Chaetomorpha

Abstract: The uptake rates and critical tissue concentrations of nitrogen and phosphorus were determined for Chaetomorpha linum and Ulva rigida , the dominant algae in Peel Inlet, Western Australia. Both species had rate-saturating mechanisms of phosphate uptake described by Michaelis-menten type functions; C. linum had the faster uptake rate (667 c.f. 272 mu g P g/dwt/h) although U. rigida had a lower half-saturation value. Both species displayed linear relationships between ammonium uptake rates and substrate concentrations with C. linum having the greater slope (4.4 c.f. 1.7). Chaetomorpha linum also had a linear increase in uptake rate with increasing concentration of nitrate, but U. rigida showed rate-saturating kinetics; below 750 mu g/L, U. rigida had the higher rate of uptake. Ulva rigida had critical tissue nitrogen and phosphorus concentrations of 20 and 0.25 mg g/dwt respectively. Corresponding concentrations for C. linum were 12 and 0.5 mg g/dwt. Ulva is frequently nitrogen limited during spring in Peel Inlet, reflecting the high nitrogen requirements of this plant compared to Chaetomorpha as well as the reduced ability of Ulva to store nutrients over winter.

Abstract: Several macroalgae from the Swedish West Coast (11 green, 5 red and 11 brown algal species) and two Ulva spp. from the Mediterranean were tested for mechanisms of HCO3 − utilization. In all except one (Palmaria palmata), photosynthesis supported by inorganic carbon (Ci) at pH 8.7 was rapidly and substantially (>50%) inhibited by acetazolamide (AZ), an inhibitor of extracellular carbonic anhydrase activity. This suggests that extracellular dehydration followed by uptake of the CO2 formed is an important component of the HCO3 − utilization mechanism(s) of these algae. In representatives of most of the green algal genera, e.g. Enteromorpha, Ulva, Chaetomorpha and Monostroma, a specific inhibitor response could be induced. This response, a sensitivity to the anion exchange inhibitor 4,4′-diisothiocyanatostilbene- 2,2′-disulphonate (DIDS) in the presence of AZ, is characteristic of an additional mechanism of HCO3 − utilization, a direct import of HCO3 − across the plasma membrane, which has been previously des...

Abstract: Seaweeds are a group of marine multicellular algae; the presence of antioxidant phytochemical constituents in Seaweed Chaetomorpha sp. extracts has received attention for their role in the prevention of human diseases. This study explores the phytochemical constituents, antioxidant, and anticancer properties of the Cladophoraceae, Chaetomorpha sp. Energy dispersive x-ray spectroscopy (EDX), and Gas chromatography-mass spectrometry (GC/MS) were performed to study the chemical structure and chemical formula. Different concentrations of ethanol and aqueous extracts of Chaetomorpha were used to estimate antioxidant activity by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity and total flavonoid, phenolic, and tannins content assays. Anti-tumor activity against breast cancer cell lines (MCF-7 and MDA-MB-231) was assessed by 3-(4,5-Dimethylthiazol-2-cyl)-2,5-Diphenyltetrazolium Bromide (MTT) assay. The EDX analysis indicated the presence of oxygen, silicon, and calcium as dominant elements. Antioxidant assays indicated that the ethanol extracts of Chaetomorpha consisted of a total of 189.14 ± 0.99 mg QE/g flavonoid content, 21.92 ± 0.43 mg GAE/g phenolic content and 21.81 ± 0.04 mg GAE/g tannins content. The DPPH radical scavenging assay exhibited higher antioxidant activity IC50 (9.41 ± 0.54 mg/mL) in the ethanol extract. Moreover, it showed high anticancer activity by growth inhibition in the MDA-MB-231 breast cancer cell line and low IC50 (225.18 ± 0.61 µg/mL). GC/MS analysis revealed the presence of Dichloracetic acid (DCA) as the active antitumor constituent of Chaetomorpha sp.; other anticancer compounds identified were Oximes and L-α-Terpinol. The results revealed that the type of Chaetomorpha sp. studied here possesses very unique and novel constituents and active potent antitumor chemical constituents and it can act as a promising antioxidant and anticancer agent for future applications in pharmaceutical industries.