2004
DOI: 10.1023/b:mici.0000032243.93917.30
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An Oligonucleotide Primer System for Amplification of the Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Genes of Bacteria of Various Taxonomic Groups

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Cited by 45 publications
(42 citation statements)
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“…The primer set RuIIF2/RuIIR2 (Spiridonova et al, 2004) used in our previous work for the detection of the cbbM gene was inefficient for the investigated strains of halophilic SOB. Better results were obtained using a combination of the newly designed forward primer RubII331f and a modified version of the reverse primer (RubII1113r) described by Elsaied et al (2007) (Table 1).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The primer set RuIIF2/RuIIR2 (Spiridonova et al, 2004) used in our previous work for the detection of the cbbM gene was inefficient for the investigated strains of halophilic SOB. Better results were obtained using a combination of the newly designed forward primer RubII331f and a modified version of the reverse primer (RubII1113r) described by Elsaied et al (2007) (Table 1).…”
Section: Resultsmentioning
confidence: 99%
“…Detection of the cbb genes in pure cultures of halophilic SOB At first, the detection of cbb genes in pure cultures of halophilic SOB was attempted using the primer set RubIgF/RubIgR specific for the 'green-like' cbbL form I (Spiridonova et al, 2004). Despite the good results previously obtained with these primers for the haloalkaliphilic SOB (Tourova et al, 2006(Tourova et al, , 2007, they gave positive amplification among the halophilic SOB only for representatives of the genera Halothiobacillus, Thiohalomonas, Thiohalophilus and Thiohalobacter.…”
Section: Resultsmentioning
confidence: 99%
“…cbbL and nifH gene fragments were amplified using specially developed and previously tested primers (Boulygina et al, 2002;Spiridonova et al, 2004;Marusina et al, 2001). PCR products were purified from lowmelting-point agarose using the Wizard PCR Preps kit (Promega).…”
Section: -1492rmentioning
confidence: 99%
“…Degenerate primers for the amplification of RuBisCO type II (cbbM) gene of the CBB cycle were used to test for the presence of the gene in the genome of strain. The designed primers were utilized as previously described (see Supplementary Information online, Table S1) 29 . The PCR amplification parameters were similar to the protocol explained above.…”
Section: Pcr Amplification Of Mam Genes and Genes Involved In Co 2 Fimentioning
confidence: 99%