Toxicity and Sorbate Sensitivity of Molds Isolated from Surplus Commodity Cheeses 1

Wei-Yun J Tsai1, Michael B Liewen1, Lloyd B Bullerman1

  • 1Department of Food Science and Technology, University of Nebraska, Lincoln, Nebraska 68583-0919.

Insights

Mold isolates from surplus cheese included four Penicillium species. Some produced mycotoxins like patulin, but no mutagenic activity was found in Ames tests.

Area of Science:

  • Food Microbiology
  • Mycology
  • Food Safety

Background:

  • Surplus cheese from government storage may harbor mold contaminants.
  • Understanding mold populations and their potential toxicity is crucial for food safety.

Purpose of the Study:

  • To identify and characterize mold species in surplus cheese.
  • To assess the mycotoxin production and toxicity of these mold isolates.

Main Methods:

  • Isolation and identification of mold species from cheese.
  • Detection of mycotoxins (patulin, penicillic acid, ochratoxin) using laboratory media.
  • Toxicity testing in chicken embryos and mutagenicity testing (Salmonella mutagenesis/Ames test).
  • Assessment of sorbate resistance in mold isolates.

Main Results:

  • 263 mold isolates identified, all belonging to the genus Penicillium (P. roqueforti, P. cyclopium, P. viridicatum, P. crustosum).
  • Approximately 10% of isolates produced mycotoxins; patulin was most common.
  • Toxicity observed in chicken embryos (10.1% on cheese, 29.7% on rice), with no correlation to mycotoxin production.
  • No mutagenic activity detected in the Ames test when grown on cheese.
  • Significant variation in sorbate resistance among isolates, unrelated to toxigenicity.

Conclusions:

  • The study identified Penicillium species in surplus cheese, with some exhibiting mycotoxin production and toxicity.
  • No mutagenic potential was found in the Ames test for these isolates on cheese.
  • Sorbate resistance varied, but did not correlate with toxic properties.

Related Concept Videos

Toxic Reactions: Overview01:26

Toxic Reactions: Overview

When toxic substances penetrate the human body, they disseminate to various tissues, undergoing metabolic changes. This process yields reactive metabolites that may covalently bind with specific target molecules, resulting in toxicity.
Toxicity falls into two primary categories: local and systemic.
Local toxicity appears at the exposure site, such as protein denaturation caused by caustic substances.
In contrast, systemic toxicity requires the toxic agent's absorption and distribution,...
1.8K
Sensitivity, Specificity, and Predicted Value01:13

Sensitivity, Specificity, and Predicted Value

In healthcare diagnostics, laboratory tests play a crucial role in identifying and diagnosing a wide range of medical conditions. However, interpreting test results is not always straightforward. An abnormal test result does not always confirm the presence of a disease, just as a normal result does not guarantee its absence. To assess the reliability of these diagnostic tools, healthcare practitioners rely on two key statistical indicators: sensitivity and specificity.
Sensitivity is the...
1.2K
SN1 Reaction: Stereochemistry02:15

SN1 Reaction: Stereochemistry

This lesson provides an in-depth discussion of the stereochemical outcomes in an SN1 reaction.
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
10.2K
SN1 Reaction: Kinetics02:05

SN1 Reaction: Kinetics

In an SN2 reaction, the reaction rate depends on both the type of nucleophile and the substrate. A hindered tertiary alkyl halide is practically inert to the SN2 mechanism despite using a strong nucleophile.
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
9.6K
SN1 Reaction: Mechanism02:25

SN1 Reaction: Mechanism

Kinetic studies of ionization of a tertiary halide in a protic solvent suggest that only the substrate participates in the rate-determining step (slow step). The nucleophile is involved only after the slowest step. The SN1 reaction takes place in a multiple-step mechanism. 
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
14.1K
Acidity of 1-Alkynes02:42

Acidity of 1-Alkynes


The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
11.1K