Roquefortine C Occurrence in Blue Cheese

2001 ◽  
Vol 64 (2) ◽  
pp. 246-251 ◽  
Author(s):  
CARLO FINOLI ◽  
ANGELA VECCHIO ◽  
ANTONIETTA GALLI ◽  
IVAN DRAGONI

Several strains of Penicillium are used for the production of mold-ripened cheeses, and some of them are able to produce mycotoxins. The aims of the research were the determination of roquefortine C and PR toxin in domestic and imported blue cheeses, the identification of the penicillia used as starter, and the investigation of their capacity for producing toxins in culture media. Roquefortine C was always found in the cheeses at levels ranging from 0.05 to 1.47 mg/kg, whereas the PR toxin was never found. The identification of the fungal strains present in the domestic cheeses included Penicillium glabrum, Penicillium roqueforti, and Penicillium cyclopium in the Gorgonzola “dolce” and Penicillium roqueforti in the Gorgonzola “naturale”; in one case, the presence of Penicillium crustosum was observed. The strains isolated from the foreign cheeses belonged to P. roqueforti. The strains were able to produce between 0.18 and 8.44 mg/liter of roquefortine in yeast extract sucrose medium and between 0.06 and 3.08 mg/liter and less than 0.05 mg/liter when inoculated in milk at 20°C for 14 days and 4°C for 24 days, respectively. Linear relations between production of roquefortine in culture media and cheeses did not emerge. PR toxin ranged from less than 0.05 to 60.30 mg/liter in yeast extract sucrose medium and was produced in milk at 20°C from only one strain. The low levels and the relatively low toxicity of roquefortine make the consumption of blue cheese safe for the consumer.

1991 ◽  
Vol 54 (7) ◽  
pp. 546-548 ◽  
Author(s):  
C. I. WEI ◽  
T. S. HUANG ◽  
J. S. CHEN ◽  
M. R. MARSHALL ◽  
K. T. CHUNG

Aspergillus candidus ATCC 44054 grown without agitation produced more kojic acid in the modified Czapek-Dox liquid medium than cultures shaken at 100 rpm. Of the three culture media tested, yeast extract-sucrose medium permitted more kojic acid production by the fungus than modified Czapek-Dox liquid medium or Tadera medium. Maximal kojic acid (57–59 mg/ml) was produced in the yeast extract-sucrose medium on days 9–12. No aflatoxin by the fungus was detected.


1998 ◽  
Vol 17 (6-7) ◽  
pp. 1215-1223 ◽  
Author(s):  
E Noroozian ◽  
F Lagerwerf ◽  
H Lingeman ◽  
U.A.TH Brinkman ◽  
M.A.T Kerkhoff

1994 ◽  
Vol 57 (3) ◽  
pp. 256-258 ◽  
Author(s):  
M. L. ABARCA ◽  
M. R. BRAGULAT ◽  
G. CASTELLÁ ◽  
F. J. CABAÑES

The mycoflora of 69 samples of animal mixed feeds were studied. Fungal counts ranged from 102 to 108 CFU/g, the lowest counts corresponding to the samples of rabbit feeds. Seventy-one fungal species belonging to 26 genera were identified. The pre- dominant species were Aspergillus flavus, Fusarium moniliforme, and Penicillium chrysogenum. Thirty-six strains of A. flavus and one strain of A. parasiticus were screened for aflatoxin production in yeast extract-sucrose medium. The final pH, weight of mycelium, and production of aflatoxins were determined after 14 days of incubation. Five strains (13.5%) were aflatoxigenic. No statistical differences were observed in mycelial dry weights and final pH between aflatoxin-producing strains and nonaflatoxigenic strains.


1985 ◽  
Vol 48 (2) ◽  
pp. 118-121 ◽  
Author(s):  
MARGARITA MEDINA ◽  
PILAR GAYA ◽  
M. NUÑEZ

PR toxin production in yeast extract-sucrose broth by 33 Penicillium roqueforti isolates from Cabrales blue cheese was quantified by a disc assay technique with Bacillus megaterium NRRL B-1368 as the test organism. Isolates from the interior of the cheese reached an average production of 1,89 mg PR toxin/100 ml, whereas the mean level of isolates from the surface was 1.64 mg/100 ml. Roquefortine production in the same broth by these isolates was quantified by a similar technique, with Bacillus stearothermophilus DSM 22 as the test organism. Mean production of roquefortine was 0.18 mg/100 ml for P. roqueforti isolates from the interior and 0.09 mg/100 ml for isolates from the surface of the cheese. If lactose or sodium lactate replaced sucrose in the growth medium, levels of both toxins decreased considerably. The identity of PR toxin and roquefortine in crude extracts was confirmed by thin-layer chromatography.


2000 ◽  
Vol 275 (33) ◽  
pp. 25533-25539 ◽  
Author(s):  
Jonathan M. Caruthers ◽  
Ilgu Kang ◽  
Michael J. Rynkiewicz ◽  
David E. Cane ◽  
David W. Christianson

1999 ◽  
Vol 20 (3) ◽  
pp. 609-619 ◽  
Author(s):  
E. Noroozian ◽  
F. Lagerwerf ◽  
H. Lingeman ◽  
U.A.T.H. Brinkman ◽  
M.A.T. Kerkhoff

2009 ◽  
Vol 2009 ◽  
pp. 1-7 ◽  
Author(s):  
Dido Maria Meimaroglou ◽  
Dia Galanopoulou ◽  
Panagiota Markaki

AflatoxinB1(AFB1) is a carcinogenic metabolite produced by certainAspergillusspecies on agricultural commodities. AFB1biosynthesis is affected by jasmonic acid and also by its methylester (MeJA), a plant growth regulator derived from linoleic acid. This study reports the effect of MeJA on the growth ofA. parasiticusand AFB1output in yeast extract sucrose (YES) medium when added at three different concentrations; namely,10−2 M,10−4 M, and10−6 M. AFB1determination was performed by immunoaffinity and HPLC. MeJA at10−4and10−6M concentrations had no significant effect on mycelial growth but did affect AFB1production after the 7th day of incubation; on the 12th day, AFB1production was increased by 212.7% and 141.6% compared to the control samples (addition of10−6 M and10−4 M MeJA, resp.). Treatment ofA. parasiticuscultures with10−2 M MeJA inhibited mycelial growth and AFB1production as well. These results suggest that the effect of MeJA on AFB1biosynthesis byA. parasiticusdepends on the MeJA concentration used.


1969 ◽  
Vol 15 (11) ◽  
pp. 1281-1285 ◽  
Author(s):  
W. van Walbeek ◽  
P. M. Scott ◽  
J. Harwig ◽  
J. W. Lawrence

Ochratoxin A has been obtained from both mycelium and culture filtrates of Penicillium viridicatum Westling grown on a yeast extract – sucrose medium. Ergosterol was also identified as a metabolite. The greatest amount of ochratoxin A was detected 9 days after inoculation. Toxin production decreased greatly after several successive subcultures. However, it was possible to obtain a strongly toxinogenic isolate again from the parent culture. Small amounts of ochratoxin A were detected in 60% whole wheat bread slices used as a substrate for P. viridicatum.


Antioxidants ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 754
Author(s):  
Sang-Eun Jung ◽  
Hui-Jo Oh ◽  
Jin-Seop Ahn ◽  
Yong-Hee Kim ◽  
Bang-Jin Kim ◽  
...  

We postulated that supplementation of antioxidant or apoptosis inhibitor in post-thaw culture media of spermatogonial stem cells (SSCs) alleviates reactive oxygen species (ROS) generation and apoptosis. Our aim was to develop an effective culture media for improving post-thaw recovery of SSCs. To determine the efficacy of supplementation with hypotaurine (HTU), α-tocopherol (α-TCP), and Z-DEVD-FMK (ZDF), we assessed the relative proliferation rate and SSC functional activity and performed a ROS generation assay, apoptosis assay, and western blotting for determination of the Bax/Bcl-xL ratio, as well as immunocytochemistry and real-time quantitative polymerase chain reaction (RT-qPCR) for SSC characterization. The relative proliferation rates with HTU 400 μM (133.7 ± 3.2%), α-TCP 400 μM (158.9 ± 3.6%), and ZDF 200 μM (133.1 ± 7.6%) supplementation were higher than that in the DMSO control (100 ± 3.6%). ROS generation was reduced with α-TCP 400 μM (0.8-fold) supplementation in comparison with the control (1.0-fold). Early apoptosis and Bax/Bcl-xL were lower with α-TCP 400 μM (2.4 ± 0.4% and 0.5-fold) and ZDF 200 μM (1.8 ± 0.4% and 0.3-fold) supplementation in comparison with the control (5.3 ± 1.4% and 1.0-fold) with normal characterization and functional activity. Supplementation of post-thaw culture media with α-TCP 400 μM and ZDF 200 μM improved post-thaw recovery of frozen SSCs via protection from ROS generation and apoptosis after cryo-thawing.


1978 ◽  
Vol 41 (5) ◽  
pp. 344-347 ◽  
Author(s):  
O. PENSALA ◽  
A. NISKANEN ◽  
S. LINDROTH

Unsweetened and sweetened (20 and 44% sucrose) black currant, blueberry and strawberry jams with spores of Aspergillus parasiticus NRRL 2999 were incubated at different temperatures and atmospheres for 0.5, 1, 2, and 6 months. Hyphal dry weight, pH of medium and aflatoxin production were examined. Also, the aflatoxin distribution between mold and jam layers was examined in jam with uncontrolled and controlled pH (initial pH 3.1–3.6 and 5.6 respectively) and in 20% yeast extract sucrose broth (initial pH 5.6) after 2 weeks of incubation. Aflatoxin was observed in black currant and strawberry jams stored at 22 and 30 C, but not in blueberry jam. Addition of sugar prevented production of aflatoxin in detectable amounts, although it enhanced fungal growth. Storage at 4 C resulted in a marked reduction in fungal growth. The high CO2 atmosphere prevented production of aflatoxin in detectable amounts in black currant and blueberry jams but not in strawberry jam. Raising the initial pH of the stored jam caused an increase in aflatoxin synthesis, although the amount of fungal mycelium, in contrast was reduced. Aflatoxin synthesis as a function of fungal growth was significantly weaker in the jams than in the yeast extract sucrose broth. The results imply that the jam raw materials, particularly blueberry, contain substances inhibiting production of atlatoxins. Alternatively, it is also possible that the jam materials contain only small amounts of nutrients necessary for synthesis of aflatoxin.


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