scholarly journals Bioactive compounds from marine Streptomyces sp.: Structure identification and biological activities

2019 ◽  
Vol 57 (5) ◽  
pp. 628-635
Author(s):  
Aya E. S. Abd-Ellatif ◽  
Ahmed S. Abdel-Razek ◽  
Abdelaaty Hamed ◽  
Maha M Soltan ◽  
Hesham S. M. Soliman ◽  
...  
Keyword(s):  
Bioactive Compounds ◽  
Biological Activities ◽  
Structure Identification ◽  
Streptomyces Sp ◽  
Marine Streptomyces

scholarly journals Generation of Unusual Aromatic Polyketides by Incorporation of Phenylamine Analogues into a C-Ring-Cleaved Angucyclinone

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1959
Author(s):  
Hua Xiao ◽  
Guiyang Wang ◽  
Zhengdong Wang ◽  
Yi Kuang ◽  
Juan Song ◽  
...  
Keyword(s):  
Natural Products ◽  
Biological Activities ◽  
Structural Diversity ◽  
Related Factor ◽  
Nuclear Factor ◽  
Streptomyces Sp ◽  
Mild Conditions ◽  
Aromatic Polyketides ◽  
Marine Streptomyces ◽  
New Compounds

Angucyclinones are aromatic polyketides that possess impressive structural diversity and significant biological activities. The structural diversity of these natural products is attributed to various enzymatic or nonenzymatic modifications on their tetracyclic benz(a)anthracene skeleton. Previously, we discovered an unusual phenylamine-incorporated angucyclinone (1) from a marine Streptomyces sp. PKU-MA00218, and identified that it was produced from the nonenzymatic conversion of a C-ring-cleaved angucyclinone (2) with phenylamine. In this study, we tested the nonenzymatic conversion of 2 with more phenylamine analogues, to expand the utility of this feasible conversion in unusual angucyclinones generation. The (3-ethynyl)phenylamine and disubstituted analogues including (3,4-dimethyl)phenylamine, (3,4-methylenedioxy)phenylamine, and (4-bromo-3-methyl)phenylamine were used in the conversion of 2, which was isolated from the fermentation of Streptomyces sp. PKU-MA00218. All four phenylamine analogues were incorporated into 2 efficiently under mild conditions, generating new compounds 3–6. The activation of 3–6 on nuclear factor erythroid 2-related factor 2 (Nrf2) transcription were tested, which showed that 4 possessing a dimethyl-substitution gave most potent activity. These results evidenced that disubstitutions on phenylamine can be roughly tolerated in the nonenzymatic reactions with 2, suggesting extended applications of more disubstituted phenylamines incorporation to generate new bioactive angucyclinones in the future.

New Anthraquinones from a Marine Streptomyces sp. – Isolation, Structure Determination and Biological Activities

2006 ◽  
Vol 61 (11) ◽  
pp. 1450-1454 ◽  
Author(s):  
Hervé M. P. Poumale ◽  
Bonaventure T. Ngadjui ◽  
Elisabeth Helmke ◽  
Hartmut Laatscha
Keyword(s):  
Acetic Acid ◽  
Carboxylic Acid ◽  
Biological Activities ◽  
Acid Methyl Ester ◽  
Streptomyces Sp ◽  
Spectroscopic Analyses ◽  
Acid Methyl ◽  
Marine Streptomyces ◽  
New Compounds ◽  
Indole 3 Acetic Acid

Two new anthraquinones were isolated from the marine Streptomyces sp. B8000, in addition to the known metabolites 3,8-dihydroxy-1-propylanthraquinone-2-carboxylic acid (1a), indole-3- carboxylic acid, 2-desoxythymidin, indole-3-acetic acid methyl ester, N-acetyltyramine, and nicotinic acid. The structures of the new compounds were established as 8-hydroxy-3-methoxy-1- propylanthraquinone (2a) and 3,8-dihydroxy-1-propylanthraquinone (2c) on the basis of extensive spectroscopic analyses. Some derivatives were prepared and their biological activities were studied.

scholarly journals MARINE Streptomyces SP. UKMCC_PT15 PRODUCING UNDECYLPRODIGIOSIN WITH ALGICIDAL ACTIVITY

2016 ◽  
Vol 78 (11-2) ◽  
Author(s):  
Zaima Azira Zainal Abidin ◽  
Asmat Ahmad ◽  
Jalifah Latip ◽  
Gires Usup
Keyword(s):  
Harmful Algal Blooms ◽  
Algal Blooms ◽  
Biological Activities ◽  
Carbon Sources ◽  
Antibacterial Activities ◽  
Tolerance Test ◽  
Algicidal Activity ◽  
Rrna Gene ◽  
Streptomyces Sp ◽  
Marine Streptomyces

Marine actinomycetes are now in demand as they are capable of producing unique and novel compounds with wide biological activities. Marine Streptomyces sp. UKMCC_PT15  previously isolated from seawater collected in Pulau Tinggi, Johor was used in this study. Molecular identification showed high similarity of Streptomyces sp. UKMCC_PT15 with Streptomyces fradiae and S. diastaticus subsp. ardesiacus based on partial sequence of 16S rRNA gene. Further characterisations of this bacterium include spore morphology using SEM, growth on various media, salt tolerance test and carbon utilisation profile. This bacterium had straight spore chain with smooth-surfaced spores and was able to tolerate up to 11% NaCl with capabilities of utilising >40 carbon sources.  Undecylprodigiosin (C25H35N3O) was successfully purified through succession of column chromatography and finally using HPLC. Structure elucidation was confirmed through NMR spectroscopy, MS and comparison with established data. This compound demonstrated strong antibacterial activities against S. aureus, B. subtilis and C. albicans but weak antibacterial activities against E. coli, P. aeruginosa and Methicillin-resistant S. aureus (MRSA), Interestingly, undecylprodigiosin also demonstrated algicidal activity when tested against toxic dinoflagellates, A. minutum and P. bahamense, both of which are responsible for harmful algal blooms (HABs). Undecylprodiogiosin with concentration of 10-100 μg/ml gave ~100% algicidal activity against both dinoflagellates. Further testing with undecylprodigiosin concentration < 10 µg/ml showed that undecylprodigision was capable of killing significantly high numbers of both dinoflagellates, giving a high algicidal activity. Findings from this study suggested the potential use of undecylprodigiosin as algicidal agent which could be used for the mitigation of HABs

Identification of Potential Antimicrobial Compounds from A Marine Streptomyces Sp. SM2.4 Strain (MH752437) Isolated from Rachgoun Island in Western Algeria

2021 ◽  
Vol 17 ◽  
Author(s):  
Nesrine Boublenza ◽  
Nadir Boudjlal Dergal ◽  
Larbi Belyagoubi ◽  
Noujoud Gabed ◽  
Djamel-Eddine Abdelouahid ◽  
...  
Keyword(s):  
Methyl Ester ◽  
Bioactive Compounds ◽  
Crude Extract ◽  
Acid Methyl Ester ◽  
Bioactive Metabolites ◽  
Streptomyces Sp ◽  
Acid Methyl ◽  
Ms Analysis ◽  
Western Algeria ◽  
Marine Streptomyces

Background: Marine actinobacteria are a potential resource for natural products; their secondary bioactive metabolites have shown several biological activities. Most of the isolated and identified actinobacteria in Algeria were usually explored from caves, Saharan soil or palm groves. The marine ecosystem is poorly explored and documented. Methods: Five Streptomyces strains producing bioactive compounds were isolated from Rachgoun Island located in Western Algeria and characterised phenotypically and genotypically using microbiological and 16S rRNA sequencing methods, respectively. The crude extract of the most representative strain “Streptomyces sp. strain SM2.4” and its seven active fractions were characterised by GC/MS analysis. Results: Streptomyces sp. strain SM2.4 revealed the strongest activity against the Gram-positive bacteria Staphylococcus aureus and Bacillus subtilis, the fungus Aspergillus niger and was inactive against Gram-negative bacteria. GC/MS analysis of the methylated crude extract of Streptomyces sp. strain SM2.4 revealed the presence of 11 major compounds including fatty acids methyl ester (12-methyltridecanoic acid methyl ester, 9-hexadecenoic acid methyl ester, hexadecanoic acid methyl ester, 14-methylhexadecanoic acid methyl ester and 16-methylheptadecanoic acid methyl ester), 2,4-di-tert-butylphenol, (4S,4aS,8aR)-4,8a-dimethyloctahydro-4a(2H)-naphthalenol (geosmin), 2,4-dimethylbenzaldehyde, 3,4-difluorobenzaldehyde, dimethylfuran-2,4-dicarboxylate and pyrrolo(1,2-a)pyrazine-1,4-dione, hexahydro-3-(2-methylpropyl)-. Partial purification of the crude extract by Thin-layer chromatography provided seven active fractions which were tested by radial diffusion assay. GC/MS analysis of the active TLC-fractions revealed the presence of a mixture of active compounds from which 2-(bromomethyl)-2-(2-methylphenyl)-1,3-dioxolane was found to be a new 1,3 dioxolane derivative. Furthermore, 3,4-dimethylbenzamide and pyrido[2,3-d] pyridazine-1,4-dione, hexahydro-3-(2-methylpropyl)-, were extracted for the first time from a natural source. Conclusion: Our study reveals that marine Streptomyces sp. strain SM2.4 has an interesting antimicrobial potential due to its panel of bioactive compounds.

scholarly journals In vitro thrombolytic potential of bioactive compounds from marine Streptomyces sp. VITJS4

2016 ◽  
pp. 1314-1323 ◽  
Author(s):  
S Jemimah Naine ◽  
C Subathra Devi ◽  
V Mohanasrinivasan
Keyword(s):  
Bioactive Compounds ◽  
Streptomyces Sp ◽  
Marine Streptomyces

Bioactive compounds from marine Streptomyces sp. VITPSA as therapeutics

2017 ◽  
Vol 12 (4) ◽  
pp. 280-289 ◽  
Author(s):  
S. Pooja ◽  
T. Aditi ◽  
S. Jemimah Naine ◽  
C. Subathra Devi
Keyword(s):  
Bioactive Compounds ◽  
Streptomyces Sp ◽  
Marine Streptomyces

Pharmacologically potentials of different substituted coumarin derivatives

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Benzene Ring ◽  
Bioactive Compounds ◽  
Biological Activities ◽  
Pharmacological Properties ◽  
Coumarin Derivatives ◽  
Wide Range ◽  
Anti Oxidant ◽  
Anti Inflammatory ◽  
Coumarin Compounds

Coumarin and its derivatives are widely spread in nature. Coumarin goes to agroup as benzopyrones, which consists of a benzene ring connected to a pyronemoiety. Coumarins displayed a broad range of pharmacologically useful profile.Coumarins are considered as a promising group of bioactive compounds thatexhibited a wide range of biological activities like anti-microbial, anti-viral,antiparasitic, anti-helmintic, analgesic, anti-inflammatory, anti-diabetic, anticancer,anti-oxidant, anti-proliferative, anti-convulsant, and antihypertensiveactivities etc. The coumarin compounds have immense interest due to theirdiverse pharmacological properties. In particular, these biological activities makecoumarin compounds more attractive and testing as novel therapeuticcompounds.

scholarly journals Cyanobacteria—From the Oceans to the Potential Biotechnological and Biomedical Applications

Marine Drugs ◽  
2021 ◽  
Vol 19 (5) ◽  
pp. 241
Author(s):  
Shaden A. M. Khalifa ◽  
Eslam S. Shedid ◽  
Essa M. Saied ◽  
Amir Reza Jassbi ◽  
Fatemeh H. Jamebozorgi ◽  
...  
Keyword(s):  
Bioactive Compounds ◽  
Biomedical Applications ◽  
Large Scale ◽  
Biological Activities ◽  
Scale Production ◽  
Pharmacological Activities ◽  
Large Scale Production ◽  
Marine Products ◽  
Hiv 1 ◽  
Successful Phase

Cyanobacteria are photosynthetic prokaryotic organisms which represent a significant source of novel, bioactive, secondary metabolites, and they are also considered an abundant source of bioactive compounds/drugs, such as dolastatin, cryptophycin 1, curacin toyocamycin, phytoalexin, cyanovirin-N and phycocyanin. Some of these compounds have displayed promising results in successful Phase I, II, III and IV clinical trials. Additionally, the cyanobacterial compounds applied to medical research have demonstrated an exciting future with great potential to be developed into new medicines. Most of these compounds have exhibited strong pharmacological activities, including neurotoxicity, cytotoxicity and antiviral activity against HCMV, HSV-1, HHV-6 and HIV-1, so these metabolites could be promising candidates for COVID-19 treatment. Therefore, the effective large-scale production of natural marine products through synthesis is important for resolving the existing issues associated with chemical isolation, including small yields, and may be necessary to better investigate their biological activities. Herein, we highlight the total synthesized and stereochemical determinations of the cyanobacterial bioactive compounds. Furthermore, this review primarily focuses on the biotechnological applications of cyanobacteria, including applications as cosmetics, food supplements, and the nanobiotechnological applications of cyanobacterial bioactive compounds in potential medicinal applications for various human diseases are discussed.

scholarly journals Pinus Species as Prospective Reserves of Bioactive Compounds with Potential Use in Functional Food—Current State of Knowledge

Plants ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1306
Author(s):  
Marcin Dziedziński ◽  
Joanna Kobus-Cisowska ◽  
Barbara Stachowiak
Keyword(s):  
Human Health ◽  
Bioactive Compounds ◽  
Functional Food ◽  
Biological Activities ◽  
Food Ingredients ◽  
Beneficial Effects ◽  
Pine Tree ◽  
Pine Trees ◽  
Health Promoting ◽  
Few Data

The pine (Pinus L.) is the largest and most heteromorphic plant genus of the pine family (Pinaceae Lindl.), which grows almost exclusively in the northern hemisphere. The demand for plant-based remedies, supplements and functional food is growing worldwide. Although pine-based products are widely available in many parts of the world, they are almost absent as food ingredients. The literature shows the beneficial effects of pine preparations on human health. Despite the wide geographical distribution of pine trees in the natural environment, there are very few data in the literature on the widespread use of pine in food technology. This study aims to present, characterise and evaluate the content of phytochemicals in pine trees, including shoots, bark and conifer needles, as well as to summarise the available data on their health-promoting and functional properties, and the potential of their use in food and the pharmaceutical industry to support health. Various species of pine tree contain different compositions of bioactive compounds. Regardless of the solvent, method, pine species and plant part used, all pine extracts contain a high number of polyphenols. Pine tree extracts exhibit several described biological activities that may be beneficial to human health. The available examples of the application of pine elements in food are promising. The reuse of residual pine elements is still limited compared to its potential. In this case, it is necessary to conduct more research to find and develop new products and applications of pine residues and by-products.

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