The taxonomy of the genus Psoroma (lichenized Ascomycota) is currently under revision, as it has long been recognized as heterogeneous. The aim of the present study was to reconstruct the phylogeny of Psoroma and related genera. The ITS region of nu-rDNA and the mtSSU rDNA from 22 collections of Psoroma and Pannaria were amplified. Sequences from GenBank were also used. For the phylogenetic analysis, direct optimization was implemented, using the program POY, and standard MP using PAUP. Both analyses resulted in similar trees. Two main clades were obtained, one including Santesoniella and most Psoroma species and the other including Pannaria and two Psoroma species, indicating that Psoroma is polyphyletic. Based on its phylogenetic position and ascus type, P. implexum is transferred to the genus Pannaria, and the new combination P. implexa is proposed. Psoroma cephalodinum clusters with Parmeliella and Degelia as a basal group within the Pannariaceae. The ascus apex of P. cephalodinum has a strong amyloid reaction revealing a compact cap-shaped plug. This differs from most of the ascus apical structures observed in the family. Both ascus internal structure and phylogenetic position suggest that P. cephalodinum is distantly related to Psoroma or Pannaria, and thus a new genus Joergensenia is proposed.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.mycres.2008.06.025 | DOI Listing |
Nat Prod Res
May 2024
Instituto de Farmacia, Facultad de Ciencias, Universidad Austral de Chile, Valdivia, Chile.
Lichens contain different types of chemical compounds with multiple biological activities that demonstrate their potential pharmacological use. This research aims to report the metabolomic identification of the ethanolic extracts of and , their antioxidant, enzyme inhibitory, and their cytoprotection activity. Sixteen metabolites were identified in and twelve in ; the extracts reported variable antioxidant activity with IC >350 µg/mL in DPPH·, values >18 µmol Trolox/g in ORAC and >40 µmol Trolox/g in FRAP and a phenolic compound content >10 mg GAE/g, as well as significant results in cholinesterases, α-glucosidase, pancreatic lipase, α-amylase, and tyrosinase enzyme inhibition activities with IC ranging from 18 to 510 µg/mL, and which were complemented by molecular docking experiments.
View Article and Find Full Text PDFMicroorganisms
March 2021
Division of Life Sciences, Korea Polar Research Institute, 26 Songdomirae-ro, Yeonsu-gu, Incheon 21990, Korea.
Biodivers Data J
August 2019
Natural History Museum, University of Oslo, Oslo, Norway Natural History Museum, University of Oslo Oslo Norway.
Background: DNA barcodes are increasingly being used for species identification amongst the lichenised fungi. This paper presents a dataset aiming to provide an authoritative DNA barcode sequence library for a wide array of Nordic lichens.
New Information: We present 1324 DNA barcode sequences (nrITS) for 507 species in 175 genera and 25 orders.
Mycol Res
December 2008
Centro Regional Universitario Bariloche, Universidad Nacional del Comahue, Quintral 1250, 8400 Bariloche, Río Negro, Argentina.
The taxonomy of the genus Psoroma (lichenized Ascomycota) is currently under revision, as it has long been recognized as heterogeneous. The aim of the present study was to reconstruct the phylogeny of Psoroma and related genera. The ITS region of nu-rDNA and the mtSSU rDNA from 22 collections of Psoroma and Pannaria were amplified.
View Article and Find Full Text PDFNew Phytol
October 2003
Botanisches Institut, Universität Kiel, Kiel, Germany.
• The cyanobionts of lichens and free-living Nostoc strains from Livingston Island (maritime Antarctica) were examined to determine both the cyanobiont specificity of lichens and the spatial distribution of Nostoc strains under extreme environmental conditions. • We collected five different lichen species with cyanobacteria as primary or secondary photobiont (Massalongia carnosa, Leptogium puberulum, Psoroma cinnamomeum, Placopsis parellina and Placopsis contortuplicata) and free-living cyanobacteria from different sample sites and analysed them using the tRNA (UAA) intron as a genetic marker to identify the cyanobacterial strains. • Our results showed that the same Nostoc strain was shared by all five lichen species and that an additional strain was present in two of the lichens.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!