Marine Algae Extracts Research Articles

Response of rice cultivation to biofertilizers in Campeche, Mexico

The activity of various biofertilizers on rice production (Sabanero A95) was evaluated in Palizada, Campeche, Mexico, in the wet season of 2009 (year one) and 2011 (year two). On year one, arbuscular mycorrhiza INIFAP? (Rhizophagus intraradices), Azospirillum brasilense plus arbuscular micorrhiza Rhizophagus sp., and chemical fertilizer (92, -92, -60 kg·ha-1) were evaluated, while on year two marine algae extracts, a consortium of growth promoting bacteria (Pseudomonas spp.) and a control (not fertilized) were evaluated. The results showed that there were no significant differences on grain yield among treatments during the year one. The average grain yield was 2,800 kg·ha-1. As for the year two, the highest grain yield was observed on plots fertilized with chemical fertilizer (3333 kg·ha-1), followed by plots treated with mycorrhiza INIFAP? (3000 kg·ha-1). The economic analysis for rice production in both years showed that the use of arbuscular mycorrhiza decreases the cost of production by 18.5% and 16.3%, which suggests that microbial inoculants might be good substitutes of chemical fertilizers in rice production.

Inhibition of the development of pathogenic fungi by extracts of some marine algae from the red sea of Jeddah, Saudi Arabia

In this study, the predominant marine algae were collected from three different sites in the coastal area of Al-Kumrah at south of the Red sea of Jeddah, during summer and autumn 2009. The different marine algae belonged to Chlorophyta ( Enteromorpha prolifera and Ulva reticulata ), Phaeophyta ( Cystoseira myrica , Padina pavonica , Sargassum portieriatum and Turbinaria triquetra ) and Rhodophyta ( Gracilaria multipartita ). Algal extraction was achieved successively by using petroleum ether, diethyl ether, ethyl acetate and methanol. The algae extracts were tested in vitro for antifungal activity against Aspergillus flavus , Aspergillus fumigatus , Aspergillus niger and the yeast Candida albican s, by using agar-well diffusion method. The crude extracts of the tested algae revealed differences in their bioactivities. The maximum growth inhibition for fungi was recorded in ethyl acetate extract of T. triquetra against C. albicans (30 mm), methanol extract of E. prolifera (29 mm) and ethyl acetate extract of Padina pavonica (28 mm) against A. fumigatus . The results clarified that Chlorophyta and Phaeophyta exhibited the highest biological activity against the tested fungi, whereas the lowest was achieved in Rhodophyta. The minimal inhibitory concentrations (MICs) of the crude extracts of the tested algae ranged from 0.5 to 3.0 μg/ml. The results confirmed the potential of seaweed extracts as a natural source of antimicrobial compounds. The antifungal activity of different extracts of marine algae which belongs to Chlorophyta, Phaeophyta and Rhodophyta were examined against A. flavus , A. fumigatus , A. niger and the yeast C. albicans . The algae belonging to Chlorophyta and Phaeophyta exhibited the highest inhibitory effect against the test pathogenic fungi. The different extracts showed different activities against fungi. The antimicrobial activity depended on both algal species and the efficiency of solvents in the extraction of bioactive substances. Keywords: Green algae, brown algae, red algae, solvent extracts, antifungal activity, minimal inhibitory concentrations (MICs)

Antibacterial activity of extracts of marine algae from the Red Sea of Jeddah, Saudi Arabia

In the present study, marine algae were collected from the southern coast of Jeddah, Saudi Arabia during summer and autumn 2009. The antibacterial activities of petroleum ether, diethyl ether, ethyl acetate and methanol extracts of marine algae belonging to the Chlorophyta, Phaeophyta and Rhodophyta were studied. Their crude extracts were tested against different types of Gram-positive bacteria (Bacillus subtilis, Methicillin-Resistant Staphylococcus aureus (MRSA) and Staphylococcus aureu) and Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae and Pseudomonas aeruginosa). All marine algae extracts tested exhibited a broad spectrum of antibacterial activity. The maximum inhibition activities were shown for extracts of Padina pavonica and Turbinaria triquetra. The growth inhibitions of bacteria by Sargassum portieriatum extracts were higher in samples collected during autumn than that investigated in summer. The maximum inhibitory effect of Gracilaria multipartita was observed in the petroleum ether extract against B. subtilis and E. coli. The ethyl acetate and petroleum ether extract of Enteromorpha prolifera and Ulva reticulata showed strong activity against the tested bacteria. The tested microorganisms that were susceptible to the most effective extracts were further tested for the minimum inhibitory concentration (MIC). The MIC of the tested microorganisms was between 0.5 and 1.25 µg/ml. The results of the present study confirmed the potential use of marine algae as a good source of antibacterial agent.

Marine algal extracts inhibit growth of the human pathogens P. falciparum, T. brucei and L. donovani

Marine algal extracts inhibit growth of the human pathogens P. falciparum, T. brucei and L. donovani

Inhibitory effect of diphlorethohydroxycarmalol on melanogenesis and its protective effect against UV-B radiation-induced cell damage

In this study, potential inhibitory effect of 21 species of marine algae on melanogenesis was assessed via tyrosinase inhibitory effect. The Ishige okamurae extract tested herein evidenced profound tyrosinase inhibitory effect, compared to that exhibited by other marine algae extracts. Thus, I. okamurae was selected for use in further experiments, and was partitioned with different organic solvents. Profound tyrosinase inhibitory effect was detected in the ethyl acetate fraction, and the active compound was identified as the carmalol derivative, diphlorethohydroxycarmalol (DPHC), which evidenced higher levels of activity than that of commercial whitening agent. Intracellular reactive oxygen species (ROS) induced by ultraviolet (UV)-B radiation was reduced by the addition of DPHC and cell viability was dose-dependently increased. Moreover, DPHC demonstrated strong protective properties against UV-B radiation via damaged DNA tail length and morphological changes in fibroblast. Hence, these results indicate that DPHC isolated from I. okamurae has potential whitening effects and prominent protective effects on UV-B radiation-induced cell damages which might be used in pharmaceutical and cosmeceutical industries.

Antilonomic Effects of Brazilian Brown Seaweed Extracts

The aim of this work was to investigate the hemolysis and blood clotting activity of Lomonia obliqua venom and the ability of some Brazilian marine algal extracts (Canistrocarpus cervicornis, Stypopodium zonale and Dictyota pfaffi) to antagonize such biological activities. L. obliqua caterpillars are dangerous to human beings and envenomation symptoms are characterized by hemorrhagic, hemolytic and blood clotting disorders, and acute renal failure, which sometimes lead to the death of the victims. Through in vitro experiments we have shown that L. obliqua venom is able to clot human plasma and hemolize human erythrocytes and that the coagulation activity of the venom is inhibited by the extracts of C. cervicornis, S. zonale and D. pfaffi. In contrast, C. cervicornis and S. zonale extracts did not inhibit the hemolytic activity of L. oblqua, as did the extract of D. pfaffi. These finding indicate that marine algae may be used as antivenoms or may contribute to the development of compounds with antilonomic effects.

In Vitro Antibacterial Activity from Marine Algal Extracts Against Virulent Bacteria

In Vitro Antibacterial Activity from Marine Algal Extracts Against Virulent Bacteria

Antiplasmodial and antimicrobial activities of South African marine algal extracts

Seventy-eight crude organic fractions from nineteen species of marine algae collected from the coast of South Africa were screened for activity against a chloroquine sensitive strain of Plasmodium falciparum (D10), Staphylococcus aureus, Klebsiella pneumoniae, Mycobacterium aurum and Candida albicans. Fifteen crude fractions showed good antiplasmodical activity (IC50 <10 μg/mL). The dichloromethane fraction from Sargassum heterophyllum (Turner) C. Agardh (Sargassaceae) was the most active with an IC50 value of 2.8 μg/mL. Eleven extracts showed MIC values ≤ 1 mg/mL against at least one of S. aureus, K. pneumoniae, M. aurum and C. albicans. The broadest spectrum of antimicrobial activity was exhibited by the aqueous-HP20 fraction of Polysiphonia incompta Harvey (Rhodomelaceae). This study shows that marine algae not only produce antimicrobial compounds but also may be a source of antimalarial lead compounds.

Antibacterial and Antifungal Eff ects of Some Marine Algae

Ethanolic crude extracts from seven marine algal species belong to Clorophyceae (Cladophora glomerata, Enteromorpha linza, Ulva rigida), Phaeophyceae (Cystoseira barbata, Padina pavonica) and Rhodophyceae (Corallina officinalis, Ceramium ciliatum) from the coast of Vona, Turkey were evaluated in vitro for the antibacterial and antifungal activity of six bacteria and two fungus with the paper disc agar diff usion methods. The marine algae analysed of Cladophora glomerata and Padina pavonica were the species with the strongest activities against the broadest spectrum of test organisms. In particular, Enteromorpha linza and Padina pavonica showed the highest antifungal activity against Aspergillus niger, while Cladophora glomerata showed the highest antibacterial activity against Staphylococcus aureus. On the other hand, it was found that extracts of all marine algae were significant antimicrobial activity against Staphylococcus aureus, Salmonella typhimurium and Aspergillus niger. The minimal inhibition concentrations (MIC) of the crude extract obtained from Enteromorpha linza and Padina pavonica ranged from 2.5 to 10 mg/ml and 1.25 to 10 mg/ml, respectively.

Evaluation of diphlorethohydroxycarmalol isolated from Ishige okamurae for radical scavenging activity and its protective effect against H 2O 2-induced cell damage

In this study, the antioxidant activities of 21 species of marine algae were assessed via an ABTS free radical scavenging assay. The Ishige okamurae extract tested herein evidenced profound free radical scavenging activity, compared to that exhibited by other marine algae extracts. Thus, I. okamurae was selected for use in further experiments, and was partitioned with different organic solvents. Profound radical scavenging activity was detected in the ethyl acetate fraction, and the active compound was identified as the carmalol derivative, diphlorethohydroxycarmalol, which evidenced higher levels of activity than that of commercial antioxidants. Moreover, the protective effects of diphlorethohydroxycarmalol against H 2O 2-induced cell damage were evaluated. Intracellular reactive oxygen species (ROS) were overproduced as the result of the addition of H 2O 2, but this ROS generation was reduced significantly after diphlorethohydroxycarmalol treatment; this corresponds to a significant enhancement of cell viability against H 2O 2-induced oxidative damage. The inhibitory effects of diphlorethohydroxycarmalol against cell damage were determined via comet assay and Hoechst staining assay, and diphlorethohydroxycarmalol was found to exert a positive dose-dependent effect. These results clearly indicate that the diphlorethohydroxycarmalol isolated from I. okamurae exerts profound antioxidant effects against H 2O 2-mediated cell damage, and treatment with this compound may be a potential therapeutic modality for the treatment or prevention of several diseases associated with oxidative stress.

Inhibitory effects of edible marine algae extracts on degranulation of RBL-2H3 cells and mouse eosinophils

Inhibitory effects on degranulation of rat basophilic leukemia (RBL-2H3) cells and mouse eosinophils by marine algae extracts were examined. More than 50% of the degranulation of RBL-2H3 cells was inhibited by water extracts of Ecklonia cava and Chrysymenia wrightii at a concentration of 100 μg/mL. More than 50% of the degranulation of RBL-2H3 cells was inhibited by methanol extracts of Petalonia binghamiae, Scytosiphon lomentaria, Undaria pinnatifida, Porphyra dentata, Codium fragile and Ulva japonica at a concentration of 200 μg/mL. Most inhibitory substances in the methanol extracts were partitioned into ethyl acetate and hexane layers. The ethyl acetate-partitioned layer of methanol extract of Petalonia binghamiae had higher inhibitory effects than the hexane-partitioned layer on the degranulation of RBL-2H3 cells. By contrast, the hexanepartitioned layer of the same extract had a higher inhibitory effect than the ethyl acetate-partitioned layer on the degranulation of mouse eosinophils. The ethyl acetate-partitioned layer of methanol extract of Petalonia binghamiae was further separated into eight fractions by silica gel column chromatography. Most inhibited the degranulation of RBL-2H3 cells, but not that of mouse eosinophils significantly. These results suggest methanol extract of Petalonia binghamiae contains materials that inhibit the degranulation of basophils and eosinophils differentially.

Antileishmanial properties of tropical marine algae extracts

Aqueous and organic extracts of twenty-seven species of marine algae (14 species of Rhodophyta, 5 species of Phaeophyta and 8 species of Chlorophyta) collected from the Gulf of Mexico and Caribbean coast of the Yucatan Peninsula (Mexico) were evaluated for their antileishmanial in vitro activity against Leishmania mexicana promastigote forms. The cytotoxicity of these extracts was also assessed using brine shrimp. Organic extracts from Laurencia microcladia (Rhodophyta), Dictyota caribaea, Turbinaria turbinata and Lobophora variegata (Phaeophyta) possessed promising in vitro activity against L. mexicana promastigotes (LC(50) values ranging from 10.9 to 49.9 microg/ml). No toxicity of algal extracts against Artemia salina was observed with LC50 ranging from 119 to >or=1000 microg/ml. Further studies on bio-guided fractionation, isolation and characterization of pure compounds from these species as well as in vivo experiments are needed and are already in progress.

Inhibitory Effects of Tunisian Marine Algal Extracts on Digestive Lipases

The lipase inhibitory activity of ethanol extracts obtained from some marine algae collected on the Tunisian coast was evaluated. Caulerpa prolifera extract markedly reduced both dog gastric (DGL) and human pancreatic lipase (HPL) activities. Generally, the inhibition reached 100% after 40 to 60 min of incubation depending on lipase types and on substrates used. Moreover, the inhibitory effect of C. prolifera extract on lipases appeared to be accelerated by adding bile salts, which likely modified the interface and allowed the inhibitory compound to inactivate the lipase. The separation of C. prolifera extract by thin-layer chromatography (TLC) resulted in eight fractions showing efficient inhibition rate against DGL, compared to the crude extract. In the case of HPL, TLC fractionation reduced the inhibitory rates, suggesting that the effect of algal extract on lipases may be caused by a synergetic action of several compounds within the extract. High-performance liquid chromatograph separation resulted in isolation of a major compound displaying high inhibition capacity of HPL activity. Caulerpa prolifera extract may therefore be useful in developing antiobesity drugs.

A SURVEY OF ANTARCTIC ALGAE FOR AGLUTININS

Normal 0 21 false false false MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Tabela normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:10.0pt; font-family:"Times New Roman"; mso-ansi-language:#0400; mso-fareast-language:#0400; mso-bidi-language:#0400;} Since the discovery of haemagglutinating activity in marine algal extracts in 1966, several algal haemagglutinins (lectins) have been detected, isolated and characterized. However, information is slowly emerging, concerning biochemical characteristics of lectins from Antarctic marine algae. Lectins are proteins or glycoproteins which bind, reversibly, to carbohydrates. Eighteen species of Antarctic marine algae have been tested for the presence of haemagglutinins against a several types of erythrocytes (rabbit, chicken, goat, sheep and ABO human blood groups). The protein extracts were prepared in phosphate buffered saline (PBS) pH 7.0. Serial doubling dilutions of extracts were prepared using 0.85% NaCl and an equal volume of 2% suspension of native or enzymatic treated erythrocytes was added to each tube, gentle mixed and left at 25 oC for 60 min before examination for agglutination. Fourteen species, among eighteen, produced haemagglutination of at least one type of blood cell tested. Protein extracts of three species were subjected to haemagglutination inhibition studies performed with a selection of sugars or glycoproteins. The activity of Adenocystis utriculares extracts was the only one inhibited by simple sugars. The other two extracts ( Georgiella confluens and Gigartina skottsbergii ) were not inhibited by mono- and polysaccharides, but were inhibited by glycoproteins.

Marine Algae

This study was done to investigate the antimicrobial potentiality of the marine algae collected from different coastal regions of Gujarat and screened for the same. Twenty-six marine algae belonging to Rhodophyceae, Chlorophyceae and Phaeophyceae were screened for their potential antibacterial activity against five clinically important bacterial strains, namely Bacillus cereus, Micrococcus flavus, Citrobacter freundii, Klebsiella pneumoniae and Pseudomonas testosterone. Acetone and methanol were used for extraction; and the extracted yield was more when the solvent used was methanol. The antibacterial activity was done by both Agar disc diffusion method and Agar ditch method. The five bacterial strains showed varied response towards marine algal extracts. The most susceptible bacteria was B. cereus followed by K. pneumoniae and C. freundii while the most resistant bacteria were M. flavus and P. testosteroni. Among the 26 algae screened, E. intestinalis was the most potent alga and thus, this alga was selected for further studies. E. intestinalis was extracted in petroleum ether, 1,4-dioxan, acetone, methanol and DMF, and their antibacterial activity was studied against the above-stated five bacterial strains using agar disc method. Maximum extractive value of E. intestinalis was in methanol (2.05%) and minimum was in acetone (0.38%). The most susceptible bacteria was K. pneumoniae and maximum antibacterial activity was shown by petroleum ether extract and minimum was shown by 1,4-dioxan extract. The most resistant bacteria were M. flavus and C. freundii. The MIC values of E. intestinalis extracts ranged from 2500-9.765 microg/0.5 ml against B. cereus and K. pneumoniae. From these results it is concluded that the acetone extract of E. intestinalis is the most potent extract and can be used as a lead molecule in drug discovery in inhibiting some of the bacterial strains. E. intestinalis can be used as a promising novel marine antimicrobial agent in the coming years.

Prevention of aflatoxin B1-initiated hepatotoxicity in rat by marine algae extracts

Chemoprevention by extracts of Laurencia obtusa (E1) and Caulerpa prolifera (E2) collected from the Egyptian coast of the Red Sea against aflatoxin B(1) (AFB(1))-initiated hepatotoxicity in female Sprague-Dawley rats has been studied. Animals were fed aflatoxin-contaminated diet (3 mg kg(-1) diet) for 6 days then treated orally with pure aflatoxin B(1) (AFB(1)) (200 microg kg(-1) b.w.) for 4 days either in combination with or before E1 or E2 administration (50 mg kg(-1) b.w.). AFB(1) resulted in a signicant increase in serum alpha fetoprotein, carcinoembryonic antigen, tumor necrosis factor alpha, nitric oxide, interleukin-1alpha, procollagen III and lipid peroxidation level in the liver. It caused a signicant decrease in food intake, body weight, serum leptin, the activities of glutathione peroxidase, superoxide dismutase and DNA and RNA concentrations in the liver. Cotreatment with AFB(1) and E1 or E2 resulted in an obvious improvement in all tested parameters. Noteworthy, E2 was more effective than E1 in the protection against AFB(1)-induced hepatotoxicity.

Induction of apoptosis by three marine algae through generation of reactive oxygen species in human leukemic cell lines.

In this study, we examined the antitumor effect of marine algae extracts on human hepatoma and leukemia cells. Ethyl acetate extracts from Colpomenia sinuosa (Cs-EA), Halimeda discoidae (Hd-EA), and Galaxaura oblongata (Go-EA) directly inhibited the growth of human hepatoma HuH-7 cells and leukemia U937 and HL-60 cells in a time- and dose-dependent manner. Specifically, these algae extracts induced apoptosis of U937 and HL-60 cells as evaluated by detection of hypodiploid cells using flow cytometry and observation of condensed and fragmented nuclei in algae extract-treated cells. Intracellular reactive oxygen species (ROS), especially hydrogen peroxide and superoxide anion, were increased about 2-3-fold in U937 cells treated with Cs-EA for 3-5 h. Interestingly, antioxidant N-acetylcysteine effectively blocked Cs-EA-, Hd-EA-, and Go-EA-induced apoptosis, suggesting that ROS is a key mediator in the apoptotic signaling pathway. In conclusion, our results show that algae extracts induce apoptosis in human leukemia cells through generation of ROS.

Capillary electrophoretic analysis of dimethylsulfoniopropionate in sugarcane and marine algal extracts

A simple and high-resolution analytical method for the determination of dimethylsulfoniopropionate (DMSP) in sugarcane and marine algae is described. Effective extraction of DMSP from plant samples was also investigated using organic solvents, 5% perchloric acid or deionised water. To increase the sensitivity, DMSP in the extracts was first converted to a phenacyl ester, and the reaction mixture was applied directly to capillary electrophoresis without any pretreatment. Water extraction followed by esterification in a pH 4 reaction buffer was found most suitable for the measurement of alkaline-labile DMSP. This method was applied to the determination of DMSP levels in marine algae samples collected from the seashore of Nagasaki, Japan. An increase in DMSP content in Ulva pertusa in the winter period was observed.

First report on the detection and quantification of arsenobetaine in extracts of marine algae using HPLC-ES-MS/MS

The detection of arsenobetaine in extracts of marine algae is reported here for the first time. The application of liquid chromatography coupled online with electrospray tandem mass spectrometry in the selected reaction monitoring mode provided improved performance for the detection of low amounts of arsenobetaine in the presence of high amounts of arsenosugars.

Inhibitory action of marine algae extracts on the Trypanosoma cruzi dihydroorotate dehydrogenase activity and on the protozoan growth in mammalian cells

Trypanosoma cruzi, the causative agent of Chagas' disease, replicates in mammalian cells and relies on the de novo pyrimidine biosynthetic pathway that supplies essential precursors for nucleic acid synthesis. The protozoan dihydroorotate dehydrogenase (DHOD), the fourth enzyme of the pathway catalyzing production of orotate from dihydroorotate, markedly differs from the human enzyme. This study was thus aimed to search for potent inhibitors against T. cruzi DHOD activity, and a number of methanol extracts prepared from green, brown, and red algae were assayed. The extracts from two brown algae, Fucus evanescens and Pelvetia babingtonii, yielded 59 and 58% decrease in the recombinant DHOD activity, respectively, at the concentration of 50 μg/ml. Inhibition by these extracts was noncompetitive with respect to dihydroorotate, with apparent K i values of 35.3±5.9 and 10.3±4.4 μg/ml, respectively. Further, in an in vitro T. cruzi–HeLa cell infection system, ethanol-reconstituted F. evanescens and P. babingtonii extracts at the concentration of 1 μg/ml, respectively, decreased significantly the infection rate of host cells and the average parasite number per infected cell. These results imply that F. evanescens and P. babingtonii contain inhibitor(s) against the T. cruzi DHOD activity and against the protozoan infection and proliferation in mammalian cells. Identification of inhibitor(s) in these two brown algae and further screening of other marine algae may facilitate the discovery of new, anti-trypanosomal lead compounds.