Abstract
AbstractLichen specific metabolites (LSMs) have interesting biological activities and quantitative variations may be present intraspecifically. For example, variations in medullary fumarprotocetraric acid (FA) and cortical usnic acid (UA) were observed in the lichen Cladonia foliacea, but the mechanism of variation is not well understood. The current study aimed to characterise the quantitative variation of FA and UA and to investigate the association between lichen metabolite content and ecological / biological variables. Fungal and algal trees were constructed using fungal (nrITS, RPB2) and algal (nrITS) loci, respectively. Using a chiral chromatographic method, the contents of (-)-UA were determined in 29 C. foliacea specimens and range from 6.88 to 34.27 mg/g dry wt. The FA contents were lower and varied from 1.44 to 9.87 mg/g dry wt. Although the fungal tree showed two well resolved clades, no significant differences of UA or FA contents were found between the two fungal clades. However, a significantly higher UA/FA ratio as well as a unique habitat were found to be associated with specimens which contained the alga Asterochloris lobophora than those specimens associated other Asterochloris algae. Taking all predictive variables into account (i.e. substrate type, elevation, collection season, photobiont identity), the multivariate data analysis indicated that photobiont identity explained most of the variance of LSM contents in C. foliacea. Thus future LSM biosynthetic studies should take the photobiont into consideration when dealing with intraspecific quantitative variation.
Funder
National Research Development and Innovation Fund
Icelandic Research Fund
University of Iceland Research Fund
Stipendium Hungaricum Scholarship
Landsvirkjun
HUN-REN Centre for Ecological Research
Publisher
Springer Science and Business Media LLC
Reference82 articles.
1. Anar M, Orhan F, Alpsoy L, Gulluce M, Aslan A, Agar G (2016) The antioxidant and antigenotoxic potential of methanol extract of Cladonia foliacea (Huds.) Willd. Toxicol Ind Health 32(4):721–729. https://doi.org/10.1177/0748233713504805
2. Armaleo D, Zhang Y, Cheung S (2008) Light might regulate divergently depside and depsidone accumulation in the lichen Parmotrema hypotropum by affecting thallus temperature and water potential. Mycologia 100(4):565–576. https://doi.org/10.3852/07-162r
3. Armaleo D, Sun X, Culberson C (2011) Insights from the first putative biosynthetic gene cluster for a lichen depside and depsidone. Mycologia 103(4):103:741-754. https://doi.org/10.3852/10-335
4. Armaleo D (1995). Factors affecting depside and depsidone biosynthesis in a cultured lichen fungus. Crypt Bot 5:14–21. https://www.researchgate.net/publication/343049771_Factors_affecting_depside_and_depsidone_biosynthesis_in_a_cultured_lichen_fungus. Accessed 30 Jan 2024
5. Arup U, Ekman S, Lindblom L, Mattsson J-E (1993) High performance thin layer chromatography (HPTLC), an improved technique for screening lichen substances. Lichenologist 25:61–71. https://doi.org/10.1006/lich.1993.1018