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1.
Toxins (Basel) ; 13(8)2021 07 27.
Artigo em Inglês | MEDLINE | ID: mdl-34437393

RESUMO

Cyanobacteria are microorganisms with photosynthetic mechanisms capable of colonizing several distinct environments worldwide. They can produce a vast spectrum of bioactive compounds with different properties, resulting in an improved adaptative capacity. Their richness in secondary metabolites is related to their unique and diverse metabolic apparatus, such as Non-Ribosomal Peptide Synthetases (NRPSs). One important class of peptides produced by the non-ribosomal pathway is anabaenopeptins. These cyclic hexapeptides demonstrated inhibitory activity towards phosphatases and proteases, which could be related to their toxicity and adaptiveness against zooplankters and crustaceans. Thus, this review aims to identify key features related to anabaenopeptins, including the diversity of their structure, occurrence, the biosynthetic steps for their production, ecological roles, and biotechnological applications.


Assuntos
Peptídeos Cíclicos , Animais , Ecologia , Estrutura Molecular , Peptídeos Cíclicos/biossíntese , Peptídeos Cíclicos/química , Peptídeos Cíclicos/toxicidade , Inibidores de Proteases/química , Inibidores de Proteases/metabolismo , Inibidores de Proteases/toxicidade
2.
Mar Drugs ; 19(1)2021 Jan 04.
Artigo em Inglês | MEDLINE | ID: mdl-33406599

RESUMO

Cyanobacteria are a rich source of secondary metabolites with a vast biotechnological potential. These compounds have intrigued the scientific community due their uniqueness and diversity, which is guaranteed by a rich enzymatic apparatus. The ribosomally synthesized and post-translationally modified peptides (RiPPs) are among the most promising metabolite groups derived from cyanobacteria. They are interested in numerous biological and ecological processes, many of which are entirely unknown. Microviridins are among the most recognized class of ribosomal peptides formed by cyanobacteria. These oligopeptides are potent inhibitors of protease; thus, they can be used for drug development and the control of mosquitoes. They also play a key ecological role in the defense of cyanobacteria against microcrustaceans. The purpose of this review is to systematically identify the key characteristics of microviridins, including its chemical structure and biosynthesis, as well as its biotechnological and ecological significance.


Assuntos
Cianobactérias/química , Inibidores de Proteases/química , Inibidores de Proteases/farmacologia , Animais , Ecologia , Humanos , Controle de Insetos , Oligopeptídeos/química , Oligopeptídeos/farmacologia
3.
Aging Cell ; 16(3): 594-597, 2017 06.
Artigo em Inglês | MEDLINE | ID: mdl-28299908

RESUMO

Aging is a major worldwide medical challenge. Not surprisingly, identifying drugs and compounds that extend lifespan in model organisms is a growing research area. Here, we present DrugAge (http://genomics.senescence.info/drugs/), a curated database of lifespan-extending drugs and compounds. At the time of writing, DrugAge contains 1316 entries featuring 418 different compounds from studies across 27 model organisms, including worms, flies, yeast and mice. Data were manually curated from 324 publications. Using drug-gene interaction data, we also performed a functional enrichment analysis of targets of lifespan-extending drugs. Enriched terms include various functional categories related to glutathione and antioxidant activity, ion transport and metabolic processes. In addition, we found a modest but significant overlap between targets of lifespan-extending drugs and known aging-related genes, suggesting that some but not most aging-related pathways have been targeted pharmacologically in longevity studies. DrugAge is freely available online for the scientific community and will be an important resource for biogerontologists.


Assuntos
Envelhecimento/efeitos dos fármacos , Antioxidantes/farmacologia , Bases de Dados de Produtos Farmacêuticos , Moduladores de Transporte de Membrana/farmacologia , Redes e Vias Metabólicas/efeitos dos fármacos , Envelhecimento/genética , Envelhecimento/metabolismo , Animais , Antioxidantes/química , Caenorhabditis elegans/efeitos dos fármacos , Caenorhabditis elegans/genética , Caenorhabditis elegans/crescimento & desenvolvimento , Caenorhabditis elegans/metabolismo , Biologia Computacional/métodos , Drosophila melanogaster/efeitos dos fármacos , Drosophila melanogaster/genética , Drosophila melanogaster/crescimento & desenvolvimento , Drosophila melanogaster/metabolismo , Geriatria/métodos , Humanos , Moduladores de Transporte de Membrana/química , Camundongos , Saccharomyces cerevisiae/efeitos dos fármacos , Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/crescimento & desenvolvimento , Saccharomyces cerevisiae/metabolismo , Interface Usuário-Computador
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