Ethanobotanical knowledge and antimicrobial activity of Pseudarthria viscida (L.)Wight & Arn., 1Ahila N*, 1Sindhu, 1Neelamegam R, and 2Siva Nadanam V 1S.T.Hindu College, Nagarcoil- 629 002, 2Lakshmipuram College of Arts and Science, Neyyoor- 629 802, *Correspoding auther email: ghanthi@gmail.com. Abstract The present work carried out on the ethanobotanical knowledge and antimicrobial activity for the leaf and stem extract of the Pseudarthria viscida (L.)Wight&Arn., Traditionally, this plant is used as cold, skin diseases, fever, headache, wounds and scabies by in an around Kalakad villager. The benzene leaf extracts showed the antibacterial activities against all the testing bacteria such as Escherichia coli, Pseudomonas …show more content…
viscida were collected from Kalakad villages in Tirunelveli District, Tamilnadu. The plant material was identified by St. Xavier’s college Herbarium (XCH) at Palayamkottai, Tirunelveli. The leaves and stem of P. viscida were a shade dried and powder with the aid of an electronic food processor. The 30 g of fine powdered materials was rolled in a filtered paper and kept in soxhlet apparatus with 250 ml of solvent (Petroleum ether, benzene, chloroform, methanol and Dis.H20 solvent) for the extract preparation at 24 h process. For antibacterial activity studies was carried by Whatman No. 1 filter paper (5 mm diameter) disc diffusion method. The selected pathogenic diluted bacteria (0.5 ml) like Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Salmonella typhii, Streptococcus pyogens, Serratia marcescens, Klebsiella pneumonia, Enterobacter aeruginosa, Proteus vulgaris, Bacillus subtilis culture was spread on sterile Muller Hinton Agar plates. The dried discs were placed on the sealed plates and gently pressed down to assure contact with the medium. Streptomycin 5 mg/ml was used as positive control and respective solvents which were used to dissolve the crude extracts served as negative control. The plates were incubated at room temperature for 24 hrs. After the incubation period the diameter of the inhibition zone around the discs were measured and recorded. Three replicates for each concentration were …show more content…
Now the extracts from stem and leaf extract of Pseudarthria viscida also exhibited better results against all the pathogens used. Ethanolic and chloroform extract of the stem showed maximum inhibitory activity when compared with other extracts. The zone of inhibition was proved that all the extracts were highly effective against several bacteria. The activity of stem extract was higher when compared with the leaf extract. The present investigation has resulted in a protocol that could be used for ex-situ conservation and true to type mass propagation of this herb of immense pharmaceutical relevance. Moreover, it can be used as an alternative source of drugs in the medicinal field. Table 1: Antimicrobial activity of leaf and stem extract of Pseudarthria viscida S.No Name of the Bacteria Petroleum ether Benzene Chloroform Methanol Dis.H20 Control Leaf Stem Leaf Stem Leaf Stem Leaf Stem Leaf Stem 01 Escherichia coli 7 - 10 - 11 - - - - - 10 02 Pseudomonas aeruginosa 8 - 12 - 12 - 18 - - - 9 03 Staphylococcus aureus 6 - 9 - 9 - 12 - - - 4 04 Salmonella typhii - - - 5 5 - 17 - - - 15 05 Streptococcus pyogens 6 4 9 4 10 6 11 6 5 - 12 06 Serratia marcescens 12 - 14 - 17 - 12 - 8 - 7 07 Klebsiella pneumoniae - - 7 - 8 - 8 - - -
After lawn inoculating a Meuller Hinton plate and placing the samples of medication, the plate was then incubated for one week at 37 degrees Celsius. The first medication choice was Trimethoprim, this produced a zone of inhibition of 16mm, therefore being sensitive to the bacteria. Antibiotic number two was nalidixic acid, this too, has a zone of inhibition of 16mm but is considered intermediate. The next antibiotic was erythromycin which produced a zone of inhibition of zero and was therefore resistant. The last antibiotic that was chosen to be used in the experiment was ciprofloxacin.
Using two separate aseptic pipettes, 250 µl of LB broth were added to each micro test tube and mixed gently. Likewise, using two separate, aseptic pipettes for each tube, 100 µl of solution was added to the appropriate agar plate. After, using a new loop for each plate, the solution was spread gently across their surfaces. Lastly, the plates were stacked, taped together, and labelled before placing them upside down in an incubator set at 37°C
Although the overall absorbance increases as more milliliters of mitochondrial suspension is added to a mixture of 0.25 mL of 0.5 mM DCIP, 0.5 mL of 50 mM sodium azide, various volumes of assay buffer (20 mM potassium
The History and Science of Healing With Essential Oils Did you know that at least 30% of prescription drugs in the United States are based on naturally occurring compounds from plants? Each year, millions of dollars are spent searching for new, undiscovered, curative elements in the bark, roots, flowers, seeds and foliage of plants from every corner of the Earth. As the most powerful part of the plant, essential oils and plant extracts have been mankind 's first medicine. History has shown and science supports that these can be used medicinally to kill bacteria and viruses.
In the laboratory, identification of an unknown bacterium is often necessary. In the lab, a random sample consisting of three different bacteria was selected. The sample contained one gram-positive, one gram-negative paracolon, and one gram-negative coliform. The purpose of the experiment is to identify each of the three species that the mixture contained. After receiving an unknown mixture, the sample was streaked for isolation onto TSA, blood agar, and MacConkey plates.
There are many things that some plants can provide. “Smudge ourselves real good with sweetgrass or cedar first. Get cleansed so we can approach it with respect” (page 166). The smoke that is given off of the burning sweetgrass is well knows to purify the body, heart, and soul. Traditional medicinal plants like the Wiike (wee-kay) root, can take away the pain from a sore throat.
The Kirby-Bauer disk diffusion method is utilized as a part of this trial so as to watch the viability of a sure anti-microbial. This strategy incorporates the spreading of the two sorts of bacteria being concentrated on an agar in a petri dish with the goal that they can produce. One agar contained Wild S. Aureus and another agar contained MRSA. Paper circles are let to absorb refined water, and equivalent centralizations of the accompanying antibiotic arrangements: Methicillin, Vancomycin and XR21347. At that point, these paper plates are put onto both agars and left as a base for bacterial development.
Meaning if the extract inhibits cilia, the affects for the human functioning airways would become weak due to cilia being the one that helps move the airway surface fluids and mucus. Providing continuous cleansing of the airway surface, which is a vital defense against inhaled particles. Materials and Methods a. experimental design: To begin the experiment we made two groups one called the control group and one called the experimental group with tobacco. For the control group we added a mixture of 20 microliters of tetrahymena, 1% India ink and 1% of glutaraldehyde to a microscope slide to create the control group . In the experimental tobacco group we added the same amount of substances only difference was 50 microliters of tobacco extract was added to the mixture.
The B. Vulgaris samples were approximately 1cm3. They were kept the same size to ensure accurate results. A control test was conducted in distilled water to obtain a result to compare. The ethanol treatments were 40% and 70%. To prepare the solutions a 70% ethanol solution was used to make 40%.
After 48 hours, I observed different growth patterns around the disks. I measured the zone of inhibition of each antibiotic and document them on Microbiology task 3
Uncontrolled Environmental conditions Atmospheric conditions The controlled variable Concentration of amylase was kept under control by measuring the amount of amylase used and also it was made sure the percentage of amylase used was 1%. The Amount of amylase/starch used were kept to 5cm3 at all times. Materials needed Beakers Bunsen burner Test tube Thermometer Stopwatch Test plate Glass rod Starch Amylase solution Water bath Iodine solution. Test tube holder Labels Marker Procedure First 5 test tubes were taken and labeled with numbers from 1 to
Sordaria fimicola is a microscopic fungal species that produces ordered tetrads. It is commonly used in classrooms because it lacks conidiospores, has a short generation time with matching genotype and phenotype, has known color genes that permit tetrad analysis, easily observable crossing over effects, and does not undergo spindle overlap. In S. fimicola, meiosis occurs in the ascus. The fungus is a haploid organism for the majority of its life. It only becomes diploid when mycelia of two unlike strains fuse.
50 μL of these dilution solutions were separated on the TLC plate coated with SNISG. The plate was developed with petroleum ether: ethyl acetate (4:1) and the movement of solvent was usually controlled at 1 cm from the upper edge. After completion, the plate was dried until no solvent smell remained. It was sprayed with an ethanol solution containing 10% sulfuric acid, and heated at an infra-red drier until obvious color came up, as shown in Fig.2 (B.ab). Simultaneously, the amount of silver nitrate in the impact of isolative effect was investigated with the sample procedure, as shown in Fig.2
For TLC profiling, 4 TLC plates were prepared for the testing of each solvent. As shown in Figure 1, the green food dye was placed at the bottom center, specifically 0.5 cm away from the bottom of the plate, with the use of a capillary tube. Each one of the silica plates were then vertically placed in a small beaker with its inside surrounded by a filter paper saturated with the solvent to be tested and a small amount of the same solvent at the bottom. The TLC plate was then taken out when the rising solvent was about to reach the top of plate. The ammonia: 1-butanol solvent was tested 7 times due to some personal