1985
DOI: 10.1007/bf02181864
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Strain identification in Rhizobium by starch gel electrophoresis of isoenzymes

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Cited by 11 publications
(8 citation statements)
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“…Furthermore, with the exceptions of the studies of Pinero et al (31) and Eardly et al (11), the reported electrophoretic studies on Rhizobium species have been based on only a few enzyme loci. However, these studies have shown that numerous allelic variants exist for those loci examined (13,14,18,27,28,45,46). In this study, we examined 44 different enzyme loci, of which 28 loci provided staining of sufficient intensity and resolution for reliable genetic interpretation.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, with the exceptions of the studies of Pinero et al (31) and Eardly et al (11), the reported electrophoretic studies on Rhizobium species have been based on only a few enzyme loci. However, these studies have shown that numerous allelic variants exist for those loci examined (13,14,18,27,28,45,46). In this study, we examined 44 different enzyme loci, of which 28 loci provided staining of sufficient intensity and resolution for reliable genetic interpretation.…”
Section: Discussionmentioning
confidence: 99%
“…The starch gel electrophoresis isoenzyme pattern types were determined on sonicated extracts of cells as described (Engvild and Nielsen, 1985). The gels were stained for esterases, 3-hydroxybutyrate dehydrogenases, arabinose dehydrogenases and sorbitol dehydrogenases.…”
Section: Lsoenzyme Electrophoresismentioning
confidence: 99%
“…These results were also found by LEMOS (1994) who confirmed the four homology groups already defined. The enzymatic polymorphism tests might be an efficient way to characterize strains and establish the genetic structure of rhizobia populations (ENGVILD & NIELSEN, 1985;ENGVILD et al, 1990). The restricted differences found in this study (only between variants of strain 5019) might be related to the small number of enzymes tested.…”
Section: Resultsmentioning
confidence: 92%
“…Isolates was grown in 50ml of tryptoneyeast medium (TY) (ENGVILD & NIELSEN, 1985) for 72 hours at 28 o C and 120rpm. After centrifugation (15,000 X g, 4 o C -20min), the bacterial pellet was washed several times in saline solution.…”
Section: Methodsmentioning
confidence: 99%