Results 61 to 70 of about 3,309 (181)

An Isotopic Ratio Outlier Analysis Approach for Global Metabolomics of Biosynthetically Talented Actinomycetes

open access: yesMetabolites, 2019
Actinomycetes are powerhouses of natural product biosynthesis. Full realization of this biosynthetic potential requires approaches for recognizing novel metabolites and determining mediators of metabolite production.
Jordan Carey   +5 more
doaj   +1 more source

A Comprehensive Overview of the Cyclodipeptide Synthase Family Enriched with the Characterization of 32 New Enzymes

open access: yesFrontiers in Microbiology, 2018
Cyclodipeptide synthases (CDPSs) use as substrates two amino acids activated as aminoacyl-tRNAs to synthesize cyclodipeptides in secondary metabolites biosynthetic pathways.
Muriel Gondry   +8 more
doaj   +1 more source

Crystal structures of the dimethyl sulfoxide solvate of 3,6-bis(indol-3-yl)-1,4-dimethylpiperazine-2,5-dione and of the dimethyl sulfoxide and tetrahydrofuran solvates of 1,4-dimethyl-3,6-bis(2-methylindol-3-yl)piperazine-2,5-dione

open access: yesActa Crystallographica Section E: Crystallographic Communications
The syntheses and structures of the dimethyl sulfoxide (DMSO) solvate of 3,6-bis(indol-3-yl)-1,4-dimethylpiperazine-2,5-dione, C11H10N2O (I), and of the dimethyl sulfoxide and tetrahydrofuran (THF) solvates of 1,4-dimethyl-3,6-bis(2-methylindol-3-yl ...
Clifford W. Padgett   +3 more
doaj   +1 more source

Inhibition of Aflatoxin Production in Aspergillus flavus by a Klebsiella sp. and Its Metabolite Cyclo(l-Ala-Gly)

open access: yesToxins
During an experiment where we were cultivating aflatoxigenic Aspergillus flavus on peanuts, we accidentally discovered that a bacterium adhering to the peanut strongly inhibited aflatoxin (AF) production by A. flavus.
Shohei Sakuda   +8 more
doaj   +1 more source

Biosynthesis of a Novel Diketopiperazine Aspkyncin Incorporating a Kynurenine Unit from Aspergillus aculeatus

open access: yesJournal of Fungi
The simplest cyclo-peptides, also known as diketopiperazines (DKPs), are widespread in nature. The growing interest in these simplest cyclo-peptides is driven by their significant potential for therapeutic applications.
Dekun Kong, Xin Wang, Li Liu
doaj   +1 more source

The diketopiperazine-fused tetrahydro-β-carboline scaffold as a model peptidomimetic with an unusual α-turn secondary structure

open access: yesBeilstein Journal of Organic Chemistry, 2013
Aiming at restricting the conformational freedom of tryptophan-containing peptide ligands, we designed a THBC (tetrahydro-β-carboline)-DKP (diketopiperazine)-based peptidomimetic scaffold capable of arranging in an unusual α-turn conformation.
Francesco Airaghi   +5 more
doaj   +1 more source

The Mode of Action of Cyclo(l-Ala-l-Pro) in Inhibiting Aflatoxin Production of Aspergillus flavus

open access: yesToxins, 2017
Cyclo(l-Ala-l-Pro) inhibits aflatoxin production in aflatoxigenic fungi without affecting fungal growth. The mode of action of cyclo(l-Ala-l-Pro) in inhibiting aflatoxin production of Aspergillus flavus was investigated. A glutathione S-transferase (GST)
Kurin Iimura   +5 more
doaj   +1 more source

Streptomyces nigra sp. nov. Is a Novel Actinobacterium Isolated From Mangrove Soil and Exerts a Potent Antitumor Activity in Vitro

open access: yesFrontiers in Microbiology, 2018
A new bacterial strain, designated 452T, was isolated from the rhizosphere soil of the mangrove Avicennia marina in China. As determined, its cell wall peptidoglycan contained LL-diaminopimelic acid; MK-9(H8) and MK-9(H6) were the major isoprenoid ...
Can Chen   +8 more
doaj   +1 more source

Solid-Phase Synthesis of Methyl N-(pyrimidin-2-yl)glycinate

open access: yesMolecules, 2003
A versatile method for the preparation of N-heteroaryl substituted aminoacid derivatives is suggested. The method avoids facile diketopiperazine formation.
Eugene V. Babaev, Denis S. Ermolat'ev
doaj   +1 more source

Synthesis and Neuroprotective Action of Optically Pure Neoechinulin A and Its Analogs

open access: yesPharmaceuticals, 2010
We developed an efficient, stereoselective synthetic method for the diketopiperazine moiety of neoechinulin A and its derivatives. The intramolecular cyclization at 80 ºC proceeded with minimal racemization of the stereogenic center at C-12 on ...
Toshiaki Aoki   +10 more
doaj   +1 more source

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