Growth and Aflatoxin Production by Aspergillus parasiticus NRRL 2999 in the Presence of Potassium Benzoate or Potassium Sorbate and at Different Initial pH Values

1987 ◽  
Vol 50 (10) ◽  
pp. 820-825 ◽  
Author(s):  
GULAM RUSUL ◽  
ELMER H. MARTH

Experiments were done to determine how different concentrations of potassium benzoate or potassium sorbate in a glucose-yeast extract-salts medium with an initial pH value of 3.5, 4.5 or 5.5 affected growth and aflatoxin production by Aspergillus parasiticus NRRL 2999. The pH of the medium, weight of mycelium and amount of aflatoxin produced were determined after 3 and 7 d of incubation. Aflatoxin was determined using reversed-phase high-performance liquid chromatography. Maximum concentrations of potassium sorbate and potassium benzoate that permitted growth were 0.2% and 0.4%, respectively, in a medium with an initial pH of 5.5. When the initial pH was 4.5, the maximum concentrations of potassium sorbate and potassium benzoate that permitted growth were 0.05% and 0.10%, respectively, but there was an extended lag phase. Increasing concentrations of potassium benzoate or potassium sorbate decreased amounts of aflatoxin B1 and G1 produced after 3 d in a medium with initial pH values of 5.5 or 4.5. Cultures growing in the medium containing 0.1, 0.15 or 0.20% potassium benzoate or potassium sorbate and with an initial pH of 5.5 were somewhat inhibited at 3 d of incubation, which was characterized by a slow decrease in pH, low mycelium dry weight and small amounts of accumulated aflatoxins. After 7 d these cultures overcame the initial inhibition and produced substantial amounts of aflatoxins and mycelium. This was also true for cultures growing in a medium with an initial pH of 4.5 and containing potassium benzoate or potassium sorbate. By decreasing the initial pH of the medium from 5.5 to 4.5, amounts of potassium benzoate or potassium sorbate required to achieve inhibition decreased by a factor of 10.

1987 ◽  
Vol 50 (11) ◽  
pp. 940-944 ◽  
Author(s):  
FATHY E. EL-GAZZAR ◽  
GULAM RUSUL ◽  
ELMER H. MARTH

Twenty-five milliliters of glucose-yeast-salts medium containing 0, 0.5, 0.75, 1.0, 1.5 and 2.0% lactic acid with an initial pH of 3.5 or 4.5 were inoculated with 1 ml of a spore suspension containing 106 conidia of Aspergillus parasiticus NRRL 2999 and incubated at 28°C for 10 d. The pH of the medium, weight of mycelium and aflatoxin production were determined after 3, 7, and 10 d of incubation. Amounts of aflatoxin produced were determined using reversed-phase high-performance liquid chromatography. Cultures grown in the presence of 0.5 and 0.75% lactic acid at an initial pH of 4.5 produced more aflatoxin B1 than did the other cultures at the end of 3 d of incubation. This was not true for aflatoxin G1; with increasing concentrations of lactic acid, cultures produced decreasing amounts of aflatoxin G1. Also, cultures growing in the medium with an initial pH of 3.5 produced more aflatoxin B1 in the presence of lactic acid at the end of 3 d of incubation than did control cultures. Cultures growing in the presence of 0.5 and 0.75% lactic acid produced the most aflatoxin. Maximum amounts of aflatoxin G1 were produced after 7 d of incubation, with cultures growing in the presence of 0.5 and 0.75% lactic acid producing the most. Lactic acid did not inhibit growth (mycelium weight) of cultures in the medium with initial pH values of 3.5 or 4.5 except there was a slight decrease in mycelial weight when the medium contained 0.5% lactic acid and had an initial pH value of 3.5.


1986 ◽  
Vol 49 (6) ◽  
pp. 461-466 ◽  
Author(s):  
FATHY E. EL-GAZZAR ◽  
GULAM RUSUL ◽  
ELMER H. MARTH

Twenty-five milliliters of glucose-yeast-salt medium containing 0, 2, 4, 6, 8, or 10% NaCl was inoculated to contain, approximately 105 or 107 conidia of Aspergillus parasiticus NRRL 2999 and then incubated at 13 or 28°C. Amounts of aflatoxin produced were determined using Reversed-Phase High Performance Liquid Chromatography (HPLC). Increasing the concentration of NaCl reduced accumulation of aflatoxin and also induced a lag in growth of the culture. At 13°C, the mold produced small amounts of aflatoxin after an extended lag phase, and NaCl was markedly more inhibitory at 13 than at 28°C.


1987 ◽  
Vol 50 (11) ◽  
pp. 909-914 ◽  
Author(s):  
GULAM RUSUL ◽  
FATHY E. EL-GAZZAR ◽  
ELMER H. MARTH

Experiments were done to determine effects of different concentrations of acetic or propionic acid in a glucose-yeast extract-salts medium with an initial pH value of 4,5 or 5.5 on growth and aflatoxin production by Aspergillus parasiticus NRRL 2999. Amounts of aflatoxin were measured with reversed-phase high-performance liquid chromatography. The maximum concentration of acetic or propionic acid that permitted growth at an initial pH of 5.5 was 1% after 7 d of incubation and 0.25% after 3 d of incubation, respectively. When the initial pH of the medium was 4.5, the maximum concentration of acetic or propionic acid that permitted growth was 0.25 or 0.1%, respectively. There was no significant difference (p>0.05) in amount of mycelial (dry weight) produced by cultures in the presence of 0.0, 0.25, 0.50 or 0.75% acetic acid. Amounts of aflatoxin B1 and G1 produced decreased with an increasing concentration of acetic acid. Increasing concentrations of propionic acid caused a decrease in the amount of mycelial dry weight and aflatoxin produced by cultures growing in the medium with an initial pH of 5.5. At an initial pH of 4.5 mycelial growth was slow and at 3 d of incubation amounts of aflatoxin B1 and G1 produced were reduced as concentrations of acetic acid increased. This also was true for propionic acid in the medium with an initial pH of 4.5. Cultures with an extended lag phase in the presence of acetic or propionic acid overcame this and then produced large amounts of aflatoxin B1 and G1 at 7 and 10 d of incubation.


1986 ◽  
Vol 49 (11) ◽  
pp. 880-885 ◽  
Author(s):  
GULAM RUSUL ◽  
FATHY E. EL-GAZZAR ◽  
ELMER H. MARTH

Twenty-five milliliters of glucose-yeast-salts medium containing 0, 2, 4, 6, 8 and 10% KCl or a mixture of NaCl (%) and KCl (%) (0:0, 1.5:0.5, 3.25:0.75, 4.75:1.25, 6.5:1.5, and 8:2) was inoculated with 1 ml of a spore suspension containing 106 conidia of Aspergillus parasiticus NRRL 2999 and incubated at 28°C for 10 d. The pH, dry weight of mycelium and aflatoxin production were determined after 3, 7 and 10 d of incubation. Amounts of aflatoxin produced were determined using reverse-phase high-performance liquid chromatography (HPLC). The mold growing in the presence of 0, 2 and 4% KCl produced maximum amounts of aflatoxin after 3 d, whereas in the presence of 6, 8 and 10% KCl it did so after 7 d. This trend was also true when the mold grew in the presence of mixtures of NaCl and KC1. Amounts of aflatoxin produced decreased with increasing concentrations of KCl or of the mixture of NaCl and KCl. The mycelial dry weight increased with increasing concentrations of KCl or the mixture of NaCl and KCl, although there was an extended lag phase at higher concentrations of both treatments.


1988 ◽  
Vol 51 (4) ◽  
pp. 263-268 ◽  
Author(s):  
FATHY E. EL-GAZZAR ◽  
ELMER H. MARTH

Hydrogen peroxide, 0.0, 0.03, 0.05, 0.3 and 0.5% was added to 25 ml of a glucose-yeast-salts medium which was inoculated with 1 ml of a spore suspension containing 106 conidia of Aspergillus parasiticus NRRL 2999 and then was incubated at 14 or 28°C. Cultures held at 28°C were analyzed after 3, 7 and 10 d for mycelial dry weight, pH and accumulation of aflatoxin B1 and G1. Incubation of some cultures at 28°C was continued for 90 d. Cultures held at 14°C were analyzed after 1, 2 and 3 months for mycelial dry weight, pH and aflatoxin production. Amounts of aflatoxin produced were determined using reversed-phase high-performance liquid chromatography (HPLC). The percentage of inhibition or stimulation by the additive was used to make comparisons between treatments and control. Overall, increasing the concentration of hydrogen peroxide to 0.3 or 0.5% completely prevented growth and aflatoxin production for up to 90 d of incubation at 14 or 28°C.


1987 ◽  
Vol 50 (4) ◽  
pp. 305-309 ◽  
Author(s):  
FATHY E. EL-GAZZAR ◽  
ELMER H. MARTH

Sodium benzoate, 0.0, 0.1, 0.2, 0.3 or 0.4%, was added to a glucose-yeast-salts medium which was inoculated with 1 ml of a spore suspension containing 108 conidia of Aspergillus parasiticus NRRL 2999 and then was incubated at 28°C. Cultures were analyzed after 3, 7 and 10 d for mycelial dry weight, pH and accumulation of aflatoxin B1 and G1. Amounts of aflatoxin produced were determined using reversed-phase high performance liquid chromatography (HPLC). The percentage of inhibition or stimulation by the additive was used to make comparisons between treatments and control. Generally, increasing the concentration of sodium benzoate increased the percentage of inhibition at the end of incubation (10 d). However, the average accumulation of mycelial dry weight was greater in the presence of benzoate than in its absence, with the greatest increase occurring when the medium contained 0.3% sodium benzoate.


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.


2013 ◽  
Vol 85 (6) ◽  
pp. 863-871 ◽  
Author(s):  
Thomas G. Palmen ◽  
Marco Scheidle ◽  
Robert Huber ◽  
Claudia Kamerke ◽  
Anja Wilming ◽  
...  
Keyword(s):  

1981 ◽  
Vol 44 (10) ◽  
pp. 736-741 ◽  
Author(s):  
AHMED E. YOUSEF ◽  
ELMER H. MARTH

Two media [basal (M1) and enriched (M2)] containing potassium sorbate (0–300 ppm as sorbic acid) were inoculated with spores (104 – 106/flask) of Aspergillus parasiticus and incubated for 5 days at 28 C. The greater the amount of sorbate added, the higher was the pH of the media after incubation and the smaller was the yield of mold mycelium. Intermediate amounts of sorbate sometimes resulted in greater accumulation of aflatoxin than when media were free of sorbate. Sorbate more effectively inhibited mold growth and aflatoxin production in medium M2 than M1 and when the small rather than the large inoculum was used. A second trial was done with 106 or 105 spores/flask of M2 (ca. 27 ml) and 105 spores/flask of M2 (ca. 27 ml) containing sorbate (200 ppm of sorbic acid). Cumulative data for mold growth. pH and content of aflatoxin in the medium showed that relative effects of different treatments changed during the incubation period. An index to measure the capacity of molds to synthesize aflatoxins was developed. Application of the index indicates that sorbate delayed mold growth but did not inhibit biosynthesis of aflatoxin. The ability to synthesize aflatoxin was greatest in the early stages of mold growth and then decreased linearly as mold growth progressed.


2019 ◽  
Vol 39 (1) ◽  
Author(s):  
Maneesh Department of Biotechnology, Mag Kumar ◽  
Harish Kumar ◽  
Roshan Kamal Topno ◽  
Jainendra Kumar

Aflatoxins are the natural carcinogens that are the best characterized as fungal secondary metabolites. The producers that are responsible for aflatoxin biosynthesis are strongly associated in toxic contamination of essential agricultural products. Aspergillus parasiticus is an exclusive fungus that participates in causing hepatic problems in humans and cattle. These mycotoxins are greatly influenced by abiotic stresses. The fungal growth, proliferation and its toxigenicity are highly influenced by these stresses. Present study aimed to restrict the mycelial growth and to prevent aflatoxin preparation in A. parasiticus under the anoxic stress. The monosporic strains of A. parasiticus were grown in two different Erlenmeyer conical flasks containing Czapek Dox Broth and Czapek Dox Agar under both aerobic and anaerobic conditions. The anoxic condition was maintained using Anaero Bag System. Aflatoxin was isolated after 10 days, and quantitative estimation was done by using High Performance Liquid Chromatography (HPLC). The experimental outcome showed that there was a drastic decrease in both the morphological growth and the aflatoxin biosynthesis of A. parasiticus in anoxic state.


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