Peter P. Wong

Investigations into the pathway of electron transport to the nitrogenase from nodule bacteroids

SummaryA series of investigations were conducted with the objective of elucidating natural pathways of electron transport from respiratory processes to the site of N2 fixation in nodule bacteroids. A survey of dehydrogenase activities in a crude extract of soybean nodule bacteroids revealed relatively high activities of NAD-specific β-hydroxybutyrate and glyceraldehyde-3-phosphate dehydrogenases. Moderate activities of NADP-specific isocitrate and glucose-6-phosphate dehydrogenases were observed. By use of the ATP-dependent acetylene reduction reaction catalyzed by soybean bacteroid nitrogenase, and enzymes and cofactors from bacteroids and other sources, the following sequences of electron transport to bacteroid nitrogenase were demonstrated: (1) H2 to bacteroid nitrogenase in presence of a nitrogenase-free extract ofC. pasteurianum; (2) β-hydroxybutyrate to bacteroid nitrogenase in a reaction containing β-hydroxybutyrate dehydrogenase, NADH dehydrogenase, NAD and benzyl viologen; (3) β-hydroxybutyrate dehydrogenase, to nitrogenase in reaction containing NADH dehydrogenase, NAD and either FMN or FAD; (4) light-dependent transfer of electrons from ascorbate to bacteroid nitrogenase in a reaction containing photosystem I from spinach chloroplasts, 2,6-dichlorophenolindophenol, and either azotoflavin from Azotobacter or non-heme iron protein from bacteroids; (5) glucose-6-phosphate to bacteroid nitrogenase in a system that included glucose-6-phosphate dehydrogenase, NADP, NADP-ferredoxin reductase from spinach, azotoflavin from Azotobacter and bacteroid non-heme iron protein. The electron transport factors, azotoflavin and bacteroid non-heme iron protein, failed to function in the transfer of electrons from an NADH-generating system to bacteroid nitrogenase. When FMN or FAD were added to systems containing azotoflavin and bacteroid non-heme iron protein, electrons apparently were transferred to the flavin-nucleotides and then nitrogenase without involvement of azotoflavin and bacteroid non-heme iron protein.Evidence is available indicating that nodule bacteroids contain flavoproteins analogous to Azotobacter, azotoflavin, and spinach ferredoxin-NADP reductase. It is concluded that physiologically important systems involved in transport of electrons from dehydrogenases to nitrogenase in bacteroids very likely will include relatively specific electron transport proteins such as bacteroid non-heme iron protein and a flavoprotein from bacteroids that is analogous to azotoflavin.

Genotypes of the Common Bean (Phaseolus vulgaris L.) Lacking the Nodule-Enhanced Isoform of Glutamine Synthetase

Glutamine synthetase (GS) is an octameric enzyme. The nodule cytosol of the common bean (Phaseolus vulgaris L.) has two major types of GS subunit polypeptides ([beta] and [gamma]). As a result, nine different isozymes containing varied proportions of [beta] and [gamma] can be generated. The isozymes are resolvable by native polyacrylamide gel electrophoresis. Staining the gel for GS activity reveals two isoforms, GSn1, which is nodule enhanced and is composed of the eight [gamma] polypeptide-containing isozymes, and GSn2, which is the isozyme [beta]8. We screened 104 cultivars and genotypes of common beans for variations in isozyme formation and found two, PI317350 and PI326054, that had no GSn1. The PI beans appeared to nodulate normally and had cytosolic protein concentrations and total GS activities similar to those of the cultivar UI-111, which has GSn1. They accumulated the [gamma] polypeptide, which had the same molecular weight (46,000) and isoelectric point (6.3) as the [gamma] polypeptide of UI-111. Experiments with extracts prepared by mixing UI-111 and the PI bean nodules suggested that the PI bean nodule extracts did not have an inhibitor or a proteolytic system that specifically inhibited or degraded GSn1. Nodules from UI-111 and the PI beans were dissected into cortex and central infection zone tissue fractions. GSn2 was found in the cortex and the central infection zone tissue of all beans. Our results suggested that the reason we were unable to detect GSn1 from the PI beans was not because their GSn1 and GSn2 had an identical electrophoretic mobility, nor was it due to an inhibited or unstable GSn1. Our results suggested that either their [gamma] gene had mutated in the region that is essential for the [gamma] polypeptide to assemble or the assembly of GS may require a chaperone. In the two PI beans, the chaperone accumulated to a lower level than it did in UI-111. This lower amount limited the assembly of the [gamma] polypeptide into GS.