• Journal of Food Hygiene and Safety
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• v.13 no.1
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• pp.47-52
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• 1998

A rice cultivar (Japonica type), Cheong-cheong, was used to examine the ability as a substrate for aflatoxin production. Brown rice samples were inoculated with Aspergillus parasiticus, stored at various conditions, and observed the production of aflatoxin $B_1$ during storage. Enzyme-linked immunosorbent assay (ELISA) was performed to detect aflatoxin $B_1$ in the samples. A temperature of $28^{\circ}C$ favored the aflatoxin production in the samples. Remoisturizing brown rice to 15.8% encouraged the fungus to produce the aflatoxin significantly (p$B_1$ production in rice, and also indicated that other factors such as husking and storage periods were also risk determinants. This study provided evidence that rice could be an efficient medium for aflatoxin production.

• Food Science and Preservation
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• v.9 no.1
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• pp.78-84
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• 2002

While rice and corn were stored at room temperature for 90 days the degree of aflatoxin production was measured without humidity and temperature control. The amount of aflatoxin production of rice and corn after 30 days was 01.1 and 0.3 ppb, respectively. The degree of aflatoxin production increased rapidly with increasing storage temperature and humidity. The optimum conditions of aflatoxin production were 25 ∼30$\^{C}$ and 80% humidity. The degree of aflatoxin production in corn was higher than in rice under the same conditions. Rice and corn were treated with 0∼0.05%(w/w) of methyl alcohol (MeOH) extract and polyphenol (PP) group materials individually respectively under the optimum conditions. As the result, the inhibition effect of aflatoxin production increased with increasing the amount of treatment. It appeared as follows: catechin (CT)

• Journal of Food Hygiene and Safety
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• v.1 no.2
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• pp.157-162
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• 1986

ABSTRACT-This study was designed to observe the effects of temperature cycling on the aflatoxin production by Aspergillus parasiticus R-716 in modified SLS medium. Temperature cycling resulted in total aflatoxin production more than did constant incubation at either $28^{\circ}C$, which was considered to be optimum for aflatoxin production, or $17.5^{\circ}C$, which had the same total thermal input as the temperature cycling. The aflatoxin biosynthesis correlated with the color intensity of media, but was controversal with lipid biosynthesis, and aflatoxin concentration is not related to changes in the fatty acid compositions of used strain.strain.

• Korean Journal of Microbiology
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• v.9 no.3
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• pp.130-138
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• 1971

In order to investigate the production of aflatoxin in various conditions such as pH, moisture and temperature, 27 smaples were inoculated with Aspergillus flavus, and in addition 3 smaples were inoculated with the mixture of Aspergillus flavus and Bacillus subtilis and cultured under the conditions such as 20.deg.C and 30% moisture contents. The following results were obtained : 1) Aflatoxin production was the highest at pH 5.0 and relatively high at pH 7.0. Its production was decreased significantly when pH reached 9.0. 2) The yield of aflatoxin was shown comparatively high level at 30% moisture contens. The higher moisture contents was, the lower aflatoxin production was. 3) The highest level of aflatoxin production was at 20.deg,C, and comparatively high level was at 30.deg.C. However, its production was fairly low at 40.deg.C. 4) The highest crude aflatoxin production was 5,093ppm (B$_{1}$, 1.912ppm ; B$_{2}$, and the lowest one 2.197 ppm (B$_{1}$, 0.793 ppm : B$_{2}$, 0.185 ppm : G$_{1}$ ,0.102 ppm G$_{2}$, 0.381ppm) at 63% moisture, pH 9.0 and 40.deg.C. 5) When Aspergillus flavus and Bacillus subilis were cultured together under the conditions such as 20.deg.C and 30% moisture, aflatoxin production was decreased by 27% comparing with the culture of Aspergillus flavus alone.

• Journal of the Korean Society of Food Science and Nutrition
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• v.13 no.1
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• pp.117-126
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• 1984

Aflatoxins are toxic and carcinogenic secondary metabolites which are produced by trains of A. flavus and A. parasiticus during their growth on foods and feedstuffs. Aflatoxins are a group of closely related heterocyclic compounds of which $B_1$, $B_2$, and $G_2$ are the major members. Aflatoxins are synthesized via a polyketide pathway in which the general steps are acetate, an-thraquinones, xanthone and aflatoxins. Aflatoxin formation is favored by high moisture or high $a_w$(0.95${\sim}$0.99). The limiting $a_w$ for aflatoxin production on agricultural commodities is 0.83. Optimum temperature for aflatoxin production by the molds is $25{\sim}30^{\circ}C$ and the incubation time for the maximum production of the toxin is 7${\sim}$15 days. The limiting temperatures for aflatoxin production are ${\leq}7.5^{\circ}C\;and\;\geq40^{\circ}C$. Cycling temperatures may or may not stimulate aflatoxin production depending on the amplitude of cycling, substrate and strains of molds. Aflatoxin pro-ducing molds are aerobic organisms and thus have a requirement for oxygen. A decreasing $O_2$ concentration and/or increasing concentrations of $CO_2$ or $N_2$ depress the mold growth and aflatoxin formation. A. flavus grows competitively or associatively in the presence of other microorganisms and occasionally loses the competition with other microorganisms. Some lactic acid bacteria have been shown to reduce growth and aflatoxin production by A. parasiticus. Carbon source is the most important nutritional factors affecting aflatoxin formation by the molds. Sucrose, fructose and glucose are the most favorable carbon sources. Food substrates of plant derived products which have high carbohydrate content such as agricultural commodities and their products are most vulnerable to contamination by aflatoxins.

• Journal of Food Hygiene and Safety
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• v.11 no.1
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• pp.35-39
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• 1996

The effect of allyisothiocyanate, the mahor compound of radish on the growth of Aspergillus parasiticus R-716 and aflatoxin production, was investigated. An increase in the level of allylisothiocyanate results in a decrease both growth and aflatoxin per myclial weight, and the addition of 125 ppm allylisothocynate completely inhibited the growth of the strain. The addition of allylisothiocyanate to the culture of R-716 strain the production of aflatoxin. The inhibition of aflatoxin was more B-group than G-group and M-group during cultural period. The growth of strain and aflatoxin production were greatly affected by the addition of allylisothiocyanate.

• Korean Journal of Microbiology
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• v.26 no.2
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• pp.143-147
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• 1988

The effect of ginseng saponin on aflatoxin(AF) production by Aspergillus parasiticus NRRL2999 and the mutagenicity of produced aflatoxin. The production of aflatoxin were decreased by the addition of ginseng saponin and the most effective concentration was 0.05%. The ratio of aflatoxin $B_{1}$ and aflatoxin $G_{1}$ were not changed by the addition of ginseng saponin. For the nutagenicity test, Ames method were adopted. Mutagenicity of mycelial aflatoxin was decreased by the addition of ginseng saponin on TA98, but not changed on TA100. Mutagenicity of excreted aflatoxin to broth was slightly increased by the saponin on TA98, but decreased on TA100.

• Journal of Environmental Health Sciences
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• v.10 no.2
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• pp.89-97
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• 1984

The possible effects of garlic (Aliium sativurn L.) extract on growth and aflatoxin production by Aspergillus parasiticus R- 716 were investigated. Various solvent extracts of garlic strongly inhibited growth and sporulation by Aspergillus parasiticus R-716, and effective solvents used for extraction of garlic were chloroform, benzene, and water-chloroform. The growth and aflatoxin production decreased with the increase in extract concentration, and extract equivalent 1.5g of raw garlic weight in 25ml SLS medium completely inhibited, and at a level of 1.25g garlic, total aflatoxin was reduced 64% (472 ${\mu}g$/25ml) of that produced in the control (1, 352 ${\mu}g$/25 ml). During cultivation inhibitory rate of growth was reduced from 89.1% to 40% and aflatoxin $B_2$, $G_1$ production increased with the laps of time. Especially garlic extract appeared to have a stimulatory effect on lipid accumulation on the contrary aflatoxin production.

• Korean Journal of Food Science and Technology
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• v.14 no.2
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• pp.162-167
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• 1982

The influence of temperature and moisture on aflatoxin production on solid substrate(barley) by Aspergillus parasiticus NRRL 2999 has been studied in some detail. The optimum temperature for production of aflatoxin under the conditions employed is 25 and $30^{\circ}C$. No aflatoxin was detected at the moisture levels of 13%, and only traces at 16% moisture. The ratio of the production of aflatoxin B to G varied with temperature and moisture level. Aflatoxin G is elabolated at a more rapid rate than B and also metabolized at a more rapid rate. Also lower temperatures favored the production of aflatoxin G. The intensity of the yellow pigment of the chloroform extracts correlated with the concentration of aflatoxin.

• Korean Journal of Microbiology
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• v.24 no.4
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• pp.352-356
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• 1986

A study was carried out to determine the effect of ginseng saponin an its related materials on aflatoxin production by Aspergillus parasiticus NRRL2999 in glucose-salts(GS) medium. Maximal growth of the mold and AF froduction in the medium occurred after 5 and 9 days at $28^{\circ}C$, respectively. When various concentrations of saponin added to the medium aflatoxin synthesis were significantly reduced (p<0.05) compared to the control after 9 days at $28^{\circ}C$. 0.05% of saponin inhibited aflatoxin production most effectively in the low concerntrations of saponin (0.01-0.2%) and the toxin synthesis reduced with an increasing concentrations of saponin in the high concentrations (0.03-5.0%). Various concentrations (0.01-1.0%) of saponin diol and triol in the media also caused to reduce aflatoxin synthesis by the mold (p<0.05). All saponin fractions were found to decrease aflatoxin production significantly. Saponin fraction numbers of 1,2,4 and 6 were shown to reduce aflatoxin production effectively, and the number 1 was the most effective. Addition of 0.05% of nucleic acid related materials to the medium reduced aflatoxin production (p<0.05). Aflatoxins could not be found in broth at all, but in mycelia when 0.05% of caffeine was added to the medium. Aflatoxin synthesis was well correlated with total lipid synthesis, growth and glucose uptake. When aflatoxin synthesis inhibited (5.0% of saponin) both total lipid synthesis and growth were stimulated and the efficiency of glucose utilization was reduced.