EXTRACTION,ASSAY AND SOME PROPERTIES OF FLORIDOSIDE PHOSPHATE SYNTHASE FROM PORPHYRA PERFORATA (RHODOPHYTA)1

A suitable method for extraction of floridoside phosphate synthase (FPS, UDP-galactose: sn-3-glycerol phosphate: 1→2′α-D-galactosyl transferase)from Porphyra perforata J. Ag. was developed. Two assay methods for enzyme activity were utilized, one measuring the amount of floridoside formed by using gas-liquid chromatography, the other measuring the sn-3-glycerol phosphate-dependent formation of UDP; both assays gave similar results. FPS is a soluble protein, and FPS activity in the extract as determined by the amount of product formed in vitro compared well with the in vivo rate of floridoside synthesis (4–7 μMmol product formed·h^?1·g^?1 fresh wt). The rate of product formation in vitro was linear up to 45 min and proportional to protein concentration in the assay mixture. The temperature optimum was 30–35° C. FPS was active over a range of pH values from 7.0–8.5. It was stable in concentrated solutions in the presence of 0.3 M ammonium sulfate, but activity was lost in diluted solution (protein concentration below 0.2 mg·mL^?1) or below 0.2 M ion strength. The data suggest that FPS may be an oligomeric protein which occurs free in the cytoplasm or loosely bound to a membrane. It may also be a regulatory protein controlling the overall rate of synthesis of floridoside in vivo.     

Glycerol‐3‐phosphate metabolism plays a role in stress response in the red alga Pyropia haitanensis

Glycerol‐3‐phosphate (G3P) has been suggested as a novel regulator of plant defense signaling, however, its role in algal resistance remains largely unknown. The glycerol kinase (also designated as NHO1) and NAD‐dependent G3P dehydrogenase (GPDH) are two key enzymes involved in the G3P biosynthesis. In our study, we cloned the full‐length cDNA of NHO1 (NHO1_Ph) and GPDH (GPDH_Ph) from the red alga Pyropia haitanensis (denoted as NHO1_Ph and GPDH_Ph) and examined their expression level under flagellin peptide 22 (flg22) stimulation or heat stress. We also measured the level of G3P and floridoside (a downstream product of G3P in P. haitanensis) under flg22 stimulation or heat stress. Both NHO1_Ph and GPDH_Ph shared high sequence identity and structural conservation with their orthologs from different species, especially from red algae. Phylogenetic analysis showed that NHO1s and GPDHs from red algae were closely related to those from animals. Under flg22 stimulation or heat stress, the expression levels of NHO1_Ph and GPDH_Ph were up‐regulated, G3P levels increased, and the contents of floridoside decreased. But the floridoside level increased in the recovery period after heat stress. Taken together, we found that G3P metabolism was associated with the flg22‐induced defense response and heat stress response in P. haitanensis, indicating the general conservation of defense response in angiosperms and algae. Furthermore, floridoside might also participate in the stress resistance of P. haitanensis.     

Floridosides in unicellular hot spring algae

Cyanidium caldarium strains RK-1, KS-1 and 001 are probably obligate autotrophs, while Chroococcidiopsis sp. strains M-8 and 002 (formerly named Cyanidium caldarium) are facultative autotrophs. The Cyanidium strains contain floridoside (2-O-glycerol-α-d-galactopyranoside) and a small amount of iso-floridoside (1-O-glycerol-α-d-galactopyranoside), both of which are known to be distributed in Rhodophyta. The Chroococcidiopsis strains also contain floridoside, but no iso-floridoside, under various culture conditions. These results indicate that Cyanidium is clearly distinguishable from Chroococcidiopsis in iso-floridoside content and nutritional properties, and suggest that all strains tested may be closely related to Rhodophyta.     

Low molecular weight carbohydrates in Cyanidium caldarium and some related algae

Floridoside (2-O-glycerol-α-d-galactopyranoside) and a small amount of iso-floridoside (1-O-glycerol-α-d- galactopyranoside) were found in Cyanidium caldarium. Floridoside was also found in the red algae Porphyridium cruentum and Porphyra yezoensis, although in the latter iso-floridoside was the main component. Sucrose and glucose were found in the green algae Chlorella pyrenoidosa and Scenedesmus obliquus, and also in a blue-green alga, Anacystis nidulans. Another blue-green alga, Phormidium foveolarum, contains mostly trehalose. From these results and from morphological considerations, it is suggested that Cyanidium caldarium belongs to the primitive Rhodophyta.     

SALINITY TOLERANCE,BILIPROTEINS, AND FLORIDOSIDE CONTENT OF COMPSOPOGON COERULEUS (RHODOPHYTA)1

The freshwater red alga Compsopogon coeruleus (Balbis) Montague is capable of growing and reproducing in salinities up to 35 ppt. Increased accumulation of floridoside (D-galactopyranosyl glycerol) parallels increase in salinity. Compsopogon phycobilisomes contain an unusual B-phycoerythrin completely lacking in phycourobilin chromophores, but with a pigmented γ subunit. The α, β, and γ subunits of this phycoerythrin all carry phycoerythrobilins. These results suggest that C. coeruleus is secondarily adapted to freshwater from marine habitats.     

NDP-sugars, floridoside and floridean starch levels in relation to activities of UDP-glucose pyrophosphorylase and UDP-glucose-4-epimerase in Solieria chorda l is (Rhodophyceae) under experimental conditions

Under limited nutrient availability (i.e. unenriched sea‐water) and under 75 mol photons m^–2 s^–1 irradiance 12:12 LD, thalli of Solieria chordalis J. Agardh accumulated floridean starch and floridoside. When they were transferred into nutrient‐enriched seawater (150 umol L^?1 NO3¹‐ and 7 umol L^?1 P0₄³i at 35 umol photons m^?2 s^?1 in irradiance 12:12 LD, starch and floridoside levels decreased. The main nucleotide diphosphate (NDP) sugars (i.e. UDP‐glucose, UDP‐galactose and ADP‐glucose) and the activities of UDP‐glucose pyrophosphorylase [Enzyme Code (EC) 2.7.7.9] and UDP‐glucose‐4‐epimerase (EC 5.1.3.2) were measured under these controlled culture conditions. Both UDP‐glucose and UDP‐galactose in the thal l i increased under conditions known to favor the accumulation of floridean starch and floridoside, whereas they decreased under conditions leading to floridean starch and floridoside breakdown. On the other hand, ADP‐glucose level only varied slightly. Although UDP‐glucose pyrophosphorylase activity rose under conditions of floridean starch synthesis, little variation was observed in UDP‐glucose‐4‐epimerase activity. These results suggest a possible enzymatic regulation of the NDP‐sugar and carbohydrate pool in which UDP‐glucose pyrophosphorylase would play a major role.     

Trehalose and (iso)floridoside production under desiccation stress in red alga Porphyra umbilicalis and the genes involved in their synthesis

The marine red alga Porphyra umbilicalis has high tolerance toward various abiotic stresses. In this study, the contents of floridoside, isofloridoside, and trehalose were measured using gas chromatography mass spectrometry (GC-MS) in response to desiccation and rehydration treatments; these conditions are similar to the tidal cycles that P. umbilicalis experiences in its natural habitats. The GC-MS analysis showed that the concentration of floridoside and isofloridoside did not change in response to desiccation as expected of compatible solutes. Genes involved in the synthesis of (iso)floridoside and trehalose were identified from the recently completed Porphyra genome, including four putative trehalose-6-phosphate synthase (TPS) genes, two putative trehalose-6-phosphate phosphatase (TPP) genes, and one putative trehalose synthase/amylase (TreS) gene. Based on the phylogenetic, conserved domain, and gene expression analyses, it is suggested that the Pum4785 and Pum5014 genes are related to floridoside and isofloridoside synthesis, respectively, and that the Pum4637 gene is probably involved in trehalose synthesis. Our study verifies the occurrences of nanomolar concentrations trehalose in P. umbilicalis for the first time and identifies additional genes possibly encoding trehalose phosphate synthases.     

Characterization of N-methyl-L-methionine sulfoxide and isethionic acid from the red alga Grateloupia doryphora

Isethionic acid (2‐hydroxyethane sulfonic acid) and N‐methyl‐L‐methionine sulfoxide (4‐methane sulfinyl‐2‐methylamino butyric acid) were isolated from the red alga Grateloupia doryphora (Cryptonemiales) collected from Brittany (France); they were identified as major organic solutes together with floridoside (α‐D‐galacto‐pyranosyl‐(1–2)‐glycerol). The presence of isethionic acid has recently been reported in certain red algae, however, the occurrence of N‐methyl‐L‐methionine sulfoxide is still very rare. This report deals with the first isolation of isethionic acid and N‐methyl‐L‐methionine sulfoxide from G. doryphora and their subsequent NMR characterization.     

Low MW carbohydrates and ions in rhodophyceae: Quantitative measurement of floridoside and digeneaside

The content of the heterosides floridoside and digeneaside and of the main ions Na⁺, K⁺, and Cl^? was estimated in 20 species of the Rhodophyceae. Methods for quantitative determination of the heterosides are described. The floridoside content is in the range of 1.5–8% on a dry weight basis (Catenella: up to 22%); the content of digeneaside, exclusively found in species of the Ceramiales, is lower, in the range of 1–2.2% on a dry weight basis. All species investigated have Cl^? as main anion, while there is a remarkable diversity in cation composition. Na⁺ was the major cation in 12 of the species investigated, the others having K⁺ as main cation.