Regulation of the Activity of Ribulose-1,5-Bisphosphate Carboxylase in Response to Changes in the Photosynthetic Source-Sink Balance in Intact Soybean Plants

Sink-limited conditions cause a reduction in the rate of photosyntheticfixation of CO₂ in single-rooted soybean leaves (Glycine max.Merr.). We suggested previously that this reduction is due tothe deactivation of ribulose-1,5-bisphosphate carboxylase (RuBPcase;EC 4.1.1.39 [EC] ) that is caused by a decrease in the level of freeP_i via a decrease in the rate of conversion of phosphorylatedintermediates to the end-product (sucrose) in sink-limited leaves[Sawada et al. (1989) Plant Cell Physiol. 30: 691, Sawada etal. (1990) Plant Cell Physiol. 31: 697, Sawada et al. (1992)Plant Cell Physiol. 33: 943]. In the present study, we investigatedwhether, in intact soybean plants, sink-limited conditions wouldalso cause a reduction in the rate of photosynthesis and whethersuch a reduction might be due to the deactivation of RuBPcasevia the same regulatory mechanism as that suggested from previousstudies with single-rooted leaves. Continuous removal of flowerbuds from intact plants brought a large decrease in ratio ofthe dry weight of sink organs (stem, roots, pods) to sourceorgan (leaves) as a result of the absence of pod formation.Pods are likely to function as the major sink at the reproductivestage. Upon continuous removal of flower buds, the treated (sink-limited)plants showed a large decrease in the rate of photosyntheticfixation of CO₂ as compared to control plants. RuBPcase in theleaves of treated plants was continuously inactivated with thedecrease in photosynthetic activity. However, the inactivatedenzyme was totally reactivated upon incubation in the presenceof 10 mM NaHCO₃ and 5 mM MgCl₂. The levels of sucrose and ribulose-1,5-bisphosphatein leaves of the treated plants increased significantly. Allthese results coincide exactly with those obtained in previousstudies of single-rooted leaves under the sink-limited conditions. (Received July 14, 1994; Accepted February 21, 1995)     

Expression of exercise-induced HSP70 in long-distance runner''s leukocytes

This study was designed to investigate the expression of heat shock protein 70 (HSP70), after acute moderate intensity exercise, in human peripheral blood leukocytes of trained runners and untrained controls. Ten male long-distance trained runners (TR) and untrained sedentary control subjects (SED) ran for 1 h at 70% of heart rate reserve (HRR). Basal HSP70 expression in TR was usually lower than that in SED, but basal HSP70 gene expression in TR was usually higher than that in SED. Although expression rates of exercise-induced HSP70 in both groups were similar, levels of HSP70 in SED were significantly higher than in TR. Significant increases in leukocytes, neutrophils, and lymphocytes after exercise were observed in both groups, but there were some differences between groups. We conclude that 1 h treadmill running at 70% HRR intensity is a sufficient stimulus to leukocytosis, neutrocytosis, lymphocytosis, and HSP70 proteins and gene expression in leukocytes. Adaptation to training was observed in TR.     

Progressive strenuous exercise induces the expression of HSP70 in rat skeletal muscles and myocardium

This study investigated the exercise-induced synthesis and accumulation of heat shock protein 70 (HSP70) after progressive strenuous exercise in rat soleus, plantaris, and myocardium. Sprague-Dawley rats were randomly assigned to one of six groups, one control group and five exercise groups, divided by intensity and duration of exercise. Skeletal muscles and heart were dissected immediately after last performance. The levels of HSP70 were analyzed by western blotting using a specific polyclonal antibody. Basal levels of HSP70 in soleus were the highest, and then followed by the myocardium and plantaris, in turn. Progressive strenuous exercise increased accumulation of HSP70 gradually in all three tissues. There were differences in patterns of increase among three tissues.     

Further Studies of the Polysaccharide of Klebsiella pneumoniae Possessing Strong Adjuvanticity: I. Production of the Adjuvant Polysaccharide by Noncapsulated Mutant

In culture fluid, Klebsiella pneumoniae type 1 Kasuya strain produces polysaccharide exhibiting a strong adjuvant effect. The active substance responsible for the strong adjuvant effect of the polysaccharide is not its acidic polysaccharide fraction (the type-specific capsular antigen) but the neutral polysaccharide fraction. In the present study, a mutant which did not produce the type-specific capsular polysaccharide was isolated from ultraviolet-irradiated cells of K. pneumoniae type 1 Kasuya strain which had been labeled with leucine-requiring marker by selecting unagglutinable cells with the antiserum to the type-specific capsular polysaccharide. Serological tests showed that the type-specific acidic capsular polysaccharide was present neither on the cells surface nor in the culture fluid of the mutant. Electron microscopically, the mutant did not possess any capsular material. On the other hand, nearly an equal amount of neutral polysaccharide antigen was produced in culture fluids of the noncapsulated mutant and the parent strain. The neutral polysaccharide antigen produced by the noncapsulated mutant exhibited the same degree of strong adjuvant effect on antibody response to bovine gammaglobulin in mice as that produced by the parent strain. The relationship between the neutral polysaccharide antigen in culture fluid and the O antigen of K. pneumoniae was discussed.     

Shear-induced arrangement of cells in cake during crossflow filtration of Escherichia coli cells

Summary The specific resistance of the cake formed in the crossflow filtration of Escherichia coli was higher than that formed in the dead-end filtration. The scanning electronmicrographs revealed that the cells in the cake formed in the crossflow filtration were oriented in the direction of the circulation flow, while the cells deposited at random in the dead-end filtration. The shear-induced arrangement of cells might increase the specific resistance of the cake in crossflow filtration.     

Stochastic tunneling in the colonization of mutualistic organisms: Primary succession by mycorrhizal plants

In mutualism under spatial structure, asynchrony between the dispersions of the interacting species can be a key determinant of their dynamics. We focused on the plant-mycorrhizal fungi system to theoretically analyze the colonization process by calculating the probability of colony establishment under environmental fluctuation. This can be considered a joint process of two sub-processes before and after the association between the host plant and the mycorrhizal fungi in a novel habitat. When colony growth undergoes environmental fluctuation, the dynamics of colony size can be considered a combination of the two stochastic sub-processes that mediated the association event between the plant and the fungi. Therefore, properties of whole system are influenced by five parameters, means and variances of colony growth rates of two sub-systems, and a rate of association of plant and fungi. For the successful establishment of a colony, the second sub-process must start before the first sub-process finishes (i.e., extinction), which we refer to as “stochastic tunneling.” Our analysis of the establishment probability of a plant colony based on this concept revealed that (1) the mean colony growth rates of the host alone and the symbiotic association affect establishment probability in different ways, (2) the variance of colony growth rate of the symbiotic association reduces the establishment probability, although the variance of growth rate of the host alone facilitates the establishment probability when the mean growth rate of the host alone is negative, and (3) a trade-off between the mean colony growth rates of the host alone and the symbiotic association could result in the evolution of either a symbiotic or parasitic relationship, based on a host decision. The model we present is widely applicable to the colonization processes of both positive and negative species relationships, where the interacting species disperse independently.     

Searching for amino acid sequence motifs among enzymes: the Enzyme-Reaction Database

Recently we have constructed a database—the Enzyme–ReactionDatabase–which links a chemical structure to amino acidsequences of enzymes that recognize the chemical structure astheir ligand. The total number of enzymes registered in thedatabase is 1103 with 6668 NBRF–PIR entry codes and 1756chemical compounds. The chemical structures and chemical namesfor 842 compounds are registered in the Chemical–StructureDatabase on the MACCS system. For each enzyme, the sequenceswere divided into clusters, and multiply aligned in each clusterto extract a conserved sequence. A total of 158 781 five–residue–longfragments were constructed from 433 conserved sequences andcompared among different clusters of different enzymes. Oneof these motifs shared by different enzymes S–G–G–L–D.The motif was conserved in both argininosuccinate synthase (EC6.3.4.5 [EC] ) and asparagine synthase (glutamine–hydrolysing)(EC 6.3.5.4 [EC] ). This result showed that the database was usefulfor the analysis of the relationship between chemical structuresand amino acid sequence motifs.