Long PCR-amplified rDNA for PCR-RFLP- and Rep-PCR-based approaches to recognize closely related microbial species

Journal of Microbiological Methods

Volumn 49, Issue 3, 2002, Pages 315-319

  Abd El Haleem, Desouky ^a,b   Layton, Alice C ^a   Sayler, Gary S ^a  

^a UNIVERSITY OF TENNESSEE   (United States)

^b Universities and Research centers District   (Egypt)

Author keywords

Long PCR; Ralstonia; Ribosomal operon

Indexed keywords

RESTRICTION ENDONUCLEASE; RIBOSOME DNA; BACTERIAL DNA; PRIMER DNA; RIBOSOMAL SPACER DNA; RNA 16S; RNA 23S;

AMPLICON; ARTICLE; BACTERIAL STRAIN; BACTERIUM IDENTIFICATION; CONTROLLED STUDY; DNA SEQUENCE; GENE AMPLIFICATION; NONHUMAN; OPERON; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; WAUTERSIA EUTROPHA; CLASSIFICATION; GENETICS; METHODOLOGY; NON-PROGRAMMATIC; SPECIES DIFFERENCE;

DNA PRIMERS; DNA, BACTERIAL; DNA, RIBOSOMAL SPACER; OPERON; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RALSTONIA EUTROPHA; RNA, RIBOSOMAL, 16S; RNA, RIBOSOMAL, 23S; SPECIES SPECIFICITY; SUPPORT, NON-U.S. GOV'T; CUPRIAVIDUS NECATOR;

BACTERIA (MICROORGANISMS); RALSTONIA; WAUTERSIA EUTROPHA;

NON-PROGRAMMATIC;

EID: 0036008796     PISSN: 01677012     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0167-7012(01)00374-8     Document Type: Article

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