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Characterization Of Recombinant Soybean Leghemoglobin A And Apolar Distal Histidine Mutants, Mark S. Hargrove, Jennifer K. Barry, Eric Allen Brucker, Michael B. Berry, George N. Phillips, Jr., John S. Olson, Raúl Arredondo-Peter, Jeanenne M. Dean, Robert V. Klucas, Gautam Sarath
Characterization Of Recombinant Soybean Leghemoglobin A And Apolar Distal Histidine Mutants, Mark S. Hargrove, Jennifer K. Barry, Eric Allen Brucker, Michael B. Berry, George N. Phillips, Jr., John S. Olson, Raúl Arredondo-Peter, Jeanenne M. Dean, Robert V. Klucas, Gautam Sarath
Gautam Sarath Publications
The cDNA for soybean leghemoglobin a (Lba) was cloned from a root nodule cDNA library and expressed in Escherichia coli. The crystal structure of the ferric acetate complex of recombinant wild-type Lba was determined at a resolution of 2.2 Å. Rate constants for O2, CO and NO binding to recombinant Lba are identical with those of native soybean Lba. Rate constants for hemin dissociation and auto-oxidation of wild-type Lba were compared with those of sperm whale myoglobin. At 37°C and pH 7, soybean Lba is much less stable than sperm whale myoglobin due both to a fourfold …