scholarly journals Antifungal activity of natamycin and development of an edible film based on hydroxyethylcellulose to avoid Penicillium spp. growth on low-moisture mozzarella cheese

LWT ◽  
2021 ◽  
pp. 112795
Author(s):  
Raquel Torrijos ◽  
Tiago Melo Nazareth ◽  
Jorge Calpe ◽  
Juan Manuel Quiles ◽  
Jordi Mañes ◽  
...  
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.


2011 ◽  
Vol 22 (3) ◽  
pp. 1-10
Author(s):  
Abdulilah S. Ismaeil ◽  
Musa I. Taha ◽  
Abdul-ghany O. Sarmamy

1993 ◽  
Vol 56 (1) ◽  
pp. 66-68 ◽  
Author(s):  
PAUL D. MATTHEWS ◽  
GERHARD J. HAAS

A number of edible plant species were investigated for antifungal agents. Whole sprouts and extracts of plant organs were tested in several assays, including bioautography. Amaranth, coffee (Coffea arabica), rice, coleus, violet, chervil, and lotus (Nelumbo nucifera) showed antifungal activity. Rhizomes of lotus had potent antifungal activity against Aspergillus niger, Trichoderma viride, and Penicillium spp. Further work is merited for characterization of this antifungal agent. Screening of sprouting plants and terrestrial aquatic plants may be a fruitful approach to finding new antimicrobials.


2015 ◽  
Vol 9 (1) ◽  
pp. 9-14
Author(s):  
Alkhazraji A.A.H Alkhazraji ◽  
Khalaf E.A Khalaf ◽  
Salman A.S Salman ◽  
Hamza E.SH Hamza ◽  
Gulboy A. Nasir Gulboy

The study was conducted to evaluate the inhibition activity of alcohol extract of Peganum harmala seeds in somepathogenic fungi (Aspergillus niger, Aspergillus flavus and Penicillium spp.), which was isolated in food researchcenter/ Ministry of Science and Technology. Results revealed that alcohol extract of Peganum harmala seeds wasinhibited the growth of all kind of fungi under study at the extract concentrations (0.012,0.05, 0.25,0.5,1,5,20,50,100 ,200 and 300 mg/ml), colonies diameters for Aspergillus niger was 27, 25 mm at the concentrations 0.012 and0.05 mg/ml respectively in the comparison with its colonies diameter in the control group which was 38 mm forboth concentrations, and it was 26,21 mm for Aspergillus flavus at the same concentration (0.012 and 0.05 mg/ml)respectively, whereas the colonies diameter was decreased to 9,7 mm for Penicillium spp. at 0.012 and 0.05 mg/mlof alcohol extract respectively. In general, the inhibition activity of Peganum harmala seeds alcohol extract wasincreased with the increasing of extract concentrations. The growth rate of all kinds of fungi under study wascompletely inhibited at 0.25mg/ml concentration and above.


2019 ◽  
Vol 25 (4) ◽  
pp. 295-302
Author(s):  
C Luz ◽  
R Torrijos ◽  
JM Quiles ◽  
J Mañes ◽  
G Meca

Molds are one of the most important spoilage organisms on cheese which can lead to economic loss as well as raising public health concerns due to the production of mycotoxins. This study investigates the use of ɛ-polylysine as natural antimicrobial to inhibit fungal growth. The minimal inhibitory concentrations and minimal fungicidal concentrations of ɛ-polylysine were determined against Penicillium roqueforti, Penicillium nordicum, and Penicillium solitum. Then, polylysine was tested as surface antimicrobial for the preservation of mozzarella slice cheese inoculated with these Penicillium spp. and stored in plastic trays during 25 days. The minimal inhibitory concentrations calculated for the three fungi tested were of 60 mg/l whereas the minimal fungicidal concentrations detected were of 125–10,000 mg/l. The shelf life observed for the control experiments was of 15 days, and just using the ɛ-polylysine at 0.00625, 0.0125, and 0.025% was evidenced a shelf life increment in comparison with the control of 1–3 days.


2012 ◽  
pp. 247-256 ◽  
Author(s):  
Suncica Kocic-Tanackov ◽  
Gordana Dimic ◽  
Dusanka Pejin ◽  
Ljiljana Mojovic ◽  
Jelena Pejin ◽  
...  

This study was aimed at investigating the antifungal potential of basil (Ocimmum basilicum L.) extract against toxin-producing Penicillium spp. (P. aurantiogriseum, P. glabrum, P. chrysogenum, and P. brevicompactum) isolated from food. The basil extract composition was determined by the GC-MS method. The major component identified in the extract was estragole (86.72%). The determination of the antifungal activity of basil extract on Penicillium spp. was performed using the agar plate method. Basil extract reduced the growth of Penicillium spp. at all applied concentration levels (0.16, 0.35, 0.70, and 1.50 mL/100mL) with the colony growth inhibition from 3.6 (for P. glabrum) to 100% (for P. chrysogenum). The highest sensitivity showed P. chrysogenum, where the growth was completely inhibited at the basil extract concentration of 1.50 mL/100mL. The growth of other Penicillium spp. was partially inhibited with the colony growth inhibition of 63.4 % (P. brevicompactum), 67.5% (P. aurantiogriseum), and 71.7% (P. glabrum). Higher concentrations (0.70 and 1.50 mL/100mL) reduced the growth of the aerial mycelium of all tested Penicillium species. In addition, at the same extract concentrations, the examination of microscopic preparation showed the deformation of hyphae with the frequent occurrence of fragmentations and thickenings, occurrence of irregular vesicle, frequently without metulae and phialides, enlarged metulae. The results obtained in this investigation point to the possibility of using basil extract for the antifungal food protection.


Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
DN Silva ◽  
MJ Gonçalves ◽  
MT Amaral ◽  
MT Batista
Keyword(s):  

Planta Medica ◽  
2013 ◽  
Vol 79 (10) ◽  
Author(s):  
JE Fierro ◽  
P Jiménez ◽  
ED Coy-Barrera

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