Table of Contents Table of Contents
Previous Page  89 / 471 Next Page
Information
Show Menu
Previous Page 89 / 471 Next Page
Page Background

Evaluation of the 3M

Petrifilm

Rapid Yeast and Mold Count

1

Plate

for the Enumeration of Yeast and Mold in Food:

2

Collaborative Study

3

4

Patrick Bird, Jonathan Flannery, Erin Crowley, James Agin, David Goins

5

Q Laboratories, Inc., 1400 Harrison Ave, Cincinnati, OH 45214

6

7

Robert Jechorek

8

3M Food Safety Department,

3MCenter – Bldg. 260-6B-01, St. Paul, MN 55144

9

10

Collaborators: D. Metzger, W. Lee, T. Hirsch, P. Fatemi, S. Spencer, J. Blumfield, B. Dieckleman,

11

K. Gonzales, C. Fagundes, J. Reed, J. Medellin, A. Hankins, R. Dermer, N. Shipley, J. Williams, A.

12

Morris, R. Brooks, K. Powers, B. Brown, K. Beers, A. Calle, J. Pickett, J. Reynolds, A. Gaydos, A.

13

Mastalerz

14

15

The 3M

Petrifilm

Rapid Yeast and Mold (RYM) Count Plate

is a simple, ready to use

16

chromogenic culture method for the rapid detection and enumeration of yeast and mold in

17

food products. The 3M Petrifilm RYM Count Plate was compared to the FDA BAM

18

Chapter 18

Yeasts, Molds and Mycotoxins

and the ISO 21527:2008

Microbiology of food and

19

animal feeding stuffs – Horizontal method for the enumeration for yeast and molds

– Part 1:

20

Colony count technique in products with water activity greater than 0,95

and Part 2:

Colony

21

count technique in products with water activity less than or equal to 0,95

reference methods

22

for raw almonds and raw frozen ground beef patties (77% lean). The 3M Petrifilm RYM

23

Count Plate was evaluated using a paired study design in a multi-laboratory collaborative

24

study following the current AOAC Validation Guidelines. Three (3) target contamination

25

levels (low, 10-100 colony forming unit (CFU)/g; medium, 100-1,000 CFU/g; high 1,000-

26

10,000 CFU/g) as well as an uninoculated control level (0 CFU/g) were evaluated for each

27

matrix. Samples evaluated by the 3M Petrifilm RYM Count Plate were prepared in

28

duplicate and incubated at both 25

o

C and 28

o

C. Plates at both temperatures were

29

enumerated after 48 and 60 hours of incubation. No significant difference was observed

30

between the 3M Petrifilm RYM Plate Count and the FDA BAM or ISO 21527 reference

31

methods for each contamination level. No statistical differences were observed between

32

samples analyzed by the 3M Petrifilm RYM Count Plate (at either 25

o

C or 28

o

C) and the

33

reference methods. No statistical significant differences were observed between

34

enumeration of colonies at 48 and 60 hours on the 3M Petrifilm RYM Count Plate and the

35

reference methods.

36

37

Foodborne yeasts and mold constitute a large and diverse group of microorganisms. Due to their

38

heterotrophic nature, these microorganisms are able to adapt and survive in a wide range of

39

environmental conditions including acidic and alkaline conditions, temperatures ranging from

40

5

o

C to 35

o

C and in low moisture products (<0.85

Aw

) [1, 2]. Many of these species cause varying

41

degrees of food decomposition leading to substantial economic loses [2]. Several foodborne

42

molds, and possibly some yeasts, may also be hazardous to human health due to their ability to

43

produce toxic metabolites [1]. The presence of these microorganisms in food commodities can

44

indicate contamination of the product, inadequately cleaned food processing equipment or

45

inadequate food storage facilities [2]. Cultural enumeration of yeasts and molds can take 5 to

46

Candidates for 2016 Method of the Year

75