Brown Algae as a Potential Source for Obtaining of High Valuable Products

2019 ◽  
Vol 800 ◽  
pp. 98-102
Author(s):  
Sarmīte Janceva ◽  
Liga Lauberte ◽  
Laima Vevere ◽  
Oskars Bikovens ◽  
Anna Andersone ◽  
...  
Keyword(s):  
Biological Activity ◽  
Brown Algae ◽  
Total Content ◽  
Sulfated Polysaccharide ◽  
Fucus Vesiculosus ◽  
Biologically Active ◽  
Germination Test ◽  
Potential Source ◽  
Good Potential ◽  
Agricultural Plants

In the present study, the Fucus vesiculosus is considered as perspective feedstock for obtaining fertilizers and valuable biologically active compounds. Polyphenols (phlorotannin) and sulfated polysaccharide (fucoidan) were isolated using sequential extraction from the above-mentioned seaweed. The total content of polyphenolics in hydrophilic extracts is 680 GAE/g. The yield of fucoidan from brown algae was 7 % on the oven dry seaweed. The assessment of biological activity of Fucus vesiculosus was performed using germination test and vegetation test. The results of the tests revealed that the Fucus vesiculosus promotes the growth of the agricultural plants, is not phytotoxic, and has a good potential in sustainable agriculture

Biologically active secondary metabolites from Actinomycetes

2012 ◽  
Vol 7 (3) ◽  
pp. 373-390 ◽  
Author(s):  
Jolanta Solecka ◽  
Joanna Zajko ◽  
Magdalena Postek ◽  
Aleksandra Rajnisz
Keyword(s):  
Biological Activity ◽  
Secondary Metabolites ◽  
Chemical Structure ◽  
Multidrug Resistant ◽  
Biologically Active ◽  
Plant Roots ◽  
Bacterial Strains ◽  
Genus Streptomyces ◽  
Gram Negative ◽  
Potential Source

AbstractSecondary metabolites obtained from Actinomycetales provide a potential source of many novel compounds with antibacterial, antitumour, antifungal, antiviral, antiparasitic and other properties. The majority of these compounds are widely used as medicines for combating multidrug-resistant Gram-positive and Gram-negative bacterial strains. Members of the genus Streptomyces are profile producers of previously-known secondary metabolites. Actinomycetes have been isolated from terrestrial soils, from the rhizospheres of plant roots, and recently from marine sediments. This review demonstrates the diversity of secondary metabolites produced by actinomycete strains with respect to their chemical structure, biological activity and origin. On the basis of this diversity, this review concludes that the discovery of new bioactive compounds will continue to pose a great challenge for scientists.

scholarly journals POLYPHENOLS OF ARCTIC BROWN ALGAE: EXTRACTION, POLYMOLECULAR COMPOSITION

2019 ◽  
pp. 65-75
Author(s):  
Konstantin Grigor'yevich Bogolitsin ◽  
Anna Sergeyevna Druzhinina ◽  
Denis Vladimirovich Ovchinnikov ◽  
Anastasiya Eduardovna Parshina ◽  
Elena Valeriyevna Shulgina ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Molecular Weight ◽  
Brown Algae ◽  
Maximum Yield ◽  
Gel Filtration ◽  
Fucus Vesiculosus ◽  
Polyphenolic Compounds ◽  
Biologically Active ◽  
Low Molecular Weight ◽  
High Biological Activity

Arctic brown algae of the species Fucus vesiculosus are characterized by a high content of polyphenolic compounds - phlorotannins, exhibiting high biological activity. The aim of this study is to develop a methodology for the isolation and analysis of biologically active polyphenolic compounds from arctic brown algae. The proposed scheme for the isolation of polyphenols from Fucus vesiculosus brown algae is based on the principles of "green chemistry" and is carried out by sequential disassembly of the biomass of the plant object with the release of associated components (lipid-pigment complex, polysaccharides, mannitol) and maximum yield of polyphenol fraction. As a result of the experimental work, the optimal parameters for carrying out each stage of the proposed scheme were determined and a stepwise assessment of its effectiveness was carried out. The extractable fraction of polyphenols contains up to 67% of polyphenols relative to their content in the initial biomass, and the proportion of polyphenols in the fraction is up to 83%. A study of the phlorotannins fraction showed that its antioxidant activity is meaningful and it was 553±24 (mg of ascorbic acid/g extract). The polymolecular composition of the target fraction was investigated by the method of exclusion gel filtration chromatography, which showed the polymodal distribution, indicating the presence of several groups of components - low molecular weight and high molecular weight phlorotannins with masses ranging from thousands to hundreds of thousands of Daltons. The data obtained using chromatography-mass spectrometry and MALDI mass spectrometry make it possible to identify the presence of low molecular weight phlorotannins in the polyphenol fraction with masses from 250 to 1638 Da, which are close analogues in structure.

Fatty Acid Composition and Biological Activity of Supercritical Extracts from Arctic Brown Algae Fucus vesiculosus

2017 ◽  
Vol 11 (7) ◽  
pp. 1144-1152 ◽  
Author(s):  
K. G. Bogolitsyn ◽  
P. A. Kaplitsin ◽  
L. K. Dobrodeeva ◽  
A. S. Druzhinina ◽  
D. V. Ovchinnikov ◽  
...  
Keyword(s):  
Biological Activity ◽  
Fatty Acid Composition ◽  
Fatty Acid ◽  
Acid Composition ◽  
Brown Algae ◽  
Fucus Vesiculosus

Isoselenocyanates: Synthesis and Their Use for Preparing Selenium-Based Heterocycles

Synthesis ◽  
2021 ◽  
Author(s):  
Stefan H. Bossmann ◽  
Raul Neri
Keyword(s):  
Biological Activity ◽  
Infectious Diseases ◽  
Cancer Cells ◽  
Multicomponent Reactions ◽  
Oxidative Cyclization ◽  
Biologically Active ◽  
Organoselenium Compounds ◽  
X Ray ◽  
Synthetic Work

AbstractIsoselenocyanates (ISCs) are a class of organoselenium compounds that have been recognized as potential chemotherapeutic and chemopreventative agents against cancer(s) and infectious diseases. ISC compounds are chemically analogous to their isosteric relatives, isothiocyanates (ITCs); however, they possess increased biological activity, such as enhanced cytotoxicity against cancer cells. ISCs not only serve as significant products, but also as precursors and essential intermediates for a variety of organoselenium compounds, such as selenium-containing heterocycles, which are biologically active. While syntheses of ISCs have become less difficult to accomplish, the syntheses of selenium-containing heterocycles are often difficult due to the use of highly toxic selenium reagents. Because of this, ISCs can serve as versatile reagents for the preparation of these heterocycles. In this review, the classical and recent syntheses of ISCs will be discussed, along with notable and recent synthetic work employing ISCs to access novel selenium-containing heterocycles.1 Introduction1.1 Selenium and Health2 Isoselenocyanates2.1 Preparation of Isoselenocyanates3 Selenium-Containing Heterocycles3.1 Notable Synthetic Work3.2 Recent Synthetic Work3.2.1 Synthesis of N-(3-Methyl-4-phenyl-3H-selenazol-2-ylidene)benzamide­ Derivatives3.2.2 Synthesis and X-ray Studies of Diverse Selenourea Derivatives3.2.3 Synthesis of Heteroarene-Fused [1,2,4]Thiadiazoles/Selenadiazoles via Iodine-Promoted [3+2] Oxidative Cyclization3.2.4 2-Amino-1,3-selenazole Derivatives via Base-Promoted Multicomponent Reactions4 Conclusion

scholarly journals Fucoidan But Not 2′-Fucosyllactose Inhibits Human Norovirus Replication in Zebrafish Larvae

Viruses ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 461
Author(s):  
Malcolm Turk Hsern Tan ◽  
Yan Li ◽  
Mohamad Eshaghi Gorji ◽  
Zhiyuan Gong ◽  
Dan Li
Keyword(s):  
Brown Algae ◽  
Disease Burden ◽  
Type A ◽  
Fucus Vesiculosus ◽  
Human Norovirus ◽  
Human Noroviruses ◽  
Molecular Weights ◽  
Zebrafish Larvae ◽  
Virus Like Particle

Human noroviruses (hNoVs) cause heavy disease burden worldwide and there is no clinically approved vaccination or antiviral hitherto. In this study, with the use of a zebrafish larva in vivo platform, we investigated the anti-hNoV potentials of fucoidan (from brown algae Fucus vesiculosus) and 2′-Fucosyllactose (2′-FL). As a result, although both fucoidan and 2′-FL were able to block hNoV GII.4 virus-like particle (VLPs) from binding to type A saliva as expected, only fucoidan, but not 2′-FL, was able to inhibit the replication of hNoV GII.P16-GII.4 in zebrafish larvae, indicating the possible needs of higher molecular weights for fucosylated carbohydrates to exert anti-hNoV effect.

scholarly journals Isolation, Structure Elucidation, and Biological Activity of a New Alkaloid from Zanthoxylum rhetsa

2011 ◽  
Vol 6 (11) ◽  
pp. 1934578X1100601
Author(s):  
Karsten Krohn ◽  
Stephan Cludius-Brandt ◽  
Barbara Schulz ◽  
Mambatta Sreelekha ◽  
Pottachola Mohamed Shafi
Keyword(s):  
Biological Activity ◽  
Carboxylic Acid ◽  
Medicinal Plant ◽  
Plant Extract ◽  
Structure Elucidation ◽  
Biologically Active ◽  
Reduction Product ◽  
Pharmacological Properties ◽  
Evergreen Tree

Several biologically active alkaloids (1-4, 6), including a new quinazoline-6-carboxylic acid (1), were isolated from the medicinal plant Zanthoxylum rhetsa, an evergreen tree, native to subtropical areas. Whereas the pharmacological properties of the plant extract and single constituents have been widely tested, we now show that all of the metabolites have antialgal activities, all but 6 are antibacterial, and 6 and the reduction product 5 (derived from 4) are also antifungal.

scholarly journals Transforming growth factor alpha: mutation of aspartic acid 47 and leucine 48 results in different biological activities.

1988 ◽  
Vol 8 (3) ◽  
pp. 1247-1252 ◽  
Author(s):  
E Lazar ◽  
S Watanabe ◽  
S Dalton ◽  
M B Sporn
Keyword(s):  
Amino Acids ◽  
Biological Activity ◽  
Amino Acid ◽  
Growth Factor ◽  
Aspartic Acid ◽  
Transforming Growth Factor ◽  
Biologically Active ◽  
Single Amino Acid ◽  
Transforming Growth Factor Alpha ◽  
Factor Alpha

To study the relationship between the primary structure of transforming growth factor alpha (TGF-alpha) and some of its functional properties (competition with epidermal growth factor (EGF) for binding to the EGF receptor and induction of anchorage-independent growth), we introduced single amino acid mutations into the sequence for the fully processed, 50-amino-acid human TGF-alpha. The wild-type and mutant proteins were expressed in a vector by using a yeast alpha mating pheromone promoter. Mutations of two amino acids that are conserved in the family of the EGF-like peptides and are located in the carboxy-terminal part of TGF-alpha resulted in different biological effects. When aspartic acid 47 was mutated to alanine or asparagine, biological activity was retained; in contrast, substitutions of this residue with serine or glutamic acid generated mutants with reduced binding and colony-forming capacities. When leucine 48 was mutated to alanine, a complete loss of binding and colony-forming abilities resulted; mutation of leucine 48 to isoleucine or methionine resulted in very low activities. Our data suggest that these two adjacent conserved amino acids in positions 47 and 48 play different roles in defining the structure and/or biological activity of TGF-alpha and that the carboxy terminus of TGF-alpha is involved in interactions with cellular TGF-alpha receptors. The side chain of leucine 48 appears to be crucial either indirectly in determining the biologically active conformation of TGF-alpha or directly in the molecular recognition of TGF-alpha by its receptor.

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