Results 31 to 40 of about 27,936 (236)

Phenazine aus Pseudomonden/Phenazines from Pseudomonads

open access: yesZeitschrift für Naturforschung B, 1981
Abstract The structure elucidation of several minor phenazine pigments of Pseudomonads is described. 4-Hydroxyphenazine-1,6-dicarboxylic acid dimethyl ester, 2,3-dihydroxyphenazine, 2,3,7-trihydroxyphenazine, 4-hydroxyphenazine-1-carboxylic acid, 2,3-dihydroxyphenazine-1-carboxylic acid, 2,6-dihydroxyphenazine-1-carboxylic acid and 2,3 ...
A. Römer, H. Scholl, H. Budzikiewicz
openaire   +1 more source

Boosting Charge Storage in Ferri/Ferrocyanide‐Based Alkaline Redox Flow Batteries

open access: yesAngewandte Chemie, EarlyView.
By modifying the solvation environment, cation engineering through Li+ substitution of traditional K+ or Na+ boosts the alkaline solubility of the ferri/ferrocyanide catholyte redox couple, providing a viable pathway to overcome the long‐standing challenge of energy density limitations for aqueous redox flow batteries (RBFs).
Mahla Sarfaraz Khabbaz   +6 more
wiley   +2 more sources

Clostridioides difficile Modifies its Aromatic Compound Metabolism in Response to Amidochelocardin-Induced Membrane Stress

open access: yesmSphere, 2022
Amidochelocardin is a broad-spectrum antibiotic with activity against many Gram-positive and Gram-negative bacteria. According to recent data, the antibiotic effect of this atypical tetracycline is directed against the cytoplasmic membrane, which is ...
Madita Brauer   +13 more
doaj   +1 more source

White light emitting molecular logic gates. [PDF]

open access: yesSmart Mol
White light emitting smart molecules with Boolean logic computing ability are surveyed. Abstract White light emitting (WLE) materials are of considerable interest with commercial and societal applications in video displays and lighting devices. A characteristic property of WLE materials is the luminescence profile spanning from 380 to 700 nm.
Tiz DB, Catania M, Magri DC.
europepmc   +2 more sources

Prophage Activation Triggers Extracellular Synthesis of DNA in Bacterial Biofilms via Rolling Circle Replication

open access: yesAngewandte Chemie, EarlyView.
Shewanella oneidensis and Bacillus subtilis, both harboring prophages, reveal a novel biosynthetic route to scalable and programmable DNA superstructures in flower‐ and wire‐like shapes, respectively. Activation of prophages is achieved via 3‐hour starvation and monitored using reporter strains.
Gabriel Antonio S. Minero   +7 more
wiley   +2 more sources

Interplay between Arabidopsis thaliana Genotype, Plant Growth and Rhizosphere Colonization by Phytobeneficial Phenazine-Producing Pseudomonas chlororaphis

open access: yesMicroorganisms, 2022
Rhizosphere colonization by phytobeneficial Pseudomonas spp. is pivotal in triggering their positive effects on plant health. Many Pseudomonas spp. Determinants, involved in rhizosphere colonization, have already been deciphered.
Antoine Zboralski   +3 more
doaj   +1 more source

Über Tetramethyldiamino‐phenazin [PDF]

open access: yesBerichte der deutschen chemischen Gesellschaft, 1916
n ...
openaire   +2 more sources

Advances in Phenazines over the Past Decade: Review of Their Pharmacological Activities, Mechanisms of Action, Biosynthetic Pathways and Synthetic Strategies

open access: yesMarine Drugs, 2021
Phenazines are a large group of nitrogen-containing heterocycles, providing diverse chemical structures and various biological activities. Natural phenazines are mainly isolated from marine and terrestrial microorganisms.
Junjie Yan   +6 more
doaj   +1 more source

Involvement of Phenazines and Anthranilate in the Antagonism of Pseudomonas aeruginosa PNA1 and Tn5 Derivatives Toward Fusarium spp. and Pythium spp.

open access: yesMolecular Plant-Microbe Interactions, 1998
Pseudomonas aeruginosa PNA1, isolated from the rhizosphere of chickpea in India, suppressed Fusarium wilt of chickpea, caused by Fusarium oxysporum f. sp. ciceris, and Pythium damping-off of bean, caused by Pythium splendens.
Vanamala Anjaiah   +6 more
doaj   +1 more source

Phenazine–naphthalene-1,5-diamine–water (1/1/2)

open access: yesActa Crystallographica Section E, 2009
The asymmetric unit of the title compound, C12H8N2·C10H10N2·2H2O, contains one half-molecule of phenazine, one half-molecule of naphthalene-1,5-diamine and one water molecule.
Maria Gdaniec, Agnieszka Czapik
doaj   +1 more source

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