In the course of investigations on peptaibol chemodiversity from marine-derived Trichoderma spp., five new 15-residue peptaibols named pentadecaibins I–V (1–5) were isolated from the solid culture of the strain Trichoderma sp. MMS1255 belonging to the T. harzianum species complex. Phylogenetic analyses allowed precise positioning of the strain close to T. lentiforme lineage inside the Harzianum clade. Peptaibol sequences were elucidated on the basis of their MS/MS fragmentation and extensive 2D NMR experiments. Amino acid configurations were determined by Marfey’s analyses. The pentadecaibins are based on the sequences Ac-Aib1-Gly2-Ala3-Leu4-Aib/Iva5-Gln6-Aib/Iva7-Val/Leu8-Aib9-Ala10-Aib11-Aib12-Aib13-Gln14-Pheol15. Characteristic of the pentadecaibin sequences is the lack of the Aib-Pro motif commonly present in peptaibols produced by Trichoderma spp. Genome sequencing of Trichoderma sp. MMS1255 allowed the detection of a 15-module NRPS-encoding gene closely associated with pentadecaibin biosynthesis. Pentadecaibins were assessed for their potential antiproliferative and antimicrobial activities.

Soybean [Glycine max (L.) Merr] is the legume with the largest cultivated area worldwide and its yield depends largely on symbiotic nitrogen fixation and root architecture. This study aimed to explore the genetic variability of root architectural traits and di-nitrogen fixing activity in a small collection of nine European cultivars belonging to the same maturity group during their early stages. New image analysis approaches were implemented to characterise root architecture at high throughput. Significant genetic variability was identified for the width of the root system, root density, and for nitrogen fixation. This study allowed us to highlight trade-offs among root and nodule traits, and structural and functional traits. Finally, both the image analysis approach and the results could be used for breeding programs of soybean, that could take into account the root system architecture, when the plant interacts in symbiosis with N2-fixing bacteria.