Screening of Anti-microbial Effect in Watermelon (Citrullus sp.)
The objective of this study was to determine the potential anti-microbial activity of aqueous ethanolic and chloroform extracts from 3 medicinal plants against bacteria and some fungal strains. The antimicrobial efficacy of Citrullus colocynthis, Citrullus lanatus and Citrullus vulgaris, was evaluated against Gram negative, positive and some fungal strains and including Esherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Bacillus subtilis and Bacillus pumilus some fungal Candida albicans, Aspergillus niger, Penicillium chrysogenum and Penicillium chrysogenum using agar well diffusion method at concentration levels (100 mg mL-1). Among the tested plants, Citrullus colonthis extract showed the highest antibacterial and anti fungal activity and all bacterial and fungal strains at 100 mg mL-1. In addition, almost all species of plants were found to have activity on at least two microbial strains. However, the diameters of inhibition zone were different according to the kinds and concentrations of plant extracts and bacterial and fungal strains. The ethanol extract of citrullus colocynthis was very active against bacterial and fungal at a concentration of 100 mg mL-1. But Trichosporon begelli showed that no zone inhibition in C. valgaries plants of ethanol and chloroform extracts.
Watermelon is one of popular fruits consumed all over the world. Beside its
juicy texture, watermelon is rich in useful antioxidant (mainly lycopene) which
has been demonstrated to inhibit growth of cancer cells (Hall,
2004). Due to its fruits property and size, genetic manipulation of this
plant will have a lot of advantages.
Watermelon is a rich source of citrulline, an amino acid that can be metabolized
to arginine, a conditionally essential amino acid for humans. Arginine is the
nitrogenous substrate used in the synthesis of nitric oxide and plays an essential
role in cardiovascular and immune functions (Collins et
al., 2007). This Cucurbitaceae is widely used in Tunisian folk medicine
and it possesses therapeutic activities against a wide range of ailments including
inflammatory disorders, arthritis and gout (Marzouk et
al., 2009). Nevertheless, a human overdose of plant immature fruits
is hazard. Intoxication is manifested by colitis, gastro-intestinal irritations,
delirium, hypothermia and cerebral congestions (Meyer, 1989;
Anti-microbial gain interest from both academic research and industry due to
their potential to provide quality and safety benefits to many materials. Anti-microbial
packaging is the packaging system that is able to kill or inhibit spoilage and
pathogenic microorganisms that are contaminating foods (Church
and Parsons, 2007; Devlieghere et al., 2000).
Microbial contamination reduces the shelf life of foods and increases the risk
of food-borne illness. The demand for minimally processed, easily prepared and
ready to eat >fresh food products, poses major challenges for
food safety and quality. Application of anti microbial treatment in food packaging
is gaining interest from researchers due to its potential to provide quality,
safety benefits and to extend the shelf life of the food. Anti-microbial food
packaging promotes safety by reducing the rate of growth of specific microorganisms
by direct contact of the package with the surface of foods (Coma
et al., 2001; Ming et al., 1997).
In the present study, we have selected Citrullus sp. like that Citrullus
colocynthis, Citrullus lanatus and Citrullus vulgaris is screened
against multi drug resistant bacteria like Bacillus subtilis, Bacillus
pumilus, Micrococcus luteus, Staphylococcus aureus, Pseudomonas
aeruginosa, Klebsiella pneumonia and Esherichia coli and some
fungal strains like Candida albicans, Aspergillus niger Penicillium
chrysogenum and Trichosporon begelli.
MATERIALS AND METHODS
The leaves of Citrullus sp. like Citrullus colocynthis, Citrullus lanatus and Citrullus vulgaris were collected from the sand dune region of Parangipettai on the Northeast coast of India, during November to December in 2009. The work was carried out of Centre of Advanced study in Marine Biology, Annamalai University, Parngipettai, Tamil nadu India.
Preparation of aqueous extracts: The aqueous extract of Citrullus. sp. leaves were prepared by squeezing the sand-free specimens in triple distilled water. The resultant solution was filtered and dialyzed by using Sigma dialysis membrane-500 (Av Flat width-24.26 mm, Av. Diameter -14.3 mm and capacity approx-1.61 mL cm-1) against D-glucose to remove the excess water. The supernatant so obtained was lyophilized (Labcono Freeze Dry System) and stored at 4°C in a refrigerator for the further use as crude aqueous extract.
Chloroform extraction: Crude toxin was extracted following the method
of Bakus et al. (1981) with certain modifications,
for chloroform extraction, the Citrullus sp. was dried in air for 2 days
and after complete drying, 10 g Citrullus sp. was put into 200 mL of
chloroform, covered and kept standing for 5 h. The solvent was then removed
after squeezing Citrullus sp. and the filtered through whatman filter
paper No 1. The solvent was evaporated at low pressure by using a Buchi Rotavapor
R-200 at 45°C in refrigerator for further use as crude chloroform extracts.
Antibacterial activity: Petri dishes with nutrient agar were inoculated with six different species of bacteria Citrullus sp. extracts were sterilized by passing each through a 0.22: m Millipore GV filter (Millipore, USA) Round paper discs with a radius of 0.8 cm were dipped into each plants extract and placed in the center on inoculated Petri dishes. Bacterial colonies were allowed to grow overnight at 37°C, then the inhibition zone around the disc was measured.
Antifungal activity: Petri dishes with Potato Dextrose agar were inoculated with three different species of fungus. Citrullus sp. extracts were sterilized by passing each through a 0.22: m Millipore GV filter (Millipore, USA) Round paper discs with a radius of 0.8 cm w ere dipped into each Citrullus sp. extract and placed in the center on inoculated petri dishes. Fungal colonies were allowed to grow 48 h at 28°C and then the inhibition zone around the disc was measured.
RESULTS AND DISCUSSION
The present study reveals that the leaves extract of Citrullus colocynthis,
Citrullus lanatus and Citrullus vulgaris were very effective against
bacteria and some fungal strains than the other species. The ethanol extract
of the leaves were more antagonistic than the respective aqueous and chloroform
extracts both bacterial and fungal tested. The ethanol leaves extracts of showed
good antifungal among the 3 plants (Table 4). The ethanol
leaves extracts of showed good anti bacterial activity among the 3 plants (Table
1-3). The zone of inhibition in bacterial maximum was
found in Esherichia coil and minimum in Staphylococcus aureus
(Table 1-3) and followed by the fungal zone
of inhibition was maximum shows in Candida albicans and minimum shows
in Trichosporon begelli for all extracts of aqueous, ethanol and chloroform
was good activity showed among the 3 plants (Table 4). In
the case of absent of zone inhibition showed that only for C. valgaries
leaves extract of ethanol and chloroform in Trichosporon begelli fungal
strains only (Table 4). Minimum zone inhibition was observed
in the bacterial strain only for the C. vulgaris leaves extracts (Table
3). Maximum zone inhibition was observed in the bacterial strain for the
C. colocynthis, C. lanatus (Table 1, 2).
||Anti bacterial activity of Citrullus colocynthis leaves
extracts and zone of inhibition
||Anti bacterial activity of Citrullus lanatus leaves
extracts and zone of inhibition
||Anti bacterial activity of Citrullus valgaries leaves
extracts and zone of inhibition
||Anti fungal activity of Citrullus sp. leaves extracts
and zone of inhibition
The present study reveals that the leaves extracts of Citrullus sp.
were very effective against bacteria such as Esherichia coli, Klebsiella
pneumoniae, Pseudomonas aeruginosa, Bacillus subtilis, Bacillus
pumilusand and some fungal Candida albicans, Aspergillus niger,
Penicillium chrysogenum, Penicillium chrysogenum than the other
species tested. The ethanol extracts of the leaves were more antagonistic than
the respective chloroform and aqueous extracts showed (Table 1).
The antibacterial activity may be due to the presence of alkaloids, flavonoids,
tannin, polyphenolic and oil as reported by Irobi and Daranola
(1994) and Brantner et al. (1996). This finding
is in agreement with the results of Agatemor (2009)
who found that ethanolic extracts of some Nigerian spices were more potent than
the aqueous extracts against common food borne microorganisms including Staphylococcus
aureus, Klebsiella pneumoniae, Proteus vulgaris and Streptococcus
faecalis. So, present result indicate the same result in r ethanol extract
for more zone inhibition when compare to other like aqueous and chloroform.
The volatile oil of Artimisia afra has greater activity as an antimycotic
than as an antibacterial agent (Graven et al., 1992).
The present study for all extract of Citrullus sp. leaves very good effective
in some fungal strains (Tabel 4). The ethanol and chloroform
extras of the citrullus sp. leaves showed low anti fungal activity against
the stains of Trichosporon begelli in C. valgaries extract Showed
(Tabel 4). The maximum zone inhibition was shows in Candida
albicans, Aspergillus niger and Penicillium chrysogenum and
minimum zone inhibition was shows in Trichosporon begelli (Table
4). It was revealed in this study, that the antifungal activity of the extracts
was enhanced by increase in the concentration of the extracts. It also supports
the earlier investigation (Banso and Adeyemo, 2007)
that the tannins isolated from the medicinal plants possess remarkable toxic
activity against bacteria and fungi and may assume pharmacological importance.
In conclusion, the studied plant could provide some activity against anti bacterial and anti fungal; however, it is not known that which component of the extract is responsible for this effect. Further studies using isolated constituents instead of the whole extract should be carried out.
The authors are grateful Thanks to the Dean, Centre of Advanced study in Marine Biology, Faculty of Marine Sciences, Annamalai University, for providing all support during the study period.
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