pseudomonas fluorescens

Benzyldodecyldimethylammonium chloride dihydrate can be used as an insecticide reagent. It can target drug-resistant bacteria, such as methicillin-resistant Staphylococcus aureus, multidrug-resistant Pseudomonas aeruginosa, etc., in a concentration-dependent manner.

Mupirocin (BRL-4910A) is a RNA synthetase inhibitor antibacterial. It has shown excellent activity against gram-positive staphylococci and streptococci.

Mupirocin calcium hydrate is an antibiotic produced by Pseudomonas fluorescens, showed a high level of activity against staphylococci and streptococci and against certain gram-negative bacteria

Galactose 1-dehydrogenase, pseudomonas fluorescens, a dehydrogenase found in Pseudomonas fluorescens, facilitates the oxidation of L-arabinose and D-galactose, utilizing NADP+ NAD+ as a cofactor. This enzyme is employed in diagnostic assays to quantify total galactose levels and serves as a biocatalyst in the production of galacturonic acid salts.

Pseudomonic acid C is the analogue of Pseudomonic Acid D which is an antibiotic agent from Pseudomonas fluorescens.

Sperabillin A (free base) is a potent antibacterial antibiotic in vivo isolated from Pseudomonas fluorescens YK-437.

Sperabillin A (HCl) is a potent antibacterial antibiotic in vivo isolated from Pseudomonas fluorescens YK-437.

Sperabillin C is a potent antibacterial antibiotic in vivo isolated from Pseudomonas fluorescens YK-437.

Safracin A is an antibiotic produced by Pseudomonas fluorescens A2-2.

Obafluorin is a β-lactone antibiotic produced by Pseudomonas fluorescens ATCC 39502, with broad-spectrum antibacterial activity, inhibiting tRNA transglycosylase, used in metabolic disease research.

MraY-IN-1 (compound 12a) is a potent inhibitor (IC50: 140 μM) of the bacterial translocase MraY. MraY-IN-1 has antibacterial activity against Escherichia coli K12 (MIC50: 7 μg ml), Bacillus subtilis W23 (MIC50: 12 μg ml) and Pseudomonas fluorescens Pf-5 (MIC50: 46 μg ml). MraY-IN-1 can be used for antimicrobial studies.

Mupirocin calcium (BRL-4910A, Pseudomonic acid), an orally active antibiotic derived from Pseudomonas fluorescens, exerts its antimicrobial effects by reversibly inhibiting isoleucyl-transfer RNA. This action impedes bacterial protein and RNA synthesis, demonstrating its effectiveness [1] [2].

MraY-IN-1 (compound 12a) is a potent inhibitor of MraY with an IC50 of 140 µM, exhibiting antimicrobial activity with MIC50 values of 7 µg/mL against Escherichia coli K12, 12 µg/mL for Bacillus subtilis W23, and 46 µg/mL for Pseudomonas fluorescens Pf-5, and is utilized in anti-bacterial research [1].

Fosfocytocin can be found in the Pseudomonas fluorescens strain PK-52 and exhibits very weak antibacterial activity.

Ferrocin B is an iron-containing cyclic decapeptide antibiotic isolated from the Pseudomonas fluorescens YK-310 strain. It exhibits strong antibacterial properties, primarily targeting Gram-negative bacteria, with a notable inhibitory effect against Pseudomonas aeruginosa. In murine infection models, the half-maximal effective dose (ED50) of Ferrocin B for P. aeruginosa is 0.593 mg/kg. Ferrocin B is applicable in anti-infective research studies.

9,17-Octadecadiene-12,14-diyne-1,11,16-triol shows antibacterial activity against Bacillus subtilis and Pseudomonas fluorescens, antifungal activity against Cladosporium cucumerinum, moiluscicidal activity against Biomphalaria glabrata at low concentratio

1. 2-endo-Hydroxy-1,8-cineole shows antimicrobial and bactericidal activities against against test bacteria (Staphylococcus aureus, Escherichia coli, and Pseudomonas fluorescens) .

Altechromone A has antimicrobial activity, it is active against Bacillus subtilis, Escherichia coli, Pseudomonas fluorescens and Candida albicans with the MICs of 3.9, 3.9, 1.8, and 3.9 ug ml, respectively.