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2002 | 05 | 2 |

Tytuł artykułu

The effect of food-processing conditions on detection of the iap gene of Listeria monocytogenes performed using polymerase chain reaction technique [PCR]

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The effect of physicochemical factors: temperature (20°C, 60°C, 100°C, 121.1°C), pH (2-9), inorganic and organic components, i.e. sodium chloride (5%, 10%, 15%, 20%), carbohydrates: glucose and starch (10%, 20%, 40%), proteins: casein (2.5%, 5%, 10%) and their combinations (e.g. prolonged incubation time at low pH) on in vitro detection of specific fragment of L. monocytogenes iap gene (453 bp) carried out using polymerase chain reaction (PCR) were examined. The possibility of detection of the iap gene during apple and tomato processing as well as in their processed products was also tested. Results showed that two factors hindering detection of the iap gene were casein at all concentrations and processing applied to apples (initial pH 2.5-3.0) and tomatoes (initial pH 4.0-4.5) as well as prolonged incubation in low pH at 60°C.

Wydawca

-

Rocznik

Tom

05

Numer

2

Opis fizyczny

http://www.ejpau.media.pl/series/volume5/issue2/food/art-08.html

Twórcy

autor
  • Agricultural University of Szczecin, Papieza Pawla VI 3, 71-459 Szczecin, Poland
autor
autor

Bibliografia

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  • Anklam E. 1999. The validation of methods based on polymerase chain reaction for the detection of genetically modified organisms in food. Anal. Chim. Acta, 393; 177-179.
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  • Chikuni K., Tabata T., Kosugiyama M., Monma M., Saito M., 1994. Polymerase chain reaction for detection of sheep and goat meats. Meat Sci., 37; 377-345.
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  • Gachet E., Martin G.G., Vigneau F., Meyer G., 1999. Detection of genetically modified organisms (GMOs) by PCR: a brief review of methodologies available. Trends Food Sci. Technol., 9; 380-388.
  • Herman L., 1997. Detection of viable and dead Listeria monocytogenes by PCR. Food Microbiol., 14; 103-110.
  • Hollricher K., Morris P., Welters P. 2000. Novel foods conquer the market. Bioforum Int., 4: 39-41.
  • Lindahl T., 1993. Instability and decay of the primary structure of DNA. Nature, 362; 709-715.
  • MacCormick C.A., Griffin H.G., Underwood H.M., Gasson M.J., 1998. Common DNA sequences with potential for detection of genetically manipulated organisms in food. J. Appl. Microbiol. 84; 969-980.
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  • Mędrala D., Dąbrowski W., Daczkowska-Kozon E., Koronkiewicz A., Czeszejko K., 2002. Comparative studies on identification of Listeria monocytogenes strains performed using a commercial APIŽLISTERIA kit and PCR technique. Pol. J. Food Nutr. Sci., 3, 11/52; 57-63.
  • Niederhauser C., Candrian U., Höfelein C., Jermini M., Bühler H.-P., Lüthy J., 1992. Use of polymerase chain reaction for detection of Listeria monocytogenes in food. Appl. Environ. Microbiol., 58; 1564-1568.
  • Palmer A.O., Lampel K.A., South P.K., Assar S.K., Carter L., Lewy D.D., 2002. Analysis of flour and food samples for cry9C from bioengineered corn. J. Food Prot., 65; 426-431.
  • Pozorski P., Pozorska A., Twardowski T., 1999. Nowa żywność – perspektywy i aspekty prawne. [Novel food – perspectives and regulatory aspects]. Przem. Spoż., 1: 7-9 [In Polsh]
  • Prince A.M., Andrus L., 1992. PCR: how to kill unwanted DNA. BioTechniques, 12; 358-360.
  • Roller S., 2001. Genetically modified foods: threat or opportunity. Food Technol. Biotechnol., 39; 259-263.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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