Browsing by Author "Odu C. E."
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Item Application of extracts of Henna (Lawsonia inamis) leaves as a counter stain(African Journal of Microbiology Research, 2011-10-09) Chukwu O. O. C.; Odu C. E.; Chukwu D. I.; Hafiz N.; Chidozie V. N.; Onyimba I. A.Aqueous (cold and hot) and ethanol extracts solutions of the Henna plant (Lawsonia inamis) leaves was adapted for the first time as a counter stain in Gram staining reaction. Different extracts of L. inamis leaves were formulated into various staining solutions of different concentrations and modified with hydrogen peroxide, ferric chloride, potassium alum and potassium permanganate. These staining solutions were used to stain both known Gram positive and Gram negative bacterial isolates using Gram staining technique. The experimental Henna plant extracts solutions were used with usual counter stains (neutral red, safranine and dilute carbol fuchsin) as positive controls. Phytochemical screening of the extracts revealed the presence of tannin (hennatonic acid or Lawsone) and saponin. The aqueous extracts of the Henna plant (cold and hot) oxidized with potassium permanganate (pH 7.00 to 7.16) gave a better staining reaction with Gram negative bacteria, while the ethanol extract oxidized with potassium permanganate (pH 6.55) had no staining reaction with Gram negative bacteria. Hence the aqueous Henna leaves extracts (cold or hot) when oxidized with potassium permanganate can be a substitute to the usual counter stains used in Gram staining procedure. The results of staining ability of the various henna leaves extracts solutions are discussed.Item Carrot (Daucus carrota), Garlic (Allium sativum) and Ginger (Zingiber officinale) Extracts as Bacteria Selective Agents in Culture Media(African Journal of Microbiology Research, 2011-12-23) Chukwu O. O. C; Odu C. E.; Chukwu I. D.; Chidozie V. N.; Onyimba I. A.; Bala Z.Extracts of carrot, garlic and ginger as selective agents in basal bacteriological media were carried out on Staphylococcus aureus ATCC 15313, Listeria monocytogenes ATCC 2522, Escherichia coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 using a standard method. Ethanolic extracts, aqueous cold and hot extracts of the experimental plant products were made at the concentration of 200 mg/ml (2 g/10 ml). The ethanolic extracts inhibited the growth of all the test bacterial isolates. The cold aqueous extracts of garlic had inhibitory effects on the S. aureus and L. monocytogenes bacterial isolates but selectively allowed the growth of E. coli. The hot aqueous extract of ginger had no effect on any of the test bacteria. The hot garlic extract selectively allowed the growth of L. monocytogenes and E. coli. Phytochemical analysis of the carrots, garlic and ginger contained saponnin, resins, alkaloids, flavonoids, steroids and terpenes in varied proportions. We assume these products may have influenced the actions of the extracts on the test organisms. The results of this preliminary study suggest that aqueous extracts of carrots, garlic and ginger when incorporated in appropriate concentrations can serve as alternative selective agents in bacteriological culture media for bacterial isolation from highly contaminated biological specimens or separation of mixed cultures of bacteria in the laboratory.