Inhibition of Growth and Aflatoxin Production of Aspergillus flavus by Lactobacillus Species†

1995 ◽  
Vol 58 (11) ◽  
pp. 1249-1256 ◽  
Author(s):  
HASSAN GOURAMA ◽  
LLOYD B. BULLERMAN

A mixture of Lactobacillus species from a commercial silage inoculum reduced mold growth and inhibited aflatoxin production by Aspergillus flavus subsp. parasiticus. Actively growing Lactobacillus spp. cells totally inhibited germination of mold spores. Culture supernatant broth from the mixture of strains inhibited mold growth but did not destroy mold spore viability. Some mold spores were observed microscopically to have germinated and produced short nonbranching germ tubes; then growth ceased. While the pH of the culture broth and supernatant were about 4.0, acidification of nonfermented broth to pH 4.0 with HCl and lactic acid did not cause a similar inhibition of spore germination. The mixture of Lactobacillus species growing in a dialysis sack inhibited aflatoxin production by the A. flavus culture growing outside of the sack in broth, whereas mold growth was not affected. The pH values outside of the dialysis sack in the control and the treatments were similar (6 to 7) throughout the incubation period. When a dialysis sack with a molecular weight cutoff (MWCO) of 1,000 was used, there was little inhibition of aflatoxin B1 production, but with MWCOs of 6,000 to 8,000 and 12,000 to 14,000 aflatoxin production was greatly inhibited. In mixed culture experiments, levels of aflatoxin B1 and G1 were depressed compared to the control (monoculture). Mold growth in this case was also reduced compared to the monoculture system. Purified isolates of Lactobacillus from the commercial mixture had a slight effect on mold growth and aflatoxin production, but supernatant liquid of one isolate was quite inhibitory to production of aflatoxins B1 and G1, without affecting mold growth.

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.


2013 ◽  
Vol 6 (1) ◽  
pp. 43-50 ◽  
Author(s):  
V. Aiko ◽  
A. Mehta

Cinnamon, cardamom, star anise and clove were studied for their effect on growth of Aspergillus flavus and aflatoxin B1 (AFB1) synthesis. The experiments were carried out in yeast extract sucrose culture broth as well as in rice supplemented with spices. AFB1 produced was analysed qualitatively and quantitatively using thin layer chromatography and high performance liquid chromatography, respectively. At a concentration of 10 mg/ml, cardamom and star anise did not exhibit any antifungal or anti-aflatoxigenic activity in culture broth, whereas cinnamon and clove inhibited A. flavus growth completely. The minimum inhibitory concentrations of cinnamon and clove were 4 and 2 mg/ml, respectively. Concentrations of cinnamon and clove below their minimum inhibitory concentrations showed enhanced fungal growth, while AFB1 synthesis was reduced. Clove inhibited the synthesis of AFB1 significantly up to 99% at concentrations ≥1.0 mg/ml. The spices also inhibited AFB1 synthesis in rice at 5 mg/g, although fungal growth was not inhibited. Clove and cinnamon inhibited AFB1 synthesis significantly up to 99 and 92%, respectively, and star anise and cardamom by 41 and 23%, respectively. The results of this study suggest the use of whole spices rather than their essential oils for controlling fungal and mycotoxin contamination in food grains.


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.


1977 ◽  
Vol 60 (1) ◽  
pp. 96-99
Author(s):  
Jo Ann L Hilldrup ◽  
Thomas Eadie ◽  
Gerald C Llewellyn

Abstract Unprocessed honey, Lilium longiflorium pollen, brood comb, whole larvae, and whole bees were inoculated with Aspergillus flavus NRRL 3251, A. flavus ATCC 15548, and A. parasiticus NRRL 2999. The fungi grew, sporulated, and produced various amounts of aflatoxin on all substrates except the unprocessed honey. The largest quantity of aflatoxin B1 was produced on whole larvae supporting A. flavus NRRL 3251 growth. A. parasiticus NRRL 2999 growing on whole larvae produced the most aflatoxin G1. Aflatoxins B2 and G2 were seldom detected. Apiarian substrates with the exception of honey seem capable of supporting fungal growth and resultant aflatoxin production.


1983 ◽  
Vol 46 (3) ◽  
pp. 210-215 ◽  
Author(s):  
JAERIM BAHK ◽  
ELMER H. MARTH

Red ginseng saponin (0.36%) inhibited mycelial growth, sporulation and aflatoxin production by Aspergillus parasificus during 9 d at 28°C. The mold caused no change in pH of the medium when it contained red ginseng saponin or ginseng tea (9%). Most ginseng products permitted mycelial growth and production of aflatoxin B1, but inhibited production of aflatoxin G1. However, when compared to the control, aflatoxin production by A. parasiticus was reduced by the presence in the medium of most of the ginseng products that were tested, Ginseng tea (9%) resulted in a higher index of maximum accumulation of aflatoxins per interval of mold growth than occurred in the control. Red ginseng was more effective than white ginseng for inhibiting mold growth and aflatoxin production.


1988 ◽  
Vol 51 (5) ◽  
pp. 361-363 ◽  
Author(s):  
MARY W. TRUCKSESS ◽  
LEONARD STOLOFF ◽  
PHILIP B. MISLIVEC

Portions of corn, a commodity in which aflatoxin is frequently found, were held at 16, 26 and 32°C after the moisture contents were adjusted to achieve water activities (aw) ranging from too low to ample for support of mold growth. Suspensions of mold spores from toxigenic cultures of Aspergillus flavus, A. ochraceus, Penicillium citrinum, P. cyclopium and P. urticae were added to the test portions, either as A. flavus alone, as A. flavus with one of the other molds or as a mixture of all 5 species. Additional water was used to obtain the proper moisture levels. A temperature of 16°C was generally too low for aflatoxin production by either the added or native strains of A. flavus, although the mold was able to grow at 16°C at aw values as low as 0.80, 0.77 and 0.85 on corn, soybeans and pinto beans, respectively. Aflatoxin production was essentially the same at 26 and 32° C with limiting aw values in the range of 0.85–0.89. Limiting aw values for mold growth at 26 and 32°C were 0.73, 0.69 and 0.75 for corn, soybeans and pinto beans, respectively. This study provided no evidence that substrate suitability at limiting temperatures and aw levels is a factor in the observed difference in the risk of aflatoxin contamination for these commodities. The study did indicate that the associated mold flora, when the seed is exposed to mold invasion, is a risk determinant.


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.


2011 ◽  
Vol 343-344 ◽  
pp. 1168-1171 ◽  
Author(s):  
Liang Bin Hu ◽  
Hong Bo Li ◽  
Jun Liang Sun ◽  
Jie Zeng

Control of aflatoxin contamination has been a worldwide problem. Laminarin from Laminaria digitata is one kind of polysaccharides with multiple biological activities. In this paper, the inhibitory effects of Laminarin on the growth and toxin production of A. flavus was studied. The results indicated that 150 and 200 µg/mL of Laminarin ccould significantly inhibit the aflatoxin production in Sabouraud liquid medium (Sab), without affecting mycelium growth. In addition, the results also showed that certain concentration Laminaria could decrease the infection of peanut seeds by A. flavus as well as the contamination by aflatoxin B1.


2018 ◽  
Vol 8 (9) ◽  
pp. 1655 ◽  
Author(s):  
Hyeong-Mi Kim ◽  
Hyunwoo Kwon ◽  
Kyeongsoon Kim ◽  
Sung-Eun Lee

Aspergillus flavus and A. parsiticus produce aflatoxins that are highly toxic to mammals and birds. In this study, the inhibitory effects of 1,8-cineole and t-cinnamaldehyde were examined on the growth of Aspergillus flavus ATCC 22546 and aflatoxin production. 1,8-Cineole showed 50% inhibition of fungal growth at a concentration of 250 ppm, while t-cinnamaldehyde almost completely inhibited fungal growth at a concentration of 50 ppm. Furthermore, no fungal growth was observed when the growth medium was treated with 100 ppm t-cinnamaldehyde. 1,8-Cineole also exhibited 50% inhibition on the production of aflatoxin B1 and aflatoxin B2 at a concentration of 100 ppm, while the addition of 100 ppm t-cinnamaldehyde completely inhibited aflatoxin production. These antiaflatoxigenic activities were related to a dramatic downregulation of the expression of aflE and aflL by 1,8-cineole, but the mode of action for t-cinnamaldehyde was unclear. Collectively, our results suggest that both of the compounds are promising alternatives to the currently used disinfectant, propionic acid, for food and feedstuff preservation.


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