[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0

Synthesis and antibacterial properties of 2,3-dideoxyglucosides of terpene alcohols and phenols.

James Bound, D. and Pushpa, S. Murthy and Srinivas, P. (2015) Synthesis and antibacterial properties of 2,3-dideoxyglucosides of terpene alcohols and phenols. Food Chemistry, 185. pp. 192-199.

[img] PDF
Food Chemistry, Volume 185, 15 October 2015, Pages 192-199.pdf - Published Version
Restricted to Registered users only

Download (2MB)

Abstract

Essential oils and their oxygenated terpene constituents possess potent antimicrobial properties. In the present study, a facile synthetic route to the 2,3-dideoxy 1-O-glucosides of important phenols and terpene alcohols in excellent yields (85–96%) has been delineated. Studies on their antimicrobial action against four food-borne pathogens – Bacillus cereus, Staphylococcus aureus, Escherichia coli and Yersinia enterocolitica – demonstrated that the zone of inhibition, in general, was higher for the 2,3-unsaturated 1-O-glucoside derivatives (1b–6b) and the corresponding saturated glucosides (1c–5c) when compared to the parent alcohols/phenols (1–6). The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values for these derivatives too were generally lower than those of the parent compounds. Furthermore, the time–kill and bacteriolysis assays too demonstrated the greater antimicrobial potential of the derivatives. The 2,3-dideoxy 1-O-glucosides of phenols and terpene alcohols were more effective in their antimicrobial action than the corresponding parent compounds. The study indicated that these novel derivatives can find useful application in control of food-related pathogenic microbes in foods.

Item Type: Article
Uncontrolled Keywords: 2,3-Dideoxyglucosides, Spices, Phenols Terpene alcohols, Synthesis, Antibacterial
Subjects: 600 Technology > 08 Food technology > 30 Spices/Condiments
Depositing User: Food Sci. & Technol. Information Services
Date Deposited: 12 Jun 2015 11:06
Last Modified: 12 Jun 2015 11:06
URI: http://ir.cftri.com/id/eprint/11789

Actions (login required)

View Item View Item