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Characterisation of Volatile Compounds and Composition of Milk of Kilis Goats Reared at Two Different Locations

PJZ_53_4_1279-1289

Characterisation of Volatile Compounds and Composition of Milk of Kilis Goats Reared at Two Different Locations

Aylin Celile Oluk1*, Ugur Serbester2, Murat Reis Akkaya3 and Oya Berkay Karaca4

1Eastern Mediterranean Agriculture Research Institute, Ministry of Food Agriculture and Livestock, 01321 Adana, Turkey

2Deptartment of Animal Science, Faculty of Agriculture, Cukurova University, 01903 Bahce, Adana, Turkey

3Deptartment of Food Engineering, Faculty of Engineering, Alpaslan Turkes Science and Technology University, Adana, Turkey

4Karatas School of Tourism and Hotel Management, Cukurova University, 01903 Bahce, Adana, Turkey

ABSTRACT

Various factors such as species, breeds, lactation stage and location affect milk composition. We evaluated the composition of Kilis goat milk in two different seasons on the basis of alcohols, ketones, aldehydes, esters, indoles, carboxylic acids, aromatic hydrocarbons and terpenes. Milk samples were collected at the early and late lactation periods from Hatay and Kilis, Turkey. During both periods, the goats consumed a diversity of plant species. Milk collected from Kilis had 15.27-16.10% total solids,5.70-6.50% fat and 4.80-5.10% protein. The lactose content did not differ significantly between milk samples from the two locations (3.90-4.20%). Total unsaturated fatty acid levels were significantly higher than total saturated fatty acid contents, irrespective of the lactation period (p<0.05). Milk from Hatay was high in saturated fatty acids, aromatic hydrocarbons and benzaldehydes, i.e. 4.50 g 100 g-1, 6.80-4.65 mg 100g-1 and 0.28-0.70 mg 100g-1, respectively. Throughout the lactation period, the levels of total solids, fat, protein, saturated and unsaturated fat, alcohol, ketones, esters and carboxylic acid increased, while indole, terpene, aromatic hydrocarbon and aldehyde contents decreased.


Article Information

Received 21 May 2019

Revised 30 July 2019

Accepted 23 April 2020

Available online 14 May 2021

Authors’ Contribution

ACO designed and performed experiments, analysed data and wrote the paper. US and MRA performed experiments. OBK analysed data.

Key words

Goat milk, Lactation, Milk composition, Volatile compounds, Indoles

DOI: https://dx.doi.org/10.17582/journal.pjz/20190521060522

* Corresponding author: [email protected]; [email protected]

0030-9923/2021/0004-1279 $ 9.00/0

Copyright 2021 Zoological Society of Pakistan



INTRODUCTION

In recent years, goat breeding has become more profitable than cattle and sheep breeding due to changes in global climate and precipitation regimes and increased soil salinity (Silanikove, 2000). Goats are more adaptable to arid environments because of their feeding behaviour, the digestion of high-fibre fodder in the rumen, their water metabolism and their capacity to store and later mobilise body reserves; they are therefore capable of adjusting the widely varying feeding situations (Morand-Fehr, 1991). About 500,000 domestic goats of the total 11 million goats in Turkey are Kilis goats. This breed is endemic and used in the southeastern regions (Kilis, Gaziantep, Hatay and Sanlıurfa) of Turkey (Daskiran et al., 2018). It has a black and brown fur coloration and long pendulous ears; its hair is straight, long and coarse. Animas of this breed are seasonal breeding animals for both meat and milk production and endangered genetic resources in Turkey (Tasdemir et al., 2011). The Kilis goat is the most important domestic goat breed for high milk yield; it is highly resistant to adverse environmental conditions and diseases (Anonymous, 2018). Milk yield and lactation time vary among different studies: 300-400 kg per lactation and 210-260 days (Iriadam, 2007), 250-400 kg and250-300 days (Cetin et al., 2009). According to the communiqué about race and line registration of domestic animals in Turkey, on average, milk yield is 217.4 kg (70.3-269.6 kg) and lactation time is 228 days (178-257 days) (Anonymous, 2018; Agaoğlu and Ertugrul, 2012).

Kilis goats reared in Hatay and Kilis are indigenous breeds and the most important source of milk for the rural population (Aslantas et al., 2005). The area contains meadows (16%), shrubland (12%) and forests (6%) and represents the transition area between the Southeast Anatolian steppe and the Mediterranean vegetation (maki), with Mediterranean vegetation being dominant in Hatay (Anonymous, 2019). Climatic and environmental conditions affect the aroma of dairy products. For example, the milk of animals grazing in meadows in a dry environment and at high elevations, rich in dicotyledon plants, has a more fruity and dried taste (Martin et al., 2005).

Milk composition varies among breeds, feeds, lactation stages, seasons, etc. (Silanikove et al., 2010). Goat milk contains twice as many short- and medium-chain fatty acids than cow milk (Raynal-Ljutovac et al., 2008). It also has a stronger flavour and aroma than other types of milk. According to previous studies, the branched and short-chain fatty acids (FAs) with less than 11 carbon atoms, such as caprylic, capric and caproic FAs, are responsible for the typical “goaty” aroma (Ha and Lindsay, 1993; Salles et al., 2002; Verruck et al., 2019). The β-oxidation of PUFA could increase the amount of degradation products such as straight-chain aldehydes and ketones, which may be converted to alcohols, forming volatile components (Cais-Sokolinska et al., 2015).

Goat milk protein is more digestible for humans than cow milk protein and has a lower amount ofαs1-casein (Costa et al., 2014). The casein micelles from goat milk are different from those of cow milk; goat milk has a low resolution, thermal stability and sedimentation rate, a high cold solubility of β-casein, a small micelle size and high calcium and phosphorus levels (Haenlein, 2004). Few studies have focused on the effects of foodstuff on goat milk composition, especially in terms of volatile compounds (Muelas et al., 2018), but no scientific data is available regarding the effects of different locations and lactation periods on the volatile profile of goat milk. In this context, we aimed to describe the changes in the composition of Kilis goat milk during the lactation period and to evaluate the influences of location and lactation periods on fatty acid and volatile profiles of the milk of Kilis goats.

MATERIALS AND METHODS

Milk of Kilis goats was collected from two separate locations (Kilis and Hatay cities) in two different periods. Kilis is located in the transition zone between the Mediterranean and Southeast region (36° 42´ 59.3136 and 37° 6´ 52.7832”) at an average elevation of 680 m above sea level. Hatay is the most southern province of Turkey (36° 0´ 47.1168” and 36° 7´ 20.1684”) and situated at an average elevation of 450 m above sea level. Milk samples (early lactation period) were collected from April 10 to 20 in Kilis and from 20 to 30 April in Hatay. Late-lactation samples were taken from October 15-20. The samples were collected from 16 Kilis goats, with three samples at regular intervals of 7 days. The milk samples were combined to obtain two samples per period, divided into two parts and immediately frozen at -18°C.

A Fourier transform infrared milk analyser (Milkoscan FT 120, FOSS Electric, Hillerød, Denmark) was used for determination of total solids, protein, fat, total saturated (SFA) and unsaturated (UFA) fatty acids, total monounsaturated fatty acids (MUFA)and polyunsaturated fatty acids (PUFA). The amounts of SFA, UFA, MUFA and PUFA were expressed as g FA/100 g milk. Volatile compounds of the goat milk samples were analysed via static headspace solid-phase micro extraction (SPME), using a gas chromatography-mass spectrometry system (Shimadzu Corporation, Kyoto, Japan) (Hayaloglu et al., 2007). A duplicate 3.0-g portion of the sample was then placed in a 15-mL vial, followed by 10 µL of internal standard containing 81 mg/kg of 2-methyl-3-heptanone in methanol (Sigma-Aldrich Co. USA) and allowed to equilibrate at 40°C for 30 min. Essentially, extraction is achieved by injecting a 2-cm 50/30 µm divinyl benzene-carboxen-polydimethylsiloxane (DVB/CAR/PDMS) fibre (Supelco, Bellefonte, PA, USA) into the vial and exposing it to the headspace for 30 min at 40°C. The fibre was positioned at 3.0 scale units in each run. Desorption of the extracted volatiles was carried out in a Shimadzu GC-2010 gas chromatography - QP-2010 mass spectrometry system (Shimadzu Corporation, Kyoto, Japan), run in splitless mode. During desorption, the fibre remained in the injector for 2 min at a temperature of 250°C, with helium as carrier gas at a flow rate of 1.0 mL/min. The volatile compounds were separated in a DB-Wax column (60 m × 0.25 mm × 0.25 um; J and W Scientific, Folsom, CA, USA). The oven temperature was held at 40°C for 2 min (desorption period), then increased at 5°C per min to 70°C and held for 1 min. The temperature was then raised at 10°C per min to 240°C to provide a run time of 30 min. The mass spectrometer was set to record at 33 to 450 amu (threshold 1,000) at a sampling rate of 1.11 scans/s. The volatile compounds were identified by calculation of the retention index (RI) of each compound, using an n-alkane series (C8 to C20) under the same conditions. The peak identifications were based on comparison of the mass spectra of unknown compounds with those in the Wiley 7 (7th edition) and NIST/EPA/NIH 02 mass spectral libraries. Identifications were also confirmed by comparing retention times with reference standards when available. About 30 authentic standard compounds (Sigma chemical Co., St. Louis, MO) were used to confirm volatiles in the obtained cheese samples. The RI values were also compared with those described in the literature, determined under the same conditions for matching the compounds. The results were calculated by comparison of the peak area of the internal standard and the unknown compounds. Each compound was expressed as mg/100 g of sample.

Statistical analysis

Variance analysis was performed by Shapiro-Wilk and Bartlett’s tests. The fixed effects were breed, lactation stage and breed x lactation stage interaction. The covariance structure was autoregressive order 1, and the degrees of freedom were adjusted by the Kenward-Rogers method. Mean separation of significant effects (P <0.05) was conducted by SAS (1999). Least squares means and SEM are reported for all data.

RESULTS AND DISCUSSION

Milk composition

At the late lactation, the levels of total solids, fat, protein, total UFA, SFA, MUFA and PUFA ratios in the goat milk were increased in both locations (Table I); this result is in agreement with previous findings (Mestawet et al., 2012; Chen et al., 2017). Total solids, fat, protein, total UFA, SFA and MUFA contents were highest in Kilis at early lactation. The total solid content of milk from Kilis was similar to the 13.88-16.27% reported by Mestawet et al. (2012), but lower than the 17.5% observed by Casey and Van Niekerk (1988). The fat and protein contents ranged between 4.2-6.5% and 3.6-5.1%, respectively. The fat content was lower than that observed in a study in South Africa with Boer goat milk, but similar to the findings of other studies, which reported7.5-6.1% fat and 4.3-5% protein, respectively (Greyling et al.,2004; Mestawet et al., 2012). These differences are most likely due to different environmental conditions and feeding strategies. At late lactation, the milk components in milk from Hatay were more highly concentrated than in milk from a cross breed in Ethiopia, with 13.88%total solids, 3.65%fat and 4.08% protein (Mestawet et al., 2012); milk from Maltese goats from Italy had relatively low levels of protein (3.4%) and fat (3.5%) (Carnicella et al., 2008). The protein and fat compounds of milk are significantly affected by the season, age and nutrition (Mestawet et al., 2012). Goats prefer leaves over stems, thick stems over thin ones and the protein parts over the carbohydrate parts (Morand-Fehr, 1991). In the early lactation period, the high protein content of goat milk from Kilis may be a result of the high protein level of the forage in this region. The lactose contents of milk samples from both regions were lower than the values found by Guo et al. (2004) with 4.47% and Prasad et al. (2005), who reported levels of well above 5.5%.

Milk FA composition is affected by rumen biohydrogenation and Δ9-desaturase enzyme conversion (C18:0 into C18:1, Bauman and Griinari, 2003), but considerable changes in the milk fat composition can be achieved by dietary changes (Liu et al., 2016). The total SFA content of goat milk was higher in milk from Hatay location than in milk from Kilis in the late lactation period. Differences in the diet can lead to differences in the saturated and unsaturated fatty acid profiles of milk (Calderon et al., 1984). We observed a significant difference (P <0.05) between total UFAs and SFA content in both early and late lactation periods. The mean contents of total SFAs (3.00-4.50 g100 g-1) were comparable to the values found in milk from Saanen or Alpine goats (3.34-4.02 g100 g-1; Le Doux et al., 2002) fed TMR or different level of forages. However, Alpine goats raised in feedlots provided milk with low total SFA contents (1.08-2.68 g100 g-1) (Bernard et al., 2005).

Unsaturated fatty acids are the precursors of dairy aromas and are reduced by microbial enzymes in the rumen (Martin et al., 2005). Total UFAs showed the highest levels (0.86 and 2.0 g100 g-1) in the milk fat of goats at different lactation stages (P <0.05); the total UFA levels were higher in milk from Kilis compared to milk from Hatay (Fig. 1), irrespective of the lactation period. This suggests that the proportion of unsaturated fatty acids is higher in milk from high elevations than in milk from low elevations. The concentration of unsaturated fatty acids in goat milk varies with fodder plants (Alvarenga et al., 2015). The UFA content of Kilis goat milk were higher than those of Saanen and Swedish Landrace goat milk samples. Yurcenko et al. (2018) reported 25.80 g 100 g-1 UFA in the total FA of Saanen goat fat, equivalent to 0.86 g 100 g-1 UFA in the total FA of goat milk. These differences might be due to the higher amount of dicotyledon species in the diet of Kilis goats.


 

The total MUFA level in goat milk from both regions ranged between 1.20-1.30 and 0.85-1.40 g 100g-1, respectively. A low monounsaturated fatty acid level in caprine milk (0.37-0.50 g 100 g-1) has been determined by Alonso et al. (1999), while Talpur et al. (2009) have reported an elevated level (4.02-4.61 g 100 g-1) in goat milk fat. There were no significant differences (P >0.05) in the total PUFAs of goat milk between the two locations and lactation periods, similar to the findings of Talpur et al. (2009) for two local breeds (Kamori and Pateri) in Pakistan. Ruminant milk fat consists of 65-70% SFA, 25-30% MUFA and 5-10% PUFA (Schwendel et al., 2014). Cais-Sokolinska et al. (2015) have reported 30.74 g 100 g-1 MUFA in the total FA of goat fat, equivalent to 1.03 g 100 g-1 MUFA in the total FA of goat milk.

Throughout the lactation stages, the milk components showed high variations in milk from Hatay at the late lactation period. The levels of total solids, fat, protein, saturated and unsaturated fatty acids were significantly higher (P <0.05) in the late lactation period than in the early lactation period; similar results have been described by Guo et al. (2004). Dry matter levels were highest at the end of the lactation period. Based on the lactation curve of goats, in the early lactation period, the total solid content is low, along with a high milk quantity. The opposite pattern was observed for the late lactation period.

The differences in the lactose contents of the milk from the same goat breed, but different locations, were not statistically significant (P >0.05). In both locations, lactose contents were high in the early lactation period, with subsequent decreases; this has also been observed by Prasad et al. (2005). The protein and total PUFA concentrations increased throughout the lactation period in both locations due to increasing herbage sugar content because of the accumulation of photosynthesis products (Avondo et al., 2008).

Volatile compounds of goat milk from different locations

All volatile compounds of milk from Kilis and Hatay are shown in Table II. A total of 58 volatile compounds were identified, including 4 indoles, 7 terpenes, 8 ketones, 5 aldehydes, 8 carboxylic acids, 7 alcohols, 18 aromatic hydrocarbons and 2 esters. Table III also shows the statistical evaluation of the differences in lactation periods and location in terms of the volatile components. Of the 58 components, 22 were present in both lactation periods and in the milk of both locations. According to Muelas et al. (2018), ketones (sweet, buttery and creamy flavours), acids and alcohols (alcoholic and floral-fruity notes) in fermented dairy products have different aroma perceptions. Acetic and lactic acids contribute to the acidic aroma, while butanoic, hexanoic and octanoic acids are responsible for the goaty and cheesy aroma. The major volatile compounds detected in Kilis goat’s milk were α- pinene, dl-limonene, cymene, capric acid, 2- octanol and 4-nonanol, irrespective of the location. The lactation period affected the amounts of volatiles in goat milk. While the amounts of terpenes, aldehyde and aromatic hydrocarbons significantly decreased during the lactation period, indoles, ketones, carboxylic acids and alcohols increased for both locations (P <0.05).

The amount of 3-methylindole (skatole), derived from tryptophan degradation, in milk from Hatay was higher than that in milk from Kilis in both lactation periods (1.77 to 0.84 mg 100 g-1). Previous studies have shownhigh amounts of skatole in the milk of grazing animals (Prache et al., 2005; Schreurs et al., 2008). In the late lactation period, 2-3-N-phenylimino indole and 1H-Indole were not detected.

The terpene content did not significantly differ between the two lactation periods (17.68 versus 8.58 mg/100 g) in milk from Kilis, but decreased significantly (P <0.05) from early to late lactation (27.36 versus 11.76 mg/100 g)in milk from Hatay location. The terpenes α-pinene, dl-limonene and β-phellandiene were the most abundant terpenes, irrespective of the location and lactation period (P<0.01). According to a previous study, higher herbage intake modifies the digestive and metabolic processes (Fedele et al., 2005), and terpenes can be used to determine the geographical origin of animals that graze pastures (Prache et al., 2005). The terpene contents of the milk samples from both locations varied, mainly because the plant species Geranium tuberosum, Arum dioscoridis, Asparagus acutifolius, Asphodelus aestivus, Gynandriris sisyrinchium and Ophrys lutea are found in Kilis grassland, while Muscari babachii, Scilla autumnalis, Gladiolus italicus, Orchis simia and Cephalanthera longifolia are more common in Hatay. Boutoial et al. (2012, 2013) have observed that addition of aromatic plants, such as rosemary and thyme, to goat diets increased the levels of PUFAs, protein, dry matter and lactose. Sant’Ana et al. (2019) have detected higher α-pinene concentrations in goat milk obtained from goats grazing native pastures of a semiarid region of Brazil compared with milk from animals kept under confinement.

In milk from Kilis, the ketone levels increased significantly (P <0.05) from early lactation (1.65 mg/100 g) to late lactation (1.76 mg 100 g-1), mainly because of the conversion of secondary alcohols to methyl ketones. 2-octanone, 4-nonanone, furanone and 3-buten-2-one compounds were found in the goat milk in both lactation period. Of these, 2-octanone, which has a fruity aroma (Fedele et al., 2005), was detected in higher concentrations in milk from the lactation period and from Kilis. The fat content seems to have an influence on the concentration of ketones (Vazquez-Landaverde et al., 2005), and in our

 

Table I. The changes in milk composition of Kilis goat breed from Hatay and Kilis locations during lactation period.

Kilis

Hatay

SEM

Location

Lactation period

Location × Lactation period

EL

LL

EL

LL

Total solids (%)

15.27

16.10

12.70

16.30

1.11

0.31

0.07

0.25

Fat (%)

5.70

6.50

4.20

6.50

1.03

0.53

0.18

0.50

Protein (%)

4.80

5.10

3.60

5.10

0.37

0.13

0.03

0.14

Lactose (%)

4.20

3.90

4.30

4.00

0.18

0.44

0.11

0.92

Total UFA (g100g-1)

1.30

2.00

0.86

1.60

0.34

0.27

0.06

0.94

Total SFA(g100g-1)

4.00

4.30

3.00

4.50

0.87

0.65

0.32

0.47

Total MUFA (g100g-1)

1.20

1.30

0.85

1.40

0.24

0.15

0.04

0.96

Total PUFA (g100g-1)

0.30

0.43

0.35

0.40

0.03

0.68

0.14

0.74

 

UFA, Unsaturated fatty acid; SFA, Saturated fatty acid; MUFA, Monounsaturated fatty acid; PUFA, Polyunsaturated fatty acid; EL, Early lactation; LL, Late lactation, SEM, Standard error of the mean.

 

Table II. All volatiles compounds (mg 100g-1, mean ± SD) during lactation period (df= 9) in Kilis breed goat milk from Hatay and Kilis.

Compounds

RI

HEL

KEL

HLL

KLL

Carboxcylic acid

Acetic acid

1467

nd

nd

0.052±0.01b

0.407±0.02a

Benzoic acid

1160

0.261±0.02c*

0.262±0.03c

0.504±0.02a

0.305±0.03b

Octanoic acid

2083

nd

0.990±0.03a

0.103±0.04c

0.220±0.02b

Caproic acid

1850

nd

0.272±0.03

nd

nd

Hexadecanoic acid

1951

0.013±0.02

nd

nd

nd

Capric acid

1809

0.346±0.04d

1.478±0.02a

0.686±0.04b

0.567±0.02c

Tetradecanoic acid

1748

nd

nd

nd

0.078±0.02

Lauric acid

1554

nd

0.052±0.03

nd

nd

Alcohols

Ethanol

931

11.457±0.09d

20.913±0.06c

25.242±0.06b

28.368±0.05a

2-Octanol

981

13.890±0.04c

16.002±0.04b

20.541±0.04a

20.560±0.04a

4-Nonanol

1076

19.156±0.04c

21.892±0.04b

28.405±0.04b

28.425±0.03a

2-Ethyl-1-hexanol

1484

0.032±0.01

nd

nd

nd

1-Butanol

1137

0.022±0.01

nd

nd

nd

Fluoren-9-ol

1108

0.051±0.01

nd

nd

0.040±0.01

1,4-Butanediol

1252

0.034±0.01

nd

nd

nd

Indoles

3-methylindole (skatole)

1070

0.835±0.03b

1.765±0.02a

0.255±0.03b

0.808±0.04b

N-ethyl-1,3-dithioisoindoline

1617

7.535±0.20a

1.092±0.05b

0.753±0.02c

1.467±0.02b

2-3-N-phenylimino indole

1085

0.160±0.02

nd

nd

nd

1H-Indole

1257

0.038±0.02b

0.190±0.03a

nd

nd

Aromatic hydrocarbon

Benzene, ethenylmethyl

1833

1.660±0.50b

3.390±0.20a

1.304±0.60c

0.568±0.40d

1-ethenyl-3-ethyl- benzene

1145

3.858±0.30a

3.145±0.60b

1.786±0.04c

0.400±0.20d

1-ethenyl-4-ethyl- benzene

1132

1.790±0.02b

2.010±0.02a

1.015±0.02c

0.540±0.04d

Aromatic hydrocarbon

Cyclopropylcarbinol

1148

nd

nd

0.217±0.01b

0.670±0.03a

Cyclobutanol

1252

0.105±0.02b

nd

0.119±0.02b

0.293±0.03a

2,4,6-Cycloheptatrien-1-one

1106

0.340±0.02b

0.072±0.04c

0.690±0.03a

nd

Ethylbenzene

843

0.016±0.01b

0.295±0.04a

nd

nd

o-Xylene

1151

0.028±0.02

nd

nd

nd

p-Xylene

1149

0.031±0.01

nd

nd

nd

3-O-5,7,3',4'-tetra o-methylquercetin

1079

0.019±0.02

nd

nd

nd

4,8,9b-Triazacyclopenta phenalene

1276

0.331±0.02a

0.293±0.02a

0,.180±0.03b

nd

Benzenesulfonylchloride

1150

0.122±0.02b

0.018±0.01c

0.035±0.02c

0.250±0.03a

2-5-thiazolyl thyocyanate

935

nd

nd

0.323±0.03a

0.170±0.02b

1-allyl-2,8-dimethoxy-9H-carbazole

1092

0.267±0.02a

0.155±0.04b

nd

0.138±0.02b

2-Chloro-4-6-pyrimidine

1221

0.063±0.02a

nd

0.042±0.02a

nd

1,3-diethenyl

1226

0.562±0.02a

0.125±0.04b

0.037±0.02c

0.025±0.02c

3-Phenylcyclopentene

981

0.043±0.03a

0.022±0.04b

nd

nd

Furanone

1530

0.027±0.04b

nd

0.013±0.01c

0.080±0.02a

5-Ethylindan

1177

0.062±0.02a

0.025±0.01c

0.041±0.01b

nd

Methoxy-phenyl- /oxime

1115

0.305±0.01c

nd

0.691±0.02b

1.195±0.05a

Esters

Hexanoic acid ethyl ester

905

nd

0.527±0.03

nd

nd

Decanoic acid ethyl ester

1823

0.037±0.04c

0.572±0.03a

nd

0.152±0.02b

Terpenes

Styrene

1273

0.705±0.01b

0.750±0.01b

0.247±0.02c

1.003±0.01a

3-Isopropoxy-1,1,1,7,7,7-hexamethy1-3,5,5, tristetrasiloxane

1400

0.257±0.02a

nd

0.071±0.01c

0.150±0.01b

Silanediol

1442

0.283±0.02a

0.152±0.03b

0.070±0.02c

nd

α-iron

1191

0.103±0.02b

0.248±0.02a

0.052±0.02c

0.030±0.01c

Ketones

2-Octanone

964

0.575±0.03c

0.560±0.01c

0.727±0.05b

0.910±0.03a

4-Nonanone

1076

0.249±0.02d

0.355±0.04c

0.727±0.04a

0.657±0.02b

2-Propanone

1201

nd

nd

0.047±0.02

nd

2-Heptanone

1175

0.406±0.02b

0.512±0.03a

nd

0.170±0.02c

2-phenyl-3,7-dimethyl-octane

1207

0.026±0.02

nd

nd

nd

Ethanone

985

0.015±0.02

nd

nd

nd

3-Buten-2-one

1014

0.199±0.01a

0.178±0.02a

nd

0.028±0.03b

2-Methylindanone

1118

0.041±0.02a

0.053±0.02a

nd

nd

Aldehydes

2-Propenal

1419

0.140±0.01a

0.093±0.02b

0.051±0,03b

nd

Benzaldehyde

941

0.509±0.02a

0.315±0.02b

0.150±0.04c

0.165±0.02c

Cinnamaldehyde

1234

0.064±0.02

0.017±0.03b

nd

nd

4-Methylcinnamaldehyde

1185

0.016±0.02

nd

nd

nd

2-Furancarboxaldehyde

1108

nd

nd

nd

0.132±0.05

 

*Means ± SD within a row with no common superscript differ (P<0,05).

Nd, not detected; RI, retention index using alkane series (C8 to C20) under the same chromatographic conditions; HEL, Hatay earllactation; KEL, Kilis early lactation; HLL, Hatay late lactation; KLL, Kilis late lactation.

 

Table III. Changes in volatile compounds (mg 100g-1, mean) of Kilis breed goat milk from Hatay and Kilis locations during both lactation period (df= 9).

 

 

Hatay

Kilis

 

SEM

 

L

 

LP

 

LxLP

EL

LL

EL

LL

3-methylindole

0.84

1.77

0.26

0.81

2.24

0.89

0.02

0.86

N-ethyl-1.3-dithioisoindoline

0.75

1.09

0.75

1.47

1.86

<0.01

0.01

0.01

Total indoles

1.59

2.86

1.01

2.28

 

 

 

 

α-pinene

7.00

2.00

15.80

2.50

1.81

0.02

<0.01

0.04

dl-limonene

4.00

1.90

3.70

2.70

0.55

0.68

0.01

0.31

β-phellandiene

2.00

2.20

1.90

2.50

0.14

0.24

0.01

0.18

Cymene

3.10

0.80

3.90

2.50

0.65

0.09

0.01

0.49

n-terpene

0.82

1.60

1.00

1.10

0.17

0.25

0.02

0.07

α-Iron

0.30

0.07

0.28

0.19

0.05

0.39

0.02

0.27

Camphene

0.46

0.01

0.78

0.27

0.31

0.39

0.18

0.92

Total terpenes

17.68

8.58

27.36

11.76

 

 

 

 

2-Octanone

0.56

0.87

0.58

0.91

0.08

0.73

<0.01

0.89

4-Nonanone

0.53

0.87

0.55

1.00

0.14

0.54

<0.01

0.61

Furanone

0.62

0.48

0.10

0.06

0.05

0.02

0.01

<0.01

3-Buten-2-one

0.05

0.51

0.45

0.14

0.29

0.96

0.80

0.22

Total ketones

1.76

2.73

1.68

2.11

 

 

 

 

Benzaldehyde

0.48

0.26

0.70

0.28

0.19

0.53

0.12

0.62

Benzoicacid

0.39

0.37

0.36

0.5

0.67

0.52

0.47

0.30

Capricacid

1.50

1.70

0.38

0.76

0.34

0.01

0.42

0.84

Total carbocylic acids

1.78

2.07

0.74

1.26

 

 

 

 

Styrene

1.10

2.00

1.00

0.90

0.29

0.05

0.19

0.13

Benzene.ethenylmethyl

3.00

1.10

1.90

2.00

0.41

0.83

0.05

0.03

1-ethenyl-4-ethyl- benzene

2.00

1.10

1.80

1.60

0.31

0.65

0.09

0.25

1.3-diethenyl benzene

0.26

0.06

2.10

0.15

0.46

0.08

0.05

0.10

Total aromatic hydrocarbons

6.36

4.26

6.80

4.65

 

 

 

 

2-Octanol

16.00

20.60

13.90

20.50

1.60

0.51

<0.01

0.52

4-Nonanol

21.90

28.40

19.20

28.40

2.39

0.57

<0.01

0.58

Total alcohols

37.90

49.00

33.10

48.90

 

 

 

 

 

EL, Early lactation; LL, Late lactation; L, Location; LP, Lactation period; SEM, Standard error of the mean.

study, the total ketone amount was higher for the 5.73% (Kilis) with respect to the 4.24% (Hatay) fat sample.

The highest amount of benzaldehyde has detected in milk from the early lactation period from Kilis, and the amount of five ketone compounds decreased during lactation, with the exception of 2-furancarboxaldehyde. However, even at low concentrations, aldehydes significantly contribute to the aroma of the milk (Vazquez-Landaverde et al., 2005).

Carboxylic acids are precursors of other aroma compounds, such as methyl ketones, alcohols, lactones, aldehydes and esters (Collins et al., 2003; Delgado et al., 2011). The amounts of carboxylic acid at the early and late lactation periods were higher in milk collected from Kilis. Previous studies have found that medium-chain fatty acids contribute to the goaty aroma (Silanikove et al., 2010), such as hexanoic (C6:0) and capric (C10:0) acid, while others have reported that octanoic acid has a rancid and pungent odour (Salles et al., 2002). Acetic acid was present in the late lactation period both locations and can be associated with the slightly tarty taste of Ibores cheese (Delgado et al., 2011). The amounts of benzoic and capric acid in milk from Hatay were relatively low in the early lactation period (Table II). Lauric acid may be the reason for bitter, rancid and unclean flavours (Clark and Mora Garcia, 2017). In milk from the early lactation period and from Kilis, the lauric acid content was 0.052 mg 100g-1. In a previous study, the amounts of hexanoic (caproic), octanoic, decanoic (capric) and dodecanoic (lauric) acids differed between Nubian and Alpine goat breeds, with Kilis goats presenting more of each of these aromatic compounds (Attaie et al., 1993).

Four aromatic hydrocarbons (styrene, benzene-ethyl methyl, 1-ethyl-4-ethyl benzene and 1.3-diethyl benzene) of the 18 components identified in milk from the two different locations were determined in both lactation periods. Aromatic hydrocarbons were identified in the milk samples, of which styrene and benzene-ethyl methyl were the most abundant ones. The levels of aromatic hydrocarbons were lower in milk from Kilis, while styrene and benzene-ethyl methyl were higher in milk from Hatay.

Ethanol, 2-octanol and 4-nonanol increased significantly (P < 0.05) throughout the lactation period in both locations. Secondary alcohols are formed by enzymatic reduction (alcoholdehydrogenase) of the corresponding methyl ketones (Molimard and Spinnler, 1996), and the increase in alcohols may be due to a reduction of grasses and an increase in the plant diversity over time (Fedele et al., 2005). Sant’Ana et al. (2019) have found 1-butanol, 1-hexanol and maltol in Sannen X American Alpine goat milk and suggested that these compounds are responsible for fruity and herbaceous flavours. Kilis goats can consume a wide range of plants due to their agility, mobile upper lips and tendency to assume a bipedal stance, apart from their higher salivary secretion and urea recycling capacity. The development of the salivary glands allows even the consumption of forage crops with bitter taste (Morand-Fehr, 1991). In cheese production, the milk type affects the volatile profile of cheeses (Delgado et al., 2011).

CONCLUSIONS

The composition of the milk from Kilis goats was significantly affected by lactation period and location. Milk from goats reared in Kilis showed a better profile in terms of total solids, fat, protein, unsaturated fat, alcohol, ketones and carboxylic acids when compared to milk from Hatay. Adequate feeding strategies for milk goats are important to improve the nutritional value of the milk and to increase economic gains. The volatile acid profile of milk varies depending on the origin of the animal.

ACKNOWLEDGMENTS

The authors thank Mustafa Cagrı Ucuk and Zeynel Gocmez (Eastern Mediterranean Agriculture Research Institute) for technical assistance.

Statement of conflict of interest

The authors have declared no conflict of interest.

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