In an effort to describe bioactive antifungal compounds from antagonistic bacteria with potential for biocontrol of plant pathogens, a strain of was collected from plant disease suppressive compost prepared from composted material of marine origin. Few natural products have been characterized from the non-filamentous Actinobacteria genus . A new cyclic tetrapeptide, cyclo-(L-Pro-L-Leu-L-γHyp-L-Tyr); arthropeptide A (), was isolated from the EtOAc soluble culture filtrate extract of M9-17 grown in MOLP broth. Its structure was confirmed by HRMS, interpretation of NMR data, and a modified Marfey's method. Arthropeptide A () displayed antifungal activity towards , the causal agent of disease in numerous host plant species, which had shown the previous susceptibility to . The newly identified compound may be responsible, in part, for the inhibitory activity of the bacterium against fungal plant pathogens.
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http://dx.doi.org/10.1080/14786419.2021.2018434 | DOI Listing |
Microorganisms
December 2024
State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Life Sciences, Yunnan University, Kunming 650091, China.
Root-knot nematodes (RKNs) are pathogens that endanger a wide range of crops and cause serious global agricultural losses. In this study, we investigated metabolites of the endoparasitic fungus YMF1.01751, with the expectation of discovering valuable biocontrol compounds.
View Article and Find Full Text PDFJ Nat Prod
December 2024
Department of Chemistry, University of Kalyani, Kalyani 741235 West Bengal, India.
A concise synthetic route to an epimer of the recently isolated biologically active cyclic tetrapeptide koshidacin B has been developed, which featured a late-stage functionalization of a macrocyclic scaffold through a cross metathesis reaction. The synthetic 9--koshidacin B showed marginal differences in spectroscopic behavior with that of the natural product but exhibited conformational preferences similar to those reported for analogous substrate chlamydocin. Moreover, it exhibited a useful level of selective inhibition of biologically relevant enzyme histone deacetylase 1 with an IC value of 0.
View Article and Find Full Text PDFbioRxiv
November 2024
James Tarpo Jr. and Margaret Tarpo Department of Chemistry, Purdue University, West Lafayette, IN 47906.
Cyclic tetrapeptides (CTPs) are a diverse class of natural products with a broad range of biological activities. However, they are extremely challenging to synthesize due to the ring strain associated with their small ring size. While chemical methods have been developed to access CTPs, they generally require the presence of certain amino acids, limiting their substrate scopes.
View Article and Find Full Text PDFInsects
September 2024
Department of Plant Medicals, Andong National University, Andong 36729, Republic of Korea.
Entomopathogenic bacteria, classified into the genus , exhibit a dual lifestyle as mutualistic symbionts to nematodes and as pathogens to a broad range of insects. Bacterial virulence depends on toxin proteins that induce toxemia and various immunosuppressive secondary metabolites that cause septicemia. Particularly, the immunosuppressive properties of bacteria determine the variability of their insecticidal activities.
View Article and Find Full Text PDFJ Nat Prod
October 2024
The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, So̷ltoft Plads, building 220, 2800 Kgs. Lyngby, Denmark.
Genome analysis of sp. CA-103260 revealed a putative lipopeptide-encoding biosynthetic gene cluster (BGC) that was cloned into a bacterial artificial chromosome (BAC) and heterologously expressed in M1152. As a result, a novel cyclic lipo-tetrapeptide containing two diaminopropionic acid residues and an exotic ,-acetonide ring, kutzneridine A (), was isolated and structurally characterized.
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