Inhibition of Mold Growth and Mycotoxin Production in High-Moisture Corn Treated with Phosphates

1989 ◽  
Vol 52 (5) ◽  
pp. 329-336 ◽  
Author(s):  
C. I. LEBRON ◽  
R. A. MOLINS ◽  
H. W. WALKER ◽  
A. A. KRAFT ◽  
H. M. STAHR

Mold growth and mycotoxin production were studied in high-moisture (20%) corn treated with tetrasodium pyrophosphate (TSPP); acid and alkaline sodium polyphosphate, glassy (SPG), also known as sodium hexametaphosphate; sodium tripolyphosphate (STPP); and tricalcium phosphate. Six mold cultures belonging to the genera Aspergillus, Fusarium, and Penicillium were tested in corn varieties highly resistant or highly susceptible to mold infection in the field, and in a mixture of five other varieties of corn. The acidic SPG, as well as TSPP and STPP totally prevented or reduced mold growth when added in powder form to corn at 1.0% or 2.0% (w/w), regardless of corn variety and high moisture content. Phosphates afforded protection in whole and damaged kernels. Similar results were obtained with 2.0% acidic SPG and TSPP when added in spray form. Whenever mold growth occurred, treatment of corn with 1.0% or 2.0% (w/w) TSPP and acidic or alkaline SPG inhibited (P<0.01) aflatoxin production by aspergilli.

1989 ◽  
Vol 52 (1) ◽  
pp. 4-6 ◽  
Author(s):  
C. I. LEBRON ◽  
R. A. MOLINS ◽  
H. W. WALKER ◽  
A. A. KRAFT ◽  
H. M. STAHR

Mycelial growth and mycotoxin production of Aspergillus flavus and A. parasiticus were studied in Sabouraud dextrose agar containing pure or blended pyro-, poly- or meta-phosphates during 9 d of incubation at 30°C. Pure tetrasodium pyrophosphate (TSPP) and sodium polyphosphate, glassy (SPG, formerly hexametaphosphate), as well as a commercial phosphate blend and three combinations all containing various proportions of sodium acid pyrophosphate (SAPP), TSPP and SPG were tested. Inhibition of growth of aspergilli was observed in media containing 2.0% TSPP and 1.0 and 2.0% SPG and 2.0% of the commercial phosphate blend. Lower concentrations of single or blended phosphates allowed only limited, atypical mycelial growth. Sporulation was totally inhibited by 2.0% concentrations of single or blended phosphates, and so was production of aflatoxins B1 and G1. TSPP or SPG at 1.0% reduced (P<0.05) aflatoxin production from parts per million (controls) to parts per billion.


1996 ◽  
Vol 59 (6) ◽  
pp. 626-630 ◽  
Author(s):  
S. KOTINEK MARSH ◽  
D. J. MYERS ◽  
H. M. STAHR

Mold growth, sporulation, and aflatoxin B1 and G1 production were studied in Sabouraud dextrose agar (SDA) and frankfurters inoculated with Aspergillus flavus or Aspergillus parasiticus. Each of four phosphates, sodium polyphosphate glassy (SPG), sodium acid pyrophosphate (SAPP), tetrasodium pyrophosphate (TSPP), and Brifisol 414 (a blend of SPG, SAPP, and TSPP) were incorporated into the SDA (1 or 2%) or used as dipping solutions (5%) for the frankfurters. In SDA at 30°C, significant (P < 0.05) reductions in aflatoxin B1 and G1 production by A. flavus and A. parasiticus occurred when 1% SPG, 1% TSPP, 1% Brifisol 414, and 2% SAPP were present. In frankfurters, A. flavus B1 aflatoxin production was increased with SAPP and TSPP.


1984 ◽  
Vol 47 (8) ◽  
pp. 637-646 ◽  
Author(s):  
LLOYD B. BULLERMAN ◽  
LISA L. SCHROEDER ◽  
KUN-YOUNG PARK

Mycotoxin production is favored by high humidity and high water activity (aw). To control mycotoxin formation on the basis of moisture, the moisture content must be maintained below a certain critical level for each commodity. Aflatoxin production is favored by temperatures of 25 to 30°C, whereas below 8 to 10°C, aflatoxin production can occur, but the amounts produced are less and the time required for production is longer. Cycling or changing temperature may or may not increase aflatoxin production, depending on the temperatures, mold species and substrates involved. Other mycotoxic molds respond to temperature differently than the aspergilli. Species of Penicillium, Fusarium and Cladosporium are capable of growing at temperatures below 5°C, and some even just below freezing. Penicillium spp. can produce patulin, penicillic acid and ochratoxin at temperatures from 0 to 31°C, whereas Aspergillus ochraceus does not produce ochratoxin or penicillic acid below 12°C. Penitrem production by Penicillium crustosum can occur at refrigeration temperature. Fusarium spp. can produce zearalenone and the trichothecenes at temperatures below 10°C and even below freezing. Maintaining storage temperatures of stored commodities at 5°C or lower will prevent the production of aflatoxins and ochratoxin by aspergilli but will not prevent the production of mycotoxins by Penicillium spp. and Fusarium spp. Mycotoxic molds may grow on a vast array of substrates, but some substrates support little or no mycotoxin production while supporting extensive mold growth. Most substrates that support aflatoxin production are plant products, such as peanuts, Brazil nuts, pecans, walnuts, almonds, filberts, pistachio nuts, cottonseed, copra, corn sorghum, millet and figs. Animal products are less likely substrates for aflatoxin production. The main source of aflatoxins in animal products are residues in milk and animal tissues as a result of consumption of toxic feed by the animal. Some herbs and spices have antifungal properties and do not support mycotoxin production. However, aside from this, most food substrates are susceptible to mold growth and mycotoxin production. Some substrates, such as cheese, cured meats and soybeans, might be less favorable for mycotoxin production, but may still support mycotoxin formation. Drought stress, insect damage and mechanical damage may increase the ability of Aspergillus flavus and other fungi to invade peanuts, cottonseed and grain. Some measure of control can be gained by minimizing drought stress through irrigation and minimizing insect and mechanical damage. Development of peanut varieties and corn hybrids that are resistant to preharvest invasion by A. flavus may also offer some measure control. Competing microorganisms tend to restrict fungal growth and mycotoxin production. Low oxygen concentration (<1%) and/or increased concentrations of other gases (i.e., >90% CO2) may depress mold growth and mycotoxin formation. Antimycotic agents can be used to control mold growth and mycotoxin production. Sorbic acid, potassium sorbate, propionic acid and propionates appear to be more effective antimycotics over a greater range of conditions than benzoates. Other substances, such as sodium diacetate and BHA, also have antifungal activity. Certain herbs and spices, particularly cinnamon, cloves and mustard, may contain enough antifungal activity to exert a protective effect at normal usage levels.


1974 ◽  
Vol 54 (4) ◽  
pp. 499-517 ◽  
Author(s):  
G. M. JONES ◽  
J. I. ELLIOT ◽  
D. N. MOWAT ◽  
E. T. MORAN Jr.

The subject is reviewed with respect to the preservation of high moisture grains with organic acids and the subsequent performance of dairy and beef cattle, swine and poultry fed rations containing this feedstuff. The importance of preventing mold growth and thereby aflatoxin production is discussed briefly. Various types of grain preservatives and application rates are examined. The economic implications of the use of grain preservatives are explored. Grain preserved in this manner has been readily accepted by livestock and has supported high levels of milk production or rapid weight gains. It is a practical method of storing high moisture grain and is competitive with artificial drying or ensiling in silos.


1996 ◽  
Vol 59 (4) ◽  
pp. 407-411 ◽  
Author(s):  
M. FERNANDA P. P. M. DE CASTRO ◽  
IVANIA A. PACHECO ◽  
LUCIA M. V. SOARES ◽  
REGINA P. Z. FURLANI ◽  
DALMO C. DE PAULA ◽  
...  

Six stacks of 36 bags containing ca. 50 kg of unshelled peanuts with moisture contents in the range of 18.0 to 21.0% (wet basis) (average 19.3%) were formed in a commercial warehouse located in a peanut-producing area in São Paulo, Brazil. Three stacks were fumigated with phosphine for 7 days. An initial dose of 3.0 g of aluminum phosphide per m3 was applied. A second and a third application of the same dose were carried out 24 and 144 h later. Before fumigation, infection by Aspergillus flavus and/or A. parasiticus was either not detected in the peanut mass or was very low (1 to 13%), but contamination with aflatoxins (up to 191 μg/kg) was found in all stacks. After the fumigation treatments, a striking increase in infection was observed in the nonfumigated stacks (73 to 100% infected kernels) while in the fumigated stacks, A. flavus and/or A. parasiticus were either not detected or were isolated in insignificant amounts, indicating that phosphine was able to control fungal development in spite of the high moisture content of the kernels. After the fumigation period, the contamination levels of aflatoxins in the treated stacks remained unchanged, while the untreated stacks showed a staggering increase (up to 10,000 μg/kg of peanuts). After a month, however, no difference was observed in aflatoxin contamination and infection by A. flavus and A. parasiticus between the untreated and the treated stacks.


1982 ◽  
Vol 45 (6) ◽  
pp. 519-526 ◽  
Author(s):  
MARTIN D. NORTHOLT ◽  
LLOYD B. BULLERMAN

Environmental conditions influence mold growth and mycotoxin production. Such things as water activity (aw), temperature, pH and atmosphere can strongly affect and profoundly alter patterns of growth and mycotoxin production. Generally, maintenance of low temperatures will prevent aflatoxin production in stored products, whereas other toxins such as penicillic acid, patulin, zearolenone and T-2 toxin may be produced at low temperatures. Toxic Penicillium and Fusarium species are generally more capable of growth at low temperatures than are toxic species of Aspergillus. Temperature interacts with aw to influence mold growth and mycotoxin production. Aflatoxin B1 can be produced at conditions of aw and temperature which are close to the minimum aw and temperature for growth. On the other hand, patulin, penicillic acid and ochratoxin A are produced within a narrower range of aw and temperature, compared with those for growth. In fact, production of patulin and penicillic acid by Penicillium species appears to be confined to high aw values only. In optimal substrates, the minima of aw and temperature for growth and toxin production may be lower than in other substrates. It appears that pH and substrate composition have no great effect on growth of toxic molds, but may have a great influence on toxin production. Presence of CO2 and O2 influences mold growth and mycotoxin production. A 20% level of CO2 in air depresses aflatoxin production and markedly depresses mold growth. Decreasing the O2 concentration of air to 10% depresses aflatoxin production, but only at O2 levels of less than 1% are growth and aflatoxin production completely inhibited. With patulin- and sterigmatocystin-producing molds, concentrations of 40% CO2 depress growth and toxin production, but a level of 90% CO2 is needed to completely inhibit production of these toxins. Decreasing O2 concentration to 2% depresses production of patulin and sterigmatocystin but does not affect fungal growth. Only at levels down to 0.2% are growth and toxin production completely inhibited. Controlled atmospheres with increased CO2 (above 10%) and decreased O2 (2%) can be used to retard mold growth. Exclusion of O2 by vacuum packaging in materials with low O2 permeability will depress or even prevent aflatoxin production. Presence of other microorganisms may also restrict fungal growth and mycotoxin production. Aflatoxin production by Aspergillus flavus in mixed cultures with Aspergillus niger is less than in pure culture. Mixtures of fungi growing in grains and nuts in competition with A. flavus seem to prevent aflatoxin production. Other organisms including Rhizopus nigricans, Saccharomyces cerevisiae, Brevibacterium linens and some lactic acid bacteria have been shown to reduce growth and aflatoxin production by Aspergillus parasiticus. In general, mold growth and mycotoxin production can be prevented by employing various measures based on knowledge of the factors involved. Choice of the measures depends upon the type of product, storage period and available techniques.


1982 ◽  
Vol 45 (10) ◽  
pp. 953-963 ◽  
Author(s):  
LISA L. RAY ◽  
LLOYD B. BULLERMAN

Mold inhibitors such as sorbates, propionates and benzoates have been used commercially for some time. Recently these and other potential inhibitors have been studied from the standpoint of their effects on growth of potentially toxic molds and mycotoxin production. In addition, other substances such as the antifungal antibiotic natamycin (pimaricin) and plant-derived products such as components of the essential oils of certain herbs and spices have recently been studied for their antifungal properties and effects on mycotoxin production. Some of these inhibitors inhibit mycotoxin production by greater than 70%, while only inhibiting growth of the mold by 25% or less. Of the organic acids, sorbic, propionic and benzoic, sorbic and its sorbate salts seems to be most effective over the widest range of conditions in preventing mold growth and mycotoxin production. Potassium sorbate is effective against toxic molds at levels of 0.10 to 0.15%. The antibiotic natamycin is very effective in preventing mold growth and toxin production at very low (0.001 to 0.005%) concentrations. A number of herbs and spices possess antifungal activity. At a level of 2.0%, in YES agar, cloves, cinnamon, mustard, allspice, garlic and oregano all completely inhibit mycotoxin production by a number of mycotoxigenic molds. Cloves, cinnamon and mustard seem to be the most effective of those tested, with complete inhibition occurring with amounts of spice less than 1%. Essential oils of orange and lemon also have antifungal properties at levels of 0.2 % and higher. Certain insecticides and fumigants also inhibit mold growth and mycotoxin production. The organophosphates naled and dichlorvos are both effective inhibitors at relatively low concentrations (0.002 to 0.01%). Phenolic antioxidants, particularly BHA, also inhibit toxic molds in concentrations of 0.025% and above. Naturally occurring methylxanthines, such as caffeine and theophylline, inhibit growth and aflatoxin production by A. parasiticus in concentrations of 0.1% and above. Chlorine, a commonly used sanitizer, will inactivate spores of toxic Aspergillus and Penicillium species at levels of residual chlorine commonly achieved with most sanitation procedures. Even though considerable information is available on inhibitory effects of a number of substances on mold growth and mycotoxin production, more work is needed to further define the conditions under which commercial antifungal agents are most effective in preventing growth of toxic molds and mycotoxin production.


2017 ◽  
Vol 12 (3) ◽  
pp. 400 ◽  
Author(s):  
Valdiney Cambuy Siqueira ◽  
Flávio Meira Borém ◽  
Guilherme Euripedes Alves ◽  
Eder Pedroza Isquierdo ◽  
Afonso Celso Ferreira Pinto ◽  
...  

Objetivou-se, com o presente trabalho, propor um novo método de processamento e secagem, assim como avaliar o comportamento dos grãos submetidos a este processo, por meio da taxa de redução de água e do ajuste de diferentes modelos matemáticos aos dados experimentais da secagem. Os frutos colhidos no estágio maduro foram divididos em três lotes. O primeiro foi seco continuamente à temperatura de 40±1 °C. O segundo consiste na secagem do café natural até os teores de água de 0,56±0,02, 0,41±0,02, 0,28±0,02 e 0,20±0,02 decimal (base seca, b.s.), seguido de beneficiamento e secagem contínua nas temperaturas de 35±1 ºC e 40±1 ºC. O terceiro lote correspondeu à secagem contínua do café descascado e desmucilado na temperatura de 40±1 °C. Em todos os lotes, a secagem foi encerrada quando os grãos atingiram o teor de água de 0,12±0,05 (b.s.). Aos dados experimentais da secagem foram ajustados dez modelos matemáticos utilizados para representação da secagem dos produtos agrícolas. Além da representação da cinética de secagem foi avaliada a taxa de redução de água dos grãos. Conclui-se que a taxa de redução de água é maior para a temperatura de secagem de 40±1 °C, especialmente para maiores teores de água. O tempo total de secagem do café beneficiado com alto teor de água é expressivamente reduzido, quando comparado ao tempo de secagem completa do café natural. O modelo de Midilli descreve satisfatoriamente a cinética de secagem do café beneficiado.


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