Rapid discrimination of psychrotolerant and mesophilic strains of the Bacillus cereus group by PCR targeting of 16S rDNA (vol 34, pg 99, 1998)

被引：0

作者：

von Stetten, F ^{[1
]}

Francis, KP ^{[1
]}

Lechner, S ^{[1
]}

Neuhaus, K ^{[1
]}

Scherer, S ^{[1
]}

机构：

[1] Tech Univ Munich, Forschungszentrum Milch & Lebensmittel, Inst Mikrobiol, D-85350 Freising, Germany

来源：

JOURNAL OF MICROBIOLOGICAL METHODS | 1999年 / 35卷 / 02期

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：185 / 185

页数：1

共 21 条

[11] Establishment of a novel multiplex PCR assay and detection of toxigenic strains of the species in the Bacillus cereus group (vol 68, pg 2123, 2005)
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[12] PCR fingerprinting of whole genomes, the spacers between the 16S and 23S rRNA genes and of intergenic tRNA gene regions reveal a different intraspecific genomic variability of Bacillus cereus and Bacillus licheniformis (vol 48, pg 107, 1998)
Daffonchio, D
Borin, S
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Manachini, PL
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INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1998, 48 : 1081 - 1081
[13] Use of 16S rRNA, 23S rRNA, and gyrB gene sequence analysis to determine phylogenetic relationships of Bacillus cereus group microorganisms (vol 42, pg 3711, 2004)
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Lysov, Yuri P.
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[14] Host range of Frankia strains isolated from actinorhizal plants growing in Japan and their relatedness based on 16S rDNA (vol 54, pg 379, 2008)
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SOIL SCIENCE AND PLANT NUTRITION, 2008, 54 (05) : 685 - 685
[15] Design and evaluation of useful bacterium-specific PCR primers that amplify genes coding for bacterial 16S rRNA (vol 64, pg 795, 1998)
Marchesi, JR
Sato, T
Weightman, AJ
Martin, TA
Fry, JC
Hiom, SJ
Dymock, D
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APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1998, 64 (06) : 2333 - 2333
[16] Bacillus cereus group strains, their hemolysin BL activity, and their detection in foods using a 16S RNA and hemolysin BL gene-targeted multiplex polymerase chain reaction system
Tsen, HY
Chen, ML
Hsieh, YM
Sheu, SJ
Chen, YL
JOURNAL OF FOOD PROTECTION, 2000, 63 (11) : 1496 - 1502
[17] Monitoring Lactobacillus plantarum in grass silages with the aid of 16S rDNA-based quantitative real-time PCR assays (vol 29, pg 49, 2006)
Klocke, Michael
Mundt, Kerstin
Idler, Christine
McEniry, Joseph
O'Kiely, Padraig
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SYSTEMATIC AND APPLIED MICROBIOLOGY, 2006, 29 (05) : 431 - 431
[18] Restriction fragment-length polymorphism analysis of 16S rDNA from oral asaccharolytic Eubacterium species amplified by polymerase chain reaction (vol 13, pg 23, 1998)
Sato, T
Sato, M
Matsuyama, J
Kalfas, S
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Hoshino, E
ORAL MICROBIOLOGY AND IMMUNOLOGY, 1998, 13 (03): : 193 - 193
[19] Absolute quantitation of microbes using 16S rRNA gene metabarcoding: A rapid normalization of relative abundances by quantitative PCR targeting a 16S rRNA gene spike-in standard (vol 9, e879, 2020)
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[20] Evaluation of numerical analysis of PFGE-DNA profiles for differentiating Campylobacter fetus subspecies by comparison with phenotypic, PCR, and 16S rDNA sequencing methods (vol 90, pg 285, 2001)
On, SLW
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JOURNAL OF APPLIED MICROBIOLOGY, 2001, 90 (04) : 676 - 676

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