Some important olive cultivars (Kilis yaglık, Halhalı, Karamani, Haşebi, Nizip yaglık) in East Mediterranean Area were studied. Olive fruits were processed on a low-scale mill equipped with a basket centrifuge. Basic quality parameters, the content of total polyphenols, o-diphenols, oxidation stability (Rancimat) and antiradical activity [1,1-diphenyl-2-picrylhydrazyl (DPPH)] were determined in oil samples. The highest induction period (IP) was 36.42 h, found in the Halhalı cultivar (from Gaziantep province), which also had strong radical scavenging activity (RSA) (96.72% in methanol:water extract and 94.91% in total oil) in all samples. The total phenol and o-diphenol content for this cultivar were 495.42 and 76.89 mg caffeic acid/kg oil, respectively. The oxidation stability and antiradical activity of the Kilis yaglık cultivar (from Kilis province) was very poor when compared to other cultivar (IP; 10.40 h, RSA in methanol: water extract; 30.94%, RSA in total oil; 52.31%). In addition total phenol and o-diphenol content for this cultivar were 38.31 and 5.03 mg caffeic acid/kg oil, respectively.

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In present study, “Saurani” Turkish olive monocultivar extra virgin olive oil (EVOO) was extracted by using Mobile Olive Oil Processing Unit (MOOPU)” (TEM Oliomio 500-2GV, Italy). Free fatty acid content, peroxide value, moisture content and UV absorbance value, minor and major components and quality characteristics changes were surveyed during a year storage. “Saurani” olive oil samples weren’t categorized as EVOO according to the trade standards of International Olive Council (IOC) based on peroxide value, UV absorbance values after five and two months of storing, respectively. Free fatty acid content of VOO samples increased during 12 months’ storage, but it was under the IOC limitation for extra virgin olive oil (< 0.8%). According to the results, color values of VOO changed from green to yellow while UV absorbance values altered during storage. Total phenol content decreased from 342.95 to 252.42 ppm in EVOO samples during a year storage time. Luteolin was the most abundant phenolic compound and its decrement was 10%. Tyrosol content of VOO samples increased from 2.80 to 8.81 ppm. Except tyrosol, other phenolic compounds’ concentration decreased after a year storage time. α-tocopherol contents of VOO sample were 324.60 ppm. After 12 months of storage, about 20.48% of α-tocopherol content was destroyed. Amounts of phenolic and tocopherol isomers decreased during storage as expected. Results of this study showed that chemical composition and oxidative stability of VOO samples changed significantly.

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