Antioxidant Activity and Inhibitory Effects of Ginger, Green tea, and Cinnamon, Alone and in Combination, on Staphylococcus aureus and Escherichia coli

Document Type : Original Article

Authors

1 Department of Dairy Science and Technology, Faculty of Agriculture, El-Shatby, Alexandria University, Alexandria, Egypt.

2 Department of Dairy Science and Technology, Faculty of Agriculture, Alexandria University, Egypt.

10.21608/asejaiqjsae.2025.457914

Abstract

Herbs and spices were used by the ancient Egyptian and have been used for centuries in India and China. Ginger, Green tea and Cinnamon were extracted and pH value of Ginger, Green tea and Cinnamon were (4.92, 5.25, 4.6) respectively, while % titratable acidity were (0.21%, 0.33%, 0.11%) respectively. Maximum value of Ferric Reducing Antioxidant Power (FRAP) observed in (Cinnamon combined with Green tea) extracts (0.25 mg GAE/g) and maximum value observed in (Cinnamon combined with Green tea) oils (0.39 mg GAE/g). Maximum total phenolic content value observed in (Cinnamon combined with Green tea) extracts (C+T) was (20.23 mg GAE/g) and maximum value observed in (Cinnamon combined with Green tea) oil (C+T) was (37.01 mg GAE/g). The antioxidants activity (DPPH) of oils are higher of extracts. The Cinnamon and Green tea oil in combination (C+T) showed the higher antioxidant activity (86.20%) comparing to the other oils. By GC-MS analysis, Zingiberene is the main constituent of essential oil of Ginger (20.52%), 1.8-Cineole is the main constituent of essential oil of Green tea (31.46%) and Cinnamaldehyde is the main constituent of essential oil of Cinnamon (30.83%). By increasing concentrations of cinnamon, Green tea and Ginger (oils and extracts) inhibition clear zone on Escherichia coli (ATTC 25922) and Staphylococcus aureus (ATTC6538) increased.
 The impact of (T+C) extract on the growth of Staphylococcus aureus (ATTC6538) was lower than Escherichia coli (ATTC 25922). There is no effect of Green tea, Ginger and Cinnamon extracts or oils separately or in-combination on the growth of yogurt starter and karish cheese starter cultures.

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