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3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures

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Chem. Listy, 102, s265–s1311 (2008) Food Chemistry & Biotechnology<br />

P63 FATTy ACIDS LIKE MARKERS OF<br />

PROCESSED ChEESE ChANGES DuRING<br />

STORAGE<br />

BLAnKA LOUPAnCOVá, EVA VíTOVá, HAnA<br />

ŠTOUDKOVá and FRAnTIŠEK BUňKA<br />

Institute of Food Science and Biotechnology, Faculty of<br />

Chemistry, Brno University of Technology, Purkyňova 118,<br />

612 00 Brno<br />

blankaloupancova@seznam.cz<br />

Introduction<br />

Pasteurized processed cheese products are cheese-based<br />

food produced by comminuting, blending and melting one or<br />

more natural cheeses and optional ingredients into a smooth<br />

homogenous blend with the aid of heat, mechanical shear and<br />

usually emulsifying salts.<br />

Optional ingredients which are determined by the product<br />

type include dairy ingredients, vegetables, meats, stabilizers,<br />

emulsifying salts, flavours, colours, preservatives<br />

and water 1,2 . Dairy ingredients means butter, cottage cheese,<br />

milk concentrates (e.g. skimmed milk powder, whey powder,<br />

caseinates).<br />

Chemical composition of processed cheese depends<br />

on a processed cheese type and raw materials used 3 .<br />

Although the dairy products fall into the class of so<br />

called non-acid foodstuffs and suitable methods must be used<br />

to prolong their durability, the processed cheese was proposed<br />

as a part of Combat Ratio. The Combat Ratio serves<br />

for nutrition of soldiers in specific combat situations such as<br />

separation from a unit, battle, etc. 3 . There are special requirements<br />

for a minimum durability of individual components of<br />

Combat Ration which has been set as 24 months depending<br />

on an ambient temperature 4 .<br />

Practically the only method of achieving the 24 month<br />

durability of processed cheese is the thermo-sterilization. In<br />

the article the effect of a defined sterilization heating and<br />

storage conditions, such as temperature and time, on changes<br />

of fatty acids contents in sterilized processed cheese was<br />

investigated.<br />

Experimental<br />

Processed cheese (40 % dry matter, 45 % fat in dry matter)<br />

was manufactured following the traditional technology<br />

process in a selected dairy. The processing temperature was<br />

91 °C, total time of heating was 5 minutes. Cheeses were than<br />

sterilized at 117 °C for 20 minutes and then cooled down to<br />

10 °C in 2 hours.<br />

Cheese samples were stored at 6 ± 2 °C, 23 ± 2 °C and<br />

40 ± 2 °C during 24 month.<br />

E x t r a c t i o n o f F a t<br />

The cheese sample (5.0 g) was heated with 15 ml of<br />

hydrochloric acid in boiling water bath until it dissolves and<br />

then still 20 minutes.<br />

s714<br />

Ethanol (15 ml), diethyl ether and petrol ether (both<br />

30 ml), were added into stirred mixture after cooling down.<br />

Closed flask was shaken and then allowed to separate the<br />

water and organic phases. The upper (organic) phase was displaced<br />

by the pipette to dried weighed flask. next the water<br />

phase was reextracted with 15 ml of diethyl ether and 15 ml<br />

of petrol ether two times.<br />

The rest of organic solvent was evaporated in 60 °C<br />

water bath (to dispose smell). Flask with fat sample was dried<br />

at 105 °C for one hour 1 .<br />

M e t h a n o l E s t e r i f i c a t i o n M e t h o d<br />

The fat sample (5.0 g) was saponified with 50 ml methanolic<br />

solution of potassium hydroxide (c = 0.5 mol dm –3 ) for<br />

30 minutes in distilling flask with condenser and was esterified<br />

after neutralization by sulphuric acid on methyl orange<br />

for 30 minutes again.<br />

After cooling methyl esters were shaken with 10 ml<br />

of heptane three times. The extract was dried by anhydrous<br />

sodium sulphate and filtered to a 50 ml volumetric flask<br />

again. Both heptane portions were rinsed with 20 ml of water<br />

twice. The extract was dried by anhydrous sodium sulphate<br />

and filtered to a 50 ml volumetric flask and filled up to the<br />

mark with heptane 5 .<br />

G C A n a l y s i s<br />

Prepared heptane methyl esters solutions were injected<br />

to gas chromatograph using autosampler.<br />

GC conditions: gas chromatograph TRACE GC (ThermoQuest<br />

Italia S. p. A., I) equipped with flame ionization detector,<br />

split/splitless injector and capillary column SPTM 2560<br />

(100 m × 0.25 mm × 0.2 μm) with the temperature programme<br />

60 °C held for 2 min, ramp 10 °C min –1 up to 220 °C, held for<br />

20 min. The injector temperature was 250 °C and the detector<br />

temperature was 220 °C. The flow rate of the carrier gas n 2<br />

was 1.2 ml min –1 .<br />

Results<br />

This work deals with the fatty acids included in processed<br />

cheese. The most abundant fatty acids such as lauric,<br />

Fig. 1. Influence of the storage time on the amount of fatty<br />

acids (cheeses stored at 6 ± 2 °C) (mg g –1 of cheese)

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