Various pathological specimens (180) were collected from patients suffering
from pseudomonas aeruginosa infections from different hospitals in Baghdad from January
to May 2011; these specimens include (Blood samples,sputum,urine and wound swabs) were
tested for pseudomonas aeruginosa producing 2-Aminoacetophenone.Wounds swabs
specially taken from burns and post surgical infections producing a higher concentration of 2-Acetophenone material than from other samples were tested for this material and most of
these were isolated bases on their distinctive grape- like odor of 2-Aminoacetophenone
production usually linked with patients whose immune system compromised by disease or
trauma, its gains access to these patients tissue through burns, although the grape odor is
sometimes difficult to detect in culture media.
These methods can be utilized to assay 2-aminoacetophenone (2AA) production in a
varies media. Its synthesis occurs relatively early in the growth cycle. It has proved easy and
convenient to detect 2-aminoacetophenone (2AA) excretion by Pseudomonas aeruginosa after
24 h of incubation on blood agar plates employing thin layer chromatography of ether extracts
of the agar medium.
2-Aminoacetophenone As A Virulent Factor For Pseudomonas Aeruginosa Causing Sever Burn And Wound Infections In Iraq
2-Aminoacetophenone
Pseudomonas Aeruginosa
gramnegative Baeteria.
Publication Date
Thu Apr 20 2023
Journal Name
Ibn Al-haitham Journal For Pure And Applied Sciences
Design of New V Shaped Thermotropic Liquid Crystals containing Heterocyclic
thiazolidine-2
4-dione
heterocyclic
thermotropic LC
V liquid crystals
The characterization and design of this study of new liquid crystals with a V shape compounds containing thiazolidine-2,4-dione and 1,3-phenylene as a core unite with mesophase properties were reported. Preparation and characterization of chloroacetic acid, water, and thiourea to produce thiazolidine-2,4-dione [I] in the presence of strong hydrochloric acid. The 4-hydreoxybenzaldehyde and n-alkyl bromide were reacted with potassium hydroxide to create the n-alkoxy benzaldehyde., then the compound [I] reacted with [II]n in presence of piperidine to produce compounds [III]n. Also, converted resorcinol to a corresponding compound [IV] by refl
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