Erratum: Corrigendum: Hu H et al. (2023) Taxonomic and phylogenetic characterisations of six species of Pleosporales (in Didymosphaeriaceae, Roussoellaceae and Nigrogranaceae) from China. MycoKeys 100: 123-151. https://doi.org/10.3897/mycokeys.100.109423.

[This corrects the article DOI: 10.3897/mycokeys.100.109423.].

Taxonomic and phylogenetic characterisations of six species of Pleosporales (in Didymosphaeriaceae, Roussoellaceae and Nigrogranaceae) from China.

Pleosporales comprise a diverse group of fungi with a global distribution and significant ecological importance. A survey on Pleosporales (in Didymosphaeriaceae, Roussoellaceae and Nigrogranaceae) in Guizhou Province, China, was conducted. Specimens were identified, based on morphological characteristics and phylogenetic analyses using a dataset composed of ITS, LSU, SSU, tef1 and rpb2 loci. Maximum Likelihood (ML) and Bayesian analyses were performed. As a result, three new species (Neokalmusiakarka, Nigrogranaschinifolium and N.trachycarpus) have been discovered, along with two new records for China (Roussoellaneopustulans and R.doimaesalongensis) and a known species (Roussoellapseudohysterioides). Morphologically similar species and phylogenetically close taxa are compared and discussed. This study provides detailed information and descriptions of all newly-identified taxa.

A 1-aminocyclopropane-1-carboxylate deaminase MrACCD from Metarhizium robertsii is associated with plant growth promotion for Metarhizium spp.

Besides killing insects, Metarhizium spp. have shown another ecological role as plant associates. Partial genra and groups of these entomopathogenic fungi act as plant growth promoters during root colonization. Here, we report that Metarhizium robertsii produces a 1-aminocyclopropane-1-carboxylate (ACC) deaminase (ACCD encoded by MracdS, MrACCD), which is involved in promoting early vegetative growth in wheat, while Metarhizium acridum lacks a functional ACCD, although a gene encoding for a putative ACCD has been identified in its genome. MracdS expression was up-regulated by a max 10.7-fold with 3 mM ACC and high ACCD enzymatic activities were induced by either ACC (7.5-fold) or wheat root (3.2-fold). In contrast, no ACCD activity was detected in M. acridum in the presence of both inducers. In pot assay, wheat seeds were treated with wild-type M. robertsii (Mr23), wild-type M. acridum (Mac324), MracdS disruption mutant (ΔMracdS) and M. acridum transformant harboring heterologous MracdS (Mac324-MracdS). Relative to the control seeds treated with heat-killed conidia, Mr23, ΔMracdS and Mac324-MracdS increased root length (by 66.2, 31.8 and 40.2%), and plant biomass (by 56.6, 42.1 and 40.9%). Nevertheless, ΔMracdS deficient in ACCD activity heavily impaired its capability of wheat growth promotion by decrease of 20.7% in root length relative to Mr23. In addition, Mr23 and Mac324-MracdS also increased shoot growth (by 42.3, and 42.7%) while ΔMracdS failed. Mac324 showed no effect on plant growth during the test. These data suggest a role for ACCD in the plant growth promotion effect by M. robertsii, which is irrelevant to Metarhizium colonization of roots since rhizosphere competency of both Mr23 and Mac324 are unaffected by the change of ACCD activity.

Cordycepin and N6-(2-hydroxyethyl)-adenosine from Cordyceps pruinosa and their interaction with human serum albumin.

Cordyceps pruinosa (CP) is often used as Traditional Chinese Medicine, but the substance basis of its medicinal properties is unclear. In this study, two compounds were isolated from CP cultures by column chromatography, and identified as cordycepin and N6-(2-hydroxyethyl)-adenosine (HEA) by Nuclear Magnetic Resonance. In order to understand the efficacy of these two substances as potential therapeutic agents, it is necessary to explore their binding with proteins. The molecular mechanisms of interaction between cordycepin, HEA and human serum albumin (HSA) were studied using UV and fluorescence spectroscopy. The bingding constants between HSA and cordycepin were 4.227, 3.573 and 3.076 × 10(3)·at 17, 27 and 37°C respectively, and that of HSA and HEA were 27.102, 19.409 and 13.002 × 10(3)·at the three tempretures respectively. Both cordycepin and HEA can quench the intrinsic fluorescence of HSA via static quenching, and they can bind with HSA to form complexes with a single binding site. The interaction forces between cordycepin and HSA were determined as electrostatic and hydrophobic, and those of HEA and HSA were hydrogen bonding and van der Waals forces. Using Foster's equation, the distance between fluorophores of cordycepin and HSA, and HEA and HSA are estimated to be 5.31 nm and 4.98 nm, respectively. In this study, cordycepin was isolated for the first time from CP, and will provide a new source of cordycepin and expand the use of this taxon. The interaction mechanisms between cordycepin and HSA was studied for the first time, which will provide a useful guide for the clinical application of cordycepin. The pharmacological importance of this study is to understand the interaction of HSA with cordycepin and HEA, which will be essential for the future designing of drugs based on the two compounds.