INTRODUCTION World Health Organization (2004) reported that infectious diseases are a major cause of morbidity and mortality worldwide and bacterial infection causes high rate of mortality in human population (Farias et al., 2000). The enhanced treatment of infectious diseases by microbicide has limitations because of its changing patterns of resistance in pathogens and side effects. These limitations demand for the identification of new antimicrobial compounds derived from natural sources especially from marine (Ballantine et al., 1987).Marine seaweeds are rich source of structurally novel and biologically active metabolites. Secondary and primary metabolites isolated from seaweeds are potentially active in the pharmaceutical industry against human and other diseases (Farias et al., 2000). Most of the secondary metabolites of marine seaweeds such as flavonoids, terpenoids, alkaloids and phenolic compounds show wide range of anti-bacterial activities against the human pathogens ( Thirumaran et al., 2006) and recent research implies that polysaccharides like inulin, oligo-fructose, galacto oligosaccharides and lactilose can also act as potent prebiotic compounds against pathogenic microbes in humans.The antimicrobial activity of seaweeds in the coastal area of Tamil Nadu is still needs to be explored. Sargassum wightii belongs to brown seaweeds and are widely found in south Indian coastal belt with remarkable biological activities.Bacillus cereus is a Gram-positive, rod-shaped aerobic bacterium with endospore (Todar, 2008) and can multiply quickly even at room temperature. B. cereus is responsible for a minority (2-5%) of food borne diseases (Todar, 2008;Davis, 2010), causing severe nausea, vomiting and diarrhea, aggressive than necrotizing fasciitis. Food poisoning is a major health problem, affecting both industrialized and developing countries.Objective of the present study was to screen the crude solvent extracts of S. wightii against the food borne pathogen B. cereus. MATERIALS AND METHODS Antibacterial assaysBacterial culture B. cereus was collected from the Rajah Muthiah Medical College, Annamalai University, Tamil Nadu, India. Collected strain was grown in Trypticase soy-polymyxin broth under aerobic conditions at 37°C in a rotary shaker at 200 rpm to reach exponential growth. Screening of antibacterial activityCrude petroleum ether, chloroform, acetone and ethanol extracts of the seaweed S. wightii were obtained by sequential solvent extraction method using a soxhlet. The antibacterial activity of crude extracts was performed by agar plate well diffusion assay on Mueller Hinton Agar (Marudhupandi and AjithKumar, 2013). Mueller Hinton agar media was prepared, sterilized and poured into sterile Petri dishes. Wells of 6 mm diameter were made on the agar plates by using sterilized well cutter. Inoculum in exponential phase of growth, equivalent to a 0.5 McFarland standard was swabbed on to the surface of the agar. Crude extracts of the solvents (petroleum ether, chloroform, acetone and ethanol) were prep...
The present work investigates the antibacterial activity of silver nanoparticles (Ag-NPs) synthesized by biological method using Sargassum wightii. The fresh live seaweed was collected from the Mandapam coast of Tamilnadu, India. Solvent extract was prepared using acetone, petroleum ether and methanol. Aqueous extract of the seaweed was also used for the synthesis of silver Ag-NPs. Seaweed extract is used as a reducing agent of 2mM silver nitrate solution for the synthesis of Ag-NPs. Periodical monitoring of reaction mixture was done using UV-vis spectroscopy at 300-750 nm. The scanning electron microscopy (SEM) of the sample confirms the presence of Ag-NPs. The antibacterial activity of solvent extract was done by Minimal inhibitory concentration (MIC) assay. The methanol extract of the seaweed at a concentration of 250µg/ml exhibited potent antimicrobial activity against the test microorganism. The zone of inhibition ranging from 8-14 mm was observed with different extracts. The antibacterial activity of the synthesized Ag-NPs against the organism was also done by MIC test. The MIC of Ag-NPs was found to be 130µg/ml for all pathogenic microorganisms selected for the study. The zone of inhibition against Bacillus cereus, Bacillus anhtracis, Staphylococcus aureus and Vibrio alginoyticus were found to be 10, 8, 10 and 9 mm, respectively. The synthesized Ag-NPs exhibited significant antimicrobial activity against the selected microorganisms than the solvent extract of seaweed.DOI: http://dx.doi.org/10.3329/icpj.v3i10.20337 International Current Pharmaceutical Journal, September 2014, 3(10): 322-325
The study is planned to find the antimicrobial activity of the extract of Jania rubens and to isolate the bioactive compound against MRSA and VRSA. Jania rubens collected from Mandapam (Pudumadam) Coastal water, East coast of India and extracted with ethanol. Antibacterial activity of J. rubens was tested against gram positive, gram negative bacteria and drug resistant bacteria). The antibacterial activities were expressed as zone of inhibition, minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) Identification of compounds from crude extract of J. rubens carried by column chromatography, thin layer chromatography and NMR analysis. Finally J. rubens could serve as useful source of new antibacterial agent.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.