scholarly journals Extracellular polysaccharide composition, ex planta nitrogenase activity, and DNA homology in Rhizobium japonicum.

1984 ◽  
Vol 158 (3) ◽  
pp. 1168-1171 ◽  
Author(s):  
T A Huber ◽  
A K Agarwal ◽  
D L Keister
1992 ◽  
Vol 38 (8) ◽  
pp. 857-861 ◽  
Author(s):  
Michael F. Dunn ◽  
Arthur L. Karr

Thirty-four strains of Bradyrhizobium japonicum were screened for the in vitro production of an extracellular polysaccharide depolymerase active against the B. japonicum acidic extracellular polysaccharide that contains mannose, glucose, galactose, and 4-O-methylgalactose as neutral sugar components. Over 90% of tested strains producing this type of extracellular polysaccharide also produced the extracellular polysaccharide depolymerase, whereas strains producing a compositionally different extracellular polysaccharide did not. In addition, representatives of species related to B. japonicum by extracellular polysaccharide composition or host range were also phenotypically depolymerase negative. Depolymerase was also present in soybean root nodules formed by B. japonicum strain 2143. In contrast to the cell-associated depolymerase activity found in free-living cells of this strain, most of the depolymerase activity present in nodules is free of the bacteroids. The widespread occurrence of the depolymerase among B. japonicum strains and the spatiotemporal distribution of its activity in planta are consistent with the enzyme playing a role in the removal of surface extracellular polysaccharide from the microorganism during the infection of nodulation process. Key words: Bradyrhizobium japonicum, soybean, extracellular polysaccharides, extracellular polysaccharide depolymerase, bacteroids.


1979 ◽  
Vol 14 (3) ◽  
pp. 253-258 ◽  
Author(s):  
Richard Storey ◽  
Kathy Rainey ◽  
Leslie Pope ◽  
Minocher Reporter

1979 ◽  
Vol 137 (1) ◽  
pp. 153-160 ◽  
Author(s):  
David W. Emerich ◽  
Tomás Ruiz-Argüeso ◽  
Te May Ching ◽  
Harold J. Evans

1975 ◽  
Vol 30 (9-10) ◽  
pp. 687-688 ◽  
Author(s):  
D. Werner ◽  
J. Wilcockson ◽  
B. Kalkowski

Induced by soy bean tissue cultures in socalled “tissue chambers”, Rhizobium japonicum str. 61-A-96 developed nitrogenase activity separated from the plant cells. The activity proceded for 48 h with a rate of 1 × 10-8 nmol C2H4 h-1 cell-1, which is about 6% of the activity measured for bacteroids from Rhizobium japonicum in nodules of Glycine max.


1978 ◽  
Vol 33 (11-12) ◽  
pp. 859-862 ◽  
Author(s):  
D. Werner

Development of nitrogenase (40 -140 nmol C2 H4 · mg protein-1· h-1) in Rhizobium japonicum 61-A-101 after transfer to special culture conditions (medium 20 P, 2% O2, 10% CO2, 88% N2 in the gas phase) is inhibited by chloramphenicol (6X 10-4 ·1O-3 м) and by rifampicin (10-5м). These concentrations do not inhibit the slow growth of the cells under these conditions with a doubling time of the cell protein and living cell number of 3 - 5 d. Nitrogenase activity of previously derepressed cells is not inhibited by chloramphenicol. Growth of the cells under air in yeast extract-mannitol-glycerol medium (8 h doubling time) is affected significantly more by chloram­phenicol (2.5 · 10-4 м) than growth under nitrogenase derepressed culture conditions.


1980 ◽  
Vol 7 (3) ◽  
pp. 251 ◽  
Author(s):  
R Storey ◽  
M Reporter

Dialysable substances capable of influencing rhizobial nitrogenase activity in vitro were obtained from Glycine max root cells during transfilter coculture with Rhizobium japonicum. These substances from the liquid plant-conditioned medium were chromatographed on Sephadex G-25, DEAE- cellulose and carboxymethylcellulose and on a concanavalin A-Sepharose column. The separated active column fractions initiated the phenotypic expression of nitrogenase activity (C2H2 reduction, H2 production) in different Rhizobium strains. Hydrolysis of these column fractions showed them to contain a small peptide and a glucan. Analysis of active fractions also showed the presence of bound copper. It was concluded that the plant fractions involved in stimulating rhizobial nitrogenase activity were peptidoglucans; at least one active fraction may also be a copper metallothionein.


1984 ◽  
Vol 62 (5) ◽  
pp. 965-971 ◽  
Author(s):  
D. B. Layzell ◽  
P. Rochman ◽  
D. T. Canvin

A continuously flowing open gas exchange system was used to monitor the rates of CO2 evolution, C2H2 reduction, and H2 evolution from intact nodulated soybean ('Harosoy 63') roots, while root temperatures were dropped from the growing temperature (25 °C) to 10 °C at the rate of 5 °C/h. Four Rhizobium japonicum inoculants were used, three of which (type S (Nitragin Co.), USDA 16, USDA 35) displayed net H2 evolution while the fourth (USDA 110) did not evolve H2. Between 25 and 15 °C, values for Q10 in the H2-evolving symbioses ranged from 2.0 to 2.7 for CO2 evolution. 1.3 to 2.4 for C2H2 reduction, and 3.2 to 3.7 for H2 evolution. Nodulated roots of USDA 110 displayed the highest Q10 values for both CO2 evolution (Q10 = 2.9) and C2H2 reduction (Q10 = 15.2). The temperature profiles of these gas exchange measurements were used to calculate both the relative efficiency (RE = 1 − (H2 evolution/C2H2 reduction)) of N2 fixation and the ratio between CO2 evolution and C2H2 reduction at temperatures between 10 and 25 °C. The effect of short-term changes on the CO2/C2H2 ratio varied with symbiotic association. In the type-S symbiosis, long-term (96 h) treatments at low root temperature (9.5 °C) decreased the amount of CO2 evolved per C2H2 reduced to 35% of the value obtained at 25 °C. This study did not determine whether these observed changes were associated with N2 fixation or growth and maintenance of the nodulated root. In all H2-evolving symbioses, the RE increased from ca. 0.6 to 0.9 in response to a temperature drop from 25 to 10 °C. Studies of net H2 uptake and 3H2 exchange at 25 and 15 °C indicated that the observed changes in relative efficiency were due to variations in electron allocation by nitrogenase rather than a relative increase in uptake hydrogenase activity. The increase in RE above 0.75 suggested that lower temperatures may have altered the minimal nitrogenase electron allocation to less than one H2 per N2 fixed. This observed increase in RE with lower temperatures indicated that, in the symbioses studied, H2 evolution may have provided a buffer which permitted the maintenance of high levels of N2 fixation during short-term or diurnal fluctuations in soil temperature.


2013 ◽  
Vol 79 (23) ◽  
pp. 7398-7412 ◽  
Author(s):  
Etienne Yergeau ◽  
John R. Lawrence ◽  
Sylvie Sanschagrin ◽  
Julie L. Roy ◽  
George D. W. Swerhone ◽  
...  

ABSTRACTSediments from the Athabasca River and its tributaries naturally contain bitumen at various concentrations, but the impacts of this variation on the ecology of the river are unknown. Here, we used controlled rotating biofilm reactors in which we recirculated diluted sediments containing various concentrations of bituminous compounds taken from the Athabasca River and three tributaries. Biofilms exposed to sediments having low and high concentrations of bituminous compounds were compared. The latter were 29% thinner, had a different extracellular polysaccharide composition, 67% less bacterial biomass per μm2, 68% less cyanobacterial biomass per μm2, 64% less algal biomass per μm2, 13% fewer protozoa per cm2, were 21% less productive, and had a 33% reduced content in chlorophyllaper mm2and a 20% reduction in the expression of photosynthetic genes, but they had a 23% increase in the expression of aromatic hydrocarbon degradation genes. Within theBacteria, differences in community composition were also observed, with relatively moreAlphaproteobacteriaandBetaproteobacteriaand lessCyanobacteria,Bacteroidetes, andFirmicutesin biofilms exposed to high concentrations of bituminous compounds. Altogether, our results suggest that biofilms that develop in the presence of higher concentrations of bituminous compounds are less productive and have lower biomass, linked to a decrease in the activities and abundance of photosynthetic organisms likely due to inhibitory effects. However, within this general inhibition, some specific microbial taxa and functional genes are stimulated because they are less sensitive to the inhibitory effects of bituminous compounds or can degrade and utilize some bitumen-associated compounds.


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