Oridamycins A and B, anti-Saprolegnia parasitica indolosesquiterpenes isolated from Streptomyces sp. KS84.

J Nat Prod

Laboratory of Microbial Chemistry, College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-Higashi, Kusatsu, Shiga 525-8577, Japan.

Published: April 2010

Oridamycins A (1) and B (2) were isolated from the fermentation broth of Streptomyces sp. strain KS84 as selective anti-Saprolegnia parasitica antibiotics. Their structures were elucidated as pentacyclic indolosesquiterpenes by the combination of NMR and spectroscopic analyses. The absolute configuration of 1 was determined by ROESY analyses after the advanced Mosher analysis. Compound 1 exhibited anti-S. parasitica activity with an MIC value of 3.0 microg/mL, but was much less active against the phytopathogenic fungus Phoma sp. and the yeast Saccharomyces cerevisiae.

Download full-text PDF

Source
http://dx.doi.org/10.1021/np1000522DOI Listing

Publication Analysis

Top Keywords

anti-saprolegnia parasitica
8
oridamycins anti-saprolegnia
4
parasitica indolosesquiterpenes
4
indolosesquiterpenes isolated
4
isolated streptomyces
4
streptomyces ks84
4
ks84 oridamycins
4
oridamycins isolated
4
isolated fermentation
4
fermentation broth
4

Similar Publications

Structure-Activity Relationship of Natural Dihydrochalcones and Chalcones, and Their Respective Oxyalkylated Derivatives as Anti- Agents.

Plants (Basel)

July 2024

Escuela de Obstetricia y Puericultura, Facultad de medicina, Campus de la Salud, Universidad de Valparaíso, Angamos 655, Reñaca, Viña del Mar 2520000, Chile.

Article Synopsis
  • A pathogenic oomycete is harming aquaculture, and current treatments are ineffective and harmful to the environment and health.
  • Researchers tested various natural and synthetic compounds for their potential as anti-pathogenic agents.
  • The most effective compounds identified were a natural dihydroxychalcone and a new oxyalkylchalcone, outperforming a commercial control substance, with molecule structure playing a key role in enhancing effectiveness.
View Article and Find Full Text PDF

This study aimed to investigate the effectiveness of five natural plant extract compounds Curcumin (CUR); Eugenol (EUG), Cinnamaldehyde (CIN), Stigmasterol (ST) and Morin (MOR), on two species of Saprolegnia; Saprolegnia parasitica and S. australis. Selective compounds were screened for the minimum inhibitory concentration, first for anti-oomycetes activity and then mycelium growth inhibition, spore germination inhibition and colonisation test.

View Article and Find Full Text PDF

Synthesis and Anti- Activity of New 2',4'-Dihydroxydihydrochalcone Derivatives.

Antibiotics (Basel)

June 2020

Laboratorio de Productos Naturales y Síntesis Orgánica (LPNSO), Departamento de Química, Facultad de Ciencias Naturales y Exactas, Universidad de Playa Ancha, Avda. Leopoldo Carvallo 270, Playa Ancha, Valparaíso 2340000, Chile.

Article Synopsis
  • The study synthesized seven derivatives of 2',4'-dihydroxydihydrochalcone and tested their anti-agent capacity against various strains of pathogens.
  • One derivative exhibited the highest effectiveness, showing minimum inhibitory concentrations (MIC) and minimum oomyceticidal concentrations (MOC) ranging from 100-175 μg/mL and 100-200 μg/mL, respectively, outperforming positive controls like bronopol and fluconazole.
  • The active compound also demonstrated the ability to damage and break down the cell membranes of all tested strains, indicating a strong antimicrobial action compared to commercial controls.
View Article and Find Full Text PDF

Isolation of anti-Saprolegnia lignans from Magnolia officinalis and SAR evaluation of honokiol/magnolol analogs.

Bioorg Med Chem Lett

February 2019

College of Animal Science and Technology, Northwest A&F University, Xinong Road 22nd, Yangling, Shaanxi 712100, China. Electronic address:

To control the fish fungal pathogen Saprolegnia, the effects of the petroleum ether extracts of Magnolia officinalis were evaluated by a rapeseed (Brassicanapus) microplate method in vitro. By loading on an open silica gel column and eluting with petroleum ether-ethyl acetate-methanol, honokiol (CHO) and magnolol (CHO) were isolated from Magnolia officinalis. Saprolegnia parasitica growth was inhibited significantly when honokiol concentration was >8.

View Article and Find Full Text PDF

Saprolegnia parasitica, belonging to oomycetes, is one of virulent pathogen of fishes such as salmon and trout, and causes tremendous damage and losses in commercial aquacultures by saprolegniasis. Previously, malachite green, an effective medicine, had been used to control saprolegniasis. However, this drug has been banned around the world due to its mutagenicity.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!