Md. Aftab Uddin*
Department of Microbiology, Stamford University Bangladesh, 51 Siddeswari Road, Dhaka 1217, Bangladesh
Khondakar Wahid Hasan
Department of Microbiology, Stamford University Bangladesh, 51 Siddeswari Road, Dhaka 1217, Bangladesh
Jubaida Binta Jamal
Department of Microbiology, Stamford University Bangladesh, 51 Siddeswari Road, Dhaka 1217, Bangladesh
Antibacterial activity; Syzygium aromaticum; Cinnamomum verum; Zingiber officinale; Laurus nobilis
Dhaka city, Bangladesh
Quality and Nutrition
Microbiological aspect, Spices
Collection of samples & processing. Sample of spices are collected for the detection of microbiological analysis and antibacterial activity from from Jatrabari bajar, Dhaka, Bangladesh within a period of July, 2017 to August, 2017. Samples were collected early in the morning and transported quickly to the laboratory according to the standard scheme. For preparing the sample suspension for microbiological examinations, 10g of each sample was weighed and homogenized in 90 ml normal saline to prepare 100ml sample suspension. Then, it was subjected to serial dilution (made up to 10-7 ) for microbiological analysis.
0.1 ml from 10-4 and 10-5 dilution of each sample was spread over nutrient agar (NA) for TVBC & 0.1 ml from 10-3 and 10-4 dilution was spread over SDA plate for the detection of total fungal load respectively (10, 11, 14). Determination of Pseudomonas spp., Staphylococcus spp. and coliform bacteria. An aliquot of 0.1 ml sample from 10-2 & 10-3 dilution was spread on Cetrimide agar, MSA(Mannitol Salt Agar), MAC (MacConkey Agar) for the determination of Pseudomonas spp., Staphylococcus spp. And coliforms, respectively and incubated overnight at 37 oC.
Detection of Vibrio spp., Salmonella spp., and Shigella spp. As Vibrio spp., Salmonella spp. and Shigella spp. remain in the environment as viable but nonculturable (VBNC) state, they do not appear readily during microbiological test procedures. Before conducting serial dilutions, 1 ml of 10-1 and 10-2 diluted samples were enriched with alkaline peptone water (APW) for Vibrio spp. and selenite cystein broth (SCB) for Salmonella spp. & Shigella spp. at 37 oC for 2-4 hrs. The samples were then spread on the XLD agar and TCBS agar for detecting Salmonella spp., Shigella spp. and Vibrio spp. (small, yellow colored colony).
Determination of antibacterial activity of the spices. The antibacterial activity of the samples was carried out by using agar well diffusion method. At first, the suspension (with standard turbidity compared to that of McFarland standard of 0.5) of each of the test bacteria (Escherichia coli, Staphylococcus spp., Vibrio spp., Salmonella spp., Pseudomonas spp., Klebsiella spp., and Bacillus spp.) were spread evenly over the MHA using cotton swab which in turn resulted into uniform lawns. Wells made in the MHA was generated by cork-borer. Each of the samples then introduced separately in the specified well along with a positive control Gentamicin (10µg) and a negative control (normal saline). Existence of clear zone surrounding the sample solution (if any) was indicative of the presence of antibacterial activity of the samples tested.
Stamford Journal of Microbiology, 2017. Vol. 7, Issue 1, p. 10-13 ISSN: 2074-5346 (Print); 2408-8846 (Online)
Journal