High pressure inactivation of byssochlamys nivea ascospores and other heat resistant moulds

The response of persistent and vegetative forms of the heat resistant mouldsByssochlamys nivea,Byssochlamys fulva,Eurotium(Aspergillus fischeri),Eupenicilliumspp. andPaecilomycesspp. to a combined pressure-temperature treatment was investigated. All vegetative forms are inactivated by 300 MPa at 25°...

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Hauptverfasser: Butz, Peter (VerfasserIn) , Funtenberger, S. (VerfasserIn) , Haberditzl, T. (VerfasserIn) , Tauscher, Bernhard (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 1996
In: LWT - food science and technology
Year: 1996, Jahrgang: 29, Heft: 5, Pages: 404-410
DOI:10.1006/fstl.1996.0062
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1006/fstl.1996.0062
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0023643896900626
Volltext
Verfasserangaben:P. Butz, S. Funtenberger, T. Haberditzl, B. Tauscher
Beschreibung
Zusammenfassung:The response of persistent and vegetative forms of the heat resistant mouldsByssochlamys nivea,Byssochlamys fulva,Eurotium(Aspergillus fischeri),Eupenicilliumspp. andPaecilomycesspp. to a combined pressure-temperature treatment was investigated. All vegetative forms are inactivated by 300 MPa at 25°C. Except forB. niveaascospores, all persistent forms are strongly reduced by treatment in the range of 300-600 MPa at 10 to 60°C. In this rangeB. fulva,EurotiumandEupenicilliumspp. show unexpected and individual pressure-temperature responses.B. niveaascospores needed pressures above 600 MPa and temperatures above 60°C for inactivation in representative studies. pH has little influence on the inactivation rate while low water activities are inhibitory. Treatment of 700 MPa at 60°C sensitizesB. niveaascospores to subsequent thermal treatment. In grape juice, the initial inactivation rate at 700 MPa and 70°C is higher than in physiological salt solution. Tissue damage to ascospores during pressure treatment are visible only after preparation for electron microscopy.
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DOI:10.1006/fstl.1996.0062