The Immunomodulating Effect of Phlorotannins from a Brown Alga,Eisenia nipponica,on Mice Stimulated with Ovalbumin through T Cell Regulation

Plant Foods for Human Nutrition - The immunomodulating effect of phlorotannin was investigated in mice stimulated by ovalbumin. When analyzing the main components of phlorotannin concentrate (PTC)...     

Thermal stress responses of a sterile mutant of Ulva pertusa (Chlorophyta)

SUMMARY: The thermal stress responses of a sterile mutant of the marine alga Ulva pertusa were investigated at 20°C and 30°C. The amounts of the photosynthetic pigments, β-carotene, chlorophylls a and b , lutein, neoxanthin, and violaxanthin, were 1.4–2.4 times higher in the 30°C-cultivated alga than in the 20°C-cultivated alga. The free amino acids, asparagine, aspartic acid, glutamine, glutamic acid, glycine, and serine, were abundant in the 20°C-cultivated alga, and increased 1.9–10.5-fold in response to thermal stress (30°C). Total carbon and nitrogen contents also increased in the 30°C-cultivated alga. Sodium dodecylsulfate-polyacrylamide gel electrophoretic patterns of total proteins extracted from both temperature-treated algae showed the increases of 20, 25, and 90 kDa proteins in the 30°C-cultivated alga. Isozyme assays for 20 enzymes showed a different banding pattern only in the case of glutamate dehydrogenase (GDH). Although it was observed that both temperature-treated algae possessed NAD⁺- and NADP⁺-specific GDH, the 30°C-cultivated alga had an additional NADP⁺-specific GDH (NADP-GDH). These results suggest that NADP-GDH compensates for the thermally induced decreases in nitrogen assimilation efficiency and thereby regulates nitrogen metabolism under conditions of temperature stress.     

Isolation and characterization of the rbcS genes from a sterile mutant of Ulva pertusa (Ulvales,Chlorophyta) and transient gene expression using the rbcS gene promoter

We isolated two different genomic DNAs (UprbcS1 and UprbcS2) encoding the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase and portions of the 5′- and 3′-flanking regions from sterile Ulva pertusa Kjellman. The UprbcS1 and UprbcS2 genes had three introns in the coding region. Each predicted UprbcS polypeptide was a 180-amino-acid (AA) residue including a 38-AA transit peptide, although the 104th AA residue was replaced. The nucleotide sequences of UprbcS cDNAs isolated from a cDNA library corresponded to that of the UprbcS1 gene, suggesting that the UprbcS1 gene was predominantly expressed in sterile U. pertusa compared to UprbcS2. Southern blot analysis showed that each UprbcS gene was a single-copy gene in the sterile U. pertusa genome. Northern hybridization indicated that the expression of UprbcS was induced and repressed by dark and light treatments, respectively. When sterile U. pertusa cells were transformed with an expression vector containing the UprbcS1 promoter and terminator sequences fused with the green fluorescent protein (GFP) gene, GFP fluorescence was observed in the cells transformed. These results suggest that the UprbcS1 gene promoter is light regulated and highly active in the sterile U. pertusa cells and is available for genetic transformation system in the alga.