cardiovascular diseases, oat β-glucans have been assigned a qualified health claim by the European Food Safety Authority and the US Food and Drug Administration.

<span class="mw-page-title-main">Botryosphaeran</span> Exopolysaccharide

Botryosphaeran is an exopolysaccharide (EPS) produced by the ascomyceteous fungus Botryosphaeria rhodina. Characterization of the chemical structure of botryosphaeran showed this EPS to be a (1→3)(1→6)-β-D-glucan. This particular β-glucan can be produced by several strains of Botryosphaeria rhodina that include: MAMB-05, DABAC-P82, and RCYU 30101. Botryosphaeran exhibits interesting rheological properties and novel biological functions including hypoglycaemia, hypocholesterolaemia, anti-atheroslerosis and anti-cancer activity, with potential commercial applications. Three cosmetic products formulated with botryosphaeran have been developed to promote skin health and treat skin conditions for future intended commercialization purposes.

<span class="mw-page-title-main">Isolichenan</span> An α-glucan occurring in certain species of lichens

Isolichenan, also known as isolichenin, is a cold-water-soluble α-glucan occurring in certain species of lichens. This lichen product was first isolated as a component of an extract of Iceland moss in 1813, along with lichenin. After further analysis and characterization of the individual components of the extract, isolichenan was named in 1881. It is the first α-glucan to be described from lichens. The presence of isolichenan in the cell walls is a defining characteristic in several genera of the lichen family Parmeliaceae. Although most prevalent in that family, it has also been isolated from members of the families Ramalinaceae, Stereocaulaceae, Roccellaceae, and Cladoniaceae. Experimental studies have shown that isolichenan is produced only when the two lichen components – fungus and alga – are growing together, not when grown separately. The biological function of isolichenan in the lichen thallus is unknown.

Ernst Adolf Raeuschel (1740–1800) was a German lichenologist, active between 1772 and 1797, specializing in bryophytes and spermatophytes. Sometimes spelled Rauschel.

<i>Punctelia perreticulata</i> Species of lichen

Punctelia perreticulata is a widely distributed species of foliose lichen in the family Parmeliaceae. It occurs in Mediterranean Europe and Russia, North America, South America, Australia, and New Zealand, where it grows on rocks, bark, or wood. Its main distinguishing features are its thallus surface, marked with many shallow depressions, grooves, or pits, and sorediate pseudocyphellae. The lower side of the thallus is ivory to tan towards the centre and the major secondary metabolite in the medulla is lecanoric acid. A lookalike species with which it has been historically confused is Punctelia subrudecta; this lichen can be distinguished from Punctelia perreticulata by the texture of the thallus surface, or, more reliably, by the length of its conidia.

<span class="mw-page-title-main">Anziaic acid</span> Carboxylate ester

Anziaic acid is a depside found in lichens. It gives a red reaction in the C test. The two phenolic rings have a pentyl side chain. It is an ester dimer of olivetolic acid.

<span class="mw-page-title-main">Salazinic acid</span> Chemical compound found in some lichens

Salazinic acid is a depsidone with a lactone ring. It is found in some lichens, and is especially prevalent in Parmotrema and Bulbothrix, where its presence or absence is often used to help classify species in those genera.

<i>Pulchrocladia retipora</i> Species of fruticose lichen

Pulchrocladia retipora, commonly known as the coral lichen, is a species of fruticose lichen in the family Cladoniaceae. Found predominantly in Australasia, its habitats range from the Australian Capital Territory to New Zealand's North and South Islands, and even the Pacific region of New Caledonia, where it grows in coastal and alpine heathlands. The lichen features coral-like branches and subbranches with numerous intricate, netlike perforations. It is known by multiple names, with some sources referring to it by its synonym Cladia retipora, or the common name lace lichen.

Lichen products, also known as lichen substances, are organic compounds produced by a lichen. Specifically, they are secondary metabolites. Lichen products are represented in several different chemical classes, including terpenoids, orcinol derivatives, chromones, xanthones, depsides, and depsidones. Over 800 lichen products of known chemical structure have been reported in the scientific literature, and most of these compound are exclusively found in lichens. Examples of lichen products include usnic acid, atranorin, lichexanthone, salazinic acid, and isolichenan, an α-glucan. Many lichen products have biological activity, and research into these effects is ongoing.

<span class="mw-page-title-main">Barbatic acid</span> Chemical compound found in some lichens

Barbatic acid is an organic compound that is made by some lichens. It is in the structural class known as depsides. It is particularly common in the genera Usnea and Cladonia.

<i>Botryolepraria</i> Genus of lichens

Botryolepraria is a genus of saxicolous (rock-dwelling), byssoid (cottony) lichens of uncertain familial placement in the order Verrucariales. It has two species. Both species grow in damp conditions, such as on cave walls, particularly in areas with minimal light.

References

  1. "Stereocaulon ramulosum". www.gbif.org. Retrieved 15 February 2021.
  2. "Stereocaulon ramulosum". Atlas of Living Australia . Retrieved February 15, 2021.
  3. 1 2 Madalena Baron, Philip A.J. Gorin, Marcello Iacomini (1988). "Isolation and identification of a linear (1→3)-linked β-d-glucan and other carbohydrate components of the lichen Stereocaulon ramulosum (SW.) Räusch". Carbohydrate Research. Elsevier. 177: 235–239. doi:10.1016/0008-6215(88)85057-2 . Retrieved February 15, 2021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. "Stereocaulon ramulosum". Australian Lichens. Australian National Herbarium . Retrieved February 15, 2021.
  5. John Walter. "Living on the Edge" (PDF). Wombat Forestcare Newsletter - September 2013. Retrieved February 15, 2021.
  6. "Stereocaulon alpinum". Association Française de Lichénologie - Les champignons lichénisés de France - AFL. Association Française de Lichénologie. Retrieved February 17, 2021.
  7. Michael L. Charters. "Calflora - Page R". Botanic Names. Retrieved February 17, 2021.
  8. Ramaut, J. L.; Serusiaux, E.; Brouers, M.; Corvisier, M. (1978). "Lichen Acids of the Stereocaulon ramulosum Group in Central East Africa". The Bryologist . 81 (3): 415. doi:10.2307/3242244. ISSN   0007-2745. JSTOR   3242244.
  9. Hickey, B.J.; Lumsden, A.J.; Cole, A.L.J.; Walker, J.R.L. (1990). "Antibiotic compounds from New Zealand plants: methyl haematommate, an anti-fungal agent from Stereocaulon ramulosum". New Zealand Natural Sci. 17: 49–53.
  10. Huneck, Siegfried; Follmann, Gerhard (1967-04-01). "Notizen: Über die Inhaltsstoffe von Usnea pusilla (RAES.) RAES., Stereocaulon ramulosum (SWANS.) RAEUSCH. und Arthothelium pacificum FOLLM". Zeitschrift für Naturforschung B (in German). 22 (4): 461. doi: 10.1515/znb-1967-0426 . ISSN   1865-7117. S2CID   98564563.
  11. Vila, Jose; Mollinedo, Patricia; Flores, Yonny; Sterner, Olov (December 2008). "1,3,7-TRIMETHYLGUANINE FROM THE LICHEN STEREOCAULON RAMULOSUM". Revista Boliviana de Química. 25 (1): 1–3. ISSN   0250-5460.
  12. Baena, Andrés; Gomez-Giraldo, Lina; Gomez, Wilton A.; Pelaez, Carlos A. (2015-07-28). "Murine invariant natural killer T cells recognize glycolipids derived from extracts of the lichen Stereocaulon ramulosum". Revista Vitae. 22 (1). doi: 10.17533/udea.vitae.v22n1a02 .