Characterization of molds from dry-cured meat products and their metabolites by micellar electrokinetic capillary electrophoresis and random amplified polymorphic DNA PCR

被引:27
作者
Martín, A [1 ]
Jurado, M [1 ]
Rodríguez, M [1 ]
Núñez, F [1 ]
Córdoba, JJ [1 ]
机构
[1] Univ Extremadura, Fac Vet, Hig Alimentos, Caceres, Spain
关键词
D O I
10.4315/0362-028X-67.10.2234
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Molds are common contaminants of dry-cured meat products in which mycotoxins could be synthesized if stored under favorable conditions. Thus, efficient and accurate characterization of the toxigenic molds from dry-cured meat products is necessary. A micellar electrokinetic capillary chromatography (MECC) method was tested to analyze secondary metabolites produced by 20 mold strains commonly found in dry-cured meat products. In addition, their random amplified polymorphic DNA (RAPD) genotypes were determined by using a PCR method. Although peak profiles of the secondary metabolites differed among mold strains of different species, they were similar in the same species. MECC analysis showed that 10 of the 20 molds tested produced mycotoxins, including patulin, penicillic acid, cyclopiazonic acid, mycophenolic acid, aflatoxin B1, sterigmatocystin, and griseofulvin. The RAPD analysis yielded a different pattern for each of the mold species tested. However, strains of the same species showed similar RAPD profiles. A high correlation between RAPD analysis and MECC was observed, since strains of the same species that showed similar RAPD patterns had similar profiles of secondary metabolites. RAPD patterns with primer GO2 and MECC profiles, either singly or combined, could be of great interest to distinguish toxigenic from nontoxigenic molds in dry-cured meat products.
引用
收藏
页码:2234 / 2239
页数:6
相关论文
共 20 条
[1]   DIFFERENTIATION OF SPECIES AND STRAINS OF ENTOMOPATHOGENIC FUNGI BY RANDOM AMPLIFICATION OF POLYMORPHIC DNA (RAPD) [J].
BIDOCHKA, MJ ;
MCDONALD, MA ;
STLEGER, RJ ;
ROBERTS, DW .
CURRENT GENETICS, 1994, 25 (02) :107-113
[2]  
CANCALON PF, 1995, FOOD TECHNOL-CHICAGO, V49, P52
[3]  
DIAZ MC, 1999, THESIS U EXTREMADURA
[4]   Molecular tools for identification of Penicillium starter cultures used in the food industry [J].
Dupont, J ;
Magnin, S ;
Marti, A ;
Brousse, M .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1999, 49 (03) :109-118
[5]   Characterization of Penicillium roqueforti strains used as cheese starter cultures by RAPD typing [J].
Geisen, R ;
Cantor, MD ;
Hansen, TK ;
Holzapfel, WH ;
Jakobsen, M .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 2001, 65 (03) :183-191
[6]  
GUTHRIE PAI, 1992, PHYTOPATHOLOGY, V82, P832, DOI 10.1094/Phyto-82-832
[7]   IDENTIFICATION OF GREMMENIELLA-ABIETINA RACES WITH RANDOM AMPLIFIED POLYMORPHIC DNA MARKERS [J].
HAMELIN, RC ;
OUELLETTE, GB ;
BERNIER, L .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (06) :1752-1755
[8]  
LOPEZCORONADO JM, 2002, CATALOGUE SPANISH TY
[9]   Distribution of Penicillium commune isolates in cheese dairies mapped using secondary metabolite profiles, morphotypes, RAPD and AFLP fingerprinting [J].
Lund, F ;
Nielsen, AB ;
Skouboe, P .
FOOD MICROBIOLOGY, 2003, 20 (06) :725-734
[10]   Micellar electrokinetic capillary chromatography of fungal metabolites - Resolution optimized by experimental design [J].
Nielsen, MS ;
Nielsen, PV ;
Frisvad, JC .
JOURNAL OF CHROMATOGRAPHY A, 1996, 721 (02) :337-344