Antifungal, physicochemical, and insect-repelling activity of the essential oil of Ocimum basilicum

1989 ◽  
Vol 67 (7) ◽  
pp. 2085-2087 ◽  
Author(s):  
S. Dube ◽  
P. D. Upadhyay ◽  
S. C. Tripathi

The essential oil of Ocimum basilicum at a dose of 1.5 mL/L completely inhibited the mycelial growth of 22 species of fungi, including the mycotoxin-producing strains of Aspergillus flavus and Aspergillus parasiticus. It also proved to repel the insect Allacophora foveicollis. The toxic dose of the oil against the test fungi was much lower than that of some commercial fungicides and fumigants, and it remains unaffected by temperature treatment, storage, and increased inoculum.

1983 ◽  
Vol 46 (11) ◽  
pp. 940-942 ◽  
Author(s):  
LLOYD B. BULLERMAN

Growth and aflatoxin production by selected strains of Aspergillus parasiticus and Aspergillus flavus in the presence of potassium sorbate at 12°C were studied. Potassium sorbate at 0.05, 0.10 and 0.15% delayed or prevented spore germination and initiation of growth, and slowed growth of these organisms in yeast-extract sucrose broth at 12°C. Increasing concentrations of sorbate caused more variation in the amount of total mycelial growth and generally resulted in a decrease in total mycelial mass. Potassium sorbate also greatly reduced or prevented production of aflatoxin B1 by A. parasiticus and A. flavus for up to 70 d at 12°C. At 0.10 and 0.15% of sorbate, aflatoxin production was essentially eliminated. A 0.05% sorbate, aflatoxin production was greatly decreased in A. flavus over the control, but only slightly decreased in A. parasiticus.


2015 ◽  
Vol 3 (3) ◽  
pp. 374-379 ◽  
Author(s):  
Neveen Helmy Abou El-Soud ◽  
Mohamed Deabes ◽  
Lamia Abou El-Kassem ◽  
Mona Khalil

BACKGROUND: The leaves of Ocimum basilicum L. (basil) are used in traditional cuisine as spices; its essential oil has found a wide application in perfumery, dental products as well as antifungal agents.AIM: To assess the chemical composition as well as the in vitro antifungal activity of O. basilicum L. essential oil against Aspergillus flavus fungal growth and aflatoxin B1 production.MATERIAL AND METHODS: The essential oil of O. basilicum was obtained by hydrodistillation and analysed using gas chromatography (GC) and GC coupled with mass spectrometry (GC/MS). The essential oil was tested for its effects on Aspergillus flavus (A. flavus) mycelial growth and aflatoxin B1 production in Yeast Extract Sucrose (YES) growth media. Aflatoxin B1 production was determined by high performance liquid chromatography (HPLC).RESULTS: Nineteen compounds, representing 96.7% of the total oil were identified. The main components were as follows: linalool (48.4%), 1,8-cineol (12.2%), eugenol (6.6%), methyl cinnamate (6.2%), α-cubebene (5.7%), caryophyllene (2.5%), β-ocimene (2.1%) and α-farnesene (2.0%).The tested oil showed significant antifungal activity that was dependent on the used oil concentration. The complete inhibition of A. flavus growth was observed at 1000 ppm oil concentration, while marked inhibition of aflatoxin B1 production was observed at all oil concentrations tested (500, 750 and 1000 ppm).CONCLUSION: These results confirm the antifungal activities of O. basilicum L. oil and its potential use to cure mycotic infections and act as pharmaceutical preservative against A. flavus growth and aflatoxin B1 production.


2009 ◽  
Vol 45 (2) ◽  
pp. 108-111 ◽  
Author(s):  
Georgia Rocha Vilela ◽  
Gustavo Steffen de Almeida ◽  
Marisa Aparecida Bismara Regitano D'Arce ◽  
Maria Heloisa Duarte Moraes ◽  
José Otávio Brito ◽  
...  

1983 ◽  
Vol 46 (3) ◽  
pp. 178-184 ◽  
Author(s):  
KUN-YOUNG PARK ◽  
LLOYD B. BULLERMAN

The effects of substrates (synthetic and semisynthetic broths and several foods) on aflatoxin production by Aspergillus parasiticus and Aspergillus flavus were studied at different temperatures. The addition of calcium lactate as a carbon source to synthetic and semisynthetic broth media was evaluated for its effect on mycelial growth and aflatoxin production. At temperatures of 15 and 25°C, lactate did not support either mycelial growth or aflatoxin production in a basal salts broth, but did support mycelial growth, though not aflatoxin production, by both molds in a semisynthetic (YEL) broth. No growth of either mold or aflatoxin production was observed at 5°C on any of the liquid media employed. Little or no aflatoxin was detected on high protein/low carbohydrate foods such as Cheddar cheese, cottage cheese, yogurt and summer sausage inoculated with A. parasiticus and held at 15°C, but substantial quantities of aflatoxins were produced on yogurt and summer sausage by A. flavus at 15°C. Cheddar and cottage cheeses were poor substrates for aflatoxin production by A. flavus at 15°C. Cheddar cheese was a favorable substrate for aflatoxin production by both molds at 25°C. Cottage cheese was a poor substrate for aflatoxin production by both organisms at 25°C. Yogurt and summer sausage were poor substrates for A. parasiticus, but favorable substrates for A. flavus for aflatoxin production at 15 and 25°C. Trace levels of aflatoxins were produced on whole soybeans by A. parasiticus, whereas high levels of aflatoxins were produced by A. flavus on soybeans at 15 and 25°C. No growth or aflatoxin production occurred on soybean blocks (Meju) at 15°C, but high levels of aflatoxins were produced at 25°C by both molds. Aflatoxins did not diffuse into the second 1-cm layer of process cheese at 15°C; however, diffusion occurred at 25°C. Process cheese appeared to be a poor substrate for aflatoxin production by both molds at 15 and 25°C. Trace levels of aflatoxins (10 to 60 ppb of aflatoxin B1) were detected on some samples of yogurt and summer sausage at 5°C, although no growth of either mold was observed.


2018 ◽  
Vol 69 (8) ◽  
pp. 1927-1933 ◽  
Author(s):  
Mariana Deleanu ◽  
Elisabeta E. Popa ◽  
Mona E. Popa

The compounds in Ginger (Zingiber officinale-Roscoe) essential oil provenience China and wild oregano (Origanum vulgare) essential oil of Romanian origin were identified by GC/MS and their antioxidant and antifungal properties were evaluated. Wild oregano oil was characterized by high content of oxygenated monoterpenes hydrocarbons (84.05%) of which carvacrol was the most abundant (73.85%) followed by b-linalool (3.46%) and thymol (2.29%). Ginger oil had a higher content of sesquiterpene hydrocarbons including zingiberene (31.47%), b-sesquiphellandrene (13.76%), a-curcumene (10.41%), a-farnesene (8.31%) and b-bisabolene (7.55%) but a lower content of oxygenated monoterpenes (7.97%). The high content of oxygenated monoterpens of wild oregano oil is in accordance with total content of polyphenols determined by the Folin�Ciocalteu method (6.71�0.73 mg of gallic acid equivalent per g oil). Ginger oil had only 1.34�0.22 mg gallic acid equivalent per g oil. Wild oregano oils exhibited appreciable in vitro antioxidant activity as assessed by 2, 2`-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging and 2,2�-azino-bis (3 ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS). The sample concentration required to scavenge 50% of the DPPH free radicals was 0.76�0.13 mg/mL for wild oregano oil compared to 20.22�2.12 mg/mL for ginger oil. Also, wild oregano oils showed significant inhibitory activity against selected pathogenic fungi (Fusarium oxysporum, Aspergillus flavus and Penicillium expansum). 1�L of oregano oil is sufficient for almost 75% growth inhibition of Aspergillus flavus compared to ginger oil which shows antifungal activity at 240�L for 78% growth inhibition. It can be concluded that wild oregano oil could be used as food preservative in some food products in which Fusarium oxysporum, Aspergillus flavus and Penicillium expansum could grow and have potential to produce health hazards mycotoxines.


Eisei kagaku ◽  
1991 ◽  
Vol 37 (2) ◽  
pp. 107-116 ◽  
Author(s):  
MITSUO NAKAZATO ◽  
SATOSHI MOROZUMI ◽  
KAZUO SAITO ◽  
KENJI FUJINUMA ◽  
TAICHIRO NISHIMA ◽  
...  

2021 ◽  
Vol 281 ◽  
pp. 109964
Author(s):  
Halime Kahveci ◽  
Nilgun Bilginer ◽  
Emel Diraz-Yildirim ◽  
Muhittin Kulak ◽  
Emre Yazar ◽  
...  

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