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   <subfield code="a">Characterization of rhizobia nodulating Lotus subbiflorus from Uruguayan soils</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[P. Irisarri, F. Milnitsky, J. Monza, E. Bedmar]</subfield>
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   <subfield code="a">Generation times, acid production, carbon utilization, immunological properties, plasmid content, protein profile and symbiotic properties of 15 isolates of rhizobia nodulating Lotus subbiflorus were studied. Based on specific growth rates, carbon source utilization and acid production, 13 out of the 15 isolates could be assigned to the slow-growing group of rhizobia (bradyrhizobia). Using antisera against whole cells of three isolates, we separated the 15 isolates into three serogroups. Only the slow-growing isolate Ls4 and the fast-growers Ls5 and Ls552 lacked cross-reactivity with any of the sera tested. Electrophoretic mobilities of whole cell protein from seven out of the eight isolates included in the serogroup represented by strain Ls31 were identical. Similarly, isolates Ls1B3 and Ls1B4, both in serogroup Ls1B3, had the same pattern of cell proteins. In contrast, isolates Ls3 and Ls7, belonging to serogroup Ls7, differed in protein profile. Plant growth experiments carried out under bacteriologically controlled conditions revealed that all of the isolates effectively nodulated L. subbiflorus and L. pedunculatus, but were unable to form effective nodules on L. tenuis and L. corniculatus. All isolates showed similar effectiveness in symbiosis with L. subbiflorus, except isolate Ls7, which gave significantly higher plant dry weight.</subfield>
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   <subfield code="a">Kluwer Academic Publishers, 1996</subfield>
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   <subfield code="a">Bradyrhizobium</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">carbon utilization</subfield>
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   <subfield code="a">ELISA</subfield>
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   <subfield code="a">Lotus subbiflorus</subfield>
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   <subfield code="a">native isolates</subfield>
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   <subfield code="a">protein profiles</subfield>
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   <subfield code="a">symbiotic effectiveness</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">ELISA : enzyme linked immuno-sorbent assay</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">kDa : kiloDalton</subfield>
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   <subfield code="a">MM : mineral medium</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PBS : phosphate-buffered saline</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">RE : relative efficiency</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SDS-PAGE : sodium dodecyl sulfate-polyacrylamide gel electrophoresis</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">YEM : deyeast extract mannitol</subfield>
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   <subfield code="u">Departamento de Bioquimica, Facultad de Agronomía, Garzón 780, 12900, Montevideo, Uruguay</subfield>
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   <subfield code="t">Plant and Soil</subfield>
   <subfield code="d">Kluwer Academic Publishers; gopher://gopher.wkap.nl</subfield>
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