Quality of Irradiated and Cooked Sausage . . .
of eight treatments, whereas the second and third batches were treatments were removed, and fermentation time recorded, as
each divided into two 8-treatment blocks with treatments ran- they reached the target pH. Sticks were weighed, and samples
domly placed on the smokehouse truck to minimize variations in were taken for moisture:protein content and texture analysis.
the thermal processing unit. The experiment used a 2 × 4 factori- The sticks were then transferred to a computer-controlled one-
al treatment design, with the treatments as follows: 1.25-kGy ir- truck environmental chamber (Alkar, Lodi, Wis., U.S.A.) operating
radiation dose; 3.0-kGy irradiation dose; nonirradiated with a at 10 °C and 75% RH until the M:P ratio reached 1.6:1. Periodic
heat treatment; control-nonirradiated without a heat treatment; samples were taken during drying for moisture:protein ratios
preblend with 1.25-kGy irradiation dose; preblend with 3.0-kGy and texture analysis (Instron Series 4500; Instron Corp. Canton,
irradiation dose; preblend (nonirradiated) with a heat treatment; Mass., U.S.A.).
preblend (nonirradiated) without a heat treatment.
Pepperoni sticks to be subjected to a heat treatment were
Fresh 80% lean pork picnic trim was purchased from local sup- placed in a computer-controlled one-truck smokehouse (Alkar,
pliers. The meat was ground through a 1.27-cm plate (Biro model Lodi, Wis.) after drying, to be heated (70 °C, 85% RH) to an inter-
7
552; The Biro Mfg Co., Marblehead, Ohio, U.S.A.), after which nal temperature of 60 °C. It should be noted that irradiation
the meat was divided into two lots for preblended and non-preb- treatments in this study did not involve the finished processed
lended treatments. The batches to be preblended were then products but rather the raw meat materials which were subse-
mixed (Leland model L-100 DA; Leland Detroit Mfg Co., Detroit, quently used to manufacture the pepperoni.
Mich., U.S.A.) with all the salt (2.1%) and one-half the cure for
approximately 5 min, after which all batches were stored in a 4 °C Proximate analysis/yield measurements
cooler. Batches (both preblended and not preblended) requiring
Proximate analysis consisted of moisture (oven drying), fat
irradiation were then boxed in fiberboard boxes with liners ap- (ether extraction), and protein (combustion method) and was
propriate for irradiation processing and received a double-sided performed according to AOAC (1993) procedures. Samples were
irradiation treatment of 1.25 or 3.0 kGy using the linear accelera- measured for proximate composition throughout the drying
tor facility (Linear Accelerator-circle III R; Saint-Aubin, France) at treatment to confirm moisture:protein ratios. All measurements
Iowa State University. Actual measured minimum doses were were performed in duplicate.
1
.24, 1.26 and 1.30 kGy in the three replications. Maximum esti-
Yields were recorded by labeling sticks of pepperoni for each
mated doses were 1.45, 1.76 and 1.88 kGy, respectively. The high- treatment and taking an initial weight immediately after stuff-
er dose treatments were measured at a minimum 2.85, 2.98 and ing. Weights were then taken periodically throughout drying and
3
.17 kGy in the three replications with estimated maximum dos- at the completion of drying and/or heat treatment.
es of 3.31, 4.17 and 4.44 kGy, respectively. Irradiation was con-
ducted at room temperature and required 8 to 10 min per treat- Texture/color analysis
ment. Product temperature did not increase by more than 1 °C
Texture measurements were recorded using both compres-
during the irradiation treatment. Doses were determined in ac- sion of sticks and puncture of slices periodically during drying
cordance with the USDA-FSIS, which reported that the D-value and at the completion of drying for each treatment. The stick
for Escherichia coli O157:H7 was 0.25 kGy for refrigerated product compression consisted of three repeated measurements taken
(
Federal Register, 1999). This requires a minimum dose of 1.25 with an Instron Universal Testing Machine (Instron Series 4500;
kGy to provide a 5-log reduction in E. coli O157:H7, as mandated Instron Corp., Canton, Mass., U.S.A.). The measurement was
by the USDA (Reed, 1995). The doses were measured by placing done by compressing a stick of pepperoni by 30% of the diameter
alanine pellet dosimeters (Bruker Instruments, Inc., Billerica, of the sausage with a 3.5-cm dia compression anvil (Model 2830-
Mass., U.S.A.) on the top and bottom of boxes for each treatment 011) attachment. The 30% compression was chosen from prelimi-
(
ASTM 1996). The dosimeters were read by electroparamagnetic nary work on commercial pepperoni which suggested that 30%
resonance (EMS 104; Bruker Analytiscne Messtechnik, Karlsruhe, was effective for detecting product differences. The Instron was
Germany). All of the treatments were then held in a 4 °C cooler equipped with a 1-KN load cell with conditions for a one-cycle
overnight, after which the 8.6-kg batches were mixed with spices, compression at 200 mm per min crosshead speed and by using a
salt, dextrose, and 78 or 156 parts per million (ppm) sodium ni- preload of 0.5 kg. The hardness of pepperoni slices was mea-
trite in a grinder-mixer (Hollymatic model 175; Hollymatic Corp., sured by the force needed to puncture a 0.2-cm slice with a 1.27-
Park Forest, Ill. U.S.A.). It is important to note that half of the cm dia probe on the Instron equipped with a 1-KN load cell. Con-
cure for the preblend treatments was added initially, with the re- ditions used for a one-cycle break of the slices were 400 mm per
maining half being added with the spices at the final mixing. Pa- min crosshead speed and a preload of 0.05 kg. Five measure-
prika oleoresin flavoring (Pepperoni Oleoresin Flavor; Chr. Hans- ments per treatment were taken for slice hardness.
en Inc., Milwaukee, Wis., U.S.A.) was added which contained an-
Color measurements of 0.2-cm slices were conducted by using
tioxidants BHA (1.12%), BHT (1.12%), and citric acid (1.12%). The a HunterLab LabScan Spectro Colorimeter (Hunter Associates
starter culture (LL2; Diversitech Inc., Gainesville, Fl., U.S.A.) was Lab, Inc., Reston, Virg., U.S.A.) with an illuminant A and 10° ob-
added last in accordance with manufacturers directions (2.95 g server light source (representing an incandescent lamp) and a
with 41 g water). The batches were then ground through a 0.318- 2.54-cm port insert. Color was first measured when the product
cm plate and vacuum-stuffed (Risco model RS 4003-165, Stough- processing was completed (drying or heating) and again after 4
ton, Mass., U.S.A.) into 1S × 30 fibrous cellulose casings. Samples wks of storage at 4 °C.
were taken during stuffing for measurement of initial pH and
proximate analysis. Initial weight of stuffed products was mea- Lipid oxidation analysis
sured after stuffing.
Samples were measured for oxidative rancidity by using the
modified 2-thiobarbituric acid (TBA) procedure of Tarladgis and
others (1960). The initial TBA measurements were done for all
treatments immediately following irradiation of appropriate
batches. Measurements were also conducted after the comple-
tion of drying and/or heating, and every 3 wk thereafter during
Pepperoni was placed in a computer-controlled one-truck
smokehouse (Alkar, Lodi, Wis., U.S.A.), which was programmed
for fermentation at 27 °C dry bulb, 26 °C wet bulb, (96% RH) until
the required pH was reached. The fermentation was considered
complete when the pH of the pepperoni declined below 5.0 as
periodically measured by a hand-held pH-Star probe (pH-Star S;
SFK Technology Inc., Cedar Rapids, Ia., U.S.A.). The pepperoni
5
-mo of storage at 4 °C. Additional samples of each treatment
were also stored at room temperature and in direct sunlight to be
Vol. 65, No. 7, 2000—JOURNAL OF FOOD SCIENCE 1261