SLIP MELTING POINT ESTIMATION OF FAT BLENDS BEFORE AND AFTER INTERESTERIFICATION BASED ON THEIR FATTY ACID COMPOSITIONS

In this study the relationship between slip melting point (SMP) and fatty acid composition of blends before and after interesterification were investigated. Forty-four blends were prepared using sunflower, canola and cottonseed oils as well as palm stearin and/or fully hydrogenated palm stearin in different proportions. Fatty acid compositions and SMP of samples were determined and then SMP of the blends before and after interesterification were defined as a function of five fatty acids. Specific constants of C_16:0, C_18:0, C_18:1, C_18:2 and C_18:3 fatty acids were determined as 0.455, 0.821, 0.622, 0.215 and -1.653, respectively, for the blends before interesterification and 0.532, 0.614, 0.399, 0.055 and -2.471, respectively, for the blends after interesterification by using least squares method. Slip melting point of blends were calculated using these constants and fatty acid compositions and then compared with the experimental values. No linear relationship existed between the calculated and experimental results of the blends before interesterification, but SMP of the blends after interesterification could be estimated with high (r=0.956) accuracy.     

EFFECT OF VITAMIN E SUPPLEMENTATION ON INTRA- AND INTERMUSCULAR FATTY ACID COMPOSITION OF AWASSI LAMBS

This research was carried out to determine the effects of vitamin E supplementation on inter- and intramuscular fatty acid composition in meat of Awassi lambs. Lambs were divided into two groups, control (CG) and experimental (VG), at the beginning of the fattening period. The CG and VG lambs were fed the same concentrate and hay. The VG also received a supplement of 45 mg vitamin E (DL-α tocopheryl acetate) per lamb per day for the 75-day fattening period prior to slaughter. After slaughtering, carcasses were stored at 4 0.5C for 24 h. Then , M. longissimus dorsi (LD) muscles were excised from carcasses, and the intra- and intermuscular fats from LD muscles were used as study material. Results showed that vitamin E supplementation had no significant effect on fatty acid composition in intra- and intermuscular fats (P < 0.05). Fatty acid content in intramuscular fats were different than those in intermuscular fats (P < 0.01) except for lauric (C₁₂), linoleic (C_18:2) and linolenic (C_18:3) acids (P < 0.05). Total saturated fatty acids in the intramuscular fats were lower than in intramuscular fats (P < 0.01). In addition, the majority of fatty acids, both intramuscular and intermuscular, in Awassi lambs were oleic (C_18:1), palmitic (C₁₆ and stearic (C₁₈) acids.     

INHIBITION OF MICROORGANISMS IN SALAD DRESSING BY SUCROSE AND METHYLGLUCOSE FATTY ACID MONOESTERS

The antimicrobial activity of sucrose and methylglucose esters of medium to long chain fatty acids was studied with two microorganisms involved in the spoilage of salad dressings, Zygosaccharomyces bailii and Lactobacillus fructivorans. The microorganisms were inhibited to various degrees by 0.1, 0.5, and 1.0% synthesized sucrose or methylglucose monoesters using a modified broth dilution method. Sucrose monoesters were most inhibitory when the esterified fatty acid was myristic (C₁₄) or palmitic acid (C₁₆). Methylglucose monoesters with lauric (C₁₂) or myristic acid (C₁₄) exhibited greater inhibition than those with longer chain fatty acids. The least inhibition was generally observed with sucrose and methylglucose oleate (C_18:1). Sucrose monoesters were usually more inhibitory than methylglucose monoesters of the same fatty acid, especially for palmitic and stearic (C₁₈) acids. In salad dressing, 1% sucrose monoesters of lauric, myristic, or palmitic acid significantly (P < 0.05) inhibited the growth of Z. bailii and L. fructivorans, and were comparable with or more effective than 0.1% sodium benzoate. Z. bailii growth was nearly completely inhibited by sucrose laurate, myristate and palmitate by 9 days of salad dressing storage. Sucrose monoesters did not delay the lag phase of L.     

Detecting vegetable oil adulteration in hazelnut paste (Corylus avellana L.)

The possibilities of detecting hazelnut paste adulterated with refined and non-refined vegetable oils have been studied. Research was focussed mainly on peanut, high oleic-acid sunflower, corn and soybean oils which have a similar composition to hazelnut oil. The analytical procedures to detect fatty acid (FA), triacylglycerol (TAG) and tocopherol profiles as indicators of adulteration were determined. The better indicators experimentally determined were seven FA (palmitic, stearic, linoleic, linolenic, arachidonic, behenic and lignoceric acids) and different TAG with three unsaturated FA (the code letters used for FA are: P = C_16:0; S = C_18:0; O = C_18:1; L = C_18:2;; L_n = C_18:3) (LLL_n, LLL and OOO), two unsaturated FA (POL, PLL and SOO), and one unsaturated FA (PPL). As expected, when refined vegetable oils were added to hazelnut paste, the increment of stigmasta-3,5-diene allowed detection at levels of 2% oil added. Limits of detection were measured using standard and adulterated hazelnut with different amounts of non-refined vegetable oils added (5%, 10%, 20% and 30%). The distribution of tocopherols and tocotrienols is highly useful, except in the case of added sunflower oil. The differences between the experimental and theoretical values of the TAG with equivalent carbon number (ΔECN) of 42 does not improve the detection limit of hazelnut paste adulterated with peanut or sunflower oils. Similarly, tocopherols usually added to refined vegetable oils as an antioxidant were also determined.     

Antioxidative Effects of Ethanol Extracts from Rhus verniciflua Stoke on Yukwa (Oil Popped Rice Snack) Base During Storage

ABSTRACT: This study was designed to evaluate the antioxidative effectiveness of ethanol extracts of Rhus verniciflua Stoke (RVE) in frying oil of Yukwa base (rice snack). RVE showed a strong antioxidant activity, but commercial antioxidants — BHA and dl-δ-tocopherol — did not demonstrate a significant ifmprovement over the control treatment (Yukwa bases prepared without any antioxidants and extracted oil from these). In particular, induction period, peroxide value, and acid value of RVE treatment exhibited a higher oxidative stability than that of the other treatments. In addition, the decrease in linoleic acid (C_18:2)/palmitic acid (C_16:0) ratio was much less than the other treatments. Texture properties (hardness and crispiness) of Yukwa base were not significantly different. Results showed strong antioxidant properties of RVE on Yukwa base during storage.     

Preparation and characterisation of the C10 to C18 even-numbered triethanolamine alkyl sulphates

The preparation and characterisation of purified C₁₀ to C₁₈ even-numbered triethano-lamine alkyl sulphates are described. Critical micelle concentrations were determined at 25°C, using both conductance and drop volume methods. The authenticity and purity of the products are established, and evidence presented for amending the accepted melting points for two of the compounds.
Preparation et identification des alkysulfates de triethanolamine en C₁₀, C₁₂, C₁₄, C₁₆, C₁₈     

SEED LIPIDS OF THE MIRACLE FRUIT (SYNSEPALUM DULCIFICUM)

The lipids from the Miracle Fruit seeds comprised 10.15% of the dry weight. The neutral lipids, phospholipids and glycolipids were separated by silicic acid chromatography and the fatty acid composition of each fraction determined. The non-saponifiable lipids, amounting to 1.6% of the neutral lipids were separated into several fractions by thin-layer chromatography and the components of each analyzed by combined gas chromatography-mass spectrometry. The hydrocarbon fraction contained the n-alkane series from C₁₇ to C₃₂ with the C₂₉ and C₃₁ members present in relatively large quantities.
The major triterpene alcohols were α-and β-amyrin and the major sterol was identified as δ⁷ spinasterol. Two short-chain alchols were also present.     

THE LIPIDS OF EGG YOLK. 5. Presence of Ceramide

SUMMARY —Ceramide (an N-acyl sphingosine) was isolated from egg yolk lipid and examined for composition of fatty acids and long-chain base constituents. Yolk ceramide was observed to contain sixteen fatty acids; C _24:0 (35.7%), C _22:0 (22.7%), C _23:0 (15.1%) and C _24:1 (13.5%) were predominant. The component long-chain bases were identified as sphingosine and dihydrosphingosine, the former being the major component (88.6%).     

The influence of fatty alcohols on the structure and stability of creams prepared with polyethylene glycol 1000 monostearate/fatty alcohols

Liquid paraffin in water emulsions stabilized by PEG 1000 monostearate and alcohols cetostearyl (c/s) myristyl (C₁₄), cetyl (C₁₆) or stearyl (C₁₈) and ternary systems prepared by dispersing each fatty alcohol and surfactant in water were examined during 30 days using a Ferranti-Shirley cone and plate viscometer. Microscopical diffusion experiments investigated interaction between PEG 1000 monostearate solution and each alcohol at high and low temperature.
The rheological properties of each ternary system and corresponding emulsion were similar. Formulations prepared from pure C₁₄, C₁₆ or c/s alcohols were semisolid immediately after preparation. Flow curves were in the form of anticlockwise hysteresis loops with spur points. On ageing for 24 h, structure built-up over a time scale similar to that observed in diffusion experiments, so that apparent viscosities increased. However, on further ageing the pure C₁₄ and C₁₆ alcohol systems were not as stable as those prepared with c/s alcohol. In contrast, the pure C₁₈ systems were mobile liquids and the emulsion cracked within days. This correlated with diffusion experiments where little interaction was observed between stearyl alcohol and PEG 1000 monostearate.
Emulsion consistencies and stabilities were related to the low temperature structures formed in the continuous phases.
L'influence des alcools gras sur la structure et la stabilité des crèmes préparées à partir de systèmes monostéarate de polyéthylène glycol 1000/alcools gras.     

CARBOISIYL AND FATTY ACID ANALYSIS OF ANTELOPE AND BEEF FAT

Characterization of kidney fat from twelve antelope and four beef was accomplished by monocarbonyl, ketoglyceride and fatty acid analysis. Antelope lipids are highly saturated, possessing strong odor and flavor characteristics which many people find objectionable. The antelope fat had a stearic acid content of 42% and an oleic acid content of only 20% while beef fat contained 28% stearic and 34% oleic acid. The lipid was further analyzed by reacting on a 2, 4-DNPH Celite impregnated column. The derivatives were separated from unreacted lip-id, and monocarbonyls and ketoglycerides fractionated using column chromatography. The ratio of monocarbonyls to ketoglycerides was about 1:3 in beef and 1:1 in antelope. Amounts of monocarbonyls average 0.70 μM/g of fat for beef and 1.47 μM/g of fat for antelope. Further analysis of the monocarbonyls indicated 7% methyl ketones, 70% saturated aldehydes, 18% enals and 6% 2,4 dienals in beef while antelope had 15%, 70%, 11% and 4%, respectively. Major constituents of the saturated aldehydes were C₂ through C₈ for both species and C₁₀ for beef while the major methyl ketones were C₃ through C₇ for both species. Methyl ketone, saturated aldehyde and enal fractions showed similar trends in composition with short-chain components higher in antelope and long-chain components higher in beef. Considerable variation occurred among animals of the same species.     

The rate of phospholipid hydrolysis in frozen fish

Summary. Phospholipid hydrolysis was studied in lemon sole and haddock between -7°C and -29°C. the rate of reaction was much faster in the Gadoid. the haddock data showed evidence for a rapid first order reaction in which lecithin and phosphatidylethanolamine containing C_16:0, C_18:1 and C_20:5 acids were preferentially hydrolysed. the reaction proceeded to an asymptote which decreased with lowering temperature. the amount of free water available in the frozen state seemed important in these hydrolytic reactions.
The relation of these findings to protein denaturation and taste panel assessment of texture are discussed.     

PROXIMATE AND LIPID COMPOSITION OF NONDAIRY IMITATION MILK IN COMPARISON WITH MILK

Comparative studies of milk and nondairy imitation milks showed that their proximate compositions were similar. Qualitative and quantitative studies revealed that saturated fatty acids were abundant in milk, while unsaturated fatty acids (C _18:1 and C _18:2 ) were predominant in nondairy imitation milks. This was confirmed by the higher melting points of the fat fractions of milk compared with those of nondairy imitation milks. Finally, lipid peroxidation level of samples were low as determined by the 2-thiobarbituric acid test.     

Specificity in Thermal Hydrolysis of Triglycerides

SUMMARY— Samples of triglycerides and triglyceride mixtures were heated in the presence of water under controlled conditions and the released fatty acids quantitatively analyzed by gas chromatography. Experiments with both a mixture of monoacyl-triglycerides and glycerides with equimolar amounts of randomly distributed fatty acids showed a preference for the hydrolysis of the shorter chain and the unsaturated fatty acids. The C₄, C₈, C₁₂, and C_18:1, fatty acids were used in the above mixtures. A trilaurin, in which the fatty acid in the P-position is labelled with C¹⁴, was synthesized. When the free acids released by heat were analyzed by a combination gas chromatographic-radioactivity detector system, no evidence for a positional specificity was apparent.     

Arabinogalactan as a potential furfural precursor in roasted coffee

A fraction C₁ which was very rich in polysaccharides and did not contain sucrose was isolated from high molecular weight water-soluble material obtained from green coffee. After roasting, furfural was identified in fraction C₁ by means of headspace-GC/MS analysis. Roasting of the fraction C₁ clearly affected the arabinogalactan promoting a high loss of arabinose residues. We suggest that furfural found in fraction C₁ originates mainly from arabinogalactan, which, together with sucrose appears to be the major furfural precursor in roasted coffee.     

Substantivity of sunscreens: an appraisal of some quaternary ammonium sunscreens

Two series of quaternary ammonium UV-B sunscreens, derived from salicylic acid (S) and from p -methoxycinnamic acid (C), and containing N-alkyl chains of different length (C₂ to C₁₆) were prepared and submitted to substantivity tests on animal (wool) keratin, and to microbiological tests. A direct correlation between substantivity and antimicrobial/antifungal activity was observed in all cases, the compounds bearing C₁₂ alkyl chains displaying peak values. The C-derivatives, when compared with the S-derivatives, showed relatively higher substantivity and sunscreen index (SI) values, coupled with lower antibacterial activity. The substantivity-microbiological activity correlations and the particular behaviour of the C₁₂ derivatives are briefly discussed in the light of the existing literature data. On the basis of the experimental results, possible guidelines for the development of substantive and non-antibacterial (and possibly, non-irritant) quaternary ammonium sunscreens are indicated.
La substantivité des filtres solaires     

CONCENTRATION OF GAMMA LINOLENIC ACID (GLA) FROM BORAGE OIL BY UREA COMPLEXATION: OPTIMIZATION OF REACTION CONDITIONS

Production of gamma-linolenic acid (GLA, 18:3ω6) concentrates from borage oil (BO) was optimized. A 3-factor-3-level face-centered cube design was used to study the effect of reaction time (X₁), reaction temperature (X₂) and urea-to-fatty acid ratio (X₃) in order to maximize the GLA content(Y). A second-order polynomial model was employed to generate a surface response. Under optimum conditions, a maximum of 91% GLA was obtained from borage oil at a reaction time of 16 h, reaction temperature of -7C and a urea-to-fatty acid ratio(w/w) of 3.7.     

PURIFICATION AND PROPERTIES OF PHOSPHOLIPASE A2 ISOZYMES FROM PYLORIC CECA OF THE STARFISH (ASTERINA PECTINIFERA)

Phospholipase A₂ isozyme II (PLA₂ II), which showed different mobility on native PAGE from that of the PLA₂ isozyme I (PLA₂ 1) isolated previously, was purified from pyloric ceca of the starfish (Asterina pectinifera). The PLA₂ II mainly released oleic acid from 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine. N-terminal amino acid sequence of the PLA₂ II was SVYQF. Temperature and pH optima of the PLA₂ II were at around 50C and pH 9.0, respectively, and the enzyme activity was enhanced by sodium deoxycholate and 1 mM or higher concentration of Ca²⁺. The PLA₂ II did not show fatty acid specificity for hydrolysis of phosphatidylcholine (PC). Specific activity of the PLA² II was about 10 times higher than that of commercially available porcine pancreatic PLA₂. The PLA₂ II hydrolyzed PC more effectively than phosphatidylethanolamine. These characteristics of the PLA₂ II were the same as those of the PLA₂ I.     

Propriétés antiélastasiques des propionylaminoacides

Antielastase activity of derivatives like 'propionylaminoacid'(C₃ prolin, C₃ hydroxyprolin, C₃ collagen) was examined for pancreatic elastase, and fibroblastic elastase production. Essential metabolic variations of normal dermal fibroblasts were evaluated: adhesion, proliferation capacity, total protein biosynthesis and collagen type I and type III production. Possible other factors such as cellular nutrients were examined by oxygen consumption evaluation.
Propionylaminoacid derivatives have antielastase activities. Pancreatic elastase showed dose related inhibition (20% to 50% inhibition for concentration from 5 to 80 mg ml⁻¹.
Moreover, fibroblastic elastase production was inhibited, cellular respiration was enhanced. A very good tolerance in vitro was observed for concentration 0–1 mg ml⁻¹ range: adhesion, proliferation capacity and collagen (type I and type III) production were not altered, and oxygen consumption was enhanced.     

Portable Electronic Nose for Detection of Spoiling Alaska Pink Salmon (Oncorhynchus gorbuscha)

ABSTRACT:  The ability of a portable hand-held electronic nose (EN) in detecting spoilage of whole Alaska pink salmon ( Oncorhynchus gorbuscha ) stored at 14 °C and in slush ice (1 °C) was investigated. Fish were sampled daily at 14 °C for up to 3 d, while fish stored in slush ice were sampled at various intervals up to 16 d. Sensory evaluations indicated that fish were rejected at day 3 when stored at 14 °C and at day 12 when stored in slush ice. Aerobic bacteria counts for fish skin at 14 °C ranged from 3.4 log₁₀ colony-forming units (CFU)/cm² (day 0) to 4.8 log₁₀ CFU/cm² (day 3) and for fish stored in slush ice ranged from 3.4 log₁₀ CFU/cm² (day 0) to 5.5 log₁₀ CFU/cm² (day 16). The correct classification rate using forward stepwise general discriminate analysis was 85% and 92% for EN analysis of belly cavity volatiles for fish held at 14 °C and in slush ice, respectively. A predictive model may be developed for spoilage of whole Alaska pink salmon by analyzing belly cavity odors using the EN.     

INFLUENCE OF TIME THICKENING ON THE WHIPPABILITY OF CREAMS

Flow properties of creams containing milk fat (Cream A), vegetable fat (Cream C), and vegetable fat plus milk fat (Cream B) were determined with a coaxial cylinder viscometer for a wide range of shear rates. All creams examined showed time thickening. The viscosity increase with shearing time was expressed by two stage equations as follows: (1) (1) where η_o and η_t are cream viscosity at zero and t shearing time, K₁ and K₂ are rate constants and C₁ and C₂ are constants. The first stage (Eq. 1) was assumed to occur in the course of primary clustering of the independent fat globules, and the second stage (Eq. 2) was assumed to occur in the course of coagulation of the fat globule clusters. Both K₁ and K₂ increased as shear rate increased.
At the same time, the whippability of each cream was determined with a household mixer to which was attached a strain gauge transducer unit for measuring consistency of the whipped creams. There was a tendency for a higher ratio of milk fat/vegetable fat in the creams to decrease the whipping time or to increase whippability of the creams.
Correlations of stability, whippability, and flow properties were examined. A cream which was high stability showed a low K₁ value, and a cream which has high whippability showed a high K₂ value. K₁ and K₂ values at a suitable shear rate will be quite helpful in the determination of the physical properties of cream.