A non-reducing disugar and amino acid were isolated in the studies on the structure of parvulomycin. The acid hydrolysis of the disugar revealed the presence of 2 moles of D-glucose. Acetylation of the disugar resulted in formation of octa-O-acetyl-alpha,alpha-tregalose, saponification of which resulted in formation of alpha,alpha-tregalose. Its physical parameters, i.e. melting point of the mixed sample, optical rotation, IR-spectrum coincided with those of the authentic alpha,alpha-tregalose. The isolated amino acid proved to be L-glutamic acid on thin-layer chromatography with witness and comparison of the physico-chemical properties of their hydrochlorides.

Download full-text PDF

Source

Publication Analysis

Top Keywords

amino acid
8
[study antibiotic
4
antibiotic parvulomycin
4
parvulomycin isolation
4
isolation alphaalpha-trehalose
4
alphaalpha-trehalose l-glutamic
4
l-glutamic acid]
4
acid] non-reducing
4
non-reducing disugar
4
disugar amino
4

Similar Publications

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!