1997Journal of Food ScienceRequires access

Inhibition of Saccharomyces Cerevisiae by Combination of Hydrostatic Pressure and Monoterpenes

G. O. Adegoke, Hitoshi Iwahashi, Yasuhiko Komatsu

Open publisher page 25 citations

Abstract

ABSTRACT Using a pressure of 1800 kg/cm 2 and 150 μg/mL of α‐terpinene for 1 hr at 25°C, growth reduction of 6 log cycles after incubation at 30°C/24h, was found with S. cerevisiae. Without pressurization, S. cerevisiae was resistant to 300 μg/mL. and 600 μg/mL α‐terpinene but was sensitive 1250 μg/mL. Reduction of 3 log cycles in viable cell counts was found when cells were exposed to pressure (1800 kg/cm 2 ) and ‐(+)‐limonene (200, 400 and 2,000 μg/mL).

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ABSTRACT Using a pressure of 1800 kg/cm 2 and 150 μg/mL of α‐terpinene for 1 hr at 25°C, growth reduction of 6 log cycles after incubation at 30°C/24h, was found with S. cerevisiae. Without pressurization, S. cerevisiae was resistant to 300 μg/mL. and 600 μg/mL α‐terpinene but was sensitive 1250 μg/mL. Reduction of 3 log cycles in viable cell counts was found when cells were exposed to pressure (1800 kg/cm 2 ) and ‐(+)‐limonene (200, 400 and 2,000 μg/mL).

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Available abstract

ABSTRACT Using a pressure of 1800 kg/cm 2 and 150 μg/mL of α‐terpinene for 1 hr at 25°C, growth reduction of 6 log cycles after incubation at 30°C/24h, was found with S. cerevisiae. Without pressurization, S. cerevisiae was resistant to 300 μg/mL. and 600 μg/mL α‐terpinene but was sensitive 1250 μg/mL. Reduction of 3 log cycles in viable cell counts was found when cells were exposed to pressure (1800 kg/cm 2 ) and ‐(+)‐limonene (200, 400 and 2,000 μg/mL).

Key concepts: Saccharomyces cerevisiae, Chemistry, Hydrostatic pressure, Incubation, Limonene, Food science, Chromatography, Biochemistry

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