Delayed inoculation of alfalfa with Sinorhizobium meliloti and Penicillium bilaiae

2015 ◽  
Vol 95 (2) ◽  
pp. 205-211 ◽  
Author(s):  
J. D. Knight

Knight, J. D. 2015. Delayed inoculation of alfalfa with Sinorhizobium meliloti and Penicillium bilaiae. Can. J. Plant Sci. 95: 205–211. The persistence of perennial forage legume crops relies on the establishment of an effective symbiotic relationship with the appropriate Rhizobium species and strain. Situations can arise where a forage legume crop fails to symbiotically fix N2. This study investigates if inoculation of alfalfa with a commercial Sinorhizobium meliloti inoculant 1 yr after seeding can induce biological N2 fixation at levels similar to those achieved when the inoculant is applied at seeding. Alfalfa (Medicago meliloti cv. Algonkwin) was grown at two sites in Saskatchewan and inoculated with S. meliloti or S. meliloti plus the P-solubilizing fungus Penicillium bilaiae. The inoculants were applied at seeding or applied 1 yr after seeding. Biological N2 fixation was measured in the fall of the delayed inoculation year as percentage of N derived from atmosphere (%Ndfa) using the 15N isotope dilution technique. Inoculation with S. meliloti increased %Ndfa at both sites relative to uninoculated and fertilized controls but had no effect on total N content or yield. Inoculating alfalfa the year after seeding increased %Ndfa relative to the controls at both sites, and at one of the sites %Ndfa in the delayed treatments was at the same levels measured in the year of seeding treatments.

1976 ◽  
Vol 31 (9-10) ◽  
pp. 509-513 ◽  
Author(s):  
D Müller-Enoch ◽  
H Thomas ◽  
W Streng ◽  
W Ildfeuer ◽  
O Haferkamp

Abstract In the yeasts C. albicans, C. tropicalis, and C. stellatoidea but not in C. krusei, R. rubra, and S. cerevisiae enzyme activity was found by which - as by the catechol-O-methyltransferase (EC 2.1.1.6) found in the liver - the O-methylation of epinephrine to metanephrine and paranephrine, of 3,4-dihydroxybenzoic acid to 4-hydroxy-3-methoxybenzoic acid and 3-hydroxy-4-methoxybenzoic acid, and of 6,7-dihydroxycoumarin to 7-hydroxy-6-methoxycoumarin and 6-hydroxy-7-methoxy-coumarin is catalysed. When the substrates 3,4-dihydroxybenzoic acid, or 6,7-dihydroxycoumarin or epinephrine were incubated in the presence of S-adenosyl-ʟ-[methyl-14C] methionine and S-adenosylmethionine hydrogensulfate with a 100 000 X g supernatant of C. albicans, C. tropicalis or C. stellatoidea the cor­responding O-methylethers were detected in the extracts of the incubation medium by thin-layer chromatography. Final identification of the isomeric radioactive O-methylethers obtained from 3,4-dihydroxy­ benzoic acid and 6,7-dihydroxycoumarin was performed after thin-layer chromatographic separation by the reversed isotope dilution technique. The radioactive m-and p-O-methyl derivatives from epinephrine were separated by thin-layer chromatography and then cleaved with periodate to the corresponding aldehydes which were also identified mainly by the reversed isotope dilution technique.


Sign in / Sign up

Export Citation Format

Share Document