Transformation of Escherichia coli in foodstuffs

被引:44
作者
Bauer, F [1 ]
Hertel, C [1 ]
Hammes, WP [1 ]
机构
[1] Univ Hohenheim, Inst Lebensmitteltechnol, D-70599 Stuttgart, Germany
关键词
Escherichia coli; foods; transformation;
D O I
10.1016/S0723-2020(99)80061-7
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
The plasmid transfer by transformation of Escherichia coli in 12 foods was investigated under conditions commonly found in processing and storage of food. Transformation occurred in all foods with frequencies of at least 10(-8) when a simplified standard transformation protocol with non-growing cells was applied. Higher rates (ca. 10(-7)) were found in milk, soy drink, tomato and orange juice. Furthermore, E. coli became transformed at temperatures below 5 degrees C, i.e. under conditions highly relevant in storage of perishable foods. In soy drink this condition resulted in frequencies which were even higher than those determined after application of a temperature shift to 37 degrees C. The transformation of cells growing in milk and carrot juice at a constantly kept temperature of 37 degrees C provides evidence for the potential of E. coli to become transformed naturally. With purified DNA frequencies were determined in these substrates of ca. 2.5 x 10(-7) and 2.5 x 10(-8), respectively. Similar frequencies were also obtained in milk containing the crude nucleic acids of homogenised cell suspensions of E. coli (pUC18). Moreover, the release of plasmid DNA from E. coli during food processing and the subsequent uptake of this DNA by growing E. coli cells was shown to take place after homogenisation in milk indicating a horizontal plasmid transfer by transformation of E. coli.
引用
收藏
页码:161 / 168
页数:8
相关论文
共 24 条
[11]   BACTERIAL GENE-TRANSFER BY NATURAL GENETIC-TRANSFORMATION IN THE ENVIRONMENT [J].
LORENZ, MG ;
WACKERNAGEL, W .
MICROBIOLOGICAL REVIEWS, 1994, 58 (03) :563-602
[12]   CALCIUM-DEPENDENT BACTERIOPHAGE DNA INFECTION [J].
MANDEL, M ;
HIGA, A .
JOURNAL OF MOLECULAR BIOLOGY, 1970, 53 (01) :159-&
[13]  
Neidhardt F.C, 1996, ESCHERICHIA COLI SAL, P2449
[14]   FACTORS AFFECTING TRANSFORMATION OF ESCHERICHIA-COLI STRAIN CHI-1776 BY PBR322 PLASMID DNA [J].
NORGARD, MV ;
KEEM, K ;
MONAHAN, JJ .
GENE, 1978, 3 (04) :279-292
[15]   CONSTRUCTION OF IMPROVED M13-VECTORS USING OLIGODEOXYNUCLEOTIDE-DIRECTED MUTAGENESIS [J].
NORRANDER, J ;
KEMPE, T ;
MESSING, J .
GENE, 1983, 26 (01) :101-106
[16]   MCRA AND MCRB RESTRICTION PHENOTYPES OF SOME ESCHERICHIA-COLI STRAINS AND IMPLICATIONS FOR GENE CLONING [J].
RALEIGH, EA ;
MURRAY, NE ;
REVEL, H ;
BLUMENTHAL, RM ;
WESTAWAY, D ;
REITH, AD ;
RIGBY, PWJ ;
ELHAI, J ;
HANAHAN, D .
NUCLEIC ACIDS RESEARCH, 1988, 16 (04) :1563-1575
[17]  
Sambrook J., 2002, MOL CLONING LAB MANU
[18]  
Souci S.W., 1994, Food composition and nutrition tables, V5th
[19]   SENSITIVITY OF ESCHERICHIA-COLI TO VIRAL NUCLEIC-ACID .7. FURTHER STUDIES ON CA2+-INDUCED COMPETENCE [J].
TAKETO, A ;
KUNO, S .
JOURNAL OF BIOCHEMISTRY, 1974, 75 (01) :59-67
[20]  
VANDIE IM, 1983, J GEN MICROBIOL, V129, P663