Antifungal Activity of Chitosan and Its Preservative Effect on Low-Sugar Candied Kumquat

1994 ◽  
Vol 57 (2) ◽  
pp. 136-140 ◽  
Author(s):  
SHAO W. FANG ◽  
CHIN F. LI ◽  
DANIEL Y. C. SHIH
Keyword(s):  
Shelf Life ◽  
Aspergillus Parasiticus ◽  
Aflatoxin Production ◽  
Inhibitory Effect ◽  
Life Extension ◽  
Potassium Sorbate ◽  
Mold Growth ◽  
Chitosan Concentration ◽  
Significant Difference ◽  
Order Polynomial

The inhibitory effect of chitosan, a deacetylated form of chitin, on the growth of Aspergillus niger and the aflatoxin production of Aspergillus parasiticus was evaluated. The inhibitory effect of chitosan against A. niger was increased as the chitosan concentration was increased from 0.1 to 5.0 mg/ml (pH 5.4). At concentrations of 4.0 or 5.0 mg/ml, chitosan was less effective than potassium sorbate in inhibiting the growth of A. niger. The greatest inhibitory effect of chitosan against A. parasiticus was found at 3.0–5.0 mg/ml. In addition, chitosan could completely prevent aflatoxin production by A. parasiticus at the concentration of 4.0–5.0 mg/ml. Chitosan (2.0 and 5.0 mg/ml) induced considerable leakage of UV-absorbing and proteinaceous material of A. niger at pH 4.8. Using the response surface methodology, a second order polynomial model was derived and used to predict the number of days to obtain visible mold growth under various combinations of chitosan concentrations and °Brix in candied kumquat. The results showed that there was no significant difference in shelf-life extension of candied kumquat at chitosan concentration of 3.5–6.5 mg/ml. However, °Brix had a significant effect on shelf life. Candied kumquat with 6.0 mg/ml chitosan concentration and 61.9° Brix had a predicted mold-free shelf life of 65.3 d.

Growth and Synthesis of Aflatoxin by Aspergillus parasiticus in the Presence of Sorbic Acid

1981 ◽  
Vol 44 (10) ◽  
pp. 736-741 ◽  
Author(s):  
AHMED E. YOUSEF ◽  
ELMER H. MARTH
Keyword(s):  
Incubation Period ◽  
Aspergillus Parasiticus ◽  
Sorbic Acid ◽  
Aflatoxin Production ◽  
Potassium Sorbate ◽  
Mold Growth ◽  
Early Stages ◽  
Cumulative Data ◽  
The Media ◽  
Growth Ph

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.

Effects of Potassium Sorbate on Growth and Aflatoxin Production by Aspergillus parasiticus and Aspergillus flavus1

1983 ◽  
Vol 46 (11) ◽  
pp. 940-942 ◽  
Author(s):  
LLOYD B. BULLERMAN
Keyword(s):  
Aspergillus Flavus ◽  
Yeast Extract ◽  
Aflatoxin B1 ◽  
Spore Germination ◽  
Mycelial Growth ◽  
Aspergillus Parasiticus ◽  
Aflatoxin Production ◽  
Potassium Sorbate ◽  
Mycelial Mass ◽  
Yeast Extract Sucrose

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.

Growth and Aflatoxin Production by Aspergillus parasiticus in a Medium Containing Plant Hormones, Herbicides or Insecticides

1987 ◽  
Vol 50 (12) ◽  
pp. 1044-1047 ◽  
Author(s):  
R. S. FARAG ◽  
M. A. EL-LEITHY ◽  
A. E. BASYONY ◽  
Z. Y. DAW
Keyword(s):  
Acetic Acid ◽  
Gibberellic Acid ◽  
Plant Hormones ◽  
Aspergillus Parasiticus ◽  
Synthetic Medium ◽  
Fungal Growth ◽  
Aflatoxin Production ◽  
Inhibitory Effect ◽  
Indol Acetic Acid ◽  
Acid Herbicides

The effect of some widely used plant hormones (indol-3-acetic acid and gibberellic acid), herbicides (gramoxone, stomp and treflan) and insecticides (malathion, actellic and guthion) on Aspergillus parasiticus growth and aflatoxin production in a synthetic medium was studied. Addition of indol acetic acid to the medium increased aflatoxin production more than gibberellic acid. Treflan at 5, 10 and 20 ppm levels caused a highly significant stimulatory effect on A. parasiticus growth and aflatoxin production. In contrast, stomp at 10 and 20 ppm produced the reverse effect. Guthion, an insecticide, caused a marked decrease in fungal growth and aflatoxin production. The inhibitory effect of insecticides under study on both fungal growth and aflatoxin production in effectiveness followed the sequence: guthion>actellic>malathion. At the recommended application rate (10 ppm), with the exception of indol acetic acid and treflan, all compounds suppressed mold growth and aflatoxin production.

Growth and Aflatoxin Production by Aspergillus parasiticus NRRL 2999 in the Presence of Acetic or Propionic Acid and at Different Initial pH Values

1987 ◽  
Vol 50 (11) ◽  
pp. 909-914 ◽  
Author(s):  
GULAM RUSUL ◽  
FATHY E. EL-GAZZAR ◽  
ELMER H. MARTH
Keyword(s):  
Acetic Acid ◽  
Propionic Acid ◽  
Aflatoxin B1 ◽  
Maximum Concentration ◽  
Aspergillus Parasiticus ◽  
Dry Weight ◽  
Aflatoxin Production ◽  
Lag Phase ◽  
Significant Difference ◽  
Initial Ph

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.

The inhibitory effect of lactic acid bacteria on aflatoxin production and expression of aflR gene in Aspergillus parasiticus

2017 ◽  
Vol 38 (1) ◽  
Author(s):  
Rooholla Ghanbari ◽  
Ebrahim Molaee Aghaee ◽  
Sassan Rezaie ◽  
Gholamreza Jahed Khaniki ◽  
Mahmoud Alimohammadi ◽  
...  
Keyword(s):  
Lactic Acid ◽  
Lactic Acid Bacteria ◽  
Aspergillus Parasiticus ◽  
Aflatoxin Production ◽  
Inhibitory Effect

scholarly journals Effect of Lactic Acid Bacteria Strains on the Growth and Aflatoxin Production Potential of Aspergillus parasiticus, and Their Ability to Bind Aflatoxin B1, Ochratoxin A, and Zearalenone in vitro

2021 ◽  
Vol 12 ◽  
Author(s):  
Cleide Oliveira de Almeida Møller ◽  
Luisa Freire ◽  
Roice Eliana Rosim ◽  
Larissa Pereira Margalho ◽  
Celso Fasura Balthazar ◽  
...  
Keyword(s):  
Lactic Acid ◽  
Lactic Acid Bacteria ◽  
Ochratoxin A ◽  
Aspergillus Parasiticus ◽  
Potassium Phosphate ◽  
Aflatoxin Production ◽  
Inhibitory Effect ◽  
Binding Studies ◽  
Aflatoxin B

The increased consumption of plant-based foods has intensified the concern related to mycotoxin intoxication. This study aimed to investigate the effect of selected lactic acid bacteria (LAB) strains on the growth of Aspergillus parasiticus NRRL 2999 and its production of aflatoxin (AF). The ability of the heat-killed (100°C for 1 h) LAB strains to bind aflatoxin M1 (AFM1) in milk and aflatoxin B1 (AFB1), ochratoxin A (OTA), and zearalenone (ZEN) in potassium phosphate buffer (PPB) was also evaluated in vitro. Ten LAB strains were tested individually, by inoculating them simultaneously with the fungus or after incubation of the fungus for 24 or 48 h at 25°C. Double layer yeast extract sucrose (YES) agar, de Man Rogosa and Sharpe (MRS) agar, and YES broth were incubated for 7 days at 25°C to follow the development of the fungus. Levilactobacillus spp. 3QB398 and Levilactobacillus brevis 2QB422 strains were able to delay the growth of A. parasiticus in YES broth, even when these strains were inoculated 24 h after the fungus. The inhibitory effect of these LAB strains was confirmed by the reduction of fungus colony size, suggesting dominance of LAB by competition (a Lotka-Voltera effect). The production of AFB1 by A. parasiticus was inhibited when the fungus was inoculated simultaneously with Lactiplantibacillus plantarum 3QB361 or L. plantarum 3QB350. No AFB1 was found when Levilactobacillus spp. 2QB383 was present, even when the LAB was inoculated 48 h after the fungus. In binding studies, seven inactivated LAB strains were able to promote a reduction of at least 50% the level of AFB1, OTA, and ZEN. This reduction varied depending on the pH of the PPB. In milk, however, only two inactivated LAB strains were able to reduce AFM1, with a reduction of 33 and 45% for Levilactobacillus spp. 3QB398 (Levilactobacillus spp.) and L. brevis 2QB422, respectively. Nevertheless, these results clearly indicate the potential of using LAB for mycotoxin reduction.

EFFECT OF POTASSIUM SORBATE AND MODIFIED ATMOSPHERE PACKAGING ON THE SHELF-LIFE EXTENSION OF SEER FISH (SCOMBEROMORUS COMMERSON)STEAKS DURING ICED STORAGE

2010 ◽  
Vol 34 (2) ◽  
pp. 399-424 ◽  
Author(s):  
POULOSE YESUDHASON ◽  
TERALANDUR KRISHNASWAMY SRINIVASA GOPAL ◽  
CHANDRAGIRI NARAYANARAO RAVISHANKAR ◽  
K.V. LALITHA ◽  
ASHOK KUMAR
Keyword(s):  
Shelf Life ◽  
Modified Atmosphere Packaging ◽  
Life Extension ◽  
Potassium Sorbate ◽  
Modified Atmosphere ◽  
Shelf Life Extension ◽  
Scomberomorus Commerson ◽  
Iced Storage ◽  
Seer Fish

Aflatoxin Production in a Meat Mix Model System in the Presence of Pediococcus and Lactobacillus

1992 ◽  
Vol 55 (8) ◽  
pp. 583-587 ◽  
Author(s):  
ROSA H. LUCHESE ◽  
JOSÉ F. P. MARTINS ◽  
WILKIE F. HARRIGAN
Keyword(s):  
Lactic Acid ◽  
Lactic Acid Bacteria ◽  
Aspergillus Parasiticus ◽  
Aflatoxin Production ◽  
Model System ◽  
Medium Composition ◽  
Mold Growth ◽  
Processing Conditions ◽  
Irradiated Meat ◽  
Incubation Temperatures

The effect on aflatoxin production by Aspergillus parasiticus of eight individual strains of Pediococcus and Lactobacillus was determined. The study was conducted in an axenic cultural system in which irradiated meat was employed in the formulation of a meat medium. The medium composition and incubation temperatures were simulations of Brazilian salami processing conditions. All single cultures of A. parasiticus supported aflatoxin production. More aflatoxin was produced in samples treated by the addition of lactic acid than in nontreated ones. Aflatoxin was not detected when A. parasiticus was grown with lactic acid bacteria, although visible mold growth was observed in all such cultures.

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