Lichen product explained

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 compounds are exclusively found in lichens. Examples of lichen products include usnic acid (a dibenzofuran), atranorin (a depside), lichexanthone (a xanthone), salazinic acid (a depsidone), and isolichenan, an α-glucan. Many lichen products have biological activity, and research into these effects is ongoing.

Biosynthesis

Most lichen products are biochemically synthesized via the acetyl-polymalonyl pathway (also known as polyketide pathway), while only a few originate from the mevalonate and shikimate biosynthetic pathways.

Occurrence

Lichen products accumulate on the outer walls of the fungal hyphae, and are quite stable. Crystal deposits can be visualised using scanning electron microscopy. For this reason, even very old herbarium specimens can be analysed. The amount of lichen products in lichen (as a percentage of dry weight) is typically between 0.1%–10%, although in some instances it may be as high as 30%. They are usually found in the medulla, or less commonly, the cortex.

In 1907, Wilhelm Zopf identified and classified about 150 lichen products. Seventy years later, this number had risen to 300, and by 1995, 850 lichen products were known; as of 2021, more than 1000 have been identified. Analytical methods were developed in the 1970s using thin-layer chromatography for the routine identification of lichen products. More recently, published techniques demonstrate ways to more efficiently harvest secondary metabolites from lichen samples.

Chemical isolateLichen sourceResearched activity and uses
AtranorinCetraria islandicaAnalgesic, anti-inflammatory, antimicrobial[1] [2]
Constipatic acidXanthoparmelia
LichexanthoneHypotrachyna osseoalba
PortentolRoccella portentosaAnticancer[3]
Salazinic acidParmotrema, BulbothrixAntibacterial[4] [5]
Usnic acidUsneaAntibacterial,[6] adrenergic activity[7]

Use in taxonomy

Lichen products play a crucial role in differentiating lichenised fungi, particularly in groups where morphological characteristics are less distinct. This approach is notably applied in the genus Lepraria, which lacks sexual reproduction and ascomata (fruiting bodies), typically key features for species identification. Similarly, in genera with more complex structures like the crustose genus Ochrolechia, and the fruticose Cladonia, the presence, absence, or substitution of specific lichen products is frequently used to distinguish species, especially when these variations align with differences in geographical distribution.

References

Cited literature

Notes and References

  1. Studzinska-Sroka . Elzbieta . Galanty . Agnieszka . Bylka . Wieslawa . 7 November 2017 . Atranorin - An Interesting Lichen Secondary Metabolite . Mini-Reviews in Medicinal Chemistry . 17 . 17 . 1633–1645 . 10.2174/1389557517666170425105727. 28443519 .
  2. Jaeck . Andreas . Atranorin . www.internetchemie.info.
  3. Cheng . Bichu . Trauner . Dirk . 2015-11-04 . A Highly Convergent and Biomimetic Total Synthesis of Portentol . Journal of the American Chemical Society . en . 137 . 43 . 13800–13803 . 10.1021/jacs.5b10009 . 26471956 . 0002-7863.
  4. Candan . Mehmet . Yılmaz . Meral . Tay . Turgay . Erdem . Murat . Türk . Ayşen Özdemir . 2007-08-01 . Antimicrobial Activity of Extracts of the Lichen Parmelia sulcata and its Salazinic Acid Constituent . Zeitschrift für Naturforschung C . en . 62 . 7–8 . 619–621 . 10.1515/znc-2007-7-827 . 17913083 . 1865-7125. free .
  5. Manojlović . Nedeljko . Ranković . Branislav . Kosanić . Marijana . Vasiljević . Perica . Stanojković . Tatjana . October 2012 . Chemical composition of three Parmelia lichens and antioxidant, antimicrobial and cytotoxic activities of some their major metabolites . Phytomedicine . en . 19 . 13 . 1166–1172 . 10.1016/j.phymed.2012.07.012. 22921748 .
  6. Web site: Wikispaces .
  7. Harris N. J. (1961), Honors Thesis, Clark University, Worcester, Massachusetts