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www.elsevier.com/locate/meatsci
Meat Science 69 (2005) 681–689
MEATSCIENCE
Chemical, physical and sensory properties of meat from pureand crossbred Podolian bulls at different ageing times
A. Braghieri, G.F. Cifuni, A. Girolami, A.M. Riviezzi, I. Marsico, F. Napolitano *
Dipartimento di Scienze delle Produzioni Animali, Universita degli Studi della Basilicata, Via dell�Ateneo Lucano 10, 85100 Potenza, Italy
Received 2 August 2004; received in revised form 24 October 2004; accepted 29 October 2004
Abstract
The present study aimed to investigate the effect of crossbreeding with Limousine sires on fatty acid profile, physical and sen-
sory properties of meat produced by Podolian young bulls. Polyunsaturated fatty acid content was influenced by crossbreeding
(P < 0.01) with Podolian bulls (P) producing beef characterised by a higher level of unsaturation in comparison with crossbred
animals (LP). As a consequence, P/S ratio was significantly higher in meat produced by P animals than LP (P < 0.01). P animals
had higher linoleic (P < 0.05), linolenic (P < 0.05), EPA (P < 0.05) and DHA acids (P < 0.001) levels than LP subjects. No breed
effect was observed for the ratio n � 6/n � 3 (P > 0.05). WBS force of LD was significantly lower in meat from crossbred subjects
(P < 0.05). Both crossbreeding with Limousine and extension of ageing from 2 to 7 days improved LD tenderness as assessed by
panel taste (P < 0.001).
� 2004 Elsevier Ltd. All rights reserved.
Keywords: Podolian cattle; Crossbreeding; Ageing; Fatty acid composition; Tenderness
1. Introduction
Meat produced by cattle are usually characterised by
a low polyunsaturated to saturated fatty acid (P:S) ratiodue to the massive hydrogenating action performed by
rumen micro-organisms on dietary fatty acids. However,
these products often show a beneficially balanced n � 6/
n � 3 ratio, which is particularly low when animals are
fed on grass based diets (Enser et al., 1998). Neverthe-
less, in addition to other factors (diet, sex, age, etc.),
the effect of breed on adipose tissue and muscle fatty
acid composition may be relevant. Numerous studieshave reported that sire breed can affect meat fatty acid
profile (Xie, Bushboom, Gaskins et al., 1996; Zembay-
0309-1740/$ - see front matter � 2004 Elsevier Ltd. All rights reserved.
doi:10.1016/j.meatsci.2004.10.019
* Corresponding author. Tel.: +39 0971 205078; fax: +39 0971
205099.
E-mail address: [email protected] (F. Napolitano).
ashi & Nishimura, 1996; Zembayashi, Nishimura, Lunt,
& Smith, 1995). Because of the low fat content of mus-
cles, lean breeds can have a different fatty acid profile
compared with meat from other breeds. In cattle, poly-unsaturated fatty acids (PUFA) are preferentially
deposited in phospholipids. As a consequence, lean
breeds tend to have a higher proportion of PUFA as
compared to fatter cattle breeds, whereas in these latter
genotypes muscles have a higher incidence of neutral
triacylglycerols (De Smet, Webb, Claeys, Uytterhaegen,
& Demeyer, 2000). The lower fat content of muscles of
lean breeds can also account for the higher ratio n � 6/n � 3 due to the greater proportion of phospholipids ob-
served in these animals. Phospholipids display lower lev-
els of linolenic and higher contents of linoleic and
arachidonic fatty acids than triacylglycerols (Bas & Sau-
vant, 2001), which in turn increase in proportion as total
lipids increase (Marmer, Maxwell, & Williams, 1984).
Previous studies reported that both double muscled
682 A. Braghieri et al. / Meat Science 69 (2005) 681–689
(De Smet et al., 2000) and Podolian cattle (Cifuni,
Napolitano, Riviezzi, Braghieri, & Girolami, 2004),
which are genetically lean breeds, show a high P:S ratio
and a correspondingly higher proportion of polar lipid
containing high levels of linoleic and arachidonic fatty
acids of the n � 6 series.The perceived healthiness of a food is of great impor-
tance for consumer preference with many consumers
concerned about the contribution of beef to their total
intake of saturated fatty acids, which have been impli-
cated in diseases associated with modern life such as cor-
onary heart disease and cancer. Consumers with a
positive perception of the product show a higher level
of acceptability for that product (Bello Acebron & Cal-vo Dopico, 2000). According to Resurreccion (2003), for
USA consumers the most important quality aspects of
beef are those in relation to healthiness (cholesterol, cal-
orie and artificial ingredient contents, etc.), whereas in
Europe consumers are also interested in other aspects
concerning the sensory properties of the product (taste,
tenderness, juiciness, etc.).
Previous studies on meat acceptability reported thatconsumers consider tenderness as the attribute most
desired when eating at the home or in the restaurant
(Huffman et al., 1996). One of the main concerns of
retailers and restaurateurs is also tenderness (Smith
et al., 1992). There are a number of factors that influ-
ence tenderness of meat, although ageing, marbling,
connective tissue content and muscle contraction can
be considered the four main aspects to be taken intoaccount.
Podolian cattle are bred using a traditional farming
system (Napolitano, Braghieri, Brancieri, Pacelli, &
Girolami, 2002) based on animals grazing green for-
ages directly from pasture at least for the first growing
period (0–10 months). Their physical activity along
with the leanness of the breed can account for the
low tenderness, which often characterises their meatand may give rise to reduced acceptability of the prod-
uct (Cifuni et al., 2004).
Previous studies focussed on fatty acid composition,
cholesterol content and sensory properties of meat pro-
duced by Podolian cattle (Cifuni, Napolitano, Pacelli,
Riviezzi, & Girolami, 2000; Cifuni et al., 2004). How-
ever, meat quality may be improved by crossbreeding
Podolian cattle with other breeds such as Limousine cat-tle (Wulf et al., 1996). Thus, crossbreeding may allow
preservation of Podolian cattle and improve some key
quality characteristics of the meat (i.e., nutritional and
sensory properties).
The present study was aimed to investigate the effect
of crossbreeding with Limousine sires on the fatty acid
profile, cholesterol and malondialdehyde contents, phys-
ical and sensory properties of meat produced by Podo-lian young bulls. The influence of ageing on meat
tenderness was also evaluated.
2. Materials and methods
2.1. Experimental design
Eight Podolian (P) and eight Limousine · Podolian
crossbred young bulls (LP) were used. Animals werereared according to the traditional local practices,
namely dam-reared to the age of natural weaning (8–9
months of age) on natural pasture of Basilicata (South-
ern Italy) where no feeding supplementation was offered
and, subsequently, moved to a straw bedded barn pro-
vided with an ample outdoor paddock. In this fattening
period the experimental subjects received a diet based on
straw offered ad libitum, 0.5 kg/100 kg LW of field beans(8%), soy (20%), corn (35%) and barley + wheat (37%)
flour and 0.5 kg/100 kg LW of a commercial pellet for
fattening cattle (14% CP). All the animals were slaugh-
tered at 18 months of age. Final live weights were ob-
tained immediately before slaughter. After removal of
skin and internal organs, carcasses were dissected into
two sides. Right and left sides from each carcass were
aged at 4 �C for 2 and 7 days post-mortem, respectively.Subsequently, sides were divided into quarters, quarters
were dissected into commercial cuts and the Longissimus
dorsi (LD) and Semimembranosus (SM) removed.
2.2. Fatty acid, cholesterol and MDA determination
Analyses for cholesterol and fatty acid contents were
performed only on samples from LD aged for 2 days.Malondialdehyde (MDA) content was determined on
LD and SM at 2 and 7 days of ageing.
Lipid was extracted according to the method of Folch,
Lees, and Stanley (1957). Gas chromatograph analysis
was performed on a Varian model Star 3400 CX instru-
ment equipped with a CP 88 capillar column, as described
by Cifuni et al. (2004). The individual fatty acid peaks
were identified by comparison of retention times withthose of known mixtures of standard fatty acids (FAME,
Sigma) rununder the sameoperating conditions.Fattyacids
were expressed as percent of total methylated fatty acids.
The determination of cholesterol was performed
using the method of Ulberth and Reich (1992). This
method involves direct saponification of the samples,
extraction of the unsaponifiable compounds with cyclo-
hexane and a subsequent enzymatic assay (Kit no.139050, Boehringer Mannheim Gmbh). The content of
cholesterol was expressed as mg/100 g of meat.
The TBA test was performed as described by Salih,
Smith, Price, and Dawson (1987). Lipid oxidation was
expressed as mg MDA/kg of meat.
2.3. Physical and sensory analyses
pH was measured at 1, 24 and 48 h post-mortem on
SM and LD (lumbar region) with a portable pH meter
A. Braghieri et al. / Meat Science 69 (2005) 681–689 683
(Hanna HI 9025), equipped with a penetrating glass
electrode.
Warner–Bratzler shear force was measured on SM
and LD cores sheared by an Instron Universal testing
machine equipped with a Warner–Bratzler shearing de-
vice at 2 and 7 days of ageing. Two 1.27 cm wide coreswere removed parallel to the muscle fibre and placed as
raw samples in the Warner–Bratzler Shear attachment,
which was attached to the model 1140 Instron texture
machine. Shear force was perpendicular to the direction
of the fibres and the force required to shear was re-
corded in kg. For each sample one mean value was cal-
culated and used for statistical analysis.
The LD muscle was also employed for sensory evalu-ation. One cm deep steaks were grilled to an internal
temperature of 75 �C, assessed using a thermocouple
probe inserted into the meat. Subsequently, 2 · 2 · 1
cm samples were cut from the muscles and offered to
the panellists. Products were rated on predetermined
scales by a panel of eight members previously selected
for their flavour and texture sensitivity. Six preliminary
sessions were used to develop attributes (flavour andtenderness) and train assessors for attribute intensity
evaluation (Napolitano et al., 2001). For each session
assessors were offered meat samples from the animals
in the experiment. After a further training for scale use
(Stone & Sidel, 1985) attributes were rated on the basis
of 10 cm unstructured lines with anchor points at each
end (0: absent and 10: very strong, therefore, higher
scores corresponded to more tender products). Scoreswere the distances (mm) from the left anchor-point.
The main trial consisted of four sessions. In each session
four samples (two for each group) were assessed with the
same frequency in each position in order to minimise the
effect of order of presentation (MacFie, Bratchell,
Greenhoff, & Vallis, 1989). Distractions to panellists
were reduced by using booths, which were illuminated
with red light to minimise bias due to possible colourdifferences.
2.4. Statistical analyses
Data were analysed with SAS statistical package
(SAS, 1990). The animal was used as the experimental
unit. Carcass traits, fatty acid profile and cholesterol
content were subjected to analysis of variance with onefactor (genotype). MDA was subjected to analysis of
variance for repeated measures with genotype as non re-
peated factor and muscle, ageing and the interactions
(first and second order) as repeated factors. pH values
were analysed using ANOVA for repeated measures
with genotype as a between-animal factor and time
(post-mortem h), muscle and the interactions (first and
second order) as within-animal factors. WBS data weresubjected to ANOVA for repeated measures with geno-
type as non-repeated factor and ageing time, muscle and
the interactions (first and second order) as repeated fac-
tors. Sensory values were normalised standardising each
assessor by his standard deviation in order to reduce the
effect of the different use of the scale (Naes, 1991). Anal-
ysis of variance with genotype (non repeated factor),
ageing and interaction (repeated factors) as the main ef-fects was performed on normalised mean values of ten-
derness and flavour intensity.
3. Results and discussion
3.1. Carcass traits
Carcass traits are displayed in Table 1. LP showed
higher live pre-slaughter and carcass weights than P
(P < 0.01). However, carcasses of both groups P and
LP were scored as 3 for fatness (corresponding to aver-
age fatness: within the thoracic cavity the muscle is
clearly visible between the ribs) and R for muscular con-
formation (well-developed topside, slightly rounded
rump, good back and fairly well developed shoulder)using the Community scale for the classification of car-
casses of adult bovine animals (SEUROP). In addition,
carcass yields were not significantly different between
groups. Values of carcass yield similar to those obtained
in the present study were found by Napolitano et al.
(2001) in Podolian young bulls of the same age.
Group P produced carcasses with a higher percent
hindquarter than LP (P < 0.001). A fast growth of theforequarters has been observed in Limousine cattle by
Robelin and Geay (1976) and Robelin, Geay, and Be-
ranger (1977). The differential growth observed in the
two genotypes (P and LP) may also explain the results
obtained for the commercial cuts: LP displayed higher
percentages of shoulder (P < 0.001) and chuck
(P < 0.01), whereas tenderloin + striploin (P < 0.10),
top side (P < 0.001) and rump cap (P < 0.05) were high-er in carcasses of P animals. No differeces between geno-
types were observed for rib-eye, rump, top beef and eye
of round (P > 0.05).
3.2. Fatty acid, cholesterol and MDA contents
Fatty acid profile of LD is depicted in Table 2. The
amounts of saturated and monounsaturated fatty acidswere not affected by genotype (P > 0.05). Both geno-
types showed high and similar levels of the saturated
stearic and monounsaturated oleic acids, which ac-
counted for over 50% of the total fatty acids. Similar
values were obtained in a previous work conducted on
Podolian beef by Cifuni et al. (2004). The stearic acid
can be easily desaturated to oleic, which in turn is con-
sidered hypolipidemic, reducing both plasma triglycer-ides and LDL-cholesterol, whereas HDL-cholesterol is
unaffected (Mattson & Grundy, 1985). Thus both acids
Table 1
Effect of genotype on pre-slaughter weight and carcass traits (means ± S.E.)
P LP Significance
Pre-slaughter weight (kg) 458.12 ± 7.82 505.00 ± 7.82 P < 0.01
Carcass weight (kg) 252.14 ± 6.41 282.76 ± 6.00 P < 0.01
Carcass yield (%) 54.86 ± 0.79 56.00 ± 0.74 NS
Forequarter (%) 47.77 ± 0.47 51.76 ± 0.44 P < 0.001
Hindquarter (%) 52.23 ± 0.48 47.36 ± 0.45 P < 0.001
Rib-eye (%) 9.21 ± 0.19 9.01 ± 0.18 NS
Chuck (%) 8.48 ± 0.39 10.42 ± 0.36 P < 0.01
Shoulder (%) 7.13 ± 0.32 9.13 ± 0.30 P < 0.001
Rump (%) 3.97 ± 0.13 4.33 ± 0.12 NS
Top beef (%) 5.91 ± 0.09 5.95 ± 0.08 NS
Rump cap (%) 7.31 ± 0.34 6.18 ± 0.31 P < 0.05
Tender loin + strip loin (%) 8.84 ± 0.22 8.21 ± 0.21 P < 0.10
Top side (%) 7.36 ± 0.14 6.52 ± 0.13 P < 0.001
Eye of round (%) 1.96 ± 0.08 1.88 ± 0.08 NS
First grade cuts (%) 52.32 ± 0.46 53.62 ± 0.43 P < 0.10
Second grade cuts (%) 33.15 ± 0.62 33.10 ± 0.58 NS
684 A. Braghieri et al. / Meat Science 69 (2005) 681–689
can be considered desirable components of the human
diet. The hyperlipidemic saturated palmitic fatty acid
C16:0 content was lower in meat produced by Podolian
cattle (P < 0.05), whereas a higher proportion of behenic
acid C22:0 was observed in the beef of purebred animals
(P < 0.05). The former is implicated in the development
of heart diseases (Bonamone & Grundy, 1988), whereas
the latter is generally regarded as safe and usually addedto oil to enable the production of semi-solid and solid
fats such as margarine.
Polyunsaturated fatty acid content was influenced by
crossbreeding (P < 0.01) with Podolian bulls producing
beef characterised by a higher level of unsaturation in
comparison with LP animals. As a consequence, P/S ra-
tio was significantly higher in meat produced by P ani-
mals than LP (P < 0.01). P/S is regarded as importantin relation to the nutritional value of foods for human
health. In the human diet, the recommended value for
P/S ratio is 0.45–0.65 (Department of Health & Social
Security, 1984) and lower ratios in the diet as a whole
may increase the incidence of cardiovascular disease.
The P/S ratio in ruminant meat is unfavourably low be-
cause dietary unsaturated fatty acids are hydrogenated
by rumen micro-organisms (Choi, Enser, Wood, & Sco-llan, 2000). Nevertheless, high P/S ratios were detected
in this trial as a consequence of the high percentages
of PUFA. This variable can be affected by the diet,
breed and type of finishing of the animals. Dietary ef-
fects on fatty acid profile of meat have been observed
by different authors (Aharoni et al., 1995; French et
al., 2000) and lipid composition tends to reflect the fatty
acid composition of the diet. However, fat content andnot diet is the primary factor leading to the variations
in P/S, therefore breed type is one of the main factors
affecting fatty acid composition, because fat deposition
differs between breeds. In lean breeds, such as the Pod-
olian, a reduced deposition of triacylglycerol fatty acids
increases the proportion of unsaturated fatty acids
which are at higher concentrations in membrane phos-
pholipids (De Smet et al., 2000). In crossbred LP sub-
jects, the proportion of membrane phospholipids may
be lower thus lowering the P/S ratio. Our results are in
agreement with those previously reported by Carnovale
and Nicoli (2000) and Cifuni et al. (2004).
Similar considerations also apply for the fatty acidsof n � 6 and n � 3 series with the meat of lean animals
characterised by high n � 6 contents (Bas & Sauvant,
2001). In the present study, although P animals had
higher linoleic acid C18:2 n � 6 levels in the meat than
LP subjects (P < 0.05), no breed effect was observed
for the ratio n � 6/n � 3 (P > 0.05), which exceeded
the recommended values for human nutrition (10:1;
Commission of European Communities, 1993) in bothgenotypes. This latter result may be attributed to the
fact that Podolian bulls showed higher levels of linolenic
C18:3 n � 3 (P < 0.05), EPA C20:5 n � 3 (P < 0.01) and
DHA C22:6 n � 3 acids (P < 0.001) than crossbred ani-
mals. Similarly, Choi et al. (2000) found higher levels of
both n � 3 and n �;6 fatty acids in both neutral and
phospholipid fractions of the leaner beef breed Welsh
Black compared to the dairy breed Holstein Friesian.No differences between P and LP animals were ob-
served in the content of iso and anteiso methyl branched
fatty acids or for trans fatty acids (P > 0.05).
Table 2 shows that intramuscular fat was unaffected
by breed-type (P > 0.05), whereas cholesterol content
was higher in Podolian beef than LP (P < 0.01).
Although in previous studies cholesterol content was
resistant to breed effect (Eichhorn et al., 1986; Wheeler,Davis, Stoecker, & Harmon, 1987 in Rule, MacNeil, &
Short, 1997), Rule et al. (1997) observed a higher choles-
terol level in the ground carcasses of steer calves pro-
duced by crossbred cows sired by Hereford bulls
(moderate growth potential) than Charolais bulls (high
Table 2
Effect of genotype on fatty acid composition (%), intramuscular fat (g/100 g) and cholesterol (mg/100 g) contents of LD muscle (means ± S.E.)
Genotype Significance
P LP
C10:0 0.03 ± 0.01 0.03 ± 0.01 NS
C12:0 0.05 ± 0.01 0.05 ± 0.01 NS
C14:0 1.73 ± 0.09 1.92 ± 0.09 NS
C14:1 trans 0.16 ± 0.01 0.18 ± 0.01 NS
C14:1 cis 0.32 ± 0.03 0.36 ± 0.02 NS
C15:0 anteiso 0.21 ± 0.01 0.22 ± 0.01 NS
C15:0 0.36 ± 0.02 0.38 ± 0.01 NS
C16:0 iso 0.20 ± 0.02 0.23 ± 0.02 NS
C16:0 22.26 ± 0.47 23.63 ± 0.44 P < 0.05
C16:1 trans 0.26 ± 0.10 0.38 ± 0.10 NS
C16:1 cis 0.38 ± 0.03 0.43 ± 0.03 NS
C17:0 anteiso 2.51 ± 0.16 2.36 ± 0.15 NS
C17:0 iso 0.91 ± 0.03 0.92 ± 0.03 NS
C17:1 0.12 ± 0.01 0.13 ± 0.01 NS
C18:0 iso 0.52 ± 0.02 0.48 ± 0.02 NS
C18:0 17.93 ± 0.63 17.68 ± 0.59 NS
C18:1 trans 2.00 ± 0.21 1.64 ± 0.20 NS
C18:1 cis 32.75 ± 0.74 33.00 ± 0.69 NS
C18:1 n � 7 0.58 ± 0.17 0.84 ± 0.16 NS
C18:2 t9t12 0.21 ± 0.01 0.14 ± 0.01 P < 0.001
C18:2c9t12 0.18 ± 0.01 0.13 ± 0.01 P < 0.05
C18:2 t9c12 0.22 ± 0.01 0.18 ± 0.01 P < 0.05
C18:2 n � 6 9.55 ± 0.37 8.37 ± 0.34 P < 0.05
C18:3 n � 6 0.26 ± 0.01 0.23 ± 0.01 NS
C18:3 n � 3 0.38 ± 0.02 0.33 ± 0.01 P < 0.05
C20:0 0.12 ± 0.04 0.16 ± 0.04 NS
C22:0 0.13 ± 0.01 0.08 ± 0.01 P < 0.01
C20:1 n � 9 0.13 ± 0.01 0.13 ± 0.01 NS
C20:2 n � 6 0.63 ± 0.05 0.54 ± 0.05 NS
C20:3 n � 6 0.07 ± 0.01 0.09 ± 0.01 NS
C20:4 n � 6 2.75 ± 0.17 2.53 ± 0.16 NS
C20:5 n � 3 EPA 0.15 ± 0.01 0.09 ± 0.01 P < 0.01
C22:4 n � 6 0.43 ± 0.04 0.41 ± 0.03 NS
C22:5 n � 3 0.46 ± 0.03 0.36 ± 0.03 P < 0.05
C22:6 n � 3 DHA 0.05 ± 0.01 0.03 ± 0.01 P < 0.001
Saturated 46.98 ± 0.63 48.16 ± 0.59 NS
Monounsaturated 36.72 ± 0.77 37.08 ± 0.72 NS
Polyunsaturated 16.30 ± 0.72 13.44 ± 0.67 P < 0.01Pn � 6/
Pn � 3 14.00 ± 0.65 15.22 ± 0.61 NS
P/S 0.35 ± 0.02 0.28 ± 0.02 P < 0.01
Trans 2.63 ± 0.21 2.33 ± 0.20 NS
Intramuscular fat 2.19 ± 0.26 2.31 ± 0.26 NS
Cholesterol 52.34 ± 1.92 44.63 ± 1.92 P < 0.05
A. Braghieri et al. / Meat Science 69 (2005) 681–689 685
growth potential). As also demonstrated by the mean fi-
nal live and carcass weights of the animals used in this
experiment, Limousine sires have a higher growth po-
tential compared to Podolian sires, which in turn pro-
duced animals with higher meat cholesterol.
MDA content (Fig. 1) was not affected by muscle
(P > 0.05), whereas it was influenced by ageing
(P < 0.01) and genotype (P < 0.05). No significant inter-actions were found. Accordingly, Cifuni et al. (2004) ob-
served a significant increase of MDA content when
ageing was changed from 8 to 15 days but no significant
variation induced by muscular anatomical location. The
effect of genotype on MDA is likely to be mediated by
the fatty acid composition observed in the two groups,
as P subjects produced meat with a higher degree of
unsaturation compared to LP and susceptibility to oxi-
dation increases with the number of double bonds in
the fat (Allen & Foegeding, 1981). The toxicity of
MDA in human nutrition is well known, however, in
the meat of both groups its level was below the threshold
value for rancidity (1–2 mg/kg of meat; Watts, 1962).
3.3. Physical and sensory properties
For both genotypes the rate of pH fall in LD and SM
is depicted in Fig. 2. The analysis of variance showed
significant effects of genotype (P < 0.05) and time
(post-mortem h; P < 0.001), whereas muscle, first and
Fig. 1. Effect of genotype and ageing on MDA content (mg/kg) of LD muscle.
Fig. 2. Effect of genotype on post-mortem pH decline of LD and SM
muscles.
Fig. 3. Genotype and ageing effects on WB shear force of LD and SM
muscles.
686 A. Braghieri et al. / Meat Science 69 (2005) 681–689
second order interactions were not significant. As ex-
pected, pH values were much lower at 24 and 48 than
at 1 h (P < 0.001) as a consequence of post-mortem gly-
colysis. pH values were higher in the meat from Podo-
lian animals than crossbred subjects. Also Ciria,
Asenjo, Beriain, and Gorraiz (2000) found significantdifferences in ultimate pH values between the cosmopol-
itan Charolais and the local Serrana Soriana breeds.
Ultimate pH can markedly affect meat quality. Watan-
abe, Daly, and Devine (1996) observed that an increase
in LD pH may be associated with increased toughness.
However, in this experiment it fell within the range
(5.5–5.8) needed to avoid dark cutting meat (Dransfield,
1981).
WBS force (Fig. 3) was affected by breed and muscle
(P < 0.001), whereas it was only slightly influenced by
ageing (P < 0.10). No significant interactions were ob-
served. In a recent study Belew, Brooks, McKenna,
and Savell (2003) evaluated the WBS values for a wide
array of bovine muscles. These authors confirmed previ-
ous works reporting that support muscles are more ten-der than locomotive muscles. Accordingly, in this study
the support LD needed a lower WBS force than the lo-
comotive SM (P < 0.001). WBS values were significantly
lower in meat from crossbred subjects (P < 0.01),
although both genotypes were below an acceptability
threshold value of 3.9 kg, as indicated by Morgan
et al. (1991). Numerous authors attributed differences
of beef tenderness in terms of WBS force to geneticallydiverse enzymatic activity, fatness or fibre type (e.g.,
Sherbeck, Tatum, Field, Morgan, & Smith, 1995). Age-
ing and the interaction ageing · genotype had no effect
Table 3
Effect of ageing and genotype on sensory attribute scores of LD muscle (mean ± S.E.)
Ageing Genotype Significance
2d 7d P LP A G A ·G
Flavour 5.21 ± 0.15 5.07 ± 0.15 5.18 ± 0.15 5.10 ± 0.15 NS NS NS
Tenderness 5.26 ± 0.18 6.15 ± 0.18 5.11 ± 0.18 6.31 ± 0.18 P < 0.001 P < 0.001 NS
A. Braghieri et al. / Meat Science 69 (2005) 681–689 687
on Warner Bratzler Shear values, although other
authors (French et al., 2001; Maria, Villaroel, Sanudo,
Olleta, & Gebresenbet, 2003; Sherbeck et al., 1995)
found a significant decrease in WBS values throughout
the ageing period, indicating a significant improvement
in meat tenderness.
Both genotype and ageing influenced LD tenderness
(Table 3) as assessed by taste panel (P < 0.001), whereasno significant interaction genotype · ageing was ob-
served. LD showed higher sensory tenderness in cross-
bred than P young bulls (P < 0.001). Although sensory
panellists scored samples from 7-day ageing as more ten-
der compared with meat aged only two days, we did not
find an effect on shear values, probably because of the
short time of ageing. The sensory evaluation of meat
tenderness by a panel is costly (meat to be purchasedand assessors to be paid) and time consuming (panel
training). However, although the Warner–Bratzler
method gives the maximal force needed to shear a core
of meat, no information on perception of meat tender-
ness during biting and mastication can be detected. As
already stated, many studies reported an effect of ageing
on beef tenderness as assessed by Warner–Bratzler
shearing. However, along with Otremba et al. (1999),what is measured by shear force may not exactly reflect
the attributes evaluated by a descriptive texture profile.
Girolami et al. (2003) stated that sensory evaluation of
meat may be more effective in detecting subtle tender-
ness differences than instrumental assessment.
The tenderisation process occurring during ageing in-
volves complex changes in muscle metabolism and is
dependent on animal breed, metabolic status and envi-ronmental factors. However, the main determinant of
ultimate tenderness appears to be the enzymatic proteol-
ysis of muscular fibres (Koohmarie, 1996). A number of
authors observed that sensory tenderness improved as
ageing time increased (Huff & Parrish, 1993; Miller
et al., 1997). In particular, for meat produced by differ-
ent continental European breeds post-mortem ageing
improved tenderness regardless of genotype (Wulf etal., 1996). In addition, Mitchell et al. (1991) observed
that the extension of the ageing period from 3 to 10 days
significantly increased sensory tenderness, whereas no
further improvement was detected at 21 day ageing. A
similar trend was found by Silva, Patarata, and Martins
(1999) for meat obtained from local Portuguese bulls,
and Xie, Bushboom, Conforth et al. (1996) for crossbred
Wagyu beef.
Numerous authors have found a significant effect of
genotype on meat sensory tenderness scores (Gregory,
Cundiff, Koch, Dikeman, & Koohmaraie, 1994; Macie
et al., 2000; O�Connor, Tatum, Wulf, Green, & Smith,
1997). In our study breed differences in muscle Zn con-
centrations may have determined higher shear values
and lower panel tenderness scores for Podolian young
bulls with higher Zn levels inhibiting post-mortem pro-teolysis (Seideman, Cross, & Crouse, 1989). In pure
and crossbred Hereford steers, Sherbeck et al. (1995) ob-
served that shear values and sensory tenderness ratings
increased as the percentage of Brahman breeding in-
creased. Accordingly, the meat of Holstein and Charo-
lais steers received poorer sensory scores compared to
Aberdeen Angus subjects (Sinclair et al., 2001). Even
within Charolais and Limousine breeds, marked geneticdifferences were observed in meat tenderness and such
results were unaffected by post-mortem ageing (Wulf
et al., 1996). Campo, Sanudo, Panea, Alberti, and
Santolaria (1999) also observed a marked effect of the
breed on meat tenderness and suggested an early con-
sumption of meat obtained from double muscle animals
and a longer ageing period for meat produced by local
and rustic breeds in order to reach tenderness values clo-ser to consumer expectations. The same authors ob-
served a significant genotype · ageing interaction with
statistical differences appearing among different geno-
types at early ageing times (1–14 days) but not at 21
day post-mortem. These results do not conflict with ours
where no interaction was found and can be explained on
the basis of the reduced ageing time used in the present
study.Although Cifuni et al. (2004) found an increased fla-
vour intensity in Podolian beef aged for longer (15 vs. 8
days), in this experiment (Table 3) the short ageing peri-
ods (7 vs. 2 days) may also account for the lack of a sig-
nificant effect (P > 0.05). No effect of breed type was
evident on the flavour intensity of the beef (P > 0.05).
4. Conclusion
In the present study crossbreeding Podolian with
Limousine cattle increased pre-slaughter weights and re-
duced cholesterol contents, but did not improve the
n � 6/n � 3 ratio, which was high and exceeded the rec-
ommended values for human nutrition in both geno-
types (P and LP). Conversely, a detrimental effect of
688 A. Braghieri et al. / Meat Science 69 (2005) 681–689
crossbreeding on the P/S ratio was observed as the meat
from Podolian young bulls showed higher and more
beneficial levels of PUFA.
The sensory panel was able to detect more subtle dif-
ferences between treatments than the Warner–Bratzler
method, possibly because panellists perceive more infor-mation during biting and mastication. The former indi-
cated that the products obtained by LP cattle and those
aged for at least 7 days were the most tender.
Therefore, the most rapid strategies available for
improving tenderness in Podolian young bulls would
be extended post-mortem ageing and the crossbreeding
with Podolian cows exceeding replacement needs with
bulls of other breeds producing more tender meat. Theinfluence of crossbreeding on beef nutritional properties
was complex, whereas the administration of forage-
based diets may be more effective in improving meat
quality in relation to human health.
Acknowledgements
Thanks are due to D. Giordano and G. D�Andrea for
help in conducting sensory analysis. This research was
financially supported by POP FESR 1999.
References
Aharoni, Y., Nachtomi, E., Holstein, P., Brosh, A., Holzer, Z., &
Nitsan, Z. (1995). Dietary effects of fat deposition and fatty acid
profiles in muscle and fat depots of Fresian bull calves. Journal of
Animal Science, 73, 2712–2720.
Allen, C. E., & Foegeding, E. A. (1981). Some lipid characteristics and
interactions in muscle foods-a review. Food Technology, 35,
253–257.
Bas, P., & Sauvant, D. (2001). Variation of lipid composition of
adipose tissues and muscles in cattle. INRA Productions Animales,
14, 311–322.
Belew, J. B., Brooks, J. C., McKenna, D. R., & Savell, J. W. (2003).
Warner–Bratzler Shear evaluations of 40 bovine muscles. Meat
Science, 64, 507–512.
Bello Acebron, L., & Calvo Dopico, D. (2000). The importance of
intrinsic and extrinsic cues to expected and experienced quality: an
empirical application for beef. Food Quality and Preference, 11,
229–238.
Bonamone, A., & Grundy, S. M. (1988). Effect of dietary stearic acid
on plasma cholesterol and lipoprotein levels. New England Journal
of Medicine, 318, 1244–1248.
Campo, M. M., Sanudo, C., Panea, B., Alberti, P., & Santolaria, P.
(1999). Breed type and ageing time effects on sensory characteristics
of beef strip loin steaks. Meat Science, 51, 383–390.
Carnovale, E., & Nicoli, S. (2000). Changes in fatty acid composition
in beef in Italy. Journal of Food Composition and Analysis, 13,
505–510.
Choi, N. J., Enser, M., Wood, J. D., & Scollan, N. D. (2000). Effect of
breed on the deposition in beef muscle and adipose tissue of dietary
n-3 polyunsaturated fatty acids. Animal Science, 71, 509–519.
Cifuni, G. F., Napolitano, F., Pacelli, C., Riviezzi, A. M., & Girolami,
A. (2000). Effect of ageing and freezing storage on fatty acid
composition and lipid oxidation of meat from Podolian bulls. In
Proceedings 4th national congress of food chemistry, 28–30 June
2000, Ferrara, Italy (pp. 189–194). .
Cifuni, G. F., Napolitano, F., Riviezzi, A. M., Braghieri, A., &
Girolami, A. (2004). Fatty acid profile, cholesterol content and
tenderness of meat from Podolian young bulls. Meat Science, 67,
289–297.
Ciria, J., Asenjo, B., Beriain, M. J., & Gorraiz, C. (2000). Influence of
breed on bovine meat quality and palatability. In Proceedings 46th
international congress of meat science and technology, 27 August–1
September 2000, Buenos Aires, Argentina (pp. 58–59). .
Commission of European Communities. (1993). Nutrients and energy
Intake for the European Community. Reports of the scientific
committee for food. Thirty-first series. Luxembourg: Office of
Official Pubblication of the European Communities.
Department of Health and Social Security. (1984). Nutritional aspects
of cardiovascular disease. Report on Health and social subjects no.
46. HMSO, London.
De Smet, S., Webb, E. C., Claeys, E., Uytterhaegen, D. I., & Demeyer,
D. I. (2000). Effect of dietary energy and protein levelson fatty acid
composition of intramuscular fat in double-muscled Belgian Blue
bulls. Meat Science, 56, 73–76.
Dransfield, E. (1981). Eating quality of the DFD beef. In P. V. Tarrant
& D. E. Wood (Eds.), The problem of dark cutting in beef
(pp. 345–361). The Hague: Martinus Nijhoff.
Eichhorn, J. M., Coleman, L. J., Wakayama, I. J., Blomquist, G. J.,
Bailey, C. M., & Jenkins, T. G. (1986). Effects od breed type and
restricted versus ad libitum feeding on fatty acid composition and
cholesterol content of muscle and adipose tissue from mature
bovine females. Journal of Animal Science, 63, 781–794.
Enser, M., Hallet, K. G., Hewett, B., Fursey, G. A. J., Wood, J. D., &
Harrington, G. (1998). The polyunsaturated fatty acid composition
of beef and lamb liver. Meat Science, 49, 321–327.
Folch, J., Lees, M., & Stanley, G. H. S. (1957). A simple method for
the isolation and purification of lipids from animal tissue. Journal
of Biological Chemistry, 226, 497–509.
French, P., O�Riordan, E. G., Monahan, F. J., Caffrey, P. J., Mooney,
M. T., Troy, D. J., et al. (2001). The eating quality of meat of
steers fed grass and/or concentrates. Meat Science, 57, 379–386.
French, P., Stanton, C., Lawless, F., O�Riordan, E. G., Monahan, F.
J., Caffrey, P. J., et al. (2000). Fatty acid composition, including
conjugated linoleic acid, of intramuscular fat from steers offered
grazed grass, grass silage, or concentrate-based diets. Journal of
Animal Science, 78, 2849–2855.
Girolami, A., Marsico, I., D�Andrea, G., Braghieri, A., Napolitano,
F., & Cifuni, G. F. (2003). Fatty acid profile, cholesterol content
and tenderness of ostrich meat as influenced by age at slaughter
and muscle type. Meat Science, 64, 309–315.
Gregory, K. E., Cundiff, L. V., Koch, R. M., Dikeman, M. E., &
Koohmaraie, M. (1994). Breed effects, retained heterosis, and
estimates of genetic and phenotypic parameters for carcass and
meat traits of beef cattle. Journal of Animal Science, 72, 1174–1183.
Huff, E. J., & Parrish, F. C. Jr., (1993). Bovine longissimus muscle
tenderness as affected by postmortem aging time, animal age and
sex. Journal of Food Science, 58, 713–716.
Huffman, K. L., Miller, M. F., Hoover, S. C., Wu, C. K., Brittin, H.
C., & Ramsey, C. B. (1996). Effect of beef tenderness on consumer
satisfaction with steaks consumed in the home and restaurant.
Journal of Animal Science, 74, 91–97.
Koohmarie, M. (1996). Biochemical factors regulating the toughening
and tenderization processes of meat. Meat Science, 43, S193.
MacFie, H. J. H., Bratchell, N., Greenhoff, K. G., & Vallis, L. V.
(1989). Design to balance the effect of order of presentation and
first-order carry over effects in hall tests. Journal of Sensory Studies,
4, 129–148.
Macie, S. E., Sanudo, C., Olleta, J. L., Panea, B., Campo, M. M., &
Alberti, P. (2000). Slaughter weight and breed group effects on
consumer beef meat quality appraisal throughout ageing. In
A. Braghieri et al. / Meat Science 69 (2005) 681–689 689
Proceedings 46th international congress of meat science and
technology, 27 August–1 September 2000, Buenos Aires, Argentina
(pp. 62–63). .
Maria, G. A., Villaroel, M., Sanudo, C., Olleta, J. L., & Gebresenbet,
G. (2003). Effect of transport time and ageing on aspects of beef
quality. Meat Science, 65, 1335–1340.
Marmer, W. N., Maxwell, R. J., & Williams, J. E. (1984). Effects of
dietary regimen and tissue site on bovine fatty acid profiles. Journal
of Animal Science, 59, 109–121.
Mattson, F. H., & Grundy, S. M. (1985). Comparison of effects of
saturated, monounsaturated and polyunsaturated fatty acids on
plasma lipids and lipoproteins in man. Journal of Lipid Research,
26, 194–202.
Miller, M. F., Kerth, C. R., Wise, J. W., Lansdell, J. L., Stowell, J. E.,
& Ramsey, C. B. (1997). Slaughter plant location, USDA quality
grade, external fat thickness, and aging time effects on sensory
characteristics of beef loin strip steak. Journal of Animal Science,
49, 662–667.
Mitchell, G. E., Giles, J. E., Rogers, S. A., Tan, L. T., Naidoo, R. J., &
Ferguson, D. M. (1991). Tenderizing, ageing, and thawing effects
on sensory, chemical, and physical properties of beef steaks.
Journal of Food Science, 56, 1125–1129.
Morgan, J. B., Savell, J. W., Hale, D. S., Miller, R. K., Griffin, D. B.,
Cross, H. R., et al. (1991). National beef tenderness survey.
Journal of Animal Science, 69, 3274–3283.
Naes, T. (1991). Handling individual differences between assessors in
sensory profiling. Food Quality and Prefence, 2, 187–199.
Napolitano, F., Carlucci, A., Braghieri, A., Cifuni, G. F., Riviezzi, A.
M., Monteleone, E., et al. (2001). Effect of ageing on meat sensory
properties of Podolian bulls. Zootecnica e Nutrizione Animale, 27,
85–89.
Napolitano, F., Braghieri, A., Brancieri, D., Pacelli, C., & Girolami,
A. (2002). The relevance of natural behaviour for Podolian cattle.
In Proceedings 48th international congress of meat science and
technology, 25–30 August 2002, Rome, Italy (pp. 718–719). .
O�Connor, S. F., Tatum, J. D., Wulf, D. M., Green, R. D., & Smith,
G. C. (1997). Genetic effects on beef tenderness in Bos indicus
composite and Bos taurus cattle. Journal of Animal Science, 75,
1822–1830.
Otremba, M. M., Dikeman, M. E., Milliken, G. A., Stroda, S. L.,
Unruh, J. A., & Chambers IV, E. (1999). Interrelationships among
evaluations of beef longissimus and semitendinosus muscles
tenderness by Warner–Bratzler Shear force, a descriptive-texture
profile sensory panel, and a descriptive attribute sensory panel.
Journal of Animal Science, 77, 865–873.
Resurreccion, A. B. A. (2003). Sensory aspects of consumer choices for
meat and meat products. Meat Science, 66, 11–20.
Robelin, J., & Geay, Y. (1976). Repartition des masses musculaires
chez le jeune bovin male entier et son evolution au cours de la
periode d�engraissiment de 9 a 15 mois. Annales de Zootechnie, 25,
273–279.
Robelin, J., Geay, Y., & Beranger, C. (1977). Evolution de la
composition corporelle des jeunes bovins males intiers de race
Limousine entre 9 et 19 mois. Annales de Zootechnie, 26, 533–546.
Rule, D. C., MacNeil, M. D., & Short, R. E. (1997). Influence of sire
growth potential, time on feed, and growing finishing strategy on
cholesterol and fatty acids of the ground carcass and longissimus
muscle of beef steers. Journal of Animal Science, 75, 1525–1533.
Salih, A. M., Smith, D. M., Price, J. F., & Dawson, L. E. (1987).
Modified extraction 2-thiobarbituric acid method for measuring
lipid oxidation in poultry. Poultry Science, 66, 1483–1488.
SAS. (1990). SAS/STAT user�s guide (Version 6). Ed. Cary: SAS
Institute, Inc.
Seideman, S. C., Cross, H. R., & Crouse, J. D. (1989). Carcass
characteristics, sensory properties and mineral content of meat
from bulls and steers. Journal of Food Quality, 11, 497–507.
Sherbeck, J. A., Tatum, J. D., Field, T. G., Morgan, J. B., & Smith, G.
C. (1995). Feedlot performance, carcass traits, and palatability
traits of Hereford and Hereford · Brahman steers. Journal of
Animal Science, 73, 3613–3620.
Sinclair, K. D., Lobley, G. E., Horgan, G. W., Kyle, D. J., Porter, A.
D., Matthews, K. R., et al. (2001). Factors influencing beef eating
quality 1. Effects of nutritional regimen and genotype on organo-
leptic properties and instrumental texture. Animal Science, 72,
269–277.
Silva, J. A., Patarata, L., & Martins, C. (1999). Influence of ultimate
pH on bovine meat tenderness during ageing. Meat Science, 52,
453–459.
Smith, G. C., Savell, J. W., Clayton, R. P., Field, T. G., Griffin, D. B.,
Hale, D. S., et al. (1992). The national beef quality audit. Ft.
Collins/Collage Station: Colorado State University/Texas A&M
University.
Stone, H., & Sidel, J. L. (1985). Sensory evaluation practices. New
York: Academic Press, Inc.
Ulberth, F., & Reich, H. (1992). Gas chromatographic determina-
tion of cholesterol in processed foods. Food Chemistry, 43,
387–391.
Watanabe, A., Daly, C. C., & Devine, C. E. (1996). The effects of
ultimate pH of meat on tenderness changes during ageing. Meat
Science, 42, 67–78.
Watts, B. M. (1962). Meat products. In A. Day & R. P. R. Simhulber
(Eds.), Symposium on food: lipids and their oxidation (pp. 202–219).
Westport: AVI Publ. Co.
Wheeler, T. L., Davis, G. W., Stoecker, B. J., & Harmon, C. J. (1987).
Cholesterol concentration of longissimus muscle, subcutaneous fat
and serum of two beef cattle breed types. Journal of Animal
Science, 65, 1531–1537.
Wulf, D. M., Tatum, J. D., Green, R. D., Morgan, J. B., Golden, B.
L., & Smith, G. C. (1996). Genetic influences on beef longissimus
palatability in Charolais and Limousine – sired steers and heifers.
Journal of Animal Science, 74, 2394–2405.
Xie, Y. R., Busboom, J. R., Gaskins, C. T., Johnson, K. A., Reeves, J.
J., Wright, R. W., et al. (1996). Effects of breed and sire on carcass
characteristics and fatty acid profiles of crossbred Wagyu and
Angus Steers. Meat Science, 43, 167–177.
Xie, Y. R., Busboom, J. R., Cornforth, D. P., Shenton, H. T., Gaskins,
C. T., Johnson, K. A., et al. (1996). Effects of time on feed and
post-mortem ageing on palatability and lipid composition of
crossbred Wagyu beef. Meat Science, 43, 157–166.
Zembayashi, M., & Nishimura, K. (1996). Genetical and nutritinal
effects on the fatty acid composition of subcutaneous and intra-
muscular lipids of steers. Meat Science, 43, 83–92.
Zembayashi, M., Nishimura, K., Lunt, D. K., & Smith, S. B. (1995).
Effect of breed type and sex on the fatty acid composition of
subcutaneous and intramuscular lipids of finishing steers and
heifers. Journal of Animal Science, 73, 3325–3332.