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Plant Physiology 72:1011-1015 (1983)
© 1983 American Society of Plant Biologists

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Articles

Host Plant Cultivar Effects on Hydrogen Evolution by Rhizobium leguminosarum1

Eulogio J. Bedmar2, Scott A. Edie3 and Donald A. Phillips

Department of Agronomy and Range Science, University of California, Davis, California 95616

The effect of host plant cultivar on H2 evolution by root nodules was examined in symbioses between Pisum sativum L. and selected strains of Rhizobium leguminosarum. Hydrogen evolution from root nodules containing Rhizobium represents the sum of H2 produced by the nitrogenase enzyme complex and H2 oxidized by any uptake hydrogenase present in those bacterial cells. Relative efficiency (RE) calculated as RE = 1 – (H2 evolved in air/C2 H2 reduced) did not vary significantly among `Feltham First,' `Alaska,' and `JI1205' peas inoculated with R. leguminosarum strain 300, which lacks uptake hydrogenase activity (Hup). That observation suggests that the three host cultivars had no effect on H2 production by nitrogenase. However, RE of strain 128C53 was significantly (P ≤ 0.05) greater in symbiosis with cultivar JI1205 than in root nodules of Feltham First. At a similar rate of C2H2 reduction on a whole-plant basis, nearly 24 times more H2 was evolved from the Feltham First/128C53 symbiosis than from the JI1205/128C53 association. Root nodules from the Alaska/128C53 symbiosis had an intermediate RE over the entire study period, which extended from 21 to 36 days after planting. Direct assays of uptake hydrogenase by two methods showed significant (P ≤ 0.05) host cultivar effects on H2 uptake capacity of both strain 128C53 and the genetically related strain 3960. The 3H2 incorporation assay showed that strains 128C53 and 3960 in symbiosis with Feltham First had about 10% of the uptake hydrogenase activity measured in root nodules of Alaska or JI1205. These data are the first demonstration of significant host plant effects on rhizobial uptake hydrogenase in a single plant species.


2 On leave from the Department of Microbiology, Estacion Experimental del Zaidin, C.S.I.C. Granada, Spain.

3 Present address: Department of Biology, Queen's University, Kingston, Ontario, Canada K7L 3N6.

1 Supported by a Fulbright Fellowship, a postgraduate fellowship from the Natural Sciences and Engineering Research Council of Canada, and the United States National Science Foundation Grant PCM 8217187.







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Copyright © 1983 by the American Society of Plant Biologists