Specific amplification of bacterial DNA by optimized so-called universal bacterial primers in samples rich of plant DNA

Journal of Microbiological Methods

Volumn 113, Issue , 2015, Pages 50-56

  Dorn In, Samart ^a,b   Bassitta, Rupert ^a   Schwaiger, Karin ^b   Bauer, Johann ^a   Hölzel, Christina S ^a,b  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

Author keywords

16S rRNA; Archaea; Bacteria; PCR; Plant; Primer

Indexed keywords

BACTERIAL DNA; FUNGAL DNA; PLANT DNA; PRIMER DNA; RNA 16S;

ARTICLE; CONTROLLED STUDY; CORYNEBACTERIUM; DNA DETERMINATION; DNA EXTRACTION; DNA FRAGMENTATION; DNA SEQUENCE; ELECTROPHORESIS; ESCHERICHIA COLI; GENE AMPLIFICATION; KLEBSIELLA PNEUMONIAE; MYCOPLASMA BOVIS; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROCESS OPTIMIZATION; PROTEIN CONFORMATION; PROTEIN POLYMORPHISM; QUANTITATIVE ANALYSIS; SINGLE STRAND CONFORMATION POLYMORPHISM; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS AGALACTIAE; TRUEPERELLA PYOGENES; VALIDATION PROCESS; ANIMAL FOOD; ARCHAEON; BACTERIAL LOAD; GENETICS; PROCEDURES; REAL TIME POLYMERASE CHAIN REACTION; RNA GENE; SENSITIVITY AND SPECIFICITY;

ANIMALIA; BACTERIA (MICROORGANISMS); EUKARYOTA; FUNGI;

ANIMAL FEED; ARCHAEA; BACTERIAL LOAD; DNA PRIMERS; DNA, BACTERIAL; DNA, FUNGAL; DNA, PLANT; GENES, RRNA; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; REAL-TIME POLYMERASE CHAIN REACTION; RNA, RIBOSOMAL, 16S; SENSITIVITY AND SPECIFICITY; SEQUENCE ANALYSIS, DNA;

EID: 84927546005     PISSN: 01677012     EISSN: 18728359     Source Type: Journal    
DOI: 10.1016/j.mimet.2015.04.001     Document Type: Article

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